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囊性纤维化相关肝病中肝纤维化的转录基础。

Transcriptional basis for hepatic fibrosis in cystic fibrosis-associated liver disease.

机构信息

The University of Queensland, Brisbane, Australia.

出版信息

J Pediatr Gastroenterol Nutr. 2012 Mar;54(3):328-35. doi: 10.1097/MPG.0b013e3182432034.

Abstract

OBJECTIVES

Liver disease contributes to significant morbidity and mortality in cystic fibrosis (CF). Although all patients with CF express the defective CF transmembrane conductance regulator in cholangiocytes, many develop asymptomatic fibrosing liver disease. Only some develop cirrhosis, with pathogenesis remaining enigmatic. Available noninvasive diagnostic tools do not identify patients at risk before development of advanced fibrosis. We conducted a pilot study to identify genes associated with hepatic injury and fibrosis on liver biopsy that may help elucidate determinants of CF-associated liver disease (CFLD).

METHODS

Liver tissue from children with CFLD with various stages of hepatic fibrosis was compared with pediatric controls using cDNA array analysis. Differential expression of genes of interest was then assessed relative to pediatric control liver and non-CF cholestatic disease control liver from patients with biliary atresia, using both real-time reverse transcription-polymerase chain reaction and immunohistochemistry.

RESULTS

cDNA array demonstrated differential expression of numerous genes associated with hepatic fibrogenesis including collagens, matrix metalloproteinases, and chemokines in CFLD versus normal controls, particularly decreased expression in tissue remodeling genes including plasminogen activator inhibitor-1 (PAI-1, up to 25-fold) and tissue inhibitor of metalloproteinase-1 (TIMP-1); this was validated by real-time reverse transcription-polymerase chain reaction (PAI-1, P = 0.004; TIMP-1, P = 0.019). No significant decrease in PAI-1 or TIMP-1 mRNA was observed in biliary atresia versus normal control. Immunohistochemistry confirmed the decreased expression of hepatic PAI-1 and TIMP-1 protein in CFLD versus both normal and biliary atresia disease controls.

CONCLUSIONS

The coordinated differential expression of these genes associated with liver fibrosis provides evidence for a transcriptional basis for the pathogenesis of CFLD and provides avenues for further study. Clarifying the pathogenesis of CFLD will facilitate techniques for early, precirrhotic detection and targeted interventions.

摘要

目的

肝脏疾病是囊性纤维化(CF)患者发病和死亡的主要原因。尽管所有 CF 患者的胆管细胞中都表达有缺陷的 CF 跨膜电导调节蛋白,但许多患者无症状性肝纤维化。只有少数患者会发展为肝硬化,其发病机制仍然难以捉摸。现有的非侵入性诊断工具无法在进展为晚期纤维化之前识别出有风险的患者。我们进行了一项试点研究,以确定与肝活检中肝损伤和纤维化相关的基因,这些基因可能有助于阐明 CF 相关肝病(CFLD)的决定因素。

方法

使用 cDNA 阵列分析比较了具有不同肝纤维化阶段的 CFLD 儿童患者的肝组织与儿科对照,然后使用实时逆转录-聚合酶链反应和免疫组织化学评估了与儿科对照肝和胆道闭锁患者胆汁淤积性疾病对照肝相比,感兴趣基因的差异表达。

结果

cDNA 阵列显示,与正常对照相比,CFLD 患者中与肝纤维化相关的许多基因的表达存在差异,包括胶原、基质金属蛋白酶和趋化因子,特别是组织重塑基因的表达降低,包括纤溶酶原激活物抑制剂-1(PAI-1,高达 25 倍)和金属蛋白酶组织抑制剂-1(TIMP-1);这通过实时逆转录-聚合酶链反应得到了验证(PAI-1,P=0.004;TIMP-1,P=0.019)。与正常对照相比,胆道闭锁患者中 PAI-1 或 TIMP-1 mRNA 无明显降低。免疫组织化学证实,与正常和胆道闭锁疾病对照相比,CFLD 患者肝 PAI-1 和 TIMP-1 蛋白表达降低。

结论

这些与肝纤维化相关的基因的协同差异表达为 CFLD 发病机制提供了转录基础的证据,并为进一步研究提供了途径。阐明 CFLD 的发病机制将有助于早期、肝硬化前检测和靶向干预技术的发展。

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