Matches in SemOpenAlex for { <https://semopenalex.org/work/W2516840018> ?p ?o ?g. }
- W2516840018 abstract "Neural stem/precursor cells (NSCs) are of particular interest because of their potential application in cell therapy for brain damage. However, most brain injury cases are followed with neuroinflammatory stress, which affects the lineage selection of grafted NSCs by promoting astrocytogenesis, thus hampering the potential for neural replacement. The present study investigated the role of miR-17-92 in protecting against detrimental effects of neuroinflammation on NSC differentiation in cell therapy. NSCs were treated with conditioned medium from lesioned astrocytes with/without neutralizing antibodies of leukemia inhibitory factor (LIF) or/and ciliary neurotrophic factor (CNTF), respectively. Afterward, the levels of p-STAT3 and p-JAK2 were determined by western blotting while expression of glial fibrillary acidic protein (GFAP) and β-tubulin III was assessed by immunostaining. The activation of JAK-STAT pathway and cell differentiation were also evaluated after we overexpressed miR-17-92 in NSCs under different neuroinflammatory conditions. After the transplantation of miR-17-92-overexpressing NSCs into injured mouse cortex, PH3, nestin, GFAP, and NeuN were analyzed by immunostaining. In addition, motor coordination of mice was evaluated by rotarod test. Conditioned medium from lesioned astrocytes activated JAK-STAT pathway and facilitated astrocytic differentiation in NSCs while neutralizing antibodies of LIF and CNTF remarkably attenuated such effects. miR-17-92 cluster repressed the expression of multiple proteins including GP130, CNTFR, JAK2, and STAT3 in JAK-STAT pathway. Overexpression of miR-17-92 in NSCs systematically blocked the activation of JAK-STAT pathway mediated by LIF and CNTF, which facilitated neuronal differentiation in vitro. Furthermore, miR-17-92 increased neuronal generation of grafted NSCs and reduced astrogliosis, which resulted in the improvement of motor coordination of brain-injured mice. Our results suggest that miR-17-92 promotes neuronal differentiation of grafted NSCs under neuroinflammatory condition via inhibition of multiple proteins in JAK-STAT pathway." @default.
- W2516840018 created "2016-09-16" @default.
- W2516840018 creator A5018244700 @default.
- W2516840018 creator A5020967361 @default.
- W2516840018 creator A5034924979 @default.
- W2516840018 creator A5036985869 @default.
- W2516840018 creator A5046605322 @default.
- W2516840018 creator A5059492103 @default.
- W2516840018 date "2016-08-27" @default.
- W2516840018 modified "2023-10-13" @default.
- W2516840018 title "miR-17-92 facilitates neuronal differentiation of transplanted neural stem/precursor cells under neuroinflammatory conditions" @default.
- W2516840018 cites W1524705340 @default.
- W2516840018 cites W1525032009 @default.
- W2516840018 cites W1824670638 @default.
- W2516840018 cites W1840012222 @default.
- W2516840018 cites W1908252718 @default.
- W2516840018 cites W1965147416 @default.
- W2516840018 cites W1966558019 @default.
- W2516840018 cites W1971598496 @default.
- W2516840018 cites W1973859136 @default.
- W2516840018 cites W1974294728 @default.
- W2516840018 cites W1975631280 @default.
- W2516840018 cites W1982649435 @default.
- W2516840018 cites W1984305500 @default.
- W2516840018 cites W1985571291 @default.
- W2516840018 cites W2021000905 @default.
- W2516840018 cites W2031503714 @default.
- W2516840018 cites W2042598724 @default.
- W2516840018 cites W2043655216 @default.
- W2516840018 cites W2045933871 @default.
- W2516840018 cites W2047804751 @default.
- W2516840018 cites W2052551969 @default.
- W2516840018 cites W2055546416 @default.
- W2516840018 cites W2058319182 @default.
- W2516840018 cites W2063638559 @default.
- W2516840018 cites W2071636817 @default.
- W2516840018 cites W2073690379 @default.
- W2516840018 cites W2076848111 @default.
- W2516840018 cites W2077845552 @default.
- W2516840018 cites W2078122037 @default.
- W2516840018 cites W2078278194 @default.
- W2516840018 cites W2095783207 @default.
- W2516840018 cites W2097387289 @default.
- W2516840018 cites W2097445408 @default.
- W2516840018 cites W2102089787 @default.
- W2516840018 cites W2110387447 @default.
- W2516840018 cites W2146546664 @default.
- W2516840018 cites W2152122421 @default.
- W2516840018 cites W2162716161 @default.
- W2516840018 cites W2163716193 @default.
- W2516840018 cites W2183908031 @default.
- W2516840018 cites W2202912080 @default.
- W2516840018 cites W2237598232 @default.
- W2516840018 cites W2244556572 @default.
- W2516840018 cites W2266755286 @default.
- W2516840018 cites W2267370441 @default.
- W2516840018 cites W2272935216 @default.
- W2516840018 cites W2285909430 @default.
- W2516840018 cites W2293347728 @default.
- W2516840018 cites W2305466441 @default.
- W2516840018 cites W2314534841 @default.
- W2516840018 cites W2346423837 @default.
- W2516840018 doi "https://doi.org/10.1186/s12974-016-0685-5" @default.
- W2516840018 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5002215" @default.
- W2516840018 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/27567678" @default.
- W2516840018 hasPublicationYear "2016" @default.
- W2516840018 type Work @default.
- W2516840018 sameAs 2516840018 @default.
- W2516840018 citedByCount "23" @default.
- W2516840018 countsByYear W25168400182016 @default.
- W2516840018 countsByYear W25168400182017 @default.
- W2516840018 countsByYear W25168400182018 @default.
- W2516840018 countsByYear W25168400182019 @default.
- W2516840018 countsByYear W25168400182020 @default.
- W2516840018 countsByYear W25168400182021 @default.
- W2516840018 countsByYear W25168400182022 @default.
- W2516840018 countsByYear W25168400182023 @default.
- W2516840018 crossrefType "journal-article" @default.
- W2516840018 hasAuthorship W2516840018A5018244700 @default.
- W2516840018 hasAuthorship W2516840018A5020967361 @default.
- W2516840018 hasAuthorship W2516840018A5034924979 @default.
- W2516840018 hasAuthorship W2516840018A5036985869 @default.
- W2516840018 hasAuthorship W2516840018A5046605322 @default.
- W2516840018 hasAuthorship W2516840018A5059492103 @default.
- W2516840018 hasBestOaLocation W25168400181 @default.
- W2516840018 hasConcept C11988809 @default.
- W2516840018 hasConcept C126322002 @default.
- W2516840018 hasConcept C136834591 @default.
- W2516840018 hasConcept C160539049 @default.
- W2516840018 hasConcept C170493617 @default.
- W2516840018 hasConcept C185592680 @default.
- W2516840018 hasConcept C203014093 @default.
- W2516840018 hasConcept C204232928 @default.
- W2516840018 hasConcept C27284151 @default.
- W2516840018 hasConcept C2776914184 @default.
- W2516840018 hasConcept C2777738006 @default.
- W2516840018 hasConcept C2778690821 @default.
- W2516840018 hasConcept C2778923194 @default.
- W2516840018 hasConcept C2780495277 @default.
- W2516840018 hasConcept C28328180 @default.