首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Differences in the Degree of Cerulein-Induced Chronic Pancreatitis in C57BL/6 Mouse Substrains Lead to New Insights in Identification of Potential Risk Factors in the Development of Chronic Pancreatitis
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Differences in the Degree of Cerulein-Induced Chronic Pancreatitis in C57BL/6 Mouse Substrains Lead to New Insights in Identification of Potential Risk Factors in the Development of Chronic Pancreatitis

机译:C57BL / 6小鼠亚种中由铜绿素诱导的慢性胰腺炎程度的差异导致鉴定慢性胰腺炎发展中潜在危险因素的新见解

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摘要

A frequently used experimental model of chronic pancreatitis (CP) recapitulating human disease is repeated injection of cerulein into mice. C57BL/6 is the most commonly used inbred mouse strain for biomedical research, but widespread demand has led to generation of several substrains with subtly different phenotypes. In this study, two common substrains, C57BL/6J and C57BL/6NHsd, exhibited different degrees of CP, with C57BL/6J being more susceptible to repetitive cerulein-induced CP as assessed by pancreatic atrophy, pancreatic morphological changes, and fibrosis. We hypothesized that the deficiency of nicotinamide nucleotide transhydrogenase (NNT) protein in C57BL/6J is responsible for the more severe C57BL/6J phenotype but the parameters of CP in NNT-expressing transgenic mice generated on a C57BL6/J background do not differ with those of wild-type C57BL/6J. The highly similar genetic backgrounds but different CP phenotypes of these two substrains presents a unique opportunity to discover genes important in pathogenesis of CP. We therefore performed whole mouse genome Affymetrix microarray analysis of pancreatic gene expression of C57BL/6J and C57BL/6NHsd before and after induction of CP. Genes with differentially regulated expression between the two substrains that might be candidates in CP progression included Mmp7, Pcolce2, Itih4, Wdfy1, and Vtn. We also identified several genes associated with development of CP in both substrains, including RIKEN cDNA 1810009J06 gene (trypsinogen 5), Ccl8, and Ccl6.
机译:重现人类疾病的慢性胰腺炎(CP)的常用实验模型是向小鼠重复注射cerulein。 C57BL / 6是用于生物医学研究的最常用的自交小鼠品系,但广泛的需求导致产生了具有不同表型的几种亚品系。在这项研究中,两个常见的亚菌株C57BL / 6J和C57BL / 6NHsd表现出不同程度的CP,通过胰腺萎缩,胰腺形态学改变和纤维化评估,C57BL / 6J更容易受到反复的轻蓝素诱导的CP的影响。我们假设C57BL / 6J中烟酰胺核苷酸转氢酶(NNT)蛋白的缺乏是造成更严重的C57BL / 6J表型的原因,但是在C57BL6 / J背景下生成的表达NNT的转基因小鼠中CP的参数与那些没有区别野生型C57BL / 6J。这两个亚种的高度相似的遗传背景但不同的CP表型为发现在CP发病机理中重要的基因提供了独特的机会。因此,我们在诱导CP前后对C57BL / 6J和C57BL / 6NHsd胰腺基因表达进行了全小鼠基因组Affymetrix微阵列分析。在两个亚菌株之间表达差异调节的基因可能是CP进展的候选基因,包括Mmp7,Pcolce2,Itih4,Wdfy1和Vtn。我们还确定了与这两个亚菌株中CP发育相关的几个基因,包括RIKEN cDNA 1810009J06基因(胰蛋白酶原5),Ccl8和Ccl6。

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