Wang Weilin, Su Zhenwei, Chen Dong, Mi Jie, Gao Hong
Key Laboratory of Health Ministry for Congenital Malformations, Shengjing Hospital of China Medical University 36 Sanhao Street Heping District, Shenyang, Liaoning, 110004, The People's Republic of China.
Department of Pediatric Surgery, Women and Children Hospital Dandong City Liaoning 118002, The People's Republic of China.
Int J Clin Exp Pathol. 2014 Apr 15;7(5):2312-8. eCollection 2014.
Hirschsprung disease (HSCR) is characterized by the absence of intramural ganglion cells in the nerve plexuses of the distal gut. Recent studies have shown that the bone morphogenetic protein receptor-type IA (BMPR1α), actinin-alpha 4 (ACTN4α) and fatty acid binding protein 7 (FABP7) play important roles in the differentiation and development of neurons. The aganglionic (stenotic) and the ganglionic (normal) colon segment tissues of 60 HSCR patients were collected to investigate the expression pattern of BMPR1α, ACTININ-4α and FABP7 using RT-PCR, quantitative real-time RT-PCR (qRT-PCR) and immunohistochemical staining. The mRNA and protein expressions of BMPR1α and ACTN4α were higher in the stenotic colon segment tissue than those in the normal colon segment tissue. However, the mRNA and protein expressions of FABP7 were lower in the stenotic colon segment tissue than those in the normal colon segment tissue. The study in HSCR patients, findings in mRNA and protein alterations to expecting provide more information to in order to find some clue for the pathomechanism of HSCR disease.
先天性巨结肠症(HSCR)的特征是远端肠道神经丛中缺乏壁内神经节细胞。最近的研究表明,骨形态发生蛋白受体IA型(BMPR1α)、肌动蛋白α4(ACTN4α)和脂肪酸结合蛋白7(FABP7)在神经元的分化和发育中起重要作用。收集60例HSCR患者的无神经节(狭窄)和有神经节(正常)结肠段组织,采用逆转录聚合酶链反应(RT-PCR)、定量实时逆转录聚合酶链反应(qRT-PCR)和免疫组织化学染色法研究BMPR1α、ACTININ-4α和FABP7的表达模式。BMPR1α和ACTN4α的mRNA和蛋白表达在狭窄结肠段组织中高于正常结肠段组织。然而,FABP7的mRNA和蛋白表达在狭窄结肠段组织中低于正常结肠段组织。对HSCR患者的研究,mRNA和蛋白改变的发现有望提供更多信息,以便为HSCR疾病的发病机制找到一些线索。