Matches in SemOpenAlex for { <https://semopenalex.org/work/W2165196402> ?p ?o ?g. }
- W2165196402 endingPage "2717" @default.
- W2165196402 startingPage "2703" @default.
- W2165196402 abstract "Bone marrow stem cells (BMSCs) have been shown to improve neurological function recovery in cerebral ischemia. Hypoxia-inducible factor-1 (HIF-1) α-AA is a more stable mutant form of HIF-1α, which is a crucial oxygen-sensitive regulator. To investigate the protective effects of HIF-1α-AA-modified BMSCs on neuron survival in cerebral ischemia models, we co-cultured HIF-1α-AA-modified BMSCs with neuron-like cells (PC12 cells) and observed a significant increase in the release of vascular endothelial growth factor (VEGF) from BMSCs, the decreased PC12 cell apoptosis, and the upregulation of Survivin expression reduced by hypoxia in PC12 cells compared to enhanced green fluorescent protein (EGFP) BMSCs. In addition, to explore whether VEGF secreted by HIF-1α-AA-modified BMSCs plays an important role in preventing hypoxia-induced apoptosis and the possible mechanism involved, exogenous VEGF were applied and the similar protective effects on PC12 cells were observed in vitro. Furthermore, hypoxia reduced the expression of phosphorylated Akt and phosphorylated FoxO1, whereas the administration of VEGF reversed these changes. Transfection of FoxO1 H215R, a DNA-binding mutant, abrogated the inhibitory ability on Survivin promoter activity, whereas FoxO1 AAA, the active form of FoxO1, presented further repression on Survivin promoter, indicating that FoxO1 directly binds on Survivin promoter as a transcriptional repressor and that phosphorylation status of FoxO1 affects its inhibition on the Survivin promoter. Transplantation of HIF-1α-AA-modified BMSCs after cerebral ischemia in vivo sufficiently reduced neurons apoptosis, decreased cerebral infarction volume, and induced a significant improvement on the modified neurological severity score compared to the EGFP BMSCs group. In conclusion, HIF-1α-AA-modified MSCs showed an obvious protective effect on neuron-like cells or neuron after ischemia in vitro and in vivo, at least in part, through the VEGF/PI3K/Akt/FoxO1 pathway." @default.
- W2165196402 created "2016-06-24" @default.
- W2165196402 creator A5021792276 @default.
- W2165196402 creator A5022977258 @default.
- W2165196402 creator A5035606496 @default.
- W2165196402 creator A5052501867 @default.
- W2165196402 creator A5072202038 @default.
- W2165196402 creator A5085084535 @default.
- W2165196402 date "2012-09-20" @default.
- W2165196402 modified "2023-09-27" @default.
- W2165196402 title "Hypoxia-Inducible Factor 1-α-AA-Modified Bone Marrow Stem Cells Protect PC12 Cells from Hypoxia-Induced Apoptosis, Partially Through VEGF/PI3K/Akt/FoxO1 Pathway" @default.
- W2165196402 cites W103851158 @default.
- W2165196402 cites W1580865462 @default.
- W2165196402 cites W1890390185 @default.
- W2165196402 cites W1894493322 @default.
- W2165196402 cites W1966841015 @default.
- W2165196402 cites W1966931906 @default.
- W2165196402 cites W1968262266 @default.
- W2165196402 cites W1972239225 @default.
- W2165196402 cites W1972986603 @default.
- W2165196402 cites W1973217010 @default.
- W2165196402 cites W1974377330 @default.
- W2165196402 cites W1989560466 @default.
- W2165196402 cites W1989648954 @default.
- W2165196402 cites W1998729124 @default.
- W2165196402 cites W2001604240 @default.
- W2165196402 cites W2002320509 @default.
- W2165196402 cites W2011849469 @default.
- W2165196402 cites W2015428837 @default.
- W2165196402 cites W2016934775 @default.
- W2165196402 cites W2017964197 @default.
- W2165196402 cites W2020397140 @default.
- W2165196402 cites W2033962191 @default.
- W2165196402 cites W2035523654 @default.
- W2165196402 cites W2040031153 @default.
- W2165196402 cites W2046297960 @default.
- W2165196402 cites W2049812302 @default.
- W2165196402 cites W2051755309 @default.
- W2165196402 cites W2052223356 @default.
- W2165196402 cites W2058896449 @default.
- W2165196402 cites W2064738912 @default.
- W2165196402 cites W2075880922 @default.
- W2165196402 cites W2078420937 @default.
- W2165196402 cites W2086812941 @default.
- W2165196402 cites W2092690603 @default.
- W2165196402 cites W2098724363 @default.
- W2165196402 cites W2101084498 @default.
- W2165196402 cites W2101717161 @default.
- W2165196402 cites W2102129021 @default.
- W2165196402 cites W2141046053 @default.
- W2165196402 cites W2142594288 @default.
- W2165196402 cites W2144503403 @default.
- W2165196402 cites W2144625075 @default.
- W2165196402 cites W2154374454 @default.
- W2165196402 cites W2163069245 @default.
- W2165196402 cites W2165085655 @default.
- W2165196402 cites W2168611216 @default.
- W2165196402 cites W2169938527 @default.
- W2165196402 cites W2170714259 @default.
- W2165196402 cites W4210973470 @default.
- W2165196402 doi "https://doi.org/10.1089/scd.2011.0604" @default.
- W2165196402 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3438847" @default.
- W2165196402 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22468883" @default.
- W2165196402 hasPublicationYear "2012" @default.
- W2165196402 type Work @default.
- W2165196402 sameAs 2165196402 @default.
- W2165196402 citedByCount "37" @default.
- W2165196402 countsByYear W21651964022012 @default.
- W2165196402 countsByYear W21651964022013 @default.
- W2165196402 countsByYear W21651964022014 @default.
- W2165196402 countsByYear W21651964022015 @default.
- W2165196402 countsByYear W21651964022016 @default.
- W2165196402 countsByYear W21651964022017 @default.
- W2165196402 countsByYear W21651964022018 @default.
- W2165196402 countsByYear W21651964022019 @default.
- W2165196402 countsByYear W21651964022020 @default.
- W2165196402 countsByYear W21651964022022 @default.
- W2165196402 crossrefType "journal-article" @default.
- W2165196402 hasAuthorship W2165196402A5021792276 @default.
- W2165196402 hasAuthorship W2165196402A5022977258 @default.
- W2165196402 hasAuthorship W2165196402A5035606496 @default.
- W2165196402 hasAuthorship W2165196402A5052501867 @default.
- W2165196402 hasAuthorship W2165196402A5072202038 @default.
- W2165196402 hasAuthorship W2165196402A5085084535 @default.
- W2165196402 hasBestOaLocation W21651964022 @default.
- W2165196402 hasConcept C104317684 @default.
- W2165196402 hasConcept C127561419 @default.
- W2165196402 hasConcept C153911025 @default.
- W2165196402 hasConcept C160450060 @default.
- W2165196402 hasConcept C190283241 @default.
- W2165196402 hasConcept C2775975398 @default.
- W2165196402 hasConcept C502942594 @default.
- W2165196402 hasConcept C54009773 @default.
- W2165196402 hasConcept C54355233 @default.
- W2165196402 hasConcept C55493867 @default.
- W2165196402 hasConcept C75217442 @default.
- W2165196402 hasConcept C81885089 @default.
- W2165196402 hasConcept C86554907 @default.