Abstract

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.

Highlights

  • Sox6, which was initially reported to be a member of the Sox gene family (Sry-type HMG box), functions as a sexdetermining SRY/Sry-related factor in humans and mice [1]

  • Our results indicate that Sox6 suppression induces retinoic acid (RA)-dependent cell death of P19 cells, mediated by bone morphogenetic protein 4 (BMP-4) expression and secretion

  • Sox proteins are known to be important factors in neurogenesis [3], and Sox2 and Sox3 are mainly expressed in the developing central nervous system, whereas Sox6 plays a role in the early stages of nervous system development, as it is expressed during the initial stage of embryogenesis [1]

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Summary

Introduction

Sox6, which was initially reported to be a member of the Sox gene family (Sry-type HMG box), functions as a sexdetermining SRY/Sry-related factor in humans and mice [1]. Our results indicate that Sox6 suppression induces RA-dependent cell death of P19 cells, mediated by BMP-4 expression and secretion. High Sox6 expression leads to RA-mediated neuronal differentiation in P19 cells; Sox6 deficiency induces production and secretion of BMP-4, which mediates selective cell death.

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