Gene Expressions for Signal Transduction under Acidic Conditions

被引:10
作者
Fukamachi, Toshihiko [1 ]
Ikeda, Syunsuke [1 ]
Wang, Xin [1 ]
Saito, Hiromi [1 ]
Tagawa, Masatoshi [2 ]
Kobayashi, Hiroshi [1 ]
机构
[1] Chiba Univ, Grad Sch Pharmaceut Sci, Chuo Ku, Chiba 2608675, Japan
[2] Chiba Canc Ctr, Res Inst, Div Pathol & Cell Therapy, Chuo Ku, Chiba 2608717, Japan
关键词
gene expression; acidic conditions; signal pathways; cancer cells; KAPPA-B-BETA; HUMAN GLIOBLASTOMA CELLS; TERMINAL REGION PROTEIN; PH; ACIDOSIS; INTERLEUKIN-32; FLUID; MICROENVIRONMENT; PROLIFERATION; ENVIRONMENTS;
D O I
10.3390/genes4010065
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Although it is now well known that some diseased areas, such as cancer nests, inflammation loci, and infarction areas, are acidified, little is known about cellular signal transduction, gene expression, and cellular functions under acidic conditions. Our group showed that different signal proteins were activated under acidic conditions compared with those observed in a typical medium of around pH 7.4 that has been used until now. Investigations of gene expression under acidic conditions may be crucial to our understanding of signal transduction in acidic diseased areas. In this study, we investigated gene expression in mesothelioma cells cultured at an acidic pH using a DNA microarray technique. After 24 h culture at pH 6.7, expressions of 379 genes were increased more than twofold compared with those in cells cultured at pH 7.5. Genes encoding receptors, signal proteins including transcription factors, and cytokines including growth factors numbered 35, 32, and 17 among the 379 genes, respectively. Since the functions of 78 genes are unknown, it can be argued that cells may have other genes for signaling under acidic conditions. The expressions of 37 of the 379 genes were observed to increase after as little as 2 h. After 24 h culture at pH 6.7, expressions of 412 genes were repressed more than twofold compared with those in cells cultured at pH 7.5, and the 412 genes contained 35, 76, and 7 genes encoding receptors, signal proteins including transcription factors, and cytokines including growth factors, respectively. These results suggest that the signal pathways in acidic diseased areas are different, at least in part, from those examined with cells cultured at a pH of around 7.4.
引用
收藏
页码:65 / 85
页数:21
相关论文
共 33 条
[11]   Interstitial pH and pO(2) gradients in solid tumors in vivo: High-resolution measurements reveal a lack of correlation [J].
Helmlinger, G ;
Yuan, F ;
Dellian, M ;
Jain, RK .
NATURE MEDICINE, 1997, 3 (02) :177-182
[12]   Extracellular acidic environments induce phosphorylation of ZAP-70 in Jurkat T cells [J].
Hirata, Satoru ;
Fukamachi, Toshihiko ;
Sakano, Hiroyuki ;
Tarora, Ayumi ;
Saito, Hiromi ;
Kobayashi, Hiroshi .
IMMUNOLOGY LETTERS, 2008, 115 (02) :105-109
[13]   Acidic stress promotes a glioma stem cell phenotype [J].
Hjelmeland, A. B. ;
Wu, Q. ;
Heddleston, J. M. ;
Choudhary, G. S. ;
MacSwords, J. ;
Lathia, J. D. ;
McLendon, R. ;
Lindner, D. ;
Sloan, A. ;
Rich, J. N. .
CELL DEATH AND DIFFERENTIATION, 2011, 18 (05) :829-840
[14]  
Ihnatko R, 2006, INT J ONCOL, V29, P1025
[15]   Exploration, normalization, and summaries of high density oligonucleotide array probe level data [J].
Irizarry, RA ;
Hobbs, B ;
Collin, F ;
Beazer-Barclay, YD ;
Antonellis, KJ ;
Scherf, U ;
Speed, TP .
BIOSTATISTICS, 2003, 4 (02) :249-264
[16]   Summaries of affymetrix GeneChip probe level data [J].
Irizarry, RA ;
Bolstad, BM ;
Collin, F ;
Cope, LM ;
Hobbs, B ;
Speed, TP .
NUCLEIC ACIDS RESEARCH, 2003, 31 (04) :e15
[17]   IL-32, a proinflammatory cytokine in rheumatoid arthritis [J].
Joosten, LAB ;
Netea, MG ;
Kim, SH ;
Yoon, DY ;
Oppers-Walgreen, B ;
Radstake, TRD ;
Barrera, P ;
van de Loo, FAJ ;
Dinarello, CA ;
van den Berg, WB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (09) :3298-3303
[18]   Acidic extracellular pH induces matrix metalloproteinase-9 expression in mouse metastatic melanoma cells through the phospholipase D-mitogen-activated protein kinase signaling [J].
Kato, Y ;
Lambert, CA ;
Colige, AC ;
Mineur, P ;
Noël, A ;
Frankenne, F ;
Foidart, JM ;
Baba, M ;
Hata, R ;
Miyazaki, K ;
Tsukuda, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (12) :10938-10944
[19]   Interleukin-32:: A cytokine and inducer of TNFα [J].
Kim, SH ;
Han, SY ;
Azam, T ;
Yoon, DY ;
Dinarello, CA .
IMMUNITY, 2005, 22 (01) :131-142
[20]   Requirement of an IκB-β COOH terminal region protein for acidic-adaptation in CHO cells [J].
Lao, QZ ;
Fukamachi, T ;
Saito, H ;
Kuge, O ;
Nishijima, M ;
Kayashi, H .
JOURNAL OF CELLULAR PHYSIOLOGY, 2006, 207 (01) :238-243