<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ying SQ</submitter><funding>Young Science and Technology Rising Star Project of Shaanxi Province</funding><funding>National Natural Science Foundation of China</funding><funding>China Postdoctoral Science Foundation</funding><pagination>521</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11363633</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(1)</volume><pubmed_abstract>Tissue-derived extracellular vesicles (EVs) are emerging as pivotal players to maintain organ homeostasis, which show promise as a next-generation candidate for medical use with extensive source. However, the detailed function and therapeutic potential of tissue EVs remain insufficiently studied. Here, through bulk and single-cell RNA sequencing analyses combined with ultrastructural tissue examinations, we first reveal that in situ liver tissue EVs (LT-EVs) contribute to the intricate liver regenerative process after partial hepatectomy (PHx), and that hepatocytes are the primary source of tissue EVs in the regenerating liver. Nanoscale and proteomic profiling further identify that the hepatocyte-specific tissue EVs (Hep-EVs) are strengthened to release with carrying proliferative message</pubmed_abstract><journal>Journal of nanobiotechnology</journal><pubmed_title>Hepatocyte-derived tissue extracellular vesicles safeguard liver regeneration and support regenerative therapy.</pubmed_title><pmcid>PMC11363633</pmcid><funding_grant_id>BX20230485</funding_grant_id><funding_grant_id>82371020</funding_grant_id><funding_grant_id>82301028</funding_grant_id><funding_grant_id>81930025</funding_grant_id><funding_grant_id>2023KJXX-027</funding_grant_id><funding_grant_id>82170988</funding_grant_id><pubmed_authors>Ying SQ</pubmed_authors><pubmed_authors>Xing SJ</pubmed_authors><pubmed_authors>Zhang K</pubmed_authors><pubmed_authors>Zhou ZK</pubmed_authors><pubmed_authors>Qiu JY</pubmed_authors><pubmed_authors>Jin Y</pubmed_authors><pubmed_authors>Zheng CX</pubmed_authors><pubmed_authors>Luo XY</pubmed_authors><pubmed_authors>Zhang XH</pubmed_authors><pubmed_authors>Jin F</pubmed_authors><pubmed_authors>Cao Y</pubmed_authors><pubmed_authors>Sui BD</pubmed_authors><pubmed_authors>Li YY</pubmed_authors><pubmed_authors>Shi K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hepatocyte-derived tissue extracellular vesicles safeguard liver regeneration and support regenerative therapy.</name><description>Tissue-derived extracellular vesicles (EVs) are emerging as pivotal players to maintain organ homeostasis, which show promise as a next-generation candidate for medical use with extensive source. However, the detailed function and therapeutic potential of tissue EVs remain insufficiently studied. Here, through bulk and single-cell RNA sequencing analyses combined with ultrastructural tissue examinations, we first reveal that in situ liver tissue EVs (LT-EVs) contribute to the intricate liver regenerative process after partial hepatectomy (PHx), and that hepatocytes are the primary source of tissue EVs in the regenerating liver. Nanoscale and proteomic profiling further identify that the hepatocyte-specific tissue EVs (Hep-EVs) are strengthened to release with carrying proliferative message</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-05-02T03:39:26.194Z</modification><creation>2025-04-05T12:30:52.245Z</creation></dates><accession>S-EPMC11363633</accession><cross_references><pubmed>39210346</pubmed><doi>10.1186/s12951-024-02790-0</doi></cross_references></HashMap>