Heterogeneous origins and functions of mouse skeletal muscle-resident macrophages.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
25 08 2020
Historique:
pubmed: 17 8 2020
medline: 29 10 2020
entrez: 16 8 2020
Statut: ppublish

Résumé

Tissue-resident macrophages can originate from embryonic or adult hematopoiesis. They play important roles in a wide range of biological processes including tissue remodeling during organogenesis, organ homeostasis, repair following injury, and immune response to pathogens. Although the origins and tissue-specific functions of resident macrophages have been extensively studied in many other tissues, they are not well characterized in skeletal muscle. In the present study, we have characterized the ontogeny of skeletal muscle-resident macrophages by lineage tracing and bone marrow transplant experiments. We demonstrate that skeletal muscle-resident macrophages originate from both embryonic hematopoietic progenitors located within the yolk sac and fetal liver as well as definitive hematopoietic stem cells located within the bone marrow of adult mice. Single-cell-based transcriptome analyses revealed that skeletal muscle-resident macrophages are distinctive from resident macrophages in other tissues as they express a distinct complement of transcription factors and are composed of functionally diverse subsets correlating to their origins. Functionally, skeletal muscle-resident macrophages appear to maintain tissue homeostasis and promote muscle growth and regeneration.

Identifiants

pubmed: 32796104
pii: 1915950117
doi: 10.1073/pnas.1915950117
pmc: PMC7456122
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

20729-20740

Subventions

Organisme : NIAMS NIH HHS
ID : R01 AR074428
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL138466
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL139714
Pays : United States
Organisme : NIDDK NIH HHS
ID : U24 DK112331
Pays : United States

Déclaration de conflit d'intérêts

The authors declare no competing interest.

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Auteurs

Xingyu Wang (X)

Department of Neurology, Boston University School of Medicine, Boston, MA 02118.

Adwait Amod Sathe (AA)

Eugene McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, TX 75390.

Gregory R Smith (GR)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY 10029.

Frederique Ruf-Zamojski (F)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY 10029.

Venugopalan Nair (V)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY 10029.

Kory J Lavine (KJ)

Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110.

Chao Xing (C)

Eugene McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, TX 75390.

Stuart C Sealfon (SC)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY 10029.

Lan Zhou (L)

Department of Neurology, Boston University School of Medicine, Boston, MA 02118; lanzhou@bu.edu.

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Classifications MeSH