The immune landscape of murine skeletal muscle regeneration and aging
Age-related alterations in the immune system are starting to emerge as key contributors to impairments found in aged organs. A decline in regenerative capacity is a hallmark of tissue aging; however, the contribution of immune aging to regenerative failure is just starting to be explored. Here, we apply a strategy combining single-cell RNA sequencing with flow cytometry, histological analysis, and functional assays to perform a complete analysis of the immune environment of the aged regenerating skeletal muscle on a time course following injury with single-cell resolution. Our results reveal an unanticipated complexity and functional heterogeneity in immune populations within the skeletal muscle that have been regarded as homogeneous. Furthermore, we uncover a profound remodeling of both myeloid and lymphoid compartments in aging. These discoveries challenge established notions on immune regulation of skeletal muscle regeneration, providing a set of potential targets to improve skeletal muscle health and regenerative capacity in aging.
Authors
- Nuno L. Barbosa‐Morais (ORCID: https://orcid.org/0000-0002-1215-0538)
- Neuza S. Sousa (ORCID: https://orcid.org/0000-0002-3433-969X)
- Inês B. Martins (ORCID: https://orcid.org/0000-0002-7937-6697)
- Inês B. Antunes (ORCID: https://orcid.org/0000-0003-1094-3144)
- Margarida F. Brás
- Joana Neves (ORCID: https://orcid.org/0000-0002-1027-3489)
- Ana Catarina Sousa (ORCID: https://orcid.org/0000-0002-8800-2195)
- Pedro Sousa‐Victor (ORCID: https://orcid.org/0000-0002-6521-7839)
- Isabel A. Encarnação
- Tiago Costa (ORCID: https://orcid.org/0000-0002-9644-3193)
- Marta Bica (ORCID: https://orcid.org/0000-0002-8453-9550)
Institutions
- University of Lisbon (PT)
- Instituto Gulbenkian de Ciência (PT)
Publication Details
- Journal
- Cell Reports
- Published
- 2024-11-01
- DOI
- https://doi.org/10.1016/j.celrep.2024.114975
- Citations
- 15
- Primary Topic
- Exercise and Physiological Responses
- Type
- article
- Field-Weighted Citation Impact
- 3.75