van den Berg Susan M, Seijkens Tom T P, Kusters Pascal J H, Beckers Linda, den Toom Myrthe, Smeets Esther, Levels Johannes, de Winther Menno P J, Lutgens Esther
Department of Medical Biochemistry, Subdivision of Experimental Vascular Biology, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands;
Department of Experimental Vascular Medicine, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands; and.
FASEB J. 2016 May;30(5):1779-88. doi: 10.1096/fj.201500175. Epub 2016 Jan 26.
Obesity is associated with chronic low-grade inflammation, characterized by leukocytosis and inflammation in the adipose tissue. Continuous activation of the immune system is a stressor for hematopoietic stem and progenitor cells (HSPCs) in the bone marrow (BM). Here we studied how diet-induced obesity (DIO) affects HSPC population dynamics in the BM. Eight groups of age-matched C57Bl/6 mice received a high-fat diet (45% kilocalories from fat) ranging from 1 d up to 18 wk. The obesogenic diet caused decreased proliferation of lineage(-)Sca-1(+)c-Kit(+) (LSK) cells in the BM and a general suppression of progenitor cell populations including common lymphoid progenitors and common myeloid progenitors. Within the LSK population, DIO induced a shift in stem cells that are capable of self-renewal toward maturing multipotent progenitor cells. The higher differentiation potential resulted in increased lymphoid and myeloid ex vivo colony-forming capacity. In a competitive BM transplantation, BM from obese animals showed impaired multilineage reconstitution when transplanted into chow-fed mice. Our data demonstrate that obesity stimulates the differentiation and reduces proliferation of HSPCs in the BM, leading to a decreased HSPC population. This implies that the effects of obesity on HSPCs hampers proper functioning of the immune system.-Van den Berg, S. M., Seijkens, T. T. P., Kusters, P. J. H., Beckers, L., den Toom, M., Smeets, E., Levels, J., de Winther, M. P. J., Lutgens, E. Diet-induced obesity in mice diminishes hematopoietic stem and progenitor cells in the bone marrow.
肥胖与慢性低度炎症相关,其特征为白细胞增多和脂肪组织炎症。免疫系统的持续激活是骨髓中造血干细胞和祖细胞(HSPCs)的应激源。在此,我们研究了饮食诱导的肥胖(DIO)如何影响骨髓中HSPC群体动态。八组年龄匹配的C57Bl/6小鼠接受了为期1天至18周的高脂饮食(45%千卡来自脂肪)。致肥胖饮食导致骨髓中谱系(-)Sca-1(+)c-Kit(+)(LSK)细胞增殖减少,并对包括普通淋巴祖细胞和普通髓系祖细胞在内的祖细胞群体产生普遍抑制。在LSK群体中,DIO诱导能够自我更新的干细胞向成熟的多能祖细胞转变。更高的分化潜能导致体外淋巴样和髓样集落形成能力增加。在竞争性骨髓移植中,肥胖动物的骨髓移植到正常饮食小鼠体内时,多谱系重建受损。我们的数据表明,肥胖刺激骨髓中HSPCs的分化并减少其增殖,导致HSPC群体减少。这意味着肥胖对HSPCs的影响会妨碍免疫系统的正常功能。——范登伯格,S.M.,塞伊肯斯,T.T.P.,库斯特斯,P.J.H.,贝克斯,L.,登图姆,M.,斯米茨,E.,莱弗尔斯,J.,德温特,M.P.J.,卢特根斯,E. 小鼠饮食诱导的肥胖会减少骨髓中的造血干细胞和祖细胞