IFN-γ downregulates expression of Na+/H+ exchangers NHE2 and NHE3 in rat intestine and human Caco-2/bbe cells

被引:103
作者
Rocha, F [1 ]
Musch, MW [1 ]
Lishanskiy, L [1 ]
Bookstein, C [1 ]
Sugi, K [1 ]
Xie, Y [1 ]
Chang, EB [1 ]
机构
[1] Univ Chicago, Martin Boyer Labs, Dept Med, Chicago, IL 60637 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2001年 / 280卷 / 05期
关键词
inflammatory bowel disease; inflammation; mucosa; sodium transport; sodium absorption; water and electrolyte transport; diarrhea; malabsorption; transporter; intestinal adaptation;
D O I
10.1152/ajpcell.2001.280.5.C1224
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Diarrhea associated with inflammatory bowel diseases has traditionally been attributed to stimulated secretion. The purpose of this study was to determine whether chronic stimulation of intestinal mucosa by interferon-gamma (IFN-gamma) affects expression and function of the apical membrane Na+/H+ exchangers NHE2 and NHE3 in rat intestine and Caco-2/bbe (C2) cells. Confluent C2 cells expressing NHE2 and NHE3 were treated with IFN-gamma for 2, 24, and 48 h. Adult rats were injected with IFN-gamma intraperitoneally for 12 and 48 h. NHE2 and NHE3 activities were measured by unidirectional Na-22 influx across C2 cells and in rat brush-border membrane vesicles. NHE protein and mRNA were assessed by Western and Northern blotting. IFN-gamma treatment of C2 monolayers caused a >50% reduction in NHE2 and NHE3 activities and protein expression. In rats, region-specific, time- and dose-dependent reductions of NHE2 and NHE3 activities, protein expression, and mRNA were observed after exposure to IFN-gamma. Chronic exposure of intestinal epithelial cells to IFN-gamma results in selective downregulation of NHE2 and NHE3 expression and activity, a potential cause of inflammation-associated diarrhea.
引用
收藏
页码:C1224 / C1232
页数:9
相关论文
共 32 条
[21]  
MUSCH MW, 1994, INFLAMM BOWEL DIS, P239
[22]  
Ruemmele FM, 1998, J CELL PHYSIOL, V176, P120, DOI 10.1002/(SICI)1097-4652(199807)176:1<120::AID-JCP14>3.0.CO
[23]  
2-B
[24]   CELLULAR BASIS FOR DEFECTIVE ELECTROLYTE TRANSPORT IN INFLAMED HUMAN COLON [J].
SANDLE, GI ;
HIGGS, N ;
CROWE, P ;
MARSH, MN ;
VENKATESAN, S ;
PETERS, TJ .
GASTROENTEROLOGY, 1990, 99 (01) :97-105
[25]   Cytosolic alkalinization increases stress-activated protein kinase/c-Jun NH2-terminal kinase (SAPK/JNK) activity and p38 mitogen-activated protein kinase activity by a calcium-independent mechanism [J].
Shrode, LD ;
Rubie, EA ;
Woodgett, JR ;
Grinstein, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (21) :13653-13659
[26]  
Sugimura K, 1999, GASTROENTEROLOGY, V116, pA827
[27]   Effect of chronic inflammation on electrolyte transport in rabbit ileal villus and crypt cells [J].
Sundaram, U ;
West, AB .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1997, 272 (04) :G732-G741
[28]   Mechanism of inhibition of Na+-glucose cotransport in the chronically inflamed rabbit ileum [J].
Sundaram, U ;
Wisel, S ;
Rajendren, VM ;
West, AB .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1997, 273 (04) :G913-G919
[29]   REGULATION OF ACTIVE SODIUM AND POTASSIUM-TRANSPORT IN THE DISTAL COLON OF THE RAT - ROLE OF THE ALDOSTERONE AND GLUCOCORTICOID RECEPTORS [J].
TURNAMIAN, SG ;
BINDER, HJ .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (06) :1924-1929
[30]   Quantitative contribution of NHE2 and NHE3 to rabbit ileal brush-border Na+/H+ exchange [J].
Wormmeester, L ;
De Medina, FS ;
Kokke, F ;
Tse, CM ;
Khurana, S ;
Bowser, J ;
Cohen, ME ;
Donowitz, M .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1998, 274 (05) :C1261-C1272