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Obesity-driven disruption of haematopoiesis and the bone marrow niche.

机译:肥胖引起的血细胞生成和骨髓生境破坏。

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摘要

Obesity markedly increases susceptibility to a range of diseases and simultaneously undermines the viability and fate selection of haematopoietic stem cells (HSCs), and thus the kinetics of leukocyte production that is critical to innate and adaptive immunity. Considering that blood cell production and the differentiation of HSCs and their progeny is orchestrated, in part, by complex interacting signals emanating from the bone marrow microenvironment, it is not surprising that conditions that disturb bone marrow structure inevitably disrupt both the numbers and lineage-fates of these key blood cell progenitors. In addition to the increased adipose burden in visceral and subcutaneous compartments, obesity causes a marked increase in the size and number of adipocytes encroaching into the bone marrow space, almost certainly disturbing HSC interactions with neighbouring cells, which include osteoblasts, osteoclasts, mesenchymal cells and endothelial cells. As the global obesity pandemic grows, the short-term and long-term consequences of increased bone marrow adiposity on HSC lineage selection and immune function remain uncertain. This Review discusses the differentiation and function of haematopoietic cell populations, the principal physicochemical components of the bone marrow niche, and how this environment influences HSCs and haematopoiesis in general. The effect of adipocytes and adiposity on HSC and progenitor cell populations is also discussed, with the goal of understanding how obesity might compromise the core haematopoietic system.
机译:肥胖症显着增加了对多种疾病的敏感性,同时破坏了造血干细胞(HSC)的生存能力和命运选择,因此破坏了对先天和适应性免疫至关重要的白细胞产生动力学。考虑到血细胞的产生和HSCs及其后代的分化部分地是由骨髓微环境发出的复杂相互作用信号精心策划的,因此扰乱骨髓结构的条件不可避免地破坏了数量和血统命运,这并不奇怪。这些关键的血细胞祖细胞。肥胖不仅会增加内脏和皮下隔室的脂肪负担,而且还会导致进入骨髓空间的脂肪细胞的大小和数量显着增加,几乎可以肯定是干扰了HSC与包括成骨细胞,破骨细胞,间充质细胞和内皮细胞。随着全球肥胖大流行的加剧,骨髓肥胖增加对HSC谱系选择和免疫功能的短期和长期后果仍然不确定。这篇综述讨论了造血细胞群的分化和功能,骨髓生境的主要理化成分,以及这种环境通常如何影响HSC和造血作用。还讨论了脂肪细胞和肥胖对HSC和祖细胞群体的影响,目的是了解肥胖如何危害核心造血系统。

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