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Microtubule deacetylases, SirT2 and HDAC6, in the nervous system
被引:113
作者:
Southwood, Cherie M.
Peppi, Marcello
Dryden, Sylvia
Tainsky, Michael A.
Gow, Alexander
机构:
[1] Wayne State Univ, Sch Med, Ctr Mol Med & Genet, Detroit, MI 48201 USA
[2] Wayne State Univ, Sch Med, Karmanos Canc Ctr, Detroit, MI 48201 USA
[3] Wayne State Univ, Sch Med, Dept Pathol, Detroit, MI 48201 USA
[4] Wayne State Univ, Sch Med, Carman & Ann Adams Dept Pediat, Detroit, MI 48201 USA
[5] Wayne State Univ, Sch Med, Dept Neurol, Detroit, MI 48201 USA
关键词:
axoglial junctions;
myelinated fibers;
central nervous system;
peripheral nervous system;
immunofluorescence;
mouse;
D O I:
10.1007/s11064-006-9127-6
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Examination of the cytoskeleton has demonstrated the pivotal role of regulatory proteins governing cytoskeletal dynamics. Most work has focused on cell cycle and cell migration regarding cancer. However, these studies have yielded tremendous insight for development, particularly in the nervous system where all major cell types remodel their shape, generate unsurpassed quantities of membranes and extend cellular processes to communicate, and regulate the activities of other cells. Herein, we analyze two microtubule regulatory alpha-tubulin deacetylases, histone deacetylase-6 (HDAC6) and SirT2. HDAC6 is expressed by most neurons but is abundant in cerebellar Purkinje cells. In contrast, SirT2 is targeted to myelin sheaths. Expression of these proteins by post-mitotic cells indicates novel functions, such as process outgrowth and membrane remodeling. In oligodendrocytes, targeting of SirT2 to paranodes coincides with the presence of the microtubule-destabilizing protein stathmin-1 during early myelinogenesis and suggests the existence of a microtubule regulatory network that modulates cytoskeletal dynamics.
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页码:187 / 195
页数:9
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