间质细胞
骨髓
造血
淋巴细胞生成
红细胞生成
生物
细胞生物学
干细胞
祖细胞
转化生长因子
癌症研究
免疫学
医学
内科学
贫血
作者
Simona Valletta,Alexander Thomas,Yiran Meng,Xiaojun Ren,Roy Drissen,Hilal Sengül,Cristina Di Genua,Claus Nerlov
标识
DOI:10.1038/s41467-020-17942-7
摘要
Hematopoietic ageing involves declining erythropoiesis and lymphopoiesis, leading to frequent anaemia and decreased adaptive immunity. How intrinsic changes to the hematopoietic stem cells (HSCs), an altered microenvironment and systemic factors contribute to this process is not fully understood. Here we use bone marrow stromal cells as sensors of age-associated changes to the bone marrow microenvironment, and observe up-regulation of IL-6 and TGFβ signalling-induced gene expression in aged bone marrow stroma. Inhibition of TGFβ signalling leads to reversal of age-associated HSC platelet lineage bias, increased generation of lymphoid progenitors and rebalanced HSC lineage output in transplantation assays. In contrast, decreased erythropoiesis is not an intrinsic property of aged HSCs, but associated with decreased levels and functionality of erythroid progenitor populations, defects ameliorated by TGFβ-receptor and IL-6 inhibition, respectively. These results show that both HSC-intrinsic and -extrinsic mechanisms are involved in age-associated hematopoietic decline, and identify therapeutic targets that promote their reversal.
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