Heme oxygenase‐1 deficiency triggers exhaustion of hematopoietic stem cells

While intrinsic changes in aging hematopoietic stem cells (HSCs) are well characterized, it remains unclear how extrinsic factors affect HSC aging. Here, we demonstrate that cells in the niche—endothelial cells (ECs) and CXCL12‐abundant reticular cells (CARs)—highly express the heme‐degrading enzyme, heme oxygenase 1 (HO‐1), but then decrease its expression with age. HO‐1‐deficient animals (HO‐1(−/−)) have altered numbers of ECs and CARs that produce less hematopoietic factors. HSCs co‐cultured in vitro with HO‐1(−/−) mesenchymal stromal cells expand, but have altered kinetic of growth and differentiation of derived colonies. HSCs from young HO‐1(−/−) animals have reduced quiescence and regenerative potential. Young HO‐1(−/−) HSCs exhibit features of premature exhaustion on the transcriptional and functional level. HO‐1(+/+) HSCs transplanted into HO‐1(−/−) recipients exhaust their regenerative potential early and do not reconstitute secondary recipients. In turn, transplantation of HO‐1(−/−) HSCs to the HO‐1(+/+) recipients recovers the regenerative potential of HO‐1(−/−) HSCs and reverses their transcriptional alterations. Thus, HSC‐extrinsic activity of HO‐1 prevents HSCs from premature exhaustion and may restore the function of aged HSCs.