<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE329nnn/GSE329536/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Macaca mulatta</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE329536</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>A single-cell transcriptomic atlas of rhesus macaque hematopoiesis reveals age-related myeloid bias and differentiation changes</name><description>Aging is accompanied by profound functional declines in the hematopoietic system, including diminished regenerative capacity and a skewing toward the myeloid lineage. While murine models have provided critical insights into hematopoietic stem cell (HSC) aging, the evolutionary distance to humans limits their translational applicability. Non-human primates, such as rhesus macaques, offer a highly relevant model, yet a comprehensive single-cell transcriptomic map of their aging hematopoietic system has been lacking. Here, we present a high-resolution single-cell RNA sequencing atlas of rhesus macaque hematopoiesis, profiling whole bone marrow, peripheral blood, and CD34-enriched progenitor cells from young and late-middle-aged cohorts. Our analysis delineates the transcriptional landscape of macaque hematopoiesis and identifies robust surface markers for prospective isolation of progenitor subpopulations. We uncover distinct, lineage-specific aging signatures, with the most profound transcriptional alterations occurring in multipotent progenitors and classical monocytes. Pseudotime and RNA velocity analyses reveal that aged HSCs reside in a more advanced state of differentiation with altered kinetics, providing a molecular basis for the observed age-related myeloid bias. Furthermore, cross-species integration with healthy human bone marrow data demonstrates profound transcriptional conservation of the stem and progenitor compartments between R. macaques and humans, with minimal species-specific divergence. These findings establish the rhesus macaque as a highly faithful surrogate for human hematopoietic aging and provide a critical resource for developing targeted interventions to rejuvenate the aging blood system.</description><dates><publication>2026/09/16</publication></dates><accession>GSE329536</accession><cross_references><GSM>GSM9705960</GSM><GSM>GSM9705920</GSM><GSM>GSM9705964</GSM><GSM>GSM9705963</GSM><GSM>GSM9705962</GSM><GSM>GSM9705961</GSM><GSM>GSM9705968</GSM><GSM>GSM9705924</GSM><GSM>GSM9705923</GSM><GSM>GSM9705967</GSM><GSM>GSM9705922</GSM><GSM>GSM9705966</GSM><GSM>GSM9705965</GSM><GSM>GSM9705921</GSM><GSM>GSM9705928</GSM><GSM>GSM9705927</GSM><GSM>GSM9705926</GSM><GSM>GSM9705925</GSM><GSM>GSM9705969</GSM><GSM>GSM9705929</GSM><GSM>GSM9705953</GSM><GSM>GSM9705952</GSM><GSM>GSM9705951</GSM><GSM>GSM9705950</GSM><GSM>GSM9705957</GSM><GSM>GSM9705956</GSM><GSM>GSM9705955</GSM><GSM>GSM9705954</GSM><GSM>GSM9705917</GSM><GSM>GSM9705916</GSM><GSM>GSM9705959</GSM><GSM>GSM9705958</GSM><GSM>GSM9705919</GSM><GSM>GSM9705918</GSM><GSM>GSM9705942</GSM><GSM>GSM9705941</GSM><GSM>GSM9705940</GSM><GSM>GSM9705946</GSM><GSM>GSM9705945</GSM><GSM>GSM9705944</GSM><GSM>GSM9705943</GSM><GSM>GSM9705949</GSM><GSM>GSM9705948</GSM><GSM>GSM9705947</GSM><GSM>GSM9705971</GSM><GSM>GSM9705970</GSM><GSM>GSM9705931</GSM><GSM>GSM9705930</GSM><GSM>GSM9705974</GSM><GSM>GSM9705973</GSM><GSM>GSM9705972</GSM><GSM>GSM9705935</GSM><GSM>GSM9705934</GSM><GSM>GSM9705933</GSM><GSM>GSM9705932</GSM><GSM>GSM9705939</GSM><GSM>GSM9705938</GSM><GSM>GSM9705937</GSM><GSM>GSM9705936</GSM><GPL>27943</GPL><GSE>329536</GSE><taxon>Macaca mulatta</taxon><PMID>[42618695]</PMID></cross_references></HashMap>