Haematopoietic stem cells

Haematopoietic stem cells (HSCs) exhibit considerable cell-intrinsic changes with age. Here the authors demonstrate that differentially accessible regions in aged HSC chromatin are enriched for stress-responsive enhancers and act as an epigenetic hub to augment transcriptional responses of aged HSCs to external stimuli.

The transcription factors, Runx1 and Runx2 are critical embryonically for generation of HSCs and osteoblasts, respectively. Here the authors show that adult mice lacking Runx1 and Runx2 in HSC-supporting CAR cells displayed an increase in fibrosis with reduced HSCs in bone marrow.

A brief, ex vivo incubation of human G-CSF-mobilized peripheral blood grafts with multimerized Fas-Ligand (CD95L), using a closed automated cell processing system, significantly reduces immunoreactivity of the graft in vitro and in vivo.

Meacham et al. report that adiponectin receptors suppress chronic inflammatory signalling by immune effector cells to prevent haematopoietic stem cell exit from quiescence and, thus, protect them from exhaustion.