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Identification of distinct non-myogenic skeletal-muscle-resident mesenchymal cell populations.
Leinroth, Abigail P; Mirando, Anthony J; Rouse, Douglas; Kobayahsi, Yoshihiko; Tata, Purushothama Rao; Rueckert, Helen E; Liao, Yihan; Long, Jason T; Chakkalakal, Joe V; Hilton, Matthew J.
Affiliation
  • Leinroth AP; Department of Cell Biology, Duke University School of Medicine, Durham, NC 27708, USA.
  • Mirando AJ; Department of Orthopaedic Surgery, Duke University School of Medicine, Durham, NC 27708, USA.
  • Rouse D; Division of Laboratory Animal Resources, Duke University School of Medicine, Durham, NC 27708, USA.
  • Kobayahsi Y; Department of Cell Biology, Duke University School of Medicine, Durham, NC 27708, USA.
  • Tata PR; Department of Cell Biology, Duke University School of Medicine, Durham, NC 27708, USA.
  • Rueckert HE; Department of Cell Biology, Duke University School of Medicine, Durham, NC 27708, USA.
  • Liao Y; Department of Pharmacology and Cancer Biology, Duke University School of Medicine, Durham, NC 27708, USA.
  • Long JT; Department of Cell Biology, Duke University School of Medicine, Durham, NC 27708, USA.
  • Chakkalakal JV; Department of Orthopaedic Surgery, Duke University School of Medicine, Durham, NC 27708, USA.
  • Hilton MJ; Department of Cell Biology, Duke University School of Medicine, Durham, NC 27708, USA; Department of Orthopaedic Surgery, Duke University School of Medicine, Durham, NC 27708, USA. Electronic address: matthew.hilton@duke.edu.
Cell Rep ; 39(6): 110785, 2022 05 10.
Article in En | MEDLINE | ID: mdl-35545045
Mesenchymal progenitors of the lateral plate mesoderm give rise to various cell fates within limbs, including a heterogeneous group of muscle-resident mesenchymal cells. Often described as fibro-adipogenic progenitors, these cells are key players in muscle development, disease, and regeneration. To further define this cell population(s), we perform lineage/reporter analysis, flow cytometry, single-cell RNA sequencing, immunofluorescent staining, and differentiation assays on normal and injured murine muscles. Here we identify six distinct Pdgfra+ non-myogenic muscle-resident mesenchymal cell populations that fit within a bipartite differentiation trajectory from a common progenitor. One branch of the trajectory gives rise to two populations of immune-responsive mesenchymal cells with strong adipogenic potential and the capability to respond to acute and chronic muscle injury, whereas the alternative branch contains two cell populations with limited adipogenic capacity and inherent mineralizing capabilities; one of the populations displays a unique neuromuscular junction association and an ability to respond to nerve injury.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Muscle, Skeletal / Muscle Development Type of study: Diagnostic_studies Limits: Animals Language: En Journal: Cell Rep Year: 2022 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Muscle, Skeletal / Muscle Development Type of study: Diagnostic_studies Limits: Animals Language: En Journal: Cell Rep Year: 2022 Document type: Article Affiliation country: United States Country of publication: United States