| Literature DB >> 33482080 |
Xia Han1, Jifan Feng1, Tingwei Guo1, Yong-Hwee Eddie Loh2, Yuan Yuan1, Thach-Vu Ho1, Courtney Kyeong Cho1, Jingyuan Li1, Junjun Jing1, Eva Janeckova1, Jinzhi He1, Fei Pei1, Jing Bi1, Brian Song1, Yang Chai1.
Abstract
Cranial neural crest (CNC) cells give rise to bone, cartilage, tendons, and ligaments of the vertebrate craniofacial musculoskeletal complex, as well as regulate mesoderm-derived craniofacial muscle development through cell-cell interactions. Using the mouse soft palate as a model, we performed an unbiased single-cell RNA-seq analysis to investigate the heterogeneity and lineage commitment of CNC derivatives during craniofacial muscle development. We show that Runx2, a known osteogenic regulator, is expressed in the CNC-derived perimysial and progenitor populations. Loss of Runx2 in CNC-derivatives results in reduced expression of perimysial markers (Aldh1a2 and Hic1) as well as soft palate muscle defects in Osr2-Cre;Runx2fl/fl mice. We further reveal that Runx2 maintains perimysial marker expression through suppressing Twist1, and that myogenesis is restored in Osr2-Cre;Runx2fl/fl;Twist1fl/+ mice. Collectively, our findings highlight the roles of Runx2, Twist1, and their interaction in regulating the fate of CNC-derived cells as they guide craniofacial muscle development through cell-cell interactions.Entities:
Keywords: Runx2; cell-cell interaction; cleft palate; cranial neural crest cells; developmental biology; mouse; muscle development
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Year: 2021 PMID: 33482080 PMCID: PMC7826157 DOI: 10.7554/eLife.62387
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140