Ambrosi Thomas H, Scialdone Antonio, Graja Antonia, Gohlke Sabrina, Jank Anne-Marie, Bocian Carla, Woelk Lena, Fan Hua, Logan Darren W, Schürmann Annette, Saraiva Luis R, Schulz Tim J
German Institute of Human Nutrition Potsdam-Rehbrücke, 14558 Nuthetal, Germany.
Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton-Cambridge CB10 1SA, UK; European Bioinformatics Institute (EMBL-EBI), European Molecular Biology Laboratory, Wellcome Genome Campus, Hinxton-Cambridge CB10 1SD, UK.
Cell Stem Cell. 2017 Jun 1;20(6):771-784.e6. doi: 10.1016/j.stem.2017.02.009. Epub 2017 Mar 16.
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.
衰老和肥胖会导致骨髓腔内异位脂肪细胞积聚。这一过程被认为会损害成骨和造血再生。在此,我们明确了骨骼中脂肪生成和成骨谱系的细胞特性。衰老会损害成骨谱系,而高脂饮食喂养会激活脂肪生成谱系的扩张,这种效应在老年动物中会显著增强。我们进一步描述了一个具有干细胞样特征的间充质亚群,它可产生这两种谱系,同时通过在致死性照射后促进竞争性再增殖,作为造血微环境的主要成分发挥作用。相反,定向分化为脂肪细胞谱系的骨驻留细胞会抑制造血和骨愈合,这可能是通过产生过量的二肽基肽酶4实现的,该蛋白酶是糖尿病治疗的靶点。这些研究明确了骨驻留脂肪细胞谱系的分子特性,并确定了其与年龄相关的骨骼和造血再生功能障碍有关。