<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(1)</volume><submitter>Jun EK</submitter><pubmed_abstract>In a previous study, we isolated human amniotic fluid (AF)-derived mesenchymal stem cells (AF-MSCs) and utilized normoxic conditioned medium (AF-MSC-norCM) which has been shown to accelerate cutaneous wound healing. Because hypoxia enhances the wound healing function of mesenchymal stem cell-conditioned medium (MSC-CM), it is interesting to explore the mechanism responsible for the enhancement of wound healing function. In this work, hypoxia not only increased the proliferation of AF-MSCs but also maintained their constitutive characteristics (surface marker expression and differentiation potentials). Notably, more paracrine factors, VEGF and TGF-β1, were secreted into hypoxic conditioned medium from AF-MSCs (AF-MSC-hypoCM) compared to AF-MSC-norCM. Moreover, AF-MSC-hypoCM enhanced the pro</pubmed_abstract><journal>International journal of molecular sciences</journal><pagination>605-28</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3907828</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Hypoxic conditioned medium from human amniotic fluid-derived mesenchymal stem cells accelerates skin wound healing through TGF-β/SMAD2 and PI3K/Akt pathways.</pubmed_title><pmcid>PMC3907828</pmcid><pubmed_authors>Park G</pubmed_authors><pubmed_authors>Kim A</pubmed_authors><pubmed_authors>Moon JH</pubmed_authors><pubmed_authors>You S</pubmed_authors><pubmed_authors>Jun EK</pubmed_authors><pubmed_authors>Lee G</pubmed_authors><pubmed_authors>Kang PJ</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors><pubmed_authors>Yoon BS</pubmed_authors><pubmed_authors>Lee JH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hypoxic conditioned medium from human amniotic fluid-derived mesenchymal stem cells accelerates skin wound healing through TGF-β/SMAD2 and PI3K/Akt pathways.</name><description>In a previous study, we isolated human amniotic fluid (AF)-derived mesenchymal stem cells (AF-MSCs) and utilized normoxic conditioned medium (AF-MSC-norCM) which has been shown to accelerate cutaneous wound healing. Because hypoxia enhances the wound healing function of mesenchymal stem cell-conditioned medium (MSC-CM), it is interesting to explore the mechanism responsible for the enhancement of wound healing function. In this work, hypoxia not only increased the proliferation of AF-MSCs but also maintained their constitutive characteristics (surface marker expression and differentiation potentials). Notably, more paracrine factors, VEGF and TGF-β1, were secreted into hypoxic conditioned medium from AF-MSCs (AF-MSC-hypoCM) compared to AF-MSC-norCM. Moreover, AF-MSC-hypoCM enhanced the pro</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Jan</publication><modification>2026-04-29T15:32:21.017Z</modification><creation>2019-03-27T01:20:59Z</creation></dates><accession>S-EPMC3907828</accession><cross_references><pubmed>24398984</pubmed><doi>10.3390/ijms15010605</doi></cross_references></HashMap>