Gene expression profiling of target genes in ventilator-induced lung injury
Author(s) -
Tamás Dolinay,
Naftali Kaminski,
Martina Felgendreher,
Hong P. Kim,
Paul R. Reynolds,
Simon C. Watkins,
Dörte Karp,
Stefan Uhlig,
Augustine M.K. Choi
Publication year - 2006
Publication title -
physiological genomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.078
H-Index - 112
eISSN - 1531-2267
pISSN - 1094-8341
DOI - 10.1152/physiolgenomics.00110.2005
Subject(s) - amphiregulin , biology , gene , gene expression profiling , gene expression , cyr61 , candidate gene , microbiology and biotechnology , immunology , ctgf , genetics , growth factor , receptor
In the lungs, high-pressure mechanical ventilation induces an inflammatory response similar to that observed in acute respiratory distress syndrome. To further characterize these responses and to compare them with classical inflammatory pathways, we performed gene expression profiling analysis of 20,000 mouse genes in isolated blood-free (to exclude genes from sequestered leukocytes) perfused mouse lungs exposed to low-pressure ventilation (10 cmH2O), high-pressure ventilation (25 cmH2O, overventilation), and LPS treatment. A large number of inflammatory and apoptotic genes were increased by both overventilation and LPS. However, certain growth factor-related genes, as well as genes related to development, cellular communication, and the cytoskeleton, were only regulated by overventilation. We validated and confirmed increased mRNA expression pattern of five genes (amphiregulin, gravin, Nur77, Cyr61, interleukin-11) by real-time PCR; furthermore, we confirmed increased protein expression of amphiregulin by immunohistochemistry and immunoblotting assays. These genes represent novel candidate genes in ventilator-induced lung injury.
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