<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/GSE316nnn/GSE316332/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Rattus norvegicus</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=GSE316332</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Nano-layered Tendon Patch to Orchestrate Timely Interactions between Tendon Stem/Progenitor Cells and Macrophages</name><description>Tendon regeneration remains limited by the unmet challenge of precisely controlling the intensity and duration of local inflammation, often resulting in scarred healing. Here, we present a novel, micro-thin, nano-layered patch that employs Layer-by-Layer (LbL) self-assembly for the precise controlled release of small molecules, Oxo-M and 4-PPBP, to address this technical challenge. This novel combination of small molecules exhibits distinct functions in modulating the polarization of macrophages and the tenogenic differentiation of tendon stem/progenitor cells (TSCs). The customized, temporal release of these small molecules effectively modulated the critical crosstalk between TSCs and macrophages, thereby promoting regenerative tendon healing. The nano-LbL tendon patch successfully mitigated early inflammation, promoted matrix synthesis, and regulated later tissue remodeling in vivo. Robust scRNA-seq and CellChat analysis delineated the temporal-orchestrated communication between cell types across healing phases, confirming the critical interplays between TSCs, tenocytes, and macrophages. Our nano-layered LbL nanopatch represents a highly translational approach for achieving scarless tendon regeneration. In addition, this study elucidated the essential signaling pathways regulating TSC-macrophage crosstalk, advancing our understanding of tendon biology and pathology.</description><dates><publication>2026/09/10</publication></dates><accession>GSE316332</accession><cross_references><GSM>GSM9449671</GSM><GSM>GSM9449669</GSM><GSM>GSM9449668</GSM><GSM>GSM9449672</GSM><GPL>25947</GPL><GSE>316332</GSE><taxon>Rattus norvegicus</taxon><PMID>[42664711]</PMID></cross_references></HashMap>