Effects of altered expression and localization of cyclophilin A on differentiation of p19 embryonic carcinoma cells

被引:17
作者
Chiu, R [1 ]
Rey, O
Zheng, JQ
Twiss, JL
Song, J
Pang, S
Yokoyama, KK
机构
[1] Univ Calif Los Angeles, Sch Dent, Dent Res Inst, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Surg Oncol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Sch Med, Dept Med, Los Angeles, CA 90024 USA
[5] Univ Calif Los Angeles, Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90024 USA
[6] RIKEN, BioResource Ctr, Tsukuba, Ibaraki 305, Japan
关键词
cyclophilin; dorsal root ganglia; p19 embryonic carcinoma cell line; retinoblastoma susceptibility gene product RB; retinoic acid;
D O I
10.1023/B:CEMN.0000005321.11544.cc
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
1. The retinoblastoma susceptibility gene product, p105Rb (RB), is an important regulator in the control of cell proliferation, differentiation, and apoptosis. Several cellular factors that complex with RB and exert their cellular regulatory functions have been identified, such as the RB: cyclophilin A (CypA) complex. 2. CypA is a cytoplasmic immunophilin and known for its involvement in T-cell differentiation and proliferation. Although CypA has a pivotal role in the immune response, its function in other signaling pathways is largely unknown. 3. In this study, we used a model of neuronal differentiation to demonstrate that the nuclear translocation of CypA, the appearance of hypophosphorylated RB and the enhancement of RB: CypA complex formation correlates with retinoic acid induced neuronal differentiation. 4. Inhibition of CypA expression results in repression of both the hypophosphorylated RB and the neuron-specific differentiation marker, class III beta tubulin. 5. The evidence of enriched CypA and colocalization of RB with CypA in the nucleus of primary adult sensory neurons substantiated the important event of RB-mediated neuronal differentiation of p19 EC cells.
引用
收藏
页码:929 / 943
页数:15
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