State Key Laboratory of Oncogenes and Related Genes, Renji-MedX Stem Cell Research Center, Ren Ji Hospital, School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai 200030, China; Med-X Research Institute & School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai 200030, China.
State Key Laboratory of Oncogenes and Related Genes, Renji-MedX Stem Cell Research Center, Ren Ji Hospital, School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai 200030, China.
Stem Cell Reports. 2017 Jul 11;9(1):231-246. doi: 10.1016/j.stemcr.2017.05.031. Epub 2017 Jun 29.
Although STAT3 signaling is demonstrated to regulate sensory cell differentiation and regeneration in the zebrafish, its exact role is still unclear in mammalian cochleae. Here, we report that STAT3 and its activated form are specifically expressed in hair cells during mouse cochlear development. Importantly, conditional cochlear deletion of Stat3 leads to an inhibition on hair cell differentiation in mice in vivo and in vitro. By cell fate analysis, inactivation of STAT3 signaling shifts the cell division modes from asymmetric to symmetric divisions from supporting cells. Moreover, inhibition of Notch signaling stimulates STAT3 phosphorylation, and inactivation of STAT3 signaling attenuates production of supernumerary hair cells induced by a Notch pathway inhibitor. Our findings highlight an important role of the STAT3 signaling during mouse cochlear hair cell differentiation and may have clinical implications for the recovery of hair cell loss-induced hearing impairment.
尽管 STAT3 信号被证明可以调节斑马鱼感觉细胞的分化和再生,但在哺乳动物耳蜗中,其确切作用仍不清楚。在这里,我们报告 STAT3 及其激活形式在小鼠耳蜗发育过程中特异性表达于毛细胞中。重要的是,条件性耳蜗中 Stat3 的缺失导致体内和体外毛细胞分化受到抑制。通过细胞命运分析,STAT3 信号的失活将细胞分裂模式从支持细胞的不对称分裂转变为对称分裂。此外,抑制 Notch 信号会刺激 STAT3 磷酸化,而抑制 STAT3 信号会减弱 Notch 通路抑制剂诱导的多余毛细胞的产生。我们的研究结果强调了 STAT3 信号在小鼠耳蜗毛细胞分化过程中的重要作用,这可能对恢复毛细胞缺失引起的听力障碍具有临床意义。