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Bone marrow Adipoq-lineage progenitors are a major cellular source of M-CSF that dominates bone marrow macrophage development, osteoclastogenesis, and bone mass.
Inoue, Kazuki; Qin, Yongli; Xia, Yuhan; Han, Jie; Yuan, Ruoxi; Sun, Jun; Xu, Ren; Jiang, Jean X; Greenblatt, Matthew B; Zhao, Baohong.
  • Inoue K; Arthritis and Tissue Degeneration Program and David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, United States.
  • Qin Y; Department of Medicine, Weill Cornell Medical College, New York, United States.
  • Xia Y; Arthritis and Tissue Degeneration Program and David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, United States.
  • Han J; Department of Medicine, Weill Cornell Medical College, New York, United States.
  • Yuan R; Arthritis and Tissue Degeneration Program and David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, United States.
  • Sun J; Department of Medicine, Weill Cornell Medical College, New York, United States.
  • Xu R; The first Affiliated Hospital of Xiamen University-ICMRS Collaborating Center for Skeletal Stem Cells, State Key Laboratory of Cellular Stress Biology, Faculty of Medicine and Life Sciences, Fujian Provincial Key Laboratory of Organ and Tissue Regeneration, School of Medicine, Xiamen University, Xia
  • Jiang JX; Arthritis and Tissue Degeneration Program and David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, United States.
  • Greenblatt MB; Department of Medicine, Weill Cornell Medical College, New York, United States.
  • Zhao B; Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, United States.
Elife ; 122023 02 13.
Article en En | MEDLINE | ID: mdl-36779851
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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Osteogénesis / Factor Estimulante de Colonias de Macrófagos Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Osteogénesis / Factor Estimulante de Colonias de Macrófagos Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Año: 2023 Tipo del documento: Article