GEOapplication/xmlftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE266nnn/GSE266509/primaryOK200TranscriptomicsMus musculusExpression profiling by high throughput sequencinghttps://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE266509GEOGSEfalseA Bcl11a-driven mechanism maintaining hematopoietic stem cell functionality gives rise to dysfunction during aging [RNA-Seq]Preserving hematopoietic stem cell (HSC) functionality is crucial for sustaining healthy blood and immune system throughout life. However, the mechanisms underlying HSC dysfunction and disruption of hematopoiesis during aging remain unclear. Utilizing an inducible mosaic mouse model, we discovered that Bcl11a levels increase in HSCs with age, mitigating functional decline while also promoting myeloid cell and IL-1β production in the bone marrow, thus accelerating HSC attrition non-cell autonomously. Notably, aging-related inflammation augments the expressions of both Bcl11a and Fc receptors (FcRs) in HSCs. FcR signaling activation induces HSC differentiation, which is counteracted by Bcl11a through repressing FcRγ expression to maintain HSC function. Deletion of FcRγ in Bcl11a-mosaic mice abolishes the non-cell autonomous effect on deteriorating HSCs. Overall, this study unveils the complex nature of HSC aging and underscores the significance of fine-tuning Bcl11a levels and FcRγ signaling strength for hematopoietic regeneration on demand and healthy blood production with age.2026/05/17GSE266509GSM8619745GSM8619746GSM8619747GSM8619748GSM8619749GSM8248649GSM8248648GSM8248647GSM8248646GSM8248645GSM8248644GSM8248643GSM8248642GSM8248641GSM8248640GSM8248639GSM8248638GSM8619750GSM8619751GSM8248637GSM8619752GSM8248636GSM8248635GSM8248634GSM8248633GSM8248632GSM8248631GSM8248630GSM8248629GSM8248628GSM8248627GSM8248626GSM8248625GSM8248624GSM8248623GSM8248622GSM8248621GSM8248620GSM8248661GSM8248660GSM8248619GSM8248618GSM8248659GSM8248658GSM8248657GSM8248656GSM8248655GSM8248654GSM8248653GSM8248652GSM8248651GSM824865024247266509Mus musculus