دورية أكاديمية

Autophagic Death of Adult Hippocampal Neural Stem Cells Following Insulin Withdrawal.

التفاصيل البيبلوغرافية
العنوان: Autophagic Death of Adult Hippocampal Neural Stem Cells Following Insulin Withdrawal.
المؤلفون: Seong-Woon Yu, Seung-Hoon Baek, Brennan, Ryan T., Bradley, Christopher J., Se Kyong Park, Yoon Sun Lee, Eun Jung Jun, Lookingland, Keith J., Eun-Kyoung Kim, Heuiran Lee, Goudreau, John L., Seong Who Kim
المصدر: Stem Cells; Oct2008, Vol. 26 Issue 10, p2602-2610, 9p, 1 Black and White Photograph, 1 Diagram, 5 Graphs
مصطلحات موضوعية: KERATINOCYTES, CELL proliferation, CELL division, CELL growth, CYTOKINES, GROWTH factors
مستخلص: Novel therapeutic approaches using stem cell transplantation to treat neurodegenerative diseases have yielded promising results. However, survival of stem cells after transplantation has been very poor in animal models, and considerable efforts have been directed at increasing the viability of engrafted stem cells. Therefore, understanding the mechanisms that regulate survival and death of neural stem cells is critical to the development of stem cell-based therapies. Hippocampal neural (HCN) stem cells derived from the adult rat brain undergo cell death following insulin withdrawal, which is associated with downregulation of antiapoptotic Bcl-2 family members. To understand the type of cell death in HCN cells following insulin withdrawal, apoptosis markers were assessed. Of note, DNA fragmentation or caspase-3 activation was not observed, but rather dying cells displayed features of autophagy, including increased expression of Beclin 1 and the type II form of light chain 3. Electron micrographs showed the dramatically increased formation of autophagic vacuoles with cytoplasmic contents. Staurosporine induced robust activation of caspase-3 and nucleosomal DNA fragmentation, suggesting that the machinery of apoptosis is intact in HCN cells despite the apparent absence of apoptosis following insulin withdrawal. Autophagic cell death was suppressed by knockdown of autophagy-related gene 7, whereas promotion of autophagy by rapamycin increased cell death. Taken together, these data demonstrate that HCN cells undergo a caspase-independent, autophagic cell death following insulin withdrawal. Understanding the mechanisms governing autophagy of adult neural stem cells may provide novel strategies to improve the survival rate of transplanted stem cells for treatment of neurodegenerative diseases. [ABSTRACT FROM AUTHOR]
Copyright of Stem Cells is the property of Oxford University Press / USA and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:10665099
DOI:10.1634/stemcells.2008-0153