Identification of macrophage genes responsive to extracellular acidification

Authors
Park, Seung-YoonKim, In-San
Issue Date
2013-04
Publisher
SPRINGER BASEL AG
Citation
INFLAMMATION RESEARCH, v.62, no.4, pp.399 - 406
Abstract
A low pH microenvironment is a characteristic feature of inflammation loci and affects the functions of immune cells. In this study, we investigated the effect of extracellular acidification on macrophage gene expression. RAW264.7 macrophages were incubated in neutral (pH 7.4) or acidic (pH 6.8) medium for 4 h. Global mRNA expression levels were determined using Affymetrix genechips. The mRNA expressions of 353 macrophage genes were significantly modified after incubation in acidic medium; 193 were up-regulated and 160 down-regulated. Differentially regulated genes were grouped into 13 classes based on the functions of the corresponding protein products. Pathway analysis revealed that differentially expressed genes are enriched in pathways related to inflammation and immune responses. Quantitative real-time PCR analysis confirmed that the expressions of CXCL10, CXCL14, IL-18, IL-4RA, ABCA1, CCL4, IL-7R, CXCR4, TLR7, and CCL3 mRNAs were regulated by extracellular acidification. The results of this study provide insights into the effects of acidic extracellular environments on macrophage gene expression.
Keywords
KAPPA-B ACTIVATION; APOPTOTIC CELLS; ALPHA-V-BETA-5 INTEGRIN; DEPENDENT PHAGOCYTOSIS; BLOOD-FLOW; PH; INFLAMMATION; NEUTROPHIL; EXPRESSION; PHOSPHATIDYLSERINE; Gene expression; Extracellular acidification; Macrophages; Microarray
ISSN
1023-3830
URI
https://pubs.kist.re.kr/handle/201004/128179
DOI
10.1007/s00011-013-0591-6
Appears in Collections:
KIST Article > 2013
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