造血
寿命
血栓反应素
血栓反应蛋白1
生物
免疫学
细胞生物学
癌症研究
遗传学
血管生成
干细胞
进化生物学
金属蛋白酶
基质金属蛋白酶
作者
Pradeep Ramalingam,Michael Gutkin,Michael G. Poulos,Agatha Winiarski,Alex Smith,Cody Carter,Chelsea Doughty,Taylor Tillery,David Redmond,Ana G. Freire,Jason M. Butler
出处
期刊:Science immunology
[American Association for the Advancement of Science (AAAS)]
日期:2025-01-03
卷期号:10 (103)
标识
DOI:10.1126/sciimmunol.ads1556
摘要
Chronic low-grade inflammation observed in older adults, termed inflammaging, is a common feature underlying a multitude of aging-associated maladies including a decline in hematopoietic activity. However, whether suppression of inflammaging can preserve hematopoietic health span remains unclear, in part because of a lack of tools to measure inflammaging within hematopoietic stem cells (HSCs). Here, we identify thrombospondin-1 (Thbs1) as an essential regulator of inflammaging within HSCs. We describe a transcriptomics-based approach for measuring inflammaging within stem cells and demonstrate that deletion of Thbs1 is sufficient to prevent HSC inflammaging. Our results demonstrate that suppression of HSC inflammaging prevents aging-associated defects in hematopoietic activity including loss of HSC self-renewal, myeloid-biased HSC differentiation, and anemia. Our findings indicate that suppression of HSC inflammaging may also prolong overall systemic health span.
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