| Literature DB >> 26221209 |
Ping Gu1, Fu-Cheng Qiu2, Rui Han3, Zhong-Xia Zhang3, Ci Dong2, Li-Na Zhang3, Yan-Yong Wang4, Qing-Ying Ma4, Bao-Yong Yan3.
Abstract
Neural stem cells (NSCs) are valuable self-renewing cells that can maintain the capacity to differentiate into specific brain cell types. NSCs may repair and even replace the brain tissue, and ultimatley promoting the central nervous system regeneration. Therefore, it is important, for scientists and pjysicians, to study the method for efficient culture and differentiation of NSCs. Our previous study demonstrated that Bone Marrow Stromal Cells (BMSCs) can directly regulate the differentiation of NSCs into neurons, and soluble molecules excreted by BMSCs played a key role in this process. Hereby, we further identified the BMSCs-induced neurons could form the synapses, convey dopamine and express voltage-depend and receptor-depend calcium channels. Moreover, the extracellular signal-regulated protein kinase ERK1/2 pathway was founded to be involved in the process of neuron differentiation and proliferation by the in vitro experiments. Finally, by using protein array, we, for the first time, found that the cytokine-induced neutrophil chemoattractant-3 (CINC-3, a small molecule cytokine) can promote the leukocytes invasion into the inflammation site, and have the ability to induce mesencephal NSCs into neurons. Consequently, these positive findings suggested that our BMSCs-induced culture system could provide a useful tool to investigate the molecular mechanisms of neural differentiation of NSCs, which may be benifical for neurodegenerative diseases in the near future.Entities:
Keywords: Neural stem cells; bone marrow stromal cells; cytokines; differentiation; neurons; protein microarray analysis
Year: 2015 PMID: 26221209 PMCID: PMC4509154
Source DB: PubMed Journal: Int J Clin Exp Med ISSN: 1940-5901