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重复 DNA 元件的转录本发出信号,阻止造血干细胞的吞噬作用。

Transcripts of repetitive DNA elements signal to block phagocytosis of hematopoietic stem cells.

机构信息

Howard Hughes Medical Institute, Boston Children's Hospital Boston, MA, USA.

Harvard Stem Cell Institute, Stem Cell and Regenerative Biology Department, Harvard University, Cambridge, MA, USA.

出版信息

Science. 2024 Sep 13;385(6714):eadn1629. doi: 10.1126/science.adn1629.

Abstract

Macrophages maintain hematopoietic stem cell (HSC) quality by assessing cell surface Calreticulin (Calr), an "eat-me" signal induced by reactive oxygen species (ROS). Using zebrafish genetics, we identified Beta-2-microglobulin (B2m) as a crucial "don't eat-me" signal on blood stem cells. A chemical screen revealed inducers of surface Calr that promoted HSC proliferation without triggering ROS or macrophage clearance. Whole-genome CRISPR-Cas9 screening showed that Toll-like receptor 3 (Tlr3) signaling regulated expression. Targeting or reduced the HSC clonality. Elevated B2m levels correlated with high expression of repetitive element (RE) transcripts. Overall, our data suggest that RE-associated double-stranded RNA could interact with TLR3 to stimulate surface expression of B2m on hematopoietic stem and progenitor cells. These findings suggest that the balance of Calr and B2m regulates macrophage-HSC interactions and defines hematopoietic clonality.

摘要

巨噬细胞通过评估细胞表面钙网蛋白(Calr)来维持造血干细胞(HSC)的质量,Calr 是一种由活性氧(ROS)诱导的“吃我”信号。利用斑马鱼遗传学,我们确定β-2-微球蛋白(B2m)是血液干细胞上的一个关键“别吃我”信号。化学筛选揭示了表面 Calr 的诱导剂,这些诱导剂促进了 HSC 的增殖,而不会引发 ROS 或巨噬细胞清除。全基因组 CRISPR-Cas9 筛选表明 Toll 样受体 3(Tlr3)信号调节 表达。靶向 或 减少了 HSC 的克隆性。B2m 水平的升高与重复元件(RE)转录本的高表达相关。总的来说,我们的数据表明,RE 相关的双链 RNA 可以与 TLR3 相互作用,刺激造血干细胞和祖细胞表面 B2m 的表达。这些发现表明,Calr 和 B2m 的平衡调节巨噬细胞-HSC 相互作用并定义造血克隆性。

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