Bone marrow Adipoq-lineage progenitors are a major cellular source of M-CSF that dominates bone marrow macrophage development, osteoclastogenesis, and bone mass.

TitleBone marrow Adipoq-lineage progenitors are a major cellular source of M-CSF that dominates bone marrow macrophage development, osteoclastogenesis, and bone mass.
Publication TypeJournal Article
Year of Publication2023
AuthorsInoue K, Qin Y, Xia Y, Han J, Yuan R, Sun J, Xu R, Jiang JX, Greenblatt MB, Zhao B
JournalElife
Volume12
Date Published2023 Feb 13
ISSN2050-084X
KeywordsAdiponectin, Animals, Bone Marrow, Bone Marrow Cells, Cell Differentiation, Humans, Macrophage Colony-Stimulating Factor, Macrophages, Mice, Mice, Inbred C57BL, Osteoclasts, Osteogenesis
Abstract

M-CSF is a critical growth factor for myeloid lineage cells, including monocytes, macrophages, and osteoclasts. Tissue-resident macrophages in most organs rely on local M-CSF. However, it is unclear what specific cells in the bone marrow produce M-CSF to maintain myeloid homeostasis. Here, we found that Adipoq-lineage progenitors but not mature adipocytes in bone marrow or in peripheral adipose tissue, are a major cellular source of M-CSF, with these Adipoq-lineage progenitors producing M-CSF at levels much higher than those produced by osteoblast lineage cells. The Adipoq-lineage progenitors with high CSF1 expression also exist in human bone marrow. Deficiency of M-CSF in bone marrow Adipoq-lineage progenitors drastically reduces the generation of bone marrow macrophages and osteoclasts, leading to severe osteopetrosis in mice. Furthermore, the osteoporosis in ovariectomized mice can be significantly alleviated by the absence of M-CSF in bone marrow Adipoq-lineage progenitors. Our findings identify bone marrow Adipoq-lineage progenitors as a major cellular source of M-CSF in bone marrow and reveal their crucial contribution to bone marrow macrophage development, osteoclastogenesis, bone homeostasis, and pathological bone loss.

DOI10.7554/eLife.82118
Alternate JournalElife
PubMed ID36779851
PubMed Central IDPMC10005769
Grant ListR01 AR071463 / AR / NIAMS NIH HHS / United States
R01 AR068970 / AR / NIAMS NIH HHS / United States
AR068970 / NH / NIH HHS / United States
AG045040 / NH / NIH HHS / United States
AR075585 / NH / NIH HHS / United States
AR071463 / NH / NIH HHS / United States
AR078212 / NH / NIH HHS / United States
R01 AR078212 / AR / NIAMS NIH HHS / United States
Related Faculty: 
Matthew B. Greenblatt, M.D., Ph.D.

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