Inactivation of STAT3 Signaling Impairs Hair Cell Differentiation in the Developing Mouse Cochlea

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. Im...

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Main Authors: Qianqian Chen, Yizhou Quan, Naitao Wang, Chengying Xie, Zhongzhong Ji, Hao He, Renjie Chai, Huawei Li, Shankai Yin, Y. Eugene Chin, Xunbin Wei, Wei-Qiang Gao
Format: Article
Language:English
Published: Elsevier 2017-07-01
Series:Stem Cell Reports
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Online Access:http://www.sciencedirect.com/science/article/pii/S2213671117302382
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spelling doaj-0bec95e0bbe14eac8583b86cb81de9152020-11-24T21:36:04ZengElsevierStem Cell Reports2213-67112017-07-019123124610.1016/j.stemcr.2017.05.031Inactivation of STAT3 Signaling Impairs Hair Cell Differentiation in the Developing Mouse CochleaQianqian Chen0Yizhou Quan1Naitao Wang2Chengying Xie3Zhongzhong Ji4Hao He5Renjie Chai6Huawei Li7Shankai Yin8Y. Eugene Chin9Xunbin Wei10Wei-Qiang Gao11State 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, ChinaState 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, ChinaState 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, ChinaMed-X Research Institute & School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai 200030, ChinaState 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, ChinaMed-X Research Institute & School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai 200030, ChinaMOE Key Laboratory of Developmental Genes and Human Disease, Institute of Life Sciences, Southeast University, Nanjing 210096, ChinaOtorhinolaryngology Department of Affiliated Eye and ENT Hospital, State Key Laboratory of Medical Neurobiology, Fudan University, Shanghai 200031, ChinaThe Affiliated Six People's Hospital, Med-X Research Institute and School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai 200030, ChinaChina Key Laboratory of Stem Cell Biology, Institute of Health Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences-Shanghai Jiao Tong University School of Medicine, Shanghai 200031, ChinaState 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, ChinaState 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, ChinaAlthough 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.http://www.sciencedirect.com/science/article/pii/S2213671117302382STAT3 signalingNotch signalingsupporting cellhair cellcell fate specificationcell division mode
collection DOAJ
language English
format Article
sources DOAJ
author Qianqian Chen
Yizhou Quan
Naitao Wang
Chengying Xie
Zhongzhong Ji
Hao He
Renjie Chai
Huawei Li
Shankai Yin
Y. Eugene Chin
Xunbin Wei
Wei-Qiang Gao
spellingShingle Qianqian Chen
Yizhou Quan
Naitao Wang
Chengying Xie
Zhongzhong Ji
Hao He
Renjie Chai
Huawei Li
Shankai Yin
Y. Eugene Chin
Xunbin Wei
Wei-Qiang Gao
Inactivation of STAT3 Signaling Impairs Hair Cell Differentiation in the Developing Mouse Cochlea
Stem Cell Reports
STAT3 signaling
Notch signaling
supporting cell
hair cell
cell fate specification
cell division mode
author_facet Qianqian Chen
Yizhou Quan
Naitao Wang
Chengying Xie
Zhongzhong Ji
Hao He
Renjie Chai
Huawei Li
Shankai Yin
Y. Eugene Chin
Xunbin Wei
Wei-Qiang Gao
author_sort Qianqian Chen
title Inactivation of STAT3 Signaling Impairs Hair Cell Differentiation in the Developing Mouse Cochlea
title_short Inactivation of STAT3 Signaling Impairs Hair Cell Differentiation in the Developing Mouse Cochlea
title_full Inactivation of STAT3 Signaling Impairs Hair Cell Differentiation in the Developing Mouse Cochlea
title_fullStr Inactivation of STAT3 Signaling Impairs Hair Cell Differentiation in the Developing Mouse Cochlea
title_full_unstemmed Inactivation of STAT3 Signaling Impairs Hair Cell Differentiation in the Developing Mouse Cochlea
title_sort inactivation of stat3 signaling impairs hair cell differentiation in the developing mouse cochlea
publisher Elsevier
series Stem Cell Reports
issn 2213-6711
publishDate 2017-07-01
description 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.
topic STAT3 signaling
Notch signaling
supporting cell
hair cell
cell fate specification
cell division mode
url http://www.sciencedirect.com/science/article/pii/S2213671117302382
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