期刊文献+

HAND2蛋白在先天性巨结肠肠壁肌间神经丛中的表达及意义 被引量:1

The expression and significance of HAND2 in the myenteric plexus of the colon in patients with Hirschsprung's disease
下载PDF
导出
摘要 目的研究HAND2蛋白在先天性巨结肠症患儿肠壁肌间神经丛的表达情况,探讨HAND2蛋白与先天性巨结肠发病的关系。方法应用免疫组化二步法染色检测46例先天性巨结肠患儿狭窄段、移行段、扩张段和正常段肠壁组织肌间神经丛中HAND2蛋白的表达,用计算机图像分析软件(Image ProPlus 6.0)计算HAND2蛋白在先天性巨结肠各段肠壁组织肌间神经丛的免疫组化阳性染色的平均光密度值。结果 HAND2蛋白在先天性巨结肠患儿正常肠壁组织的肌间神经丛有阳性表达,多呈强阳性;环形肌及纵行肌亦有表达,多呈中等强度阳性。狭窄段肌间神经丛中,未见有阳性染色的神经节细胞,可见肌间神经纤维表达呈弱阳性或阴性;在移行段与扩张段肌间神经丛中,可见较多阳性表达肌间神经节或神经纤维。分别与移行段、扩张段及正常段比较,狭窄段的平均光密度明显降低,差异有统计学意义(P<0.01)。结论狭窄段肠壁肌间神经丛中HAND2蛋白表达量降低,HAND2蛋白表达改变可能是先天性巨结肠的发病因素之一。 Objective To investigate the expression of HAND2 in the myenteric plexus of the colon in patients with Hirschsprung's disease (HD), thus to study correlation between HAND2 and pathogenesis of HD. Methods The aganglionic, transitional, dilated and normal segments from the resected colon specimens of 46 patients with HD were col- lected for study. Immunohistochemistry was applied to assess the protein expression of HAND2. Results In normal seg- ments, HAND2 was strong positive in the myenteric plexus and median positive in muscle layers, including circular and longitudinal layers. No HAND2 positive ganglion cell was observed in the myenteric plexus in aganglionie segments, though weak positive or negative nerve fibers could be observed. HAND2 positive myenteric plexus were also observed in the transitional and dilated segments. Significant reduction in optical density of HAND2 was revealed in myenteric plexus in aganglionic segments when comparing with those in transitional, dilated and normal segments (P 〈 0. 01 ). Conclusion HAND2 is down - regulated in the myenteric plexus of the aganglionic segment of HD patients, suggesting it is involved its pathogenesis.
出处 《广东医学》 CAS CSCD 北大核心 2013年第10期1513-1515,共3页 Guangdong Medical Journal
基金 广东省自然科学基金面上项目(编号:S2012010008947)
关键词 先天性巨结肠 HAND2 免疫组化 肌间神经丛 Hirschsprung's disease HAND2 immunohistochemistry myenteric plexus
  • 相关文献

参考文献9

  • 1PAN Z W, LI J C. Advances in molecular genetics of Hirschs- prung's disease[J]. Anat Rec(Hoboken) , 2012, 295 (10) : 1628 - 1638.
  • 2KENNY S E, TAM P K, GARCIA BARCELO M. Hirschsprung's disease[J]. Semin Pediatr Surg, 2010, 19(3) : 194-200.
  • 3IKLE J M, ARTINGER K B, CLOUTHIER D E. Identification and characterization of the zebrafish pharyngeal arch - specific en- hancer for the basic helix - loop - helix transcription factor Hand2 [J]. DevBiol, 2012, 368(1): 118-126.
  • 4贺强,王立峰.bHLH蛋白家族的功能[J].国外医学(生理病理科学与临床分册),2004,24(6):545-547. 被引量:8
  • 5LIU N, BARBOSA A C, CHAPMAN S L, et al. DNA binding- dependent and - independent functions of the Hand2 transcription factor during mouse embryogenesis[ J]. Development, 2009, 136 (6) : 933 - 942.
  • 6HENDERSHOT T J, LIU H, SARKAR A A, et al. Expression of Hand2 is sufficient for neurogenesis and cell type - specific gene expression in the enteric nervous system [ J]. Dev Dyn, 2007, 236( 1 ) : 93 - 105.
  • 7HOWARD M, FOSTER D N, CSERJESI P. Expression of HAND gene products may be sufficient for the differentiation of avian neu- ral crest - derived cells into catecholaminergic neurons in culture [J]. DevBiol, 1999, 215(1): 62-77.
  • 8LEI J, HOWARD M J. Targeted deletion of Hand2 in enteric neu- ral precursor ceils affects its functions in neurogenesis, neurotrans- ndtter specification and gangliogenesis, causing functional agangli- onosis[ J]. Development, 2011, 138(21 ) : 4789 -4800.
  • 9D'AUTRIEAUX F, MORIKAWA Y, CSERJESI P, et al. Hand2 is necessary for terminal differentiation of enteric neurons from crest - derived precursors but not for their migration into the gut or for formation of glia[J]. Development, 2007, 134(12): 2237- 2249.

二级参考文献15

  • 1Fischer A, Leimeister C, Winkler C, et al. Hey bHLH factors in cardiovascular development[J]. Cold Spring Harb Symp Quant Biol, 2002,67(6) :63-70.
  • 2Allan DW, Thor S. Together at last: bHLH and LIM-HD regulators cooperate to specify motor neurons [ J ]. Neuron, 2003,38 ( 5 ) :675-677.
  • 3Dambly-Chaudiere C, Vervoort M. The bHLH genes in neural development [ J ]. Int J Dev Biol, 1998,42 (3) :269-273.
  • 4Lees MJ, Whitelaw ML. Effect of ARA9 on dioxin receptor mediated transcription[ J]. Toxicology, 2002,27 (12): 143-146.
  • 5Greenbaum S, Zhuang Y. Regulation of early lymphocyte development by E2A family proteins[ J ]. Semin Immunol, 2002,14 (6):405-414.
  • 6Kageyama R, Ohtsuka T, Tomita K, et al. The bHLH gene Hesl regulates differentiation of multiple cell types [ J ]. Mol Cells, 2000,29(1) :1-7
  • 7Guillemot F. Vertebrate bHLH genes and the determination of neuronal fates[J]. Exp Cell Res, 1999,253(2):357-364.
  • 8Olson EN, Arnold HH, Rigby PW, et al. Know your neighbors:three phenotypes in null mutants of the myogenic bHLH gene MRF4[J]. Genes Dev,1994,8(1) :1-8.
  • 9Bray SJ. Expression and function of Enhancer of split bHLH proteins during Drosophila neurogenesis[ J]. Perspect Dev Neurobiol,1997,4(4) :313-323.
  • 10Fisher A, Caudy M. The function of hairy-related bHLH repressor proteins in cell fate decisions [ J ]. Bioessays, 1998,20 ( 4 ): 298-306.

共引文献7

同被引文献16

  • 1杜勇,施诚仁,潘骏,张文竹.先天性巨结肠HuD蛋白表达的实验研究[J].临床小儿外科杂志,2005,4(5):345-348. 被引量:4
  • 2崔新海,陈雨历,张蕾,张唐山,刘园园.先天性巨结肠突触素免疫组织化学研究[J].中国现代普通外科进展,2006,9(6):340-342. 被引量:2
  • 3孙树敏,刘皓.神经生长相关蛋白与突触可塑性[J].天津医科大学学报,2007,13(1):118-121. 被引量:8
  • 4Mckeown SJ,Stamp L,Hao MM,et al.Hirschsprung disease: a developmental disorder of the enteric nervous system.Wiley Interdiscip Rev Dev Biol,2013,2(1): 113-129.
  • 5Pan ZW,Li JC.Advances in molecular genetics of Hirschsprung’s disease.Anat Rec (Hoboken),2012,295(10): 1628-1638.
  • 6Sharkey KA,Coggin PJ,Tetzlaff W,et al.Distribution of troth-associated protein,B-50 (GAP-43) in the mammalian enteric nervous system.Neuroscience,1990,38(1): 13-20.
  • 7Andreasen TJ,Luetje CW,Heideman W,et al.Purification of a novel calmodulin binding protein from bovine cerebral cortex membranes.Biochemistry,1983,22(20): 4615-4618.
  • 8Pascale A,Gusev PA,Amadio M,et al.Increase of the RNA-binding protein HuD and posttranscriptional up-regulation of the GAP-43 gene during spatial memory.Proc Natl Acad Sci U S A,2004,101(5): 1217-1222.
  • 9Smith CL,Afroz R,Bassell GJ,et al.GAP-43 mRNA in growth cones is associated with HuD and ribosomes.J Neurobiol,2004,61(2): 222-235.
  • 10Kobayashi H,Hirakawa H,Puri P.Is intestinal neuronal dysplasia a disorder of the neuromuscular junction?.J Pediatr Surg,1996,31(4): 575-579.

引证文献1

二级引证文献1

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