期刊文献+

The development of colon innervation in trisomy 16 mice and Hirschsprung’s disease 被引量:3

The development of colon innervation in trisomy mice and Hirschsprungs disease
下载PDF
导出
摘要 AIM To study the colon innervation of trisomy 16 mouse, an animal model for Downs syndrome, and the expression of protein gene product 9.5 (PGP 9.5) in the stenosed segment of colon in Hirschsprungs disease (HD). METHODS Trisomy 16 mouse breeding; cytogenetic analysis of trisomy 16 mice; and PGP 9.5 immunohistochemistry of colons of trisomy 16 mice and HD were carried out. RESULTS Compared with their normal littermates, the nervous system of colon in trisomy 16 mice was abnormally developed. There existed developmental delay of muscular plexuses of colon, no submucosal plexus was found in the colon, and there was 5mm aganglionic bowel aparting from the anus in trisomy 16 mice. The mesentery nerve fibers were as well developed as shown in their normal littermates. Abundant proliferation of PGP 9.5 positive nerve fibers was revealed in the stenosed segment of HD colon. CONCLUSION Trisomy 16 mice could serve as an animal model for Hirschsprung s disease for aganglionic bowel in the distal part of colon. Abundant proliferation of PGP 9.5 positive fibers resulted from extrinsic nerve compensation, since no ganglionic cells were observed in the stenosed segment of the colon in HD. HD has a genetic tendency. AIM To study the colon innervation of trisomy16 mouse, an animal model for Downssyndrome, and the expression of protein geneproduct 9.5 ( PGP 9.5) in the stenosed segmentof colon in Hirschsprungs disease (HD).METHODS Trisomy 16 mouse breeding;cytogenetic analysis of trisomy 16 mice; andPGP 9.5 immunohistochemistry of colons oftrisomy 16 mice and HD were carried out.RESULTS Compared with their normalIittermates, the nervous system of colon intrisomy 16 mice was abnormally developed.There existed developmental delay of muscularplexuses of colon, no submucosal plexus wasfound in the colon, and there was 5mmaganglionic bowel aparting from the anus intrisomy 16 mice. The mesentery nerve fiberswere as well developed as shown in their normallittermates. Abundant proliferation of PGP 9.5positive nerve fibers was revealed in thestenosed segment of HD colon.CONCLUSION Trisomy 16 mice could serve asaganglionic bowel in the distal part of colon.Abundant proliferation of PGP 9.5 positive fibersresulted from extrinsic nerve compensation,since no ganglionic cells were observed in thestenosed segment of the colon in HD. HD has agenetic tendency.
机构地区 Institute of Antomy
出处 《World Journal of Gastroenterology》 SCIE CAS CSCD 2001年第1期16-21,共6页 世界胃肠病学杂志(英文版)
基金 Project supported by the Grants of Analysis and Measurement of Zhejiang Province and Education Committee of Zhejiang Province.
关键词 Hirschsprungs disease COLON down syndrome IMMUNOHISTOCHEMISTRY nervous system TRISOMY 16 MOUSE Hirschsprungs disease colon down syndrome immunohistochemistry nervous system trisomy 16 mouse
  • 相关文献

参考文献12

  • 1Michael V. Zaragoza,Patricia A. Jacobs,Rowena S. James,Peter Rogan,Stephanie Sherman,Terry Hassold.Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns[J].Human Genetics.1994(4)
  • 2Chang-Jiang Zheng,Breck Byers.Oocyte selection: a new model for the maternal-age dependence of Down syndrome[J].Human Genetics (-).1992(1-2)
  • 3Epstein ML,Poulsen KT,Thiboldeaux R.Formation of ganglia in the gut of the chick embryo[].Journal of Comparative Neurology.1991
  • 4Epstein ML,Poulsen KT,Thiboldeaux R.Formation of ganglia in the gut of the chick embryo[].Journal of Comparative Neurology.1991
  • 5Leffler A,Ludwig M,Schmitt O,Bush LC.Germ cell migration and early development of the gonads in the trisomy 16 mouse-an animal model for Downs syndrome[].Anatomischer Anzeiger.1999
  • 6Webb S,Brown NA,Anderson RH.Cardiac morphology at late fetal stages in the mouse with trisomy 16: consequences for different formation of the atrioventricular junction when compared to humans with trisomy 21[].Cardiovascular Research.1997
  • 7Barone V,Weber D,Luo Y,Brancolini V,Devoto M,Romeo G.Exclusion of linkage between RET and neuronal intestinal dysplasia type B[].American Journal of Medical Genetics.1996
  • 8Wedel T,Krammer HJ,Kuhnel W,Sigge W.Alterations of the enteric nervous system in neonatal necrotizing enterocolitis revealed by whole-mount immunohistochemistry[].Pediatric Pathology.1998
  • 9Kapur RP,Yost C,Palmiter RD.A transgenic model for studying development of the enteric nervous system in normal and aganglionic mice[].Development.1992
  • 10Hoehner JC,Wester T,Pahlman S,Olsen L.Localization of neurotrophins and their high-affinity receptors during human enteric nervous system development[].Gastroenterology.1996

同被引文献3

引证文献3

二级引证文献18

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部