Abstract:【Objective】 To establish the method for culturing and purifying enteric neural stem cells (ENSCs) derived from rat and to investigate the effect of miR-145-3p on proliferation and differentiation of ENSCs. 【Methods】 ENSCs which primarily extracted from 18-days SD rats embryos, were observed by cytological characteristics and identified by Nestin and GFAP immunofluorescence staining. The liposome transfection and lentivirus transfection were used to transfect the ENSCs. Overexpression of miR-145-3p in ENSCs was transfected through liposome and infected with lentivirus with miR-145-3p, which followed by fluorescence microscope and qRT-PCR measurement. Edu cell proliferation assay was used to analyze proliferating cells by recording the proportion of Edu/DAPI in each group. The neurospheres was differentiated by differentiation medium and the GFAP/DAPI ratio of differentiated cells was recorded. 【Results】 Primary culture of ENSCs showed the formation of a large number of neurosphere-like structures (undifferentiated neurospheres). The immunofluorescence showed that Nestin and GFAP were positive in these cells. The qRT-PCR showed that the relative expression level of miR-145-3p in overexpression group was 3.52±0.24 significantly higher than the negative control group 0.01±0.01, the difference was statistically significant (P<0.01). It indicated that lentivirus was successfully transfected into ENSCs. Edu cell infiltration showed that the positive rate of Edu in the miR-145-3p overexpression group was (15.23±1.17) %, while the negative control group was (22.38±1.52) % (P<0.05). After NESCs cells were exposed to the differentiation medium, the proportion of GFAP positive cells in the miR-145-3p overexpression group was (21.47±1.98)%, which was lower than that in the negative cell control group(33.86±2.52)% (P<0.05). 【Conclusions】 Lentivirus transfection is a high efficient transfection method in ENSCs. Overexpression of miR-145-3p inhibits the proliferation and differentiation of ENSCs, which may play an important role in the development of enteric nervous system.
陈钦明, 杨六成, 王健俊, 何继贤, 路羿, 余岱岳, 吴凯. miR-145-3p对大鼠肠神经干细胞增殖与分化的影响[J]. 医学临床研究, 2022, 39(5): 652-655.
CHEN Qin-ming, YANG Liu-cheng, WANG Jian-jun, et al. Effects of MiR-145-3p on Proliferation and Differentiation of Enteric Neural Stem Cells. JOURNAL OF CLINICAL RESEARCH, 2022, 39(5): 652-655.
[1] SCHNEIDER S, WRIGHT C M, HEUCKEROTH R O. Unexpected roles for the second brain:enteric nervous system as master regulator of bowel function[J].Annu Rev Physiol,2019,81:235-259.
[2] 张金哲. 张金哲小儿外科学[M]. 北京:人民卫生出版社,2013:1078-1079.
[3] MURRAY M J, NICHOLSON J C, COLEMAN N. Biology of childhood germ cell tumours, focussing on the significance of microRNAs[J].Andrology,2015,3(1):129-139.
[4] 赵海军, 吴凯, 王健俊, 等. 应用微阵列芯片技术分析先天性巨结肠微小 RNAs 表达谱差异[J].中华实用儿科临床杂志,2016,31(6):462-465.
[5] PAN W, YU H, ZHENG B, et al. Upregulation of MiR-369-3p suppresses cell migration and proliferation by targeting SOX4 in Hirschsprung's disease[J].J Pediatr Surg,2017,52(8):1363-1370.
[6] LIU W, ZHANG L, WU R. Enteric neural stem cells expressing insulin-like growth factor 1:a novel cellular therapy for hirschsprung's disease in mouse model[J].DNA Cell Biol,2018,37(7):642-648.
[7] HEUCKEROTH R O. Hirschsprung disease-integrating basic science and clinical medicine to improve outcomes[J].Nat Rev Gastroenterol Hepatol,2018,15(3):152-167.
[8] WEI R, QIU X, WANG S, et al. NEDL2 is an essential regulator of enteric neural development and GDNF/Ret signaling[J].Cell Signal,2015,27(3):578-586.
[9] TAM P K, GARCIA-BARCELÓ M. Genetic basis of Hirschsprung's disease[J].Pediatr Surg Int,2009,25(7):543-558.
[10] TANG W, QIN J, TANG J, et al. Aberrant reduction of MiR-141 increased CD47/CUL3 in Hirschsprung's disease[J].Cell Physiol Biochem,2013,32(6):1655-1667.
[11] LEI H, TANG J, LI H, et al. MiR-195 affects cell migration and cell proliferation by down-regulating DIEXF in Hirschsprung's disease[J].BMC Gastroenterol,2014,14:123.
[12] WANG X, CHAN A K, SHAM M H, et al. Analysis of the sacral neural crest cell contribution to the hindgut enteric nervous system in the mouse embryo[J].Gastroenterology,2011,141(3):992-1002.
[13] 陈东, 弭杰, 付冬辉, 等. 大鼠胚胎肠神经干细胞体外培养的时间选择及鉴定[J].中华小儿外科杂志,2015,36(3):226-229.
[14] 潘伟康, 郑百俊, 高亚, 等. bFGF联合EGF对人肠神经嵴前体细胞增殖及分化能力的影响[J].中华小儿外科杂志,2014,35(7):509-513.