Identification of distinct non-myogenic skeletal-muscle-resident mesenchymal cell populations.
| dc.contributor.author | Leinroth, Abigail P | |
| dc.contributor.author | Mirando, Anthony J | |
| dc.contributor.author | Rouse, Douglas | |
| dc.contributor.author | Kobayahsi, Yoshihiko | |
| dc.contributor.author | Tata, Purushothama Rao | |
| dc.contributor.author | Rueckert, Helen E | |
| dc.contributor.author | Liao, Yihan | |
| dc.contributor.author | Long, Jason T | |
| dc.contributor.author | Chakkalakal, Joe V | |
| dc.contributor.author | Hilton, Matthew J | |
| dc.date.accessioned | 2023-10-01T13:41:03Z | |
| dc.date.available | 2023-10-01T13:41:03Z | |
| dc.date.issued | 2022-05 | |
| dc.date.updated | 2023-10-01T13:41:02Z | |
| dc.description.abstract | 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. | |
| dc.identifier | S2211-1247(22)00552-6 | |
| dc.identifier.issn | 2211-1247 | |
| dc.identifier.issn | 2211-1247 | |
| dc.identifier.uri | ||
| dc.language | eng | |
| dc.publisher | Elsevier BV | |
| dc.relation.ispartof | Cell reports | |
| dc.relation.isversionof | 10.1016/j.celrep.2022.110785 | |
| dc.subject | Muscle, Skeletal | |
| dc.subject | Animals | |
| dc.subject | Mice | |
| dc.subject | Cell Differentiation | |
| dc.subject | Muscle Development | |
| dc.subject | Adipogenesis | |
| dc.subject | Muscle Fibers, Skeletal | |
| dc.title | Identification of distinct non-myogenic skeletal-muscle-resident mesenchymal cell populations. | |
| dc.type | Journal article | |
| duke.contributor.orcid | Tata, Purushothama Rao|0000-0003-4837-0337 | |
| duke.contributor.orcid | Chakkalakal, Joe V|0000-0002-8440-7312 | |
| duke.contributor.orcid | Hilton, Matthew J|0000-0003-3165-267X | |
| pubs.begin-page | 110785 | |
| pubs.issue | 6 | |
| pubs.organisational-group | Duke | |
| pubs.organisational-group | School of Medicine | |
| pubs.organisational-group | Basic Science Departments | |
| pubs.organisational-group | Clinical Science Departments | |
| pubs.organisational-group | Institutes and Centers | |
| pubs.organisational-group | Cell Biology | |
| pubs.organisational-group | Medicine | |
| pubs.organisational-group | Orthopaedic Surgery | |
| pubs.organisational-group | Medicine, Pulmonary, Allergy, and Critical Care Medicine | |
| pubs.organisational-group | Duke Cancer Institute | |
| pubs.organisational-group | Regeneration Next Initiative | |
| pubs.publication-status | Published | |
| pubs.volume | 39 |
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