Protein composition of liver cyst fluid from the BALB/c-cpk/+ mouse model of autosomal recessive polycystic kidney disease

被引:5
作者
Lai, Xianyin
Blazer-Yost, Bonnie L. [2 ,3 ]
Gattone, Vincent H., II [2 ]
Muchatuta, Monalisa N. [3 ]
Witzmann, Frank A. [1 ]
机构
[1] Indiana Univ, Sch Med, Dept Cellular & Integrat Physiol, Biotechnol Res & Training Ctr, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Dept Anat & Cell Biol, Indianapolis, IN 46202 USA
[3] Indiana Univ Purdue Univ, Dept Biol, Indianapolis, IN 46205 USA
关键词
Autosomal recessive polycystic kidney disease; LC-MS/MS; Liver cyst fluid; HUMAN BILE; EXTRACELLULAR-MATRIX; PROTEOMIC ANALYSIS; STATISTICAL-MODEL; MESSENGER-RNA; IN-VITRO; DOMINANT; MICE; CELLS; GENE;
D O I
10.1002/pmic.200800379
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cysts arising from hepatic bile ducts are a common extra-renal pathology associated with polycystic kidney disease in humans. As an initial step in identifying active components that could contribute to disease progression, we have investigated the protein composition of hepatic cyst fluid in an orthologous animal model of autosomal recessive polycystic kidney disease, heterozygous (BALB/c-cpk/+) mice. Proteomic analysis of cyst fluid tryptic digests using LC-MS/MS identified 303 proteins, many of which are consistent with enhanced inflammatory cell processes, cellular proliferation, and basal laminar fibrosis associated with the development of hepatic bile duct cysts. Protein identifications have been submitted to the PRIDE database (http://www.ebi.ac.uk/pride), accession number 9227.
引用
收藏
页码:3775 / 3782
页数:8
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