Sox6 suppression induces RA-dependent apoptosis mediated by BMP-4 expression during neuronal differentiation in P19 cells

被引:11
|
作者
Hamada-Kanazawa, Michiko [1 ]
Ogawa, Daisuke [1 ]
Takano, Masaoki [1 ]
Miyake, Masaharu [1 ]
机构
[1] Kobe Gakuin Univ, Fac Pharmaceut Sci, Div Biopharmaceut Sci, Chuo Ku, Kobe, Hyogo 6508586, Japan
关键词
Sox6; P19; BMP-4; Retinoic acid; Apoptosis; BMPRIB; EMBRYONIC STEM-CELLS; RETINOIC ACID; NEURAL DIFFERENTIATION; CARCINOMA-CELLS; GENE SOX6; DEATH; PROTEIN; MOUSE; SRY; REQUIRES;
D O I
10.1007/s11010-015-2607-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Sox6 is a transcription factor that induces neuronal differentiation in P19 cells; its suppression not only inhibits neuronal differentiation but also induces retinoic acid (RA)-dependent apoptosis of P19 cells. In the present study, we found that Sox6 suppression-induced apoptosis was mediated by activation of caspase 9 and 3. Moreover, we noted a weak leakage of cytochrome c into the cytoplasm from the mitochondria, indicating that apoptosis occurs through a mitochondrial pathway in Sox6-suppressed P19 (P19[anti-Sox6]) cells. Sox6 suppression in the presence of RA also induced the expression and secretion of bone morphogenetic protein 4 (BMP-4). Addition of an anti-BMP-4 antibody for neutralization increased cell viability and led to RA-dependent death of P19[anti-Sox6] cells. Our results indicate that Sox6 suppression induces RA-dependent cell death of P19 cells, mediated by BMP-4 expression and secretion. Normally, high Sox6 expression leads to RA-mediated neuronal differentiation in P19 cells; however, Sox6 deficiency induces production and secretion of BMP-4, which mediates selective cell death. Our findings suggest that Sox6 contributes to cell survival by suppressing BMP-4 transcription during neuronal differentiation.
引用
收藏
页码:49 / 57
页数:9
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