Robust differentiation of human pluripotent stem cells into mural progenitor cells via transient activation of NKX3.1

Mural cells are central to vascular integrity and function. In this study, we demonstrate the innovative use of the transcription factor NKX3.1 to guide the differentiation of human induced pluripotent stem cells into mural progenitor cells (iMPCs). By transiently activating NKX3.1 in mesodermal intermediates, we developed a method that diverges from traditional growth factor-based differentiation techniques. This approach efficiently generates a robust iMPC population capable of maturing into diverse functional mural cell subtypes, including smooth muscle cells and pericytes. These iMPCs exhibit key mural cell functionalities such as contractility, deposition of extracellular matrix, and the ability to support endothelial cell-mediated vascular network formation in vivo. Our study not only underscores the fate-determining significance of NKX3.1 in mural cell differentiation but also highlights the therapeutic potential of these iMPCs. We envision these insights could pave the way for a broader use of iMPCs in vascular biology and regenerative medicine.

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Publication Details

Journal
Nature Communications
Published
2024-09-30
DOI
https://doi.org/10.1038/s41467-024-52678-8
Citations
12
Primary Topic
Pluripotent Stem Cells Research
Type
article
Field-Weighted Citation Impact
2.81

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article

Robust differentiation of human pluripotent stem cells into mural progenitor cells via transient activation of NKX3.1

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12 citations
Nature Communications
Pluripotent Stem Cells Research
2.81
article

Robust differentiation of human pluripotent stem cells into mural progenitor cells via transient activation of NKX3.1

Miao Cui, Yunhye Kim, Kaifu Chen, Minglin Ma, Yonglin Zhu, Daniel M. Tremmel, Juan M. Melero‐Martin, Liyan Gong, Allen Chilun Luo, Victoria Sofia Villarreal, Yadong Zhang, Kai Wang, Xi Wang, Ke Yuan, Ruei-Zeng Lin, Umji Lee
article en
12 citations

Abstract

Mural cells are central to vascular integrity and function. In this study, we demonstrate the innovative use of the transcription factor NKX3.1 to guide the differentiation of human induced pluripotent stem cells into mural progenitor cells (iMPCs). By transiently activating NKX3.1 in mesodermal intermediates, we developed a method that diverges from traditional growth factor-based differentiation techniques. This approach efficiently generates a robust iMPC population capable of maturing into diverse functional mural cell subtypes, including smooth muscle cells and pericytes. These iMPCs exhibit key mural cell functionalities such as contractility, deposition of extracellular matrix, and the ability to support endothelial cell-mediated vascular network formation in vivo. Our study not only underscores the fate-determining significance of NKX3.1 in mural cell differentiation but also highlights the therapeutic potential of these iMPCs. We envision these insights could pave the way for a broader use of iMPCs in vascular biology and regenerative medicine.

Nature CommunicationsVol. 15(1)
Boston Children's Hospital (US), Harvard University (US), Peking University (CN), Cornell University (US), Boston Children's Museum (US), Harvard Stem Cell Institute (US)
Harvard University, National Institutes of Health
Zero hunger
Openalex Percentile: Top 9%
Pluripotent Stem Cells Research
2.81
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