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