GIMM - Gulbenkian Institute for Molecular Medicine, 1649-035 Lisbon, Portugal; Faculdade de Medicina, Universidade de Lisboa, 1649-028 Lisbon, Portugal.
GIMM - Gulbenkian Institute for Molecular Medicine, 1649-035 Lisbon, Portugal.
Cell Rep. 2024 Nov 26;43(11):114975. doi: 10.1016/j.celrep.2024.114975. Epub 2024 Nov 15.
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.
随着年龄相关的免疫系统改变开始成为导致老年器官功能障碍的关键因素,再生能力的下降是组织衰老的一个标志;然而,免疫衰老对再生衰竭的贡献才刚刚开始被探索。在这里,我们应用了一种结合单细胞 RNA 测序和流式细胞术、组织学分析和功能测定的策略,以单细胞分辨率在损伤后对衰老再生骨骼肌的免疫环境进行全面分析。我们的结果揭示了在骨骼肌中被认为是同质的免疫群体中出乎意料的复杂性和功能异质性。此外,我们还揭示了衰老过程中骨髓和淋巴器官的深刻重塑。这些发现挑战了关于免疫调节骨骼肌再生的既定观念,为改善衰老时骨骼肌健康和再生能力提供了一系列潜在的靶点。