Division of Endocrinology, Diabetes and Metabolism, Mayo Clinic, Rochester, MN, USA.
Robert and Arlene Kogod Center On Aging, Mayo Clinic, Rochester, MN, USA.
Curr Osteoporos Rep. 2023 Dec;21(6):771-778. doi: 10.1007/s11914-023-00820-8. Epub 2023 Sep 9.
The purpose of this review is to discuss the role of macrophages in the regulation of skeletal health with age, particularly in regard to both established and unexplored mechanisms in driving inflammation and senescence.
A multitude of research has uncovered mechanisms of intrinsic aging in macrophages, detrimental factors released by these immune cells, and crosstalk from senescent mesenchymal cell types, which altogether drive age-related bone loss. Furthermore, bone marrow macrophages were recently proposed to be responsible for the megakaryocytic shift during aging and overall maintenance of the hematopoietic niche. Studies on extra-skeletal macrophages have shed light on possible conserved mechanisms within bone and highlight the importance of these cells in systemic aging. Macrophages are a critically important cell type in maintaining skeletal homeostasis with age. New discoveries in this area are of utmost importance in fully understanding the pathogenesis of osteoporosis in aged individuals.
本文讨论了巨噬细胞在骨骼健康随年龄变化中的作用,尤其讨论了驱动炎症和衰老的既定和未探索机制。
大量研究揭示了巨噬细胞内在衰老的机制、这些免疫细胞释放的有害因子,以及衰老间充质细胞类型的串扰,这些共同导致了与年龄相关的骨丢失。此外,最近有研究提出骨髓巨噬细胞负责衰老过程中的巨核细胞转移和造血龛的整体维持。对骨骼外巨噬细胞的研究揭示了骨骼中可能存在的保守机制,并强调了这些细胞在全身衰老中的重要性。巨噬细胞是维持骨骼内稳态的关键细胞类型。该领域的新发现对于充分理解老年个体骨质疏松症的发病机制至关重要。