| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2786183 | International Journal of Developmental Neuroscience | 2013 | 6 Pages |
Bone marrow mesenchymal stem cells (MSCs) are known to differentiate into neurons in vitro. However, the mechanism underlying MSC differentiation remains controversial. A recent analysis has shown that Notch signaling is involved in regulating the differentiation of MSCs. This study examines the potential mechanism of the differentiation of MSCs into neurons, and it considers the role of caveolin-1 in this process. We investigated neuron differentiation and Notch signaling by detecting the expression levels of microtubule-associated protein 2 (MAP-2), Neuron-specific Enolase (NSE), Notch-1, Notch intracellular domain (NICD) and hairy enhancer of split 5 (Hes5). We found that by down-regulating caveolin-1 during induction, MSCs were prone to neural differentiation and expressed high levels of neuronal markers. Meanwhile, the expression levels of Notch-1, NICD and Hes5 decreased. Our results indicate that down-regulation of caveolin-1 promotes the neuronal differentiation of MSCs by modulating the Notch signaling pathway.
► Caveolin-1 can regulate the neural differentiation of MSCs. ► The down-regulation of caveolin-1 inhibited Notch signaling in MSCs. ► The expression of caveolin-1 increased during the neural differentiation of MSCs. ► Caveolin-1 promoted the neural differentiation of MSCs by modulating Notch signaling.
