IRF7 suppresses hematopoietic regeneration under stress via CXCR4. (9th December 2020)

• Record Type: Journal Article
• Authors: Chen, Ying-Ying; Liu, Yu-Feng; Liu, Yong-Dong; Deng, Xiao-Hui; Zhou, Jie
• Is Part Of: Stem cells. Volume 39:Number 2(2021)
• Page Start: 183
• Page End: 195
• Publication Date: 2020-12-09
• Subjects: CXCR4 -- hematopoietic stem and progenitor cells -- hematopoietic stress -- human umbilical cord blood -- interferon regulatory factor 7 -- regeneration; Cloning -- Periodicals; Clone cells -- Periodicals; Stem cells -- Periodicals; Cell Differentiation -- Periodicals; Cell Division -- Periodicals; Clone Cells -- Periodicals; Hematopoietic Stem Cells -- Periodicals; Stem Cells -- Periodicals; 571.84
• DOI: 10.1002/stem.3308
• Languages: English
• ISSNs: 1066-5099

Abstract

Abstract: Hematopoietic stem cells (HSCs) maintain quiescence under steady state; however, they are compelled to proliferate and expand to replenish the blood system under stress. The molecular basis underlying stress hematopoiesis remains to be fully understood. In this study, we reported that IRF7 represents an important regulator of stress hematopoiesis. Interferon regulatory factor 7 (IRF7) was dispensable for normal hematopoiesis, whereas its deficiency significantly enhanced hematopoietic stem and progenitor cells (HSPCs) regeneration and improved long-term repopulation of HSCs under stress. Mechanistic studies showed that CXCR4 was identified as a downstream target of IRF7. Overexpression of CXCR4 abrogated the enhanced proliferation and regeneration of IRF7-deficient HSPCs under stress. Similar results were obtained in HSCs from human umbilical cord blood. These observations demonstrated that IRF7 plays an important role in hematopoietic regeneration under stress. Abstract :