Transcription factor TEAD1 is essential for vascular development by promoting vascular smooth muscle differentiation

TEAD1 (TEA domain transcription factor 1), a transcription factor known for the functional output of Hippo signaling, is important for tumorigenesis. However, the role of TEAD1 in the development of vascular smooth muscle cell (VSMC) is unknown. To investigate cell-specific role of Tead1 , we genera...

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Veröffentlicht in:Cell death and differentiation 2019-12, Vol.26 (12), p.2790-2806
Hauptverfasser: Wen, Tong, Liu, Jinhua, He, Xiangqin, Dong, Kunzhe, Hu, Guoqing, Yu, Luyi, Yin, Qin, Osman, Islam, Peng, Jingtian, Zheng, Zeqi, Xin, Hongbo, Fulton, David, Du, Quansheng, Zhang, Wei, Zhou, Jiliang
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container_end_page 2806
container_issue 12
container_start_page 2790
container_title Cell death and differentiation
container_volume 26
creator Wen, Tong
Liu, Jinhua
He, Xiangqin
Dong, Kunzhe
Hu, Guoqing
Yu, Luyi
Yin, Qin
Osman, Islam
Peng, Jingtian
Zheng, Zeqi
Xin, Hongbo
Fulton, David
Du, Quansheng
Zhang, Wei
Zhou, Jiliang
description TEAD1 (TEA domain transcription factor 1), a transcription factor known for the functional output of Hippo signaling, is important for tumorigenesis. However, the role of TEAD1 in the development of vascular smooth muscle cell (VSMC) is unknown. To investigate cell-specific role of Tead1 , we generated cardiomyocyte (CMC) and VSMC-specific Tead1 knockout mice. We found CMC/VSMC-specific deletion of Tead1 led to embryonic lethality by E14.5 in mice due to hypoplastic cardiac and vascular walls, as a result of impaired CMC and VSMC proliferation. Whole transcriptome analysis revealed that deletion of Tead1 in CMCs/VSMCs downregulated expression of muscle contractile genes and key transcription factors including Pitx2c and myocardin. In vitro studies demonstrated that PITX2c and myocardin rescued TEAD1-dependent defects in VSMC differentiation. We further identified Pitx2c as a novel transcriptional target of TEAD1, and PITX2c exhibited functional synergy with myocardin by directly interacting with myocardin, leading to augment the differentiation of VSMC. In summary, our study reveals a critical role of Tead1 in cardiovascular development in mice, but also identifies a novel regulatory mechanism, whereby Tead1 functions upstream of the genetic regulatory hierarchy for establishing smooth muscle contractile phenotype.
doi_str_mv 10.1038/s41418-019-0335-4
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However, the role of TEAD1 in the development of vascular smooth muscle cell (VSMC) is unknown. To investigate cell-specific role of Tead1 , we generated cardiomyocyte (CMC) and VSMC-specific Tead1 knockout mice. We found CMC/VSMC-specific deletion of Tead1 led to embryonic lethality by E14.5 in mice due to hypoplastic cardiac and vascular walls, as a result of impaired CMC and VSMC proliferation. Whole transcriptome analysis revealed that deletion of Tead1 in CMCs/VSMCs downregulated expression of muscle contractile genes and key transcription factors including Pitx2c and myocardin. In vitro studies demonstrated that PITX2c and myocardin rescued TEAD1-dependent defects in VSMC differentiation. We further identified Pitx2c as a novel transcriptional target of TEAD1, and PITX2c exhibited functional synergy with myocardin by directly interacting with myocardin, leading to augment the differentiation of VSMC. 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However, the role of TEAD1 in the development of vascular smooth muscle cell (VSMC) is unknown. To investigate cell-specific role of Tead1 , we generated cardiomyocyte (CMC) and VSMC-specific Tead1 knockout mice. We found CMC/VSMC-specific deletion of Tead1 led to embryonic lethality by E14.5 in mice due to hypoplastic cardiac and vascular walls, as a result of impaired CMC and VSMC proliferation. Whole transcriptome analysis revealed that deletion of Tead1 in CMCs/VSMCs downregulated expression of muscle contractile genes and key transcription factors including Pitx2c and myocardin. In vitro studies demonstrated that PITX2c and myocardin rescued TEAD1-dependent defects in VSMC differentiation. We further identified Pitx2c as a novel transcriptional target of TEAD1, and PITX2c exhibited functional synergy with myocardin by directly interacting with myocardin, leading to augment the differentiation of VSMC. 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subjects 13/44
14/19
14/35
14/63
631/208/135
631/208/200
64/60
96/109
96/31
Animals
Apoptosis
Biochemistry
Biomedical and Life Sciences
Cardiomyocytes
Cell Biology
Cell Cycle Analysis
Cell Differentiation - physiology
Clonal deletion
DNA-Binding Proteins - genetics
DNA-Binding Proteins - metabolism
Embryos
Female
Gene Deletion
Gene expression
Lethality
Life Sciences
Male
Mice
Mice, Knockout
Muscle contraction
Muscle, Smooth, Vascular - cytology
Muscle, Smooth, Vascular - growth & development
Muscle, Smooth, Vascular - metabolism
Phenotypes
Smooth muscle
Stem Cells
TEA Domain Transcription Factors
Transcription factors
Transcription Factors - genetics
Transcription Factors - metabolism
Tumorigenesis
title Transcription factor TEAD1 is essential for vascular development by promoting vascular smooth muscle differentiation
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