MicroRNA-132 directs human periodontal ligament-derived neural crest stem cell neural differentiation

被引:18
|
作者
Ng, Tsz Kin [1 ,2 ,3 ,4 ,5 ]
Yang, Qichen [4 ]
Fortino, Veronica R. [6 ,7 ]
Lai, Nikky Yuk-Ki [4 ]
Carballosa, Carlos M. [6 ]
Greenberg, Jordan M. [6 ]
Choy, Kwong Wai [8 ]
Pelaez, Daniel [5 ,9 ]
Pang, Chi Pui [1 ,2 ,4 ]
Cheung, Herman S. [5 ,6 ]
机构
[1] Shantou Univ, Joint Shantou Int Eye Ctr, Shantou, Guangdong, Peoples R China
[2] Chinese Univ Hong Kong, Shantou, Guangdong, Peoples R China
[3] Shantou Univ, Med Coll, Shantou, Guangdong, Peoples R China
[4] Chinese Univ Hong Kong, Dept Ophthalmol & Visual Sci, Kowloon, Peoples R China
[5] Miami Vet Affairs Med Ctr, Geriatr Res Educ & Clin Ctr, 1201 NW 16th St, Miami, FL 33125 USA
[6] Univ Miami, Dept Biomed Engn, Coll Engn, Coral Gables, FL 33124 USA
[7] Nova Southeastern Univ, Dept Biol Sci, Ft Lauderdale, FL 33314 USA
[8] Chinese Univ Hong Kong, Dept Obstet & Gynaecol, Shatin, Hong Kong, Peoples R China
[9] Univ Miami, Dept Ophthalmol, Bascom Palmer Eye Inst, Miami, FL USA
关键词
microRNAs; neural crest stem cells; neural differentiation; neurons; periodontal ligament; ZEB2; NEURONAL DIFFERENTIATION; GENE-EXPRESSION; MIR-200; FAMILY; PROMOTES; NEUROGENESIS; GROWTH; OVEREXPRESSION;
D O I
10.1002/term.2759
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Neurogenesis is the basis of stem cell tissue engineering and regenerative medicine for central nervous system (CNS) disorders. We have established differentiation protocols to direct human periodontal ligament-derived stem cells (PDLSCs) into neuronal lineage, and we recently isolated the neural crest subpopulation from PDLSCs, which are pluripotent in nature. Here, we report the neural differentiation potential of these periodontal ligament-derived neural crest stem cells (NCSCs) as well as its microRNA (miRNA) regulatory mechanism and function in NCSC neural differentiation. NCSCs, treated with basic fibroblast growth factor and epidermal growth factor-based differentiation medium for 24 days, expressed neuronal and glial markers (beta III-tubulin, neurofilament, NeuN, neuron-specific enolase, GFAP, and S100) and exhibited glutamate-induced calcium responses. The global miRNA expression profiling identified 60 upregulated and 19 downregulated human miRNAs after neural differentiation, and the gene ontology analysis of the miRNA target genes confirmed the neuronal differentiation-related biological functions. In addition, overexpression of miR-132 in NCSCs promoted the expression of neuronal markers and downregulated ZEB2 protein expression. Our results suggested that the pluripotent NCSCs from human periodontal ligament can be directed into neural lineage, which demonstrate its potential in tissue engineering and regenerative medicine for CNS disorders.
引用
收藏
页码:12 / 24
页数:13
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