Temporal dynamics of TNF-mediated changes in hematopoietic stem cell function and recovery

While tumor necrosis factor (TNF) is a critical mediator of appropriate immune response and tissue repair, its misregulation is linked to cancer, autoimmunity, bone marrow failure, and aging. Understanding the context-dependent roles of TNF is essential for elucidating normal and pathogenic conditions and to guide clinical therapy advancements. Prior studies suggested that TNF restricts the self-renewal capacity of hematopoietic stem cells (HSCs), but its long-term effect on HSCs remains unclear. Here, we demonstrate that in vivo TNF administration results in a transient exit of HSCs from quiescence, which coincides with a compromised repopulation capacity. These functional changes are; however, fully reversible even following prolonged/chronic transient exposure to TNF. Notably, antagonizing TNF signaling in transplantation recipients enhances donor HSC reconstitution. Our findings provide molecular and functional insight into HSC regulation, with implications for both acute and chronic inflammatory conditions. [Display omitted] •Temporary TNF exposure results in reversible HSC repopulation capacity reductions•TNF-induced repopulation impairments coincide with altered quiescence status•TNF signaling inhibition enhances HSC reconstitution in transplantation recipients Biological sciences; Cell biology; Molecular biology; Stem cells research