Properties of secondary and tertiary human enteric nervous system neurospheres

被引:39
|
作者
Lindley, Richard M. [1 ,2 ]
Hawcutt, Daniel B. [1 ]
Connell, M. Gwen [1 ]
Edgar, David H. [3 ]
Kenny, Simon E. [1 ]
机构
[1] Univ Liverpool, Royal Liverpool Childrens NHS Fdn Trust Alder Hey, Dept Paediat Surg, Inst Child Hlth, Liverpool L12 2AP, Merseyside, England
[2] Nottingham Univ Hosp NHS Trust, Dept Paediat Surg, Queens Med Ctr, Nottingham NG7 2UH, England
[3] Univ Liverpool, Dept Human Anat & Cell Biol, Liverpool L69 3GE, Merseyside, England
基金
英国医学研究理事会;
关键词
Enteric nervous system; Neurosphere; Transplantation; Stem cell; Secondary; Tertiary; CREST-DERIVED CELLS; STEM-CELLS; PRECURSOR CELLS; TRANSPLANTATION; RECOVERY; NEURONS; MODEL; BOWEL; GLIA;
D O I
10.1016/j.jpedsurg.2009.02.048
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Advances in enteric nervous system (ENS) stem cell biology have raised the possibility of treating Hirschsprung's disease with ENS stem/progenitor cell (ENSPC) transplantation. This study aimed to expand ENSPC numbers by the growth and redissociation of neurospheres and assess their differential potential. Methods: Human ENS neurospheres were cultured as previously described and redissociated to generate secondary and tertiary neurospheres. Neurospheres were assessed for the presence of neuronal (PGP9.5), glial (S100), and stem cell (p75, nestin markers). The degree of immunofluorescence was quantified using the ImageJ program. Secondary/tertiary neurospheres were transplanted into Mouse distal colon grown in tissue Culture. Results: Secondary/tertiary neurospheres could be generated with exponentially increasing numbers. Tertiary neurospheres showed a significant increase in the proportion of p75 staining but a significant decrease in the proportion of S100 staining. After transplantation, secondary/tertiary neurosphere-derived cells positive for PGP9.5 and S100 Could be identified. Conclusions: It is possible to exponentially expand neurosphere and therefore ENSPC numbers by repeated dissociation and culture. There is a loss of S100-positive cells in secondary/tertiary neurospheres, but the ENSPCs remain capable of differentiating into neurons and glia when transplanted into an embryonic gut environment. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:1249 / 1256
页数:8
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