OSP/claudin-11 forms a complex with a novel member of the tetraspanin super family and β1 integrin and regulates proliferation and migration of oligodendrocytes

被引:146
作者
Tiwari-Woodruff, SK
Buznikov, AG
Vu, TQ
Micevych, PE
Chen, K
Kornblum, HI
Bronstein, JM
机构
[1] Univ Calif Los Angeles, Sch Med, Dept Neurol, Los Angeles, CA 90024 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Neurobiol, Los Angeles, CA 90024 USA
[3] Univ Calif Los Angeles, Sch Med, Dept Mol & Med Pharmacol & Pediat, Los Angeles, CA 90024 USA
[4] Univ Calif Los Angeles, Sch Med, Inst Brain Res, Los Angeles, CA 90024 USA
关键词
tight junctions; myelin; TM4SF; brain; OAP-1;
D O I
10.1083/jcb.153.2.295
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Oligodendrocyte-specific protein (OSP)/claudin-11 is a major component of central nervous system myelin and forms tight junctions (TJs) within myelin sheaths. TJs are essential for forming a paracellular barrier and have been implicated in the regulation of growth and differentiation via signal transduction pathways. We have identified an OSP/claudin-11-associated protein (OAP)1, using a yeast two-hybrid screen. OAP-1 is a novel member of the tetraspanin superfamily, and it is widely expressed in several cell types, including oligodendrocytes, OAP-1, OSP/claudin-11, and beta1 integrin form a complex as indicated by coimmunoprecipitation and confocal immunocytochemistry. Overexpression of OSP/claudin-11 or OAP-1 induced proliferation in an oligodendrocyte cell line. Anti-OAP-1, anti-OSP/claudin-11, and anti-beta1 integrin antibodies inhibited migration of primary oligodendrocytes, and migration was impaired in OSP/claudin-11-deficient primary oligodendrocytes. These data suggest a role for OSP/claudin-11, OAP-1, and beta1 integrin complex in regulating proliferation and migration of oligodendrocytes, a process essential for normal myelination and repair.
引用
收藏
页码:295 / 305
页数:11
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