| Literature DB >> 31474563 |
Stephen Li1, Dileep Karri1, Efrain Sanchez-Ortiz1, Priscilla Jaichander1, Rhonda Bassel-Duby1, Ning Liu2, Eric N Olson3.
Abstract
We previously identified a unique population of interstitial muscle progenitors, marked by expression of the Twist2 transcription factor, which fuses specifically to type IIb/x fast-twitch myofibers. Tw2+ progenitors are distinct from satellite cells, a muscle progenitor that expresses Pax7 and contributes to all myofiber types. Through RNA sequencing and immunofluorescence, we identify the membrane receptor, Nrp1, as a marker of Tw2+ cells but not Pax7+ cells. We also found that Sema3a, a chemorepellent ligand for Nrp1, is expressed by type I and IIa myofibers but not IIb myofibers. Using stripe migration assays, chimeric cell-cell fusion assays, and a Sema3a transgenic mouse model, we identify Sema3a-Nrp1 signaling as a major mechanism for Tw2+ cell fiber-type specificity. Our findings reveal an extracellular signaling mechanism whereby a cell-surface receptor for a chemorepellent confers specificity of intercellular fusion of a specific muscle progenitor with its target tissue.Entities:
Keywords: Twist2; chemorepulsion; fiber-type specificity; fusion; muscle stem cell; plexin; semaphorin; stripe assay
Mesh:
Substances:
Year: 2019 PMID: 31474563 PMCID: PMC6783380 DOI: 10.1016/j.devcel.2019.08.002
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270