Correlation Engine 2.0
Clear Search sequence regions

Sizes of these terms reflect their relevance to your search.

Hematopoietic stem cells (HSCs) are capable of entering the cell cycle to replenish the blood system in response to inflammatory cues; however, excessive proliferation in response to chronic inflammation can lead to either HSC attrition or expansion. The mechanism(s) that limit HSC proliferation and expansion triggered by inflammatory signals are poorly defined. Here, we show that long-term HSCs (HSCLT) rapidly repress protein synthesis and cell cycle genes following treatment with the proinflammatory cytokine interleukin (IL)-1. This gene program is associated with activation of the transcription factor PU.1 and direct PU.1 binding at repressed target genes. Notably, PU.1 is required to repress cell cycle and protein synthesis genes, and IL-1 exposure triggers aberrant protein synthesis and cell cycle activity in PU.1-deficient HSCs. These features are associated with expansion of phenotypic PU.1-deficient HSCs. Thus, we identify a PU.1-dependent mechanism triggered by innate immune stimulation that limits HSC proliferation and pool size. These findings provide insight into how HSCs maintain homeostasis during inflammatory stress. © 2021 Chavez et al.


James S Chavez, Jennifer L Rabe, Dirk Loeffler, Kelly C Higa, Giovanny Hernandez, Taylor S Mills, Nouraiz Ahmed, Rachel L Gessner, Zhonghe Ke, Beau M Idler, Katia E Niño, Hyunmin Kim, Jason R Myers, Brett M Stevens, Pavel Davizon-Castillo, Craig T Jordan, Hideaki Nakajima, John Ashton, Robert S Welner, Timm Schroeder, James DeGregori, Eric M Pietras. PU.1 enforces quiescence and limits hematopoietic stem cell expansion during inflammatory stress. The Journal of experimental medicine. 2021 Jun 07;218(6)

Expand section icon Mesh Tags

Expand section icon Substances

PMID: 33857288

View Full Text