The aim of the present investigation is to studythe effects of DEX or E2 treatment during differentiation towards neural cell line of rat BM-MSCs in culture. Inorder to better characterize biochemically our in vitromodel, we evaluate by western blotting and immunocytochemical analysis some neural lineage markers (nestin, neurofilament, beta-tubulin) and MAP-Kinases. An enhancedexpression of the neural markers and MAP-Kinase in DEX-treated BM-MSCs cultures is found. In addition, E2-treatment increases MAP-Kinase and beta-tubulin expression, but it decreases nestin and neurofilament expression. In conclusion,our findings highlight a significant up and downmodulation of nestin, neurofilament, beta-tubulin and MAP-Kinases expression in neurosteroids-treated BM-MSCs. In particular, our results clarify the molecular mechanism involved during eventual differentiation of these stem cells treated with DEX and E2, addressed towards a neural cell line, that may express neurotrophic receptors and releaseneurotrophines particularly implicated during neurogenesisprocesses.

Neural markers espression in rat bone marrow mesenchymal stem cell cultures treated with neurosteroids

BRONZI, D;BRAMANTI, V;LAUREANTI,F;GRASSO, S;AVOLA ,R.
2010-01-01

Abstract

The aim of the present investigation is to studythe effects of DEX or E2 treatment during differentiation towards neural cell line of rat BM-MSCs in culture. Inorder to better characterize biochemically our in vitromodel, we evaluate by western blotting and immunocytochemical analysis some neural lineage markers (nestin, neurofilament, beta-tubulin) and MAP-Kinases. An enhancedexpression of the neural markers and MAP-Kinase in DEX-treated BM-MSCs cultures is found. In addition, E2-treatment increases MAP-Kinase and beta-tubulin expression, but it decreases nestin and neurofilament expression. In conclusion,our findings highlight a significant up and downmodulation of nestin, neurofilament, beta-tubulin and MAP-Kinases expression in neurosteroids-treated BM-MSCs. In particular, our results clarify the molecular mechanism involved during eventual differentiation of these stem cells treated with DEX and E2, addressed towards a neural cell line, that may express neurotrophic receptors and releaseneurotrophines particularly implicated during neurogenesisprocesses.
2010
Mesenchymal stem cells; Neural markers; Dexamethasone
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11769/25689
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