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Mesenchymal Stem Cells in Immune-Mediated Bone Marrow Failure Syndromes

机译:免疫介导的骨髓衰竭综合征的间充质干细胞

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Immune-mediated bone marrow failure syndromes (BMFS) are characterized by ineffective marrow haemopoiesis and subsequent peripheral cytopenias. Ineffective haemopoiesis is the result of a complex marrow deregulation including genetic, epigenetic, and immune-mediated alterations in haemopoietic stem/progenitor cells, as well as abnormal haemopoietic-to-stromal cell interactions, with abnormal release of haemopoietic growth factors, chemokines, and inhibitors. Mesenchymal stem/stromal cells (MSCs) and their progeny (i.e., osteoblasts, adipocytes, and reticular cells) are considered as key cellular components of the bone marrow haemopoietic niche. MSCs may interfere with, haemopoietic as well as immune regulation. Evidence suggests that bone marrow MSCs may be involved in immune-mediated BMFS underlying pathophysiology, harboring either native abnormalities and/or secondary defects, caused by exposure to activated marrow components. This review summarizes previous as well as more recent information related to the biologic/functional characteristics of bone marrow MSCs in myelodysplastic syndromes, acquired aplastic anemia, and chronic idiopathic neutropenia.
机译:免疫介导的骨髓衰竭综合征(BMFS)的特征是无效的骨髓造血和随后的外周血细胞减少。无效的造血是复杂的骨髓失调导致的,包括造血干/祖细胞的遗传,表观遗传和免疫介导的改变,以及造血与基质之间的异常相互作用,以及造血生长因子,趋化因子和抑制剂。间充质干/基质细胞(MSCs)及其子代(即成骨细胞,脂肪细胞和网状细胞)被认为是骨髓造血生境的关键细胞成分。 MSC可能干扰造血以及免疫调节。有证据表明,骨髓间充质干细胞可能参与了免疫介导的BMFS潜在的病理生理学,具有暴露于活化的骨髓成分引起的天然异常和/或继发性缺陷。这篇综述总结了以前和最近有关骨髓增生异常综合征,获得性再生障碍性贫血和慢性特发性中性粒细胞减少症的骨髓MSCs的生物学/功能特征的信息。

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