miR-381 Regulates Neural Stem Cell Proliferation and Differentiation via Regulating Hes1 Expression
Author(s) -
Xiaodong Shi,
Chunhua Yan,
Baoquan Liu,
Chunxiao Yang,
Xuedan Nie,
Xiaokun Wang,
Jiaolin Zheng,
Yue Wang,
Yulan Zhu
Publication year - 2015
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0138973
Subject(s) - neural stem cell , stem cell , hes1 , biology , neurosphere , neuroepithelial cell , microbiology and biotechnology , cellular differentiation , neurogenesis , adult stem cell , multipotent stem cell , microrna , neural development , progenitor cell , signal transduction , genetics , gene , notch signaling pathway
Neural stem cells are self-renewing, multipotent and undifferentiated precursors that retain the capacity for differentiation into both glial (astrocytes and oligodendrocytes) and neuronal lineages. Neural stem cells offer cell-based therapies for neurological disorders such as Alzheimer's disease, Parkinson's disease, Huntington's disease and spinal cord injuries. However, their cellular behavior is poorly understood. MicroRNAs (miRNAs) are a class of small noncoding RNAs involved in cell development, proliferation and differentiation through regulating gene expression at post-transcriptional level. The role of miR–381 in the development of neural stem cells remains unknown. In this study, we showed that overexpression of miR–381 promoted neural stem cells proliferation. It induced the neural stem cells differentiation to neurons and inhibited their differentiation to astrocytes. Furthermore, we identified HES1 as a direct target of miR–381 in neural stem cells. Moreover, re-expression of HES1 impaired miR-381-induced promotion of neural stem cells proliferation and induce neural stem cells differentiation to neurons. In conclusion, miR–381 played important role in neural stem cells proliferation and differentiation.
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