Volume 7 Supplement 1

Proceedings of the 2011 International Conference on Molecular Neurodegeneration

Open Access

C-terminal part of alpha-synuclein mediates its activity in promoting proliferation of dopaminergic cells

  • Juanjuan Yin1,
  • Tao Wang1,
  • Junyan Han1,
  • Chen Zhang1,
  • Qiulan Ma1,
  • Xin Li1,
  • Furong Cheng1,
  • Guangwei Liu1,
  • Yaohua Li1,
  • Kenji Uéda1, 3,
  • Piu Chan1 and
  • Shun Yu1, 2
Contributed equally
Molecular Neurodegeneration20127(Suppl 1):S21

DOI: 10.1186/1750-1326-7-S1-S21

Published: 7 February 2012

Background

Although abnormal aggregation of alpha-synuclein (α-syn) is involved in several neurodegenerative diseases, its biological functions remain poorly understood, which limits our understanding of its pathogenic mechanisms. α-Syn has been shown to exhibit a MAP-like activity and promote the assembly of microtubules. Since microtubules play a pivotal role in proliferative cell division, it is possible that α-syn affects cell proliferation by facilitating microtubule assembly. The role of α-syn in promoting cell proliferation was reported previously in PC12 dopaminergic cells overexpressing α-syn. Here, we extended this study aiming at finding the association between the cell proliferation effect of α-syn and its microtubule assembly activity, and identifying the potential active domain for the effect α-syn on cell proliferation.

Method

By exploiting the property that the 11-mer repeats of synuclein molecules are able to mediate a rapid intracellular translocation of these proteins across the plasma membrane without being degraded by the cellular proteolytic system, we added recombinant full-length α-syn (wild type and A53T and A30P mutants) and β-syn to the culture medium of MES23.5 dopaminergic cells, and observed their intracellular translocation, subcellular distribution and effects on cell proliferation.

Result

We found that all the synuclein molecules could enter the cells where they were localized in both the cytoplasm and nucleus. However, only the wild-type α-syn, which had been shown to have microtubule assembly activity, was able to promote proliferation of the MES23.5 cells. The A53T and A30P mutant α-syn as well as β-syn, which had been proved not to possess microtubule assembly activity, did not exhibit any effect on cell proliferation. Since the α-syn activity in microtubule assembly was shown to be related to its specific functional domain, we then generated different functional fragments (N-terminal 1-65aa, NAC 66-95aa and C-terminal 96-140aa) and tested their activities in cell proliferation. We showed that all the α-syn fragments could enter the cells, but with different subcellular localizations. The N-terminal and NAC fragments were localized in the cytoplasm and the C-terminal fragment mainly in the nucleus. In accordance with the activity for the C-terminal part of α-syn in microtubule assembly, only the NAC and C-terminal fragments exhibited the activity in cell proliferation. The N-terminal fragment without microtubule assembly activity did not promote cell proliferation.

Conclusion

The above results suggest that the α-syn function in promoting cell proliferation is associated with its microtubule assembly activity with the functional domain localized in its C-terminal part.

Notes

Authors’ Affiliations

(1)
Department of Neurobiology and Sino-Japan Joint Laboratory for Neurodegenerative Diseases, Beijing Institute of Geriatrics, Xuanwu Hospital of China Capital Medical University
(2)
Institute for Hypoxia Medicine, Xuanwu Hospital of China Capital Medical University
(3)
Division of Psychobiology, Tokyo Institute of Psychiatry

Copyright

© Yin et al; licensee BioMed Central Ltd. 2012

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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