Young Kira, Borikar Sneha, Bell Rebecca, Kuffler Lauren, Philip Vivek, Trowbridge Jennifer J
The Jackson Laboratory for Mammalian Genetics, Bar Harbor, ME 04609.
The Jackson Laboratory for Mammalian Genetics, Bar Harbor, ME 04609
J Exp Med. 2016 Oct 17;213(11):2259-2267. doi: 10.1084/jem.20160168. Epub 2016 Oct 10.
Declining immune function with age is associated with reduced lymphoid output of hematopoietic stem cells (HSCs). Currently, there is poor understanding of changes with age in the heterogeneous multipotent progenitor (MPP) cell compartment, which is long lived and responsible for dynamically regulating output of mature hematopoietic cells. In this study, we observe an early and progressive loss of lymphoid-primed MPP cells (LMPP/MPP4) with aging, concomitant with expansion of HSCs. Transcriptome and in vitro functional analyses at the single-cell level reveal a concurrent increase in cycling of aging LMPP/MPP4 with loss of lymphoid priming and differentiation potential. Impaired lymphoid differentiation potential of aged LMPP/MPP4 is not rescued by transplantation into a young bone marrow microenvironment, demonstrating cell-autonomous changes in the MPP compartment with aging. These results pinpoint an age and cellular compartment to focus further interrogation of the drivers of lymphoid cell loss with aging.
免疫功能随年龄下降与造血干细胞(HSCs)的淋巴输出减少有关。目前,人们对异质性多能祖细胞(MPP)细胞区室随年龄的变化了解甚少,该细胞区室寿命长,负责动态调节成熟造血细胞的输出。在本研究中,我们观察到随着年龄增长,淋巴样启动的MPP细胞(LMPP/MPP4)早期且逐渐减少,同时造血干细胞数量增加。单细胞水平的转录组和体外功能分析显示,衰老的LMPP/MPP4细胞周期同时增加,伴有淋巴样启动和分化潜能丧失。将衰老的LMPP/MPP4移植到年轻的骨髓微环境中并不能挽救其受损的淋巴样分化潜能,这表明随着年龄增长,MPP区室存在细胞自主性变化。这些结果确定了一个年龄和细胞区室,以便进一步探究衰老导致淋巴细胞丢失的驱动因素。
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