RETRACTED ARTICLE: Calcium-dependent cytosolic phospholipase A₂ activation is implicated in neuroinflammation and oxidative stress associated with ApoE4

Abstract

Background

Apolipoprotein E4 (APOE4) is associated with a greater response to neuroinflammation and the risk of developing late-onset Alzheimer’s disease (AD), but the mechanisms for this association are not clear. The activation of calcium-dependent cytosolic phospholipase A₂ (cPLA2) is involved in inflammatory signaling and is elevated within the plaques of AD brains. The relation between APOE4 genotype and cPLA2 activity is not known.

Methods

Mouse primary astrocytes, mouse and human brain samples differing by APOE genotypes were collected for measuring cPLA2 expression, phosphorylation, and activity in relation to measures of inflammation and oxidative stress.

Results

Greater cPLA2 phosphorylation, cPLA2 activity and leukotriene B₄ (LTB4) levels were identified in ApoE4 compared to ApoE3 in primary astrocytes, brains of ApoE-targeted replacement (ApoE-TR) mice, and in human brain homogenates from the inferior frontal cortex of patients with AD carrying APOE3/E4 compared to APOE3/E3. Greater cPLA2 phosphorylation was also observed in human postmortem frontal cortical synaptosomes and primary astrocytes after treatment with recombinant ApoE4 ex vivo. In ApoE4 astrocytes, the greater levels of LTB4, reactive oxygen species (ROS), and inducible nitric oxide synthase (iNOS) were reduced after cPLA2 inhibition.

Conclusions

Our findings implicate greater activation of cPLA2 signaling system with APOE4, which could represent a potential drug target for mitigating the increased neuroinflammation with APOE4 and AD.

Background

The enzyme phospholipase A₂ (PLA2) catalyzes the hydrolysis of the stereospecifically numbered (sn-2) ester bond of substrate phospholipids in the cell membrane to produce a free fatty acid and a lysophospholipid [1]. Calcium-independent PLA₂ (iPLA2) has a greater affinity for releasing docosahexaenoic acid (DHA, 22:6 n-3), which acts as a signaling molecule during neurotransmission and as the precursor of anti-inflammatory and antioxidant resolvins [2, 3]. Calcium-dependent cytosolic phospholipase A₂ (cPLA2) releases arachidonic acid (AA, 20:4 n-6), which plays important functions in storing energy, as a second messenger in neurotransmission, and as the precursor of eicosanoids [4, 5]. Free AA can be oxidized by cyclooxygenase (COX) or lipoxygenase (LOX) to produce prostaglandins or leukotrienes, which are potent mediators of inflammation [1, 6]. In astrocytes, cPLA2 interacts with mitochondrial antiviral-signaling protein (MAVS) to boost nuclear factor kappa-light-chain-enhancer of activated B cell (NF-κB)-driven inflammatory responses [7]. In microglia, cPLA2 and AA metabolic pathways contribute to reactive oxygen species (ROS) and nitric oxide (NO) production during cell activation [8]. cPLA2 activity depends on its phosphorylation, regulated by mitogen-activated protein kinase (MAPK) pathways [9, 10].

A lower amount of Aβ oligomers and the absence of glial activation markers in both astrocytes and microglia distinguish the brains of individuals with greater brain Aβ plaques and tangles but resilience to AD dementia from those with dementia [11]. cPLA2 activation is one of the pathways that activates microglia and astrocytes in the brain. The cPLA2 gene, protein levels, and phosphorylated form are increased around AD brains’ plaques compared to healthy controls [12,13,14]. Increased activation of cPLA2 is observed in the hippocampus of human amyloid precursor protein (hAPP) transgenic mice [14]. The activation of cPLA2 by Aβ oligomers contributes to dysregulation of fatty acid metabolism and promotes neurodegeneration [15, 16]. Overexpression of p25 (Protein 25, a cyclin-dependent kinase 5 activator) in neurons increases the expression of cPLA2, leading to lysophosphatidylcholine (LPC) secretion and the activation of astrocytes and production of proinflammatory cytokines [17]. Conversely, cPLA2 deficiency in AD mouse models ameliorates the memory impairment and hyperactivated glial cells observed in AD mouse models [14, 18]. Knocking out cPLA2 in microglia decreases lipopolysaccharide (LPS) induced oxidative stress and inflammatory response [8].

Carrying the APOE4 allele is the strongest genetic risk factor for late-onset AD. The ApoE4 protein seems to have proinflammatory and/or reduced anti-inflammatory functions, which could exacerbate AD pathology. This ApoE4 effect on inflammation was clearly demonstrated in the Framingham cohort, where participants with APOE4 and elevated plasma C-reactive protein (CRP) levels had a greater risk of developing late-onset AD than age and sex-matched APOE2 and APOE3 carriers [19]. In the brains of participants with AD, APOE4 is associated with greater levels of lipid peroxidation, eicosanoids, and oxidative stress markers [20], but the mechanisms for these observations are not clear. Here, we hypothesized that ApoE4 activates cPLA2 to enhance AA release and eicosanoid levels, leading to an enhanced inflammatory and oxidative stress response. Accordingly, we examined cPLA2 expression and activation in mouse primary astrocytes, and in mouse and human brain samples that differed by APOE genotype and determined the cellular effects of cPLA2 inhibition on measurements of neuroinflammation and oxidative stress.

Results

cPLA2 and phosphorylated cPLA2 are increased in ApoE4 mouse primary astrocytes

We previously found that DHA/AA ratio in cerebrospinal fluid (CSF) is lower in APOE4/E4 carriers compared to APOE3/E3 carriers [21, 22]. Since astrocytic cPLA2 and iPLA2 enzymes are important determinants of brain AA and DHA metabolism [2, 23], these enzymes’ expression and activity were first examined in primary astrocytes from ApoE-TR mice. ApoE4 astrocytes had greater mRNA and protein levels of cPLA2 and phosphorylated cPLA2 (p-cPLA2) compared with ApoE3 astrocytes (Fig. 1a, b). In contrast, iPLA2 mRNA and protein levels did not differ between ApoE4 and ApoE3 primary astrocytes (Fig. 1c, d). These measures were also significantly greater in ApoE4 immortalized astrocytes compared to ApoE3 (Fig. S1A and S1B). No differences were found in p-cPLA2 and total cPLA2 levels between ApoE3 and ApoE4 primary microglial cells from ApoE-TR mice (Fig. S1C). To identify cellular cPLA2 localization, cytosolic and membrane fractions were obtained from primary ApoE astrocytes. As expected, the majority of cPLA2 was present in the cytosol. Both cytosolic and membrane-bound cPLA2 levels were greater in ApoE4 compared to ApoE3 (Fig. S2). To further explore the activities of cPLA2 and iPLA2, the efflux of ³H-AA or ¹⁴C-DHA from ApoE3 and ApoE4 primary astrocyte cells to media with or without ATP stimulation for 15 min was examined. ³H-AA efflux was significantly greater in stimulated ApoE4 compared to ApoE3 primary astrocytes (Fig. 1e), whereas ¹⁴C-DHA efflux showed no difference between ApoE4 and ApoE3 (Fig. 1f). To confirm the ApoE protein’s effect, cultured primary astrocytes from C57BL/6 mice were labeled with ³H-AA or ¹⁴C-DHA and then treated with 0.2 μM rApoE3 or rApoE4 proteins for 24 h under similar conditions to primary astrocytes cultured from ApoE-TR mice. ³H-AA efflux was greater after rApoE4 than rApoE3 treatment (Fig. 1g), whereas DHA efflux did not differ between rApoE4 and rApoE3 treatments (Fig. 1h). Taken together, these results confirmed that cPLA2 expression and activity were greater in ApoE4 compared to ApoE3 astrocytes.

Fig. 1

ApoE4 increases cPLA2 but not iPLA2 expression in mouse primary astrocytes. a, cPLA2 mRNA levels in primary astrocytes from APOE3-TR and APOE4-TR mice. b, cPLA2, and phosphorylated cPLA2 (p-cPLA2) protein levels in primary astrocytes from APOE3-TR and ApoE4-TR mice (left) were detected by WB. c, iPLA2 mRNA levels in primary astrocytes from ApoE3-TR and ApoE4-TR mice. d, iPLA2 protein levels in primary astrocyte cultures from APOE3-TR and ApoE4-TR mice were detected by WB. e, f, Primary astrocytes from APOE3-TR and ApoE4-TR mice were incubated with ³H-labelled AA (e) or ¹⁴C-labeled DHA (f) for 24 h, followed by induction by 100 nM ATP for 15 min. The efflux of ³H-AA (e) and ¹⁴C-DHA (f) from cells to media was measured by scintillation counting. g, h, Primary astrocytes from C57BL/6 wild type mice were labeled with ³H-AA (g) or ¹⁴C-DHA (h) for 24 h and then treated with recombinant ApoE3 or ApoE4 for 24 h, followed by induction with 100 nM ATP for 15 min. ³H-AA (g) and ¹⁴C-DHA (h) efflux were measured by scintillation counting. WB: western blot

Phosphorylated cPLA2 and cPLA2 activity are increased in APOE4 mouse brains

To investigate the effect of the ApoE isoforms on cPLA2 in vivo, mRNA, total protein, and phosphorylated protein levels of cPLA2 were measured in the cerebral cortex from 8-month-old ApoE3-TR and ApoE4-TR mice. There was no difference in cortical cPLA2 mRNA levels between ApoE3-TR and ApoE4-TR mice (Fig. 2a). Since p-cPLA2 levels were too low to detect in total brain homogenates, cPLA2 was enriched by immunoprecipitation with a cPLA2 antibody using 500 μg of cortical homogenate, and total cPLA2 and p-cPLA2 levels were measured by Western blot. Total cPLA2 levels did not differ between ApoE3-TR and ApoE4-TR mouse cortex (Fig. 2b, c). However, p-cPLA2 was significantly increased in the ApoE4-TR mouse cortex compared to the ApoE3-TR mouse cortex (Fig. 2b, c). Consistent with these observations, cortical cPLA2 activity (based on the hydrolysis of the arachidonoyl thioester bond to release a detectable free thiol by endogenous brain PLA2) and leukotriene B₄ (LTB4) levels (downstream product of AA release after cPLA2 activation) were higher in ApoE4-TR than ApoE3-TR mice (Fig. 2d, e).

Fig. 2

cPLA2 and p-cPLA2 levels in 8-month old ApoE3-TR and ApoE4-TR mouse brains. The cortex of 8-month old APOE3-TR and ApoE4-TR mice were collected. a, cPLA2 mRNA level in the cortex was detected by qPCR. b, p-cPLA2 and total cPLA2 protein levels in the cortex were detected by western blot. c. Densitometric quantification from b. d, cPLA2 activity in mouse cortex homogenates were measured by cPLA2 activity assay kit. e, LTB4 levels in mouse cortical homogenates were measured by LTB4 assay kit. (n = 5 for each genotype, 3 males and 2 females)

p38 MAPK but not ERK1/2 is increased in ApoE4 mouse primary astrocytes

Phosphorylation of cPLA2 is regulated by MAPK pathways, including p38 MAPK and ERK1/2 MAPK [10, 24, 25]. We tested the phosphorylation of p38 and ERK1/2 in primary astrocytes and mouse cortex from ApoE3 or ApoE4-TR mice by immunoblot using antibodies against total and phosphorylated proteins. Total p38 and ERK1/2 proteins did not differ between ApoE3 and ApoE4 primary astrocytes (Fig. 3a). Interestingly, only phosphorylated p38 (p-p38), but not phosphorylated ERK1/2 (p-ERK1/2), was significantly greater in ApoE4 primary astrocytes than ApoE3 primary astrocytes (Fig. 3a). In agreement, greater p38 phosphorylation but not ERK1/2 was evident in the cerebral cortex of 8-months old ApoE4-TR mice compared to ApoE3-TR mice (Fig. 3b). To test whether cPLA2 activation is dependent on p38 MAPK signaling, we treated ApoE4 primary astrocytes with two different p38 MAPK pathway inhibitors (SB202190 and SB203580) prior to the induction of cPLA2 activation with TNFα and IFNγ. The results showed that SB202190 significantly reduced p-cPLA2 (activated cPLA2) levels (Fig. 3c). Interestingly, SB203580 had no inhibitory effects on cPLA2 activation (Fig. 3c), as SB203580 inhibited MAPKAPK-2 activity but not phosphorylation of p38 MAPK itself [26]. cPLA2 was found to be complexed with p38 as indicated by p38 co-immunoprecipitating with cPLA2 by anti-cPLA2 antibodies in immortalized ApoE4 astrocytes (Fig. 3d). These observations confirmed that p38 MAPK but not the ERK1/2 MAPK pathway can directly regulate cPLA2 phosphorylation in ApoE4 astrocytes.

Fig. 3

Increased p-cPLA2 in APOE4 is mediated by p38 MAPK. a, Phosphorylated and total p38 and ERK levels in primary astrocyte from ApoE3-TR and ApoE4-TR mice were detected by WB. b, Phosphorylated and total p38 and ERK levels in cortical homogenates from APOE3-TR and APOE4-TR mice were detected by WB. c, ApoE4 primary astrocytes from mouse were pre-treated with p38 inhibitors SB 202190 (10 μM) or SB 203580 (10 μM) for 20 min and then treated with medium or TNFα plus IFNγ together for 30 min. The total and phosphorylated cPLA2 and p38 were detected in the cell lysate by WB. d, cPLA2 bound with p38. Immunoprecipitation was performed in the cell lysate of immortalized ApoE4 astrocytes using anti-cPLA2 antibody or species-matched IgG. cPLA2 and p38 were co-detected after immunoprecipitation by WB. WB: Western Blot

Phosphorylated cPLA2 is increased in APOE4 human brains

To determine whether these findings can be demonstrated in human brains, we compared p-cPLA2 and total cPLA2 in the inferior frontal cortex of persons with a similar clinical diagnosis but with different APOE genotypes. Characteristics of brain samples tested are summarized in Table 1. After enrichment of cPLA2 from the cortex, p-cPLA2 and total cPLA2 levels were measured by western blot. In the NCI group, total cPLA2 did not significantly differ between the APOE3/E3 and APOE3/E4 carriers, while the p-cPLA2 level showed a trend increase in APOE3/E4 carriers compared to APOE3/E3 carriers (Fig. 4a). In patients with AD, p-cPLA2 levels were significantly greater in APOE3/E4 carriers compared with APOE3/E3 carriers (p = 0.039), while the total cPLA2 levels did not differ between the two groups (Fig. 4b). Greater cPLA2 phosphorylation in the APOE3/E4 group was not affected by sex, age, or Braak stage. A nonsignificant difference in soluble Aβ₄₂ monomers (p = 0.12) was observed in the brains of APOE3/E4 carriers compared with APOE3/E3 carriers with AD (Fig. S3).

Table 1 Characteristics of clinical samples

Fig. 4

cPLA2 and p-cPLA2 levels in the brains of persons with different APOE genotypes. a, p-cPLA2, and cPLA2 protein levels in the inferior frontal cortex from persons with NCI were detected by WB (left). Densitometric quantification of the blotting (right). b, p-cPLA2, and cPLA2 protein levels in the inferior frontal cortex from AD patients were detected by WB. Densitometric quantification of the blotting (right). WB: Western Blot

p38 MAPK is increased in APOE4 human brain samples

Previous results from mouse astrocyte and cortex showed increased p38 activation in ApoE4-TR compared to ApoE3-TR mice. Phosphorylated and total p38 levels did not differ between no cognitive impairment (NCI) APOE3/E3 and NCI APOE3/E4 groups (Fig. 5a), while total p38 level was significantly greater in the AD APOE3/E4 group compared with the AD APOE3/E3 group (Fig. 5b). In a second brain cohort from the USC ADRC neuropathology core (Supplementary table 1), nonsignificant differences were observed in p-cPLA2/total cPLA2 in the hippocampus of the APOE4/E4 AD group compared to the APOE3/E3 NCI group (Fig. S4A), despite a significantly greater ratio of p-p38/ total p38 in the APOE4/E4 AD group (Fig. S4B). These results supported the greater activation of p38 MAPK pathway with ApoE4 that was most prominent in persons with AD.

Fig. 5

p38 levels in the brains of humans with different APOE genotypes. a, p-p38 and p38 protein levels in inferior frontal cortex from persons with NCI were detected by WB. Densitometric quantification of the blotting (right). b, p-p38 and p38 protein level in inferior frontal cortex from AD patients were detected by WB. Densitometric quantification of the blotting (right). WB: Western blot

LTB4 levels are increased in APOE4 human brain samples

AA is released by cPLA2 hydrolysis of membrane phospholipids, and then can be rapidly oxidized by COX or LOX enzymes to prostaglandins or leukotrienes (LTB4 and PGE2), potent mediators of inflammation and signal transduction [2]. To test the effect of the greater cPLA2 phosphorylation in APOE4 AD brains, PGE2 and LTB4 levels were assayed in brain homogenates from the inferior frontal cortex. LTB4 levels were significantly greater in the AD APOE3/E4 group compared with the AD APOE3/E3 group (p = 0.01) (Fig. 6a), while PGE2 levels did not differ between the two groups (Fig. 6b). The greater LTB4 levels in the APOE3/E4 group were also not affected by sex, age, or Braak stage. No significant differences were found in either LTB4 or PGE2 levels between the NCI APOE3/E3 and NCI APOE3/E4 groups (Fig. 6c and d). The expression of 5-LOX and COX-2 did not differ between the AD APOE3/3 and AD APOE3/E4 groups (Fig. 6e). These results indicated that ApoE4’s activation of cPLA2 in AD selectively increased LTB4 levels in the AD brain.

Fig. 6

LTB4 and PGE2 levels in the cortex of humans with different APOE genotypes. LTB4 (a, c) and PGE2 (b, d) levels in the inferior frontal cortex of AD patients (a, b) and NCI participants (c, d) with different APOE genotypes. e, 5-Lipoxygenase and COX-2 protein levels in inferior frontal cortex from AD patients were detected by WB. (n = 12 (F6/M6) for NCI E3/E3; n = 10 (F5/M5) for NCI E3/E4; n = 12 (F5/M7) for AD E3/E3; n = 10 (F6/M4) for AD E3/E4). WB: Western blot

The NF-κB inflammasome is not induced in the APOE4 brain

It is not clear whether APOE4 can induce neuroinflammation via activation of the NF-κB inflammasome in vivo, and whether cPLA2 is involved in this pathway. Although we found greater TNFα mRNA levels in ApoE4 than in ApoE3 astrocytes, IL1β, IL6 and Ccl2 did not differ between ApoE3 and ApoE4 astrocytes (Fig. 7a). In addition, the protein levels of these cytokines and chemokines were comparable in different APOE genotypes in the mouse brains (Fig. 7b) or the human brain samples (Fig. 7d). Similarly, the abundance of glial fibrillary acid protein (GFAP) in astrocytes and ionized calcium binding adaptor molecule 1 (Iba1) in microglia also did not differ by genotype (Fig. 7d-e). No associations were found between the p-cPLA2/cPLA2 ratio and the GFAP or Iba1 levels in human cortex samples (Fig. S5). The greater LTB4 levels in APOE3/E4 group were also not affected by sex, age, or Braak stage. These results indicated that neuroinflammation with APOE4 does not favor the NF-κB inflammatory response pathway.

Fig. 7

Inflammatory responses in primary astrocytes, mouse, and human cortex with different APOE genotypes. a, mRNA levels of proinflammatory markers in the primary astrocyte from ApoE3-TR or ApoE4-TR mice. b, mRNA levels of proinflammatory cytokines in the cortex of ApoE3-TR or ApoE4-TR mice. c, GFAP, and Iba1 expression in the cortex of ApoE3-TR or ApoE4-TR mice. (n = 5, 3 males and 2 females for b and c). d, mRNA levels of proinflammatory markers in inferior frontal cortex from AD patients. e, GFAP and Iba1 expression in inferior frontal cortex from AD patients. (n = 12 (F5/M7) for AD E3/E3; n = 10 (F6/M4) for AD E3/E4)

cPLA2 is involved in the ApoE4 mediated up-regulation of LTB4 and ROS

To explore whether cPLA2 inhibition mitigates the downstream effects of LTB4 production on ROS and iNOS, ApoE3 and ApoE4 primary astrocytes were treated with the cPLA2 inhibitor pyrrophenone (Fig. 8a). Treatment with pyrrophenone reduced LTB4 levels in ApoE3 and ApoE4 astrocytes, but to a greater extent in ApoE4 astrocytes (Fig. 8b). Furthermore, cPLA2 inhibition significantly decreased iNOS and ROS levels in ApoE3 and ApoE4 primary astrocytes (Fig. 8c, d). These results indicated that greater cPLA2 activity promoted greater levels of iNOS and ROS in the ApoE4 group and can be reduced with cPLA2 inhibition. To confirm the specific effect of cPLA2 on LTB4 production, we knocked down cPLA2 by small interfering RNA (siRNA) in ApoE4 primary astrocytes (Fig. 8e). In agreement, LTB4 levels were significantly decreased in the cPLA2 siRNA treatment group compared to the non-target siRNA treatment group (Fig. 8f).

Fig. 8

Inhibition of cPLA2 reduces ApoE4 mediated up-regulation of LTB4, ROS, and iNOS levels. a-c ApoE3 and ApoE4 primary astrocytes from mice were pre-treated with cPLA2 inhibitor- pyrrophenone (500 nM) for 30 min and then treated with medium or TNFα plus IFNγ together for 18 h. Total and p-cPLA2 in the cell lysate were detected by WB (a). LTB4 levels in the culture medium were measured by the assay kit (b). iNOS expression in cell lysate was detected by WB (c). d, ApoE3, and ApoE4 primary astrocyte were pre-treated with cPLA2 inhibitor-pyrrophenone (1 μM) for 30 min and then treated with medium or TNFα plus IFNγ together for 24 h. The ROS level were detected by the DCFDA probe. e, f, ApoE4 primary astrocytes were transfected with cPLA2 siRNA (10 nM) or Non-target (NT) siRNA (10 nM) for 48 h and then treated with medium or TNFα plus IFNγ together for 24 h. cPLA2 protein levels in cell lysate were detected by WB (e). LTB4 levels in the culture medium were measured by the assay kit (f). Two-way ANOVA was used in a, c, and d for group comparisons. WB: Western blot

ApoE4 and Aβ induce cPLA2 activation in human postmortem frontal cortical synaptosomes

Since cPLA2 was shown to be expressed in neurons and activated by Aβ monomers [27], we examined the effect of exogenous Aβ₄₂ and ApoE on its activation in synaptosomes from human postmortem frontal cortices obtained from control participants without AD pathology. The results showed that treatment with Aβ₄₂, ApoE4, ApoE4/Aβ₄₂ or ApoE3 individually had no effect on cPLA2 activation and distribution in the cytosol and membrane of the synaptosomes (Fig. 9a, b). However, pretreatment with Aβ₄₂, ApoE4 and Aβ₄₂ plus ApoE4 significantly prevented TNFa+IFNγ-evoked cPLA2 cytosol to membrane translocation leading to an increase in p-cPLA2/cPLA2 ratio in the membranous fraction of synaptosome but a decrease in the cytosolic p-cPLA2/cPLA2 ratio. ApoE3 had no effect on cPLA2 activation (Fig. 9a, c). In contrast to TNFα+IFNγ, ceramide-1-phosphate did not alter cPLA2 cellular distribution. Aβ₄₂, ApoE4 and Aβ₄₂ plus ApoE4 significantly enhanced p-cPLA2 levels in the cytosol but had no effect on membranous cPLA2 (Fig. 9a, d). Taken together, these results indicated that ApoE4 and Aβ₄₂ could induce cPLA2 activation in neurons and astrocytes, suggesting that greater cPLA2 activitation in the human cortex of AD APOE3/APOE4 compared to AD APOE3/APOE3 might arise from the combined effects of ApoE4 and greater Aβ₄₂ accumulation.

Fig. 9

ApoE4 and Aβ42 induced cPLA2 activation in human postmortem frontal cortical synaptosomes. a, Synaptosomes were incubated in oxygenated Kreb’s Ringer with different reagents: rApoE3, rApE4, Aβ42, Aβ42/rApoE4 for 30 min, followed by 15 min incubation with Kreb’s-Ringer (control), TNFα/IFNγ or ceramide-1-phosphate, respectively. The synaptosomes were harvested and homogenized, and the membrane and cytosolic fractions of synaptosomes were isolated by centrifugation. cPLA2 was enriched in both fractions by immunoprecipitation with anti-cPLA2 antibodies, and the p-cPLA2 and total cPLA2 were detected by western blot. b-d, Densitometric quantification of blotting shown in A

Discussion

Despite multiple past observations associating APOE4 with greater neuroinflammatory and oxidative stress response than APOE2 or APOE3 (Table 2), the underlying mechanisms are not clearly understood. Here, we identify a plausible mechanism where APOE4 induces greater activation of the cPLA2 system in both astrocytes and synaptosomes, with greater release of AA, LTB4, and iNOS, and generation of ROS in astrocytes. The increase in LTB4 in APOE4 was corroborated in human brain samples matched by disease state. Inhibition of cPLA2 activity lowered the greater neuroinflammation associated with APOE4, reinforcing the candidacy of cPLA2 as a therapeutic target for mitigating the increase in AD risk conferred by carrying APOE4.

Table 2 Summary of the association of APOE4 with greater neuroinflammation

There is evidence from clinical studies implicating greater cPLA2 activation around AD brain plaques [12]. cPLA2 activity is also increased in the CSF of patients with AD [41]. cPLA2 activation can be indirectly assessed by the release of AA from membrane phospholipids [2]. ¹¹C AA brain uptake by PET and unesterified AA/DHA measurement in CSF are surrogate brain cPLA2 activity markers. Indeed, greater incorporation coefficients of ¹¹C AA by PET scans were observed in the grey matter of the brain of AD patients compared to control subjects [42]. Moreover, a greater AA/DHA ratio in both CSF and plasma was present in APOE4 carriers with mild AD compared to APOE3 carriers after DHA supplementation [21]. A greater AA/DHA ratio in plasma phospholipids in cognitively healthy APOE4 carriers was associated with greater conversion to MCI/AD [43]. The greater plasma AA/DHA in APOE4 suggests a systemic (for example, in the liver) activation of cPLA2 that is not just confined to the brain.

Our studies in human brains revealed that carrying an APOE4 allele is not sufficient to activate cPLA2. This is not surprising as not all APOE4 carriers develop AD pathology. cPLA2 activation was significantly greater in APOE4 carriers compared to APOE3 carriers with AD, but not in those with NCI. We also found recombinant ApoE4 and Aβ42 induced greater activation of cPLA2 in postmortem frontal lobe synaptosomes (Fig. 9). One biological explanation is that the effects of soluble Aβ oligomers in AD is additively intensified by ApoE4 to promote a neuroinflammatory phenotype. We speculate that treatments which reduce activation of cPLA2 especially in APOE4 carriers can protect these subjects from neuroinflammation and neurodegeneration, but this hypothesis is yet to be proven. In contrast to observations made in human brains, the activation of cPLA2 in APOE4-TR mouse models in both primary astrocytes and animal brains was measured independent of Aβ. The APOE4-TR mouse models used here are APOE4 homozygous and are maintained under a controlled environment that can allow for observing a greater APOE4 effect than observed in human studies.

Greater cPLA2 activation is mechanistically involved in AD pathology and may represent one pathophysiological link between Aβ oligomers and neuroinflammatory responses [44]. An increase in p-cPLA2 but not in total cPLA2 was observed in the brains of AD mouse models compared with WT mice [14]. In vitro studies suggested that Aβ oligomers can trigger cPLA2 activation and PGE2 production in neurons, eventually leading to neurodegeneration [27, 45]. Inhibition of cPLA2 prevented synaptic loss and memory deficits induced by Aβ oligomers in mice [46]. Similar to Aβ, there is evidence that human prion peptide can also induce neurotoxicity by activating cPLA2, which can be prevented by cPLA2 inhibition [47]. In support of greater cPLA2 activity, hippocampal levels of AA and AA-derived metabolites were much greater in hAPP mice than in non-transgenic control mice [14].

The pattern of enhanced neuroinflammation of the APOE4 AD brains observed in this study does not support the induction of the NF-ĸB inflammasome by cytokines or chemokines such as TNFα, IL1β, IL6, and Ccl2, as past findings supporting these activation patterns were mostly a result of high-dose LPS injections in cell culture and in vivo animal models (summarized in Table 2). Instead, we found a greater level of LTB4 in the cerebral cortex of AD with APOE3/E4 carriers compared to APOE3/E3 carriers and ApoE4 astrocytes, which was associated with the greater phosphorylation of cPLA2. These observations provide a mechanism for the greater levels of oxidative stress in the APOE4 brain [20, 37]. It is plausible that astrocytes contribute to greater LTB4, ROS, and iNOS production with APOE4. An extensive recent proteomic and lipidomic investigation in animal brains of ApoE-TR mice corroborates the enhanced eicosanoid signaling with APOE4 [48]. LTB4 signaling may have a prominent role in inducing oxidative stress. Chuang et al. reported that ROS and NO production during microglia activation is reduced by inhibition of lipoxygenase but not COX [8], suggesting induced LOX signaling as the primary driver of oxidative stress.

Activation of cPLA2 may differ by cell type and within cellular compartments. Recently, astrocytic activation of cPLA2 bound directly with MAVS enhanced NF-ĸB pathways to produce proinflammatory factors such as Ccl2 and Nos2 in an animal model of multiple sclerosis (MS) [7]. The fact that we did not observe greater Ccl2 or Nos2 expression in APOE4 astrocytes, mouse, or human brains in our current study suggests the selective activation cPLA2 by location within the astrocyte leading to a distinct neuroinflammatory phenotype. In addition to MS, the increase in AA release and its metabolism to prostaglandins and leukotrienes have been observed in cancers and other neurodegeneration diseases [49,50,51]. For example, PIK3CA mutant breast cancer tumor cells displayed dramatically elevated AA and eicosanoid levels, promoting tumor cell proliferation [50].

The activation of MAPK system by ApoE4 likely involves complex set of ApoE receptors or signaling pathways. In neurons, ApoE4 was shown to produce greater activation of the MAPK/ERK system (isoform dependent manner) to induce greater production of APP [52], however, it was not clear if this activation involved ApoE signaling receptors (e.g., ApoER2 and VLDLR) or metabolic receptors (e.g., LRP1 and LDLR). Further studies are needed to sort out the receptor(s) involved in different cell types. This could help elucidate the physiological and pathological pathways relevant to ApoE and/or the receptors and their effect of p38-cPLA2 signaling.

Activation of cPLA2 is associated with its phosphorylation [10]. cPLA2 phosphorylation is regulated by ERKs and p38 MAPK pathways, which phosphorylates cPLA2 at Ser-505 and increases its enzymatic activity [9]. cPLA2 phosphorylation and AA release in response to PMA and ATP stimulation in mouse astrocytes are mediated by ERKs and p38 MAPK pathways [10]. In the platelets, cPLA2 phosphorylation was induced by p38 MAPK activation [24]. Here, we found that ApoE4 selectively activated p38 but not ERKs, and inhibition of p38 in ApoE4 astrocytes decreased cPLA2 activation. This activation of p38 is consistent with a previous report of greater p38 activation but not ERKs pathway in ApoE4-TR mice [53]. Interestingly, p38 inhibitors are involved in drug development pipelines for AD [54].

Our study has several strengths and some limitations. We confirmed our findings of greater cPLA2 activation in several independent models: primary cells, synaptosomes, in ApoE-TR animal models, and in human brains matched by disease stage and differing by genotype. We identified the signaling pathway involved in cPLA2 activation (MAPK-p38) and validated this in both animal and human brains. Some of the limitations include not defining the cell-specific cPLA2 activation profile in vivo (whether derived from astrocytes, microglia, neurons and oligodendrocytes). In the clinical cohort, we did not study cPLA2 expression in APOE4 homozygote patients without cognitive impairment, as this condition is infrequent. We also acknowledge that the small sample sizes the human brain cohort can preclude the full examination of the effect of sex and other AD risk factors on the association between APOE4 and neuroinflammation. Future studies should include larger sample sizes and more specific approaches (such as single-cell sequencing) to capture cPLA2’s activation fingerprint on different brain cell types.

Conclusions

Overall, using multiple approaches, our study has identified that the activation of cPLA2 is implicated in neuroinflammation and oxidative stress associated with APOE4 (Fig. 10). Our findings support the induction of the MAPK-p38 pathway as the driving factor for the activation of the cPLA2-LTB4 signaling cascade, and our cellular studies prioritize astrocytes as the target cell type. Inhibition of brain cPLA2 signaling may provide an attractive strategy to reduce the risk of AD dementia associated with carrying the APOE4 allele.

Fig. 10

Illustration of ApoE4 in astrocytes and neurons inducing greater cPLA2 activation than ApoE3 through p38 MAPK pathway, leading to more LTB4, iNOS, and ROS production, increased oxidative stress and neuroinflammation

Materials and methods

Clinical samples

The frozen hippocampi of AD patients with APOE4/E4 carriers (N = 9) and no-cognitive impairment (NCI) with APOE3/E3 carriers (N = 7) were collected from the University of Southern California (USC) Alzheimer Disease Research Center (ADRC) Neuropathology core, which was approved by USC’s Institutional Review Board (IRB) protocol (HS-16-00888). The frozen inferior frontal lobe (Brodmann area 10) of the individuals with NCI and the APOE3/E3 carriers (N = 12) and APOE3/E4 carriers (N = 10) and AD patients and the APOE3/E3 (N = 12) and APOE3/E4 genotypes (N = 10) were obtained from the Rush Alzheimer’s Disease Center (RADC) at the Rush University Medical Center. Rush Memory and Aging Project was approved by an Institutional Review Board (IRB) of Rush University Medical Center.

Animals

ApoE3-TR and ApoE4-TR mice were a generous gift from Dr. Patrick Sullivan. The endogenous mouse ApoE was replaced by either human APOE3 or APOE4, created by gene targeting, as described previously [55]. All experiments were performed on age-matched male animals (8 months of age) and were approved by the USC Animal Care Committee. Every effort was made to reduce animal stress and to minimize animal usage. The mice were anesthetized with isoflurane and perfused with PBS. The brains were split in half for further analysis.

Cell cultures

Primary astrocytes were obtained from C57JB6, ApoE3-TR, and ApoE4-TR mice pups and cultured, as described previously [56]. Briefly, cerebral cortices from each 1 to 3 day-old neonatal mouse were dissected in ice-cold Hanks’ Balanced Salt Solution (HBSS) (Corning, 21–021-CV) and digested with 0.25% trypsin for 20 min at 37 °C. Trypsinization was stopped by the addition of a 2-fold volume of DMEM (Corning, 10–013) with 10% fetal bovine serum (FBS) (Omega Scientific, FB-12) and 1% antibiotic-antimycotic (Anti-anti) (Thermo Fisher, 15,240,062). The cells were dispersed into a single-cell level by repeated pipetting and filtered through 100 μm cell strainers (VWR, 10199–658). After filtering, cells were centrifuged for 5 min at 1000 rpm and resuspended in a culture medium supplemented with 10% FBS and antibiotics. Then, cells were seeded in a 75 cm² flask and cultured at 37 °C in 5% CO₂. The medium was changed the next day and then replaced every 3 days. These mixed glia cultures reached confluence after 7–10 days. The cells were then shaken at 250 rpm for 16 h at 37 °C to remove microglia and oligodendrocyte progenitor cells. The remaining cells were harvested by digestion with trypsin. At this stage, the culture contained 95% astrocytes and was used for further experiments.

Immortalized mouse astrocytes derived from human APOE3-TR and APOE4-TR mice [57] were gifts from Dr. David Holtzman and grown in DMEM/F12 (Corning, MT10090CV) containing 10% FBS, 1 mM sodium pyruvate (Thermo Fisher, 11,360,070), 1 mM geneticin (Thermo Fisher, 10,131–035) and 1% anti-anti.

Cell lysate and brain homogenate preparation

The immortalized or primary astrocytes were lysed with 1x RIPA buffer (Cell Signaling Technology, CST 9806) containing protease inhibitor cocktail (Sigma, P8340) and phosphatase inhibitor cocktail (Sigma, P0044), followed by centrifugation at 14,000 gs for 10 min at 4 °C. The supernatant was collected for further analysis.

The mouse cerebral cortex, human hippocampus, and inferior frontal cortex were weighed, then RIPA buffer containing protease inhibitor cocktail and phosphatase inhibitor cocktail was added as 1:30 (w/v). The tissue was then homogenized using a 2 mL glass Dounce tissue grinder, followed by centrifugation with 14,000 gs for 10 min at 4 °C. The supernatant was collected, and the concentration was measured by BCA kit.

cPLA2 protein enrichment

To detect p-cPLA2 in mouse cortex homogenates, cPLA2 protein was enriched by immunoprecipitation. For each mouse sample, 5 μg of cPLA2 antibody (Santa Cruz Biotechnology, sc-376,618) was conjugated to 50 μL Dynabeads Protein G (Thermo Scientific, 10003D) for 1 h at room temperature, then 500 μg total protein in 500 μL RIPA was added to the cPLA2-beads complex and incubated with rotation overnight at 4 °C. The beads were washed with 0.1% PBST 3 times by rotation for 5 min. After washing, 30 μL of 1x sample buffer (Bio-Rad, 1,610,747) was added to the beads and heated for 10 min at 100 °C. The supernatant was collected by magnetic force and used for the further Western blot assay.

Western blot

The cell lysates, cortex homogenate, and enriched cPLA2 proteins were separated by 4–15% mini-precast protein gels (Bio-Rad, 4,561,086) under reducing conditions and then transferred onto nitrocellulose membranes (Bio-Rad, 1,704,270). After transfer, membranes were blocked with 5% fat-free milk (Bio-Rad, 1,706,404) in TBST for 1 h at room temperature, followed by overnight incubation with the primary antibody in 5% BSA at 4 °C. Then, the membranes were incubated with HRP conjugated secondary antibody for 1 h at room temperature. Chemiluminescent HRP substrate (Millipore, WBKLS0500) was used for detection. Fujifilm LAS-4000 imager system was used to capture images, and the densitometric quantification was done by Gel Quant NET software.

The following antibodies and dilution factors were used: cPLA2 antibody (Santa Cruz Biotechnology, sc-376,618) (1:200), phospho-cPLA2 (Ser505) antibody (CST, 53044) (1:1000), phospho-ERK1/2 antibody (CST, 4370) (1:1000), ERK1/2 antibody (CST, 4595) (1:1000), p38 antibody (CST, 9212) (1:1000), phospho-p38 antibody (CST, 4511) (1:1000), GFAP antibody (CST, 12389) (1:1000), Iba1 antibody (GeneTex, GTX100042) (1:1000), iNOS antibody (CST, 13120) (1:1000), GAPDH antibody (CST, 5174) (1:1000), ApoE4 antibody (CST, 8941) (1:1000), β-actin antibody (CST, 3700) (1:1000), β-tubulin antibody (CST, 2146) (1:1000), HRP-linked anti-mouse IgG (CST, 7076) (1:2000), HRP-linked anti-rabbit IgG (CST, 7074) (1:2000).

qPCR

The cells and brain specimens were harvested, and RNA was extracted using an RNA extraction kit (Thermo Fisher, K0731). Synthesis of cDNA was done using High-Capacity cDNA Reverse Transcription Kit (Thermo Fisher, 4368814). qPCR was performed using the PowerUp SYBR Green Master Mix (Thermo Fisher, A25742). The following primers were synthesized by Integrated DNA Technologies. The cPLA2 sense (5′-CTGCAAGGCCGAGTGACA-3′) and antisense (5′-TTCGCCCACTTCTCTGCAA-3′); mouse Tnfα sense (5′-GCCTCTTCTCATTCCTGCTTG-3′) and antisense (5′-CTGATGAGAGGGAGGCCATT-3′); mouse Il1β sense (5′-GCAACTGTTCCTGAACTCAACT-3′) and antisense (5′-ATCTTTTGGGGTCCGTCAACT-3′); mouse Il6 sense (5′-TAGTCCTTCCTACCCCAATTTCC-3′) and antisense (5′-TTGGTCCTTAGCCACTCCTTC-3′); mouse Ccl2 sense (5′-GTCCCTGTCATGCTTCTGG-3′) and antisense (5′-GCTCTCCAGCCTACTCATTG-3′); mouse Mip1α sense (5′- TGAAACCAGCAGCCTTTGCTC-3′) and antisense (5′-AGGCATTCAGTTCCAGGTCAGTG-3′); mouse Mip2 sense (5′-ATCCAGAGCTTGAGTGTGACGC-3′) and antisense (5′- AAGGCAAACTTTTTGACCGCC-3′); mouse β-actin sense (5′-ACCTTCTACAATGAGCTGCG-3′) and antisense (5′-CTGGATGGCTACGTACATGG-3′); human TNFα sense (5′-ACTTTGGAGTGATCGGCC-3′) and antisense (5′-GCTTGAGGGTTTGCTACAAC-3′); human IL1β sense (5′-ATGCACCTGTACGATCACTG-3′) and antisense (5′-ACAAAGGACATGGAGAACACC-3′);

human IL6 sense (5′-CCACTCACCTCTTCAGAACG-3′) and antisense (5′-CATCTTTGGAAGGTTCAGGTTG-3′); human Ccl2 sense (5′- TGTCCCAAAGAAGCTGTGATC-3′) and antisense (5′-ATTCTTGGGTTGTGGAGTGAG-3′); human GAPDH sense (5′-ACATCGCTCAGACACCATG-3′) and antisense (5′-TGTAGTTGAGGTCAATGAAGGG-3′).

AA and DHA efflux assays

To investigate arachidonic acid (AA) and docosahexaenoic acid (DHA) release by cPLA2 and iPLA2 activation, respectively, we performed an AA and DHA efflux assay as described previously [2]. ApoE3 and ApoE4 primary astrocytes were seeded at 5000 cells/well in 96-well plates. After 24 h, the culture medium was changed with serum-free DMEM containing fatty acid-free BSA (5 mg/mL) (Sigma, A9647) and ³H-AA (0.1 μCi/mL) or ¹⁴C-DHA (0.1 μCi/mL) (Moravek) for 24 h. The cells were then washed twice with 100 μL of DMEM, and 100 μL of DMEM containing BSA (5 mg/mL) was added. After 30 min, the medium was removed, and 100 μL of ATP (100 μM) in DMEM without BSA was added. After 15 min, the cell culture medium was collected and transferred to scintillation vials filled with 3 mL of scintillation cocktail. The cells were solubilized in 90 μL of NaOH (0.5 N) for 5 min, neutralized with 60 μL PBS, and then transferred to scintillation vials filled with 3 mL scintillation cocktail. After rigorous mixing, the vials were counted in a Beckman LS6500 liquid scintillation counter (Beckman Coulter). The efflux of AA and DHA were assessed by the ratio of the corresponding fatty acid in the medium to total (medium and cell lysate). The change of AA and DHA efflux was calculated by subtracting the levels of AA and DHA in the ATP treated group to ATP non-treated group for each genotype. WT primary astrocytes were plated and labeled with ³H-AA (0.1 μCi/mL) or ¹⁴C-DHA (0.1 μCi/mL) as described above. Then, the cells were washed twice with 100 μL of DMEM. After wash, 10 μL of DMEM containing BSA and 0.2 μM recombinant ApoE3 or ApoE4 protein were added. After 24 h, the medium was removed, and 100 μL of ATP (100 μM) in DMEM without BSA was added. The AA and DHA efflux were measured as described above after 15 min.

cPLA2 activity assay

cPLA2 activity was detected by the cPLA2 activity assay kit (Cayman Chemical, 765,021). The mouse cortex was homogenized into HEPES buffer (50 mM, pH 7.4, containing 1 mM EDTA) as 1:10 (w/v), and the supernatant was collected after centrifuged and used for cPLA2 activity detection.

Immunoprecipitation

Immortalized ApoE4 astrocytes were cultured in a 100-mm dish for 18 h and then were lysed with RIPA containing protease and phosphatase inhibitors. The lysates were used for immunoprecipitation with an anti-cPLA2 antibody or species-matched IgG. After elution, cPLA2 and p38 were detected by Western blot.

p38 MAPK inhibiton experiment

ApoE4 primary astrocytes were seeded in a 24 wells plate with the intensity of 100,000 cells per well. Forty-eight hours later, cells were pre-treated with p38 MAPK inhibitors – SB202190 (10 μM, Sigma, S7076) or SB203580 (10 μM, Sigma, S8307) in the DMEM culture medium without FBS for 20 min, followed by the treatment with vehicle or TNFα (10 ng/mL) (R&D Systems, 210-TA-005) plus IFNγ (100 ng/mL) (Sigma, SRP3058) together for 30 min. Then, the cells were lysed with RIPA. Total and phosphorylated cPLA2 and p38 were detected by Western blot.

LTB4 and PGE2 measurement

For the LTB4 and PGE2 measurements in the human brain samples, brain tissue was weighed, then PBS containing 1 mM EDTA, 10 μM indomethacin (Cox inhibitor, Sigma I8280), and 10 μM NDGA (Lox inhibitor, Sigma 479,975) as 1:10 (w/v) were added. The tissue was then homogenized using a 2 mL glass Dounce tissue grinder, followed by centrifugation with 8000 x g for 10 min at 4 °C. The supernatant was collected, and the protein concentration was measured using a BCA kit. LTB4 and PGE2 levels were detected by the assay kit (LTB4 ELISA Kit, Cayman Chemical, 10,009,292; PGE2 ELISA Kit, Cayman Chemical, 500,141).

For the LTB4 measurement in the cells, ApoE3 and ApoE4 primary astrocytes were seeded in a 24-wells plate with the intensity of 100,000 cells per well. Forty-eight hours later, cells were pre-treated with cPLA2 inhibitor-Pyrrophenone (500 nM, Sigma, 5,305,380,001) in the DMEM culture medium without FBS but containing N2 supplement for 30 min, followed by the treatment with vehicle or TNFα (10 ng/mL) (R&D Systems, 210-TA-005) plus IFNγ (100 ng/mL) (Sigma, SRP3058) together for 18 h. Then, the culture media and cell lysate were collected. LTB4 levels were measured in a 4-fold concentrated medium using the assay kit.

ApoE4 primary astrocytes were seeded in a 24-wells plate with the intensity of 100,000 cells per well. Forty-eight hours later, cells were transfected with cPLA2 or non-target (NT) siRNA (10 nM) for 48 h, followed by the treatment with vehicle or TNFα (10 ng/mL) plus IFNγ (100 ng/mL) together for 24 h. Then, the culture media and cell lysate were collected. LTB4 levels were measured in a 4-fold concentrated medium by the assay kit.

ROS measurement

ROS were detected by the DCFDA cellular ROS detection assay kit (Abcam, ab113851). ApoE3 and ApoE4 primary astrocytes were seeded in dark, clear bottom 96-wells plate with the intensity of 20,000 cells per well. Forty-eight hours later, cells were pre-treated with cPLA2 inhibitor (1 μM) in the DMEM culture medium without FBS but containing N₂ supplement for 30 min, followed by the treatment with vehicle or TNFα (10 ng/mL) plus IFNγ (100 ng/mL) together for 24 h. After removing the media and washing plate once with 1x assay buffer, the cells were stained with DCFDA solution (100 μL/well) for 45 min at 37 °C in the dark. Then, the DCFDA solution was removed, and the 1x assay buffer (100 μL/well) was added to the plate. ROS levels were measured using a fluorescent plate reader at Excision/Emission = 485/585 nm.

Assessment of activation and cellular distribution of cPLA2 in synaptosomes

Synaptosomes prepared from postmortem human frontal cortices using an established method with minor modification [58]. Briefly, thawed postmortem human frontal cortical slices (about 20 mg) were homogenized in 10 volume of ice-cold homogenization buffer (10 mM HEPES, pH 7.4, 0.32 M sucrose, 0.1 mM EDTA containing EDTA-free protease inhibitor cocktail (Roche, 04693159001) and 0.2% 2-mercaptoethanol) using a Teflon/glass homogenizer (10 strokes). The homogenates were cleared by centrifugation (1000 x g for 10 min), and the supernatants were centrifuged at 15,000 x g at 4 °C for 30 min to pellet the synaptosomes (P2 fraction). The synaptosomes were washed twice at 4 °C in 1 mL of ice-cold oxygenated K-R (Kreb’s-Ringer) solution (25 mM HEPES, pH 7.4, 118 mM NaCl, 4.8 mM KCl, 25 mM NaHCO₃, 1.3 mM CaCl₂, 1.2 mM MgSO₄, 1.2 mM KH₂PO₄, 10 mM glucose, 100 μM ascorbic acid, EDTA-free protease inhibitor cocktail). The synaptosomes were then resuspended in 1 mL of K-R solution, and the protein concentrations were determined by the BCA kit. Two hundred μg synaptosomes were incubated with 0.1 μM of Aβ₄₂, rApoE3, rApoE4 or Aβ₄₂ + rApoE4 in 200 μL oxygenated Kreb’s-Ringer for 30 min at 37 °C followed by incubation with 1 μM A23187 (Santa Cruz Biotechnology, sc-3591), 5 ng/mL TNFα+ 10 ng/mL IFNɣ or 2.5 μM ceramide-1-phosphate (Sigma, C4832) for 15 min (oxygenated with 95% O2/5% CO2 for 1 min every 10 min). Upon completion of incubation, an ice-cold protein phosphatase inhibitor cocktail (Roche, 04906837001) is added and placed on ice for 5 min, and synaptosomes were pelleted by centrifugation.

The cytosolic and membranous fractions of the synaptosomes were prepared as established previously with minor modifications [59]. The synaptosomes were briefly sonicated (Kontes Micro Cell Disrupter) in 250 μL of immunoprecipitation buffer (25 mM HEPES, pH 7.5, 200 mM NaCl, 1 mM EDTA, protease and protein phosphatase inhibitor cocktails, and 0.02% 2-mercaptoethanol and centrifuged at 48,000 x g for 15 min. The resultant supernatant was removed as the cytosolic fraction, and the pellet was briefly sonicated in 200 μL immunoprecipitation buffer as the membranous fraction. Both cytosolic and membranous fractions were solubilized with 0.5% digitonin, 0.2% sodium cholate, and 0.5% NP-40 (total incubation volume was 220 μL and incubated at 4 °C with end-to-end shaking for 1 h. After dilution with 780 μL of ice-cold immunoprecipitation buffer and centrifugation (4 °C) to remove insoluble debris. cPLA2 were isolated by immunoprecipitation with 16 h incubation at 4 °C with anti-cPLA2 antibodies (Santa Cruz Bio-technology, sc-376,618, and sc-137,069) covalently linked protein A/G-conjugated agarose beads. The resultant immunocomplexes were pelleted by centrifugation at 4 °C. After three washes with 1 mL of ice-cold PBS, pH 7.2, and centrifugation, the isolated cPLA2 was eluted with 90 μl IgG elution buffer (Thermo Fisher, 21,004), neutralized by 10 μL 1.5 M Tris-HCl (pH 9.0) and then solubilized by boiling for 5 min with 17 μL of 6X SDS-PAGE sample preparation buffer. The contents of activated cPLA2 (p-cPLA2) and total cPLA2 in 50% of the obtained anti-cPLA2 immunoprecipitants were determined respectively by Western blot with p-cPLA2 (Cell Signaling Technologies, 53,044) and anti-cPLA2 (Santa Cruz Biotechnology, sc-376,618) antibodies.

Statistical analysis

Descriptive results are presented as the mean ± SD. Data were analyzed using Student’s unpaired t-test or ANOVA. The cPLA2 phosphorylation was compared in APOE groups using a linear regression model, adjusting for age, sex, and Braak stage. Non-parametric tests were used for non-normally distributed data. Statistical significance was present at p < 0.05. Statistical program R, version 3.5 was used. Quantification of WB gels was conducted on three independent experiments.