Gene expression alterations during HGF-induced dedifferentiation of a renal tubular epithelial cell line (MDCK) using a novel canine DNA microarray

被引:28
作者
Balkovetz, DF
Gerrard, ER
Li, SX
Johnson, D
Lee, J
Tobias, JW
Rogers, KK
Snyder, RW
Lipschutz, JH
机构
[1] Univ Alabama Birmingham, Dept Med, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Cell Biol, Birmingham, AL 35294 USA
[3] Vet Adm Med Ctr, Birmingham, AL 35294 USA
[4] Univ Alabama Birmingham, Dept Surg, Birmingham, AL 35294 USA
[5] Univ Penn, Genom Inst, Philadelphia, PA 19104 USA
[6] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[7] Univ Penn, Cell & Mol Biol Grad Grp, Philadelphia, PA 19104 USA
关键词
hepatocyte growth factor; Madin-Darby canine kidney cells;
D O I
10.1152/ajprenal.00270.2003
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Hepatocyte growth factor (HGF) elicits a broad spectrum of biological activities, including epithelial cell dedifferentiation. One of the most widely used and best-studied polarized epithelial cell lines is the Madin-Darby canine kidney (MDCK) cell line. Here, we describe and validate the early response of polarized monolayers of MDCK cells stimulated with recombinant HGF using a novel canine DNA microarray designed to query 12,473 gene sequences. In our survey, eight genes previously implicated in the HGF signaling pathway were differentially regulated, demonstrating that the system was responsive to HGF. Also identified were 117 genes not previously known to be involved in the HGF pathway. The results were confirmed by real-time PCR or Western blot analysis for 38 genes. Of particular interest were the large number of differentially regulated genes encoding small GTPases, proteins involved in endoplasmic reticulum translation, proteins involved in the cytoskeleton, the extracellular matrix, and the hematopoietic and prostaglandin systems.
引用
收藏
页码:F702 / F710
页数:9
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