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LepR+ 巢细胞衍生的 AREG 在 DNA 修复缺陷和衰老条件下损害造血干细胞的维持。

LepR+ niche cell-derived AREG compromises hematopoietic stem cell maintenance under conditions of DNA repair deficiency and aging.

机构信息

Division of Hematology and Oncology, University of Pittsburgh School of Medicine, Pittsburgh, PA.

Genome Stability Program, UPMC Hillman Cancer Center, Pittsburgh, PA.

出版信息

Blood. 2023 Nov 2;142(18):1529-1542. doi: 10.1182/blood.2022018212.

Abstract

The cross talk between extrinsic niche-derived and intrinsic hematopoietic stem cell (HSC) factors controlling HSC maintenance remains elusive. Here, we demonstrated that amphiregulin (AREG) from bone marrow (BM) leptin receptor (LepR+) niche cells is an important factor that mediates the cross talk between the BM niche and HSCs in stem cell maintenance. Mice deficient of the DNA repair gene Brca2, specifically in LepR+ cells (LepR-Cre;Brca2fl/fl), exhibited increased frequencies of total and myeloid-biased HSCs. Furthermore, HSCs from LepR-Cre;Brca2fl/fl mice showed compromised repopulation, increased expansion of donor-derived, myeloid-biased HSCs, and increased myeloid output. Brca2-deficient BM LepR+ cells exhibited persistent DNA damage-inducible overproduction of AREG. Ex vivo treatment of wild-type HSCs or systemic treatment of C57BL/6 mice with recombinant AREG impaired repopulation, leading to HSC exhaustion. Conversely, inhibition of AREG by an anti-AREG-neutralizing antibody or deletion of the Areg gene in LepR-Cre;Brca2fl/fl mice rescued HSC defects caused by AREG. Mechanistically, AREG activated the phosphoinositide 3-kinases (PI3K)/AKT/mammalian target of rapamycin (mTOR) pathway, promoted HSC cycling, and compromised HSC quiescence. Finally, we demonstrated that BM LepR+ niche cells from other DNA repair-deficient and aged mice also showed persistent DNA damage-associated overexpression of AREG, which exerts similar negative effects on HSC maintenance. Therefore, we identified an important factor that regulates HSCs function under conditions of DNA repair deficiency and aging.

摘要

外源性龛衍生和内源性造血干细胞 (HSC) 因子之间的串扰控制 HSC 维持仍然难以捉摸。在这里,我们证明了骨髓 (BM) 瘦素受体 (LepR+) 龛细胞中的表皮生长因子 (AREG) 是一种重要的因子,可介导 BM 龛与 HSC 之间在干细胞维持中的串扰。特异性缺失 DNA 修复基因 Brca2 的 LepR+ 细胞(LepR-Cre;Brca2fl/fl)的小鼠表现出总 HSC 和偏骨髓 HSC 的频率增加。此外,LepR-Cre;Brca2fl/fl 小鼠的 HSCs 表现出受损的重编程能力、供体衍生的偏骨髓 HSC 的过度扩增以及髓系输出增加。Brca2 缺陷的 BM LepR+ 细胞表现出持续的 DNA 损伤诱导的 AREG 过度产生。野生型 HSCs 的体外处理或重组 AREG 的全身治疗会损害重编程能力,导致 HSC 衰竭。相反,用抗 AREG 中和抗体抑制 AREG 或在 LepR-Cre;Brca2fl/fl 小鼠中缺失 Areg 基因可挽救 AREG 引起的 HSC 缺陷。从机制上讲,AREG 激活了磷脂酰肌醇 3-激酶 (PI3K)/AKT/雷帕霉素靶蛋白 (mTOR) 通路,促进了 HSC 循环,并损害了 HSC 的静止状态。最后,我们证明其他 DNA 修复缺陷和衰老小鼠的 BM LepR+ 龛细胞也表现出与持续的 DNA 损伤相关的 AREG 过度表达,这对 HSC 维持产生类似的负面影响。因此,我们确定了一种在 DNA 修复缺陷和衰老条件下调节 HSCs 功能的重要因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b15/10656728/47b5fa294677/BLOOD_BLD-2022-018212-ga1.jpg

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