生物
骨髓
造血
再生(生物学)
干细胞
细胞生物学
间充质干细胞
脂肪生成
免疫学
内分泌学
造血干细胞
作者
Thomas H. Ambrosi,Antonio Scialdone,Antonia Graja,Sabrina Gohlke,Anne‐Marie Jank,Carla Bocian,Lena Woelk,Hua Fan,Darren W. Logan,Annette Schürmann,Luís R. Saraiva,Tim J. Schulz
出处
期刊:Cell Stem Cell
[Elsevier BV]
日期:2017-03-16
卷期号:20 (6): 771-784.e6
被引量:701
标识
DOI:10.1016/j.stem.2017.02.009
摘要
Aging and obesity induce ectopic adipocyte accumulation in bone marrow cavities. This process is thought to impair osteogenic and hematopoietic regeneration. Here we specify the cellular identities of the adipogenic and osteogenic lineages of the bone. While aging impairs the osteogenic lineage, high-fat diet feeding activates expansion of the adipogenic lineage, an effect that is significantly enhanced in aged animals. We further describe a mesenchymal sub-population with stem cell-like characteristics that gives rise to both lineages and, at the same time, acts as a principal component of the hematopoietic niche by promoting competitive repopulation following lethal irradiation. Conversely, bone-resident cells committed to the adipocytic lineage inhibit hematopoiesis and bone healing, potentially by producing excessive amounts of Dipeptidyl peptidase-4, a protease that is a target of diabetes therapies. These studies delineate the molecular identity of the bone-resident adipocytic lineage, and they establish its involvement in age-dependent dysfunction of bone and hematopoietic regeneration.
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