SIGNALING AND GROWTH-RESPONSES OF LLC-PK1/CL-4 CELLS TRANSFECTED WITH THE RABBIT AT(1) ANG-II RECEPTOR

被引:23
作者
BURNS, KD
HARRIS, RC
机构
[1] UNIV OTTAWA, DEPT MED, OTTAWA, ON K1H 8M5, CANADA
[2] UNIV OTTAWA, DEPT PHYSIOL, OTTAWA, ON K1H 8M5, CANADA
[3] OTTAWA GEN HOSP, OTTAWA, ON K1H 8M5, CANADA
[4] VANDERBILT UNIV, DEPT MED, NASHVILLE, TN 37232 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 1995年 / 268卷 / 04期
关键词
PROXIMAL TUBULE; POLARITY; HYPERTROPHY; KINASES;
D O I
10.1152/ajpcell.1995.268.4.C925
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Angiotensin II (ANG II) receptors of the AT(1) subtype are present on the apical and basolateral membranes of renal proximal tubule cells. Cells of the proximal tubulelike cell line, LLC-PK1/Cl-4, were transfected with an expression plasmid containing cDNA encoding the rabbit AT(1) ANG II receptor. In transfected cells, specific binding of I-125-ANG II was detected on both apical and basolateral membranes; wild-type LLC-PK1/Cl-4 cells did not express ANG II receptors. In transfected cells, apical or basolateral ANG II increased both S6 kinase activity and incorporation of [H-3]leucine. In cells pretreated with pertussis toxin, the stimulatory effect of apical or basolateral ANG II on [H-3]leucine incorporation was abolished. In contrast, ANG II did not affect mitogenesis, determined by [H-3]thymidine incorporation. Apical or basolateral ANG II (10(-6) M) stimulated phosphoinositide turnover by 13.4 +/- 4.4% (n = 8) and 16.3 +/- 4.2% (n = 9), respectively. The activity of protein kinase C, determined by phosphorylation of a specific protein kinase C peptide substrate, was also stimulated by ANG II in transfected cells. Apical or basolateral ANG II had no significant effect on cellular adenosine 3',5'-cyclic monophosphate levels. In permeabilized transfected cells, apical ANG II (10(-6) M) inhibited the phosphorylation of a specific peptide substrate of protein kinase A; lower apical concentrations or basolateral ANG II were without significant effect. These results indicate that AT(1) ANG II receptors sort to both apical and basolateral membranes in renal epithelial cells and are coupled to activation of phospholipase C. ANG II stimulates protein synthesis by binding to either apical or basolateral receptors; this effect requires coupling to G proteins and may be mediated by activation of S6 kinase. Because high concentrations of ANG II exist in proximal tubule, binding to apical and basolateral receptors may regulate proximal tubule cell growth under physiological conditions.
引用
收藏
页码:C925 / C935
页数:11
相关论文
共 37 条
[2]   PROXIMAL TUBULAR SECRETION OF ANGIOTENSIN-II IN RATS [J].
BRAAM, B ;
MITCHELL, KD ;
FOX, J ;
NAVAR, LG .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (05) :F891-F898
[3]   ANGIOTENSIN-II-BINDING SITES IN RAT AND PRIMATE ISOLATED RENAL TUBULAR BASOLATERAL MEMBRANES [J].
BROWN, GP ;
DOUGLAS, JG .
ENDOCRINOLOGY, 1983, 112 (06) :2007-2014
[4]   ANGIOTENSIN-II BINDING-SITES ON ISOLATED RAT RENAL BRUSH-BORDER MEMBRANES [J].
BROWN, GP ;
DOUGLAS, JG .
ENDOCRINOLOGY, 1982, 111 (06) :1830-1836
[5]  
BURNS KD, 1993, SEMIN NEPHROL, V13, P13
[6]   REGULATION OF NA+-H+ EXCHANGE BY ATP DEPLETION AND CALMODULIN ANTAGONISM IN RENAL EPITHELIAL-CELLS [J].
BURNS, KD ;
HOMMA, T ;
HARRIS, RC .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (04) :F607-F616
[7]   CLONING OF A RABBIT KIDNEY CORTEX AT(1) ANGIOTENSIN-II RECEPTOR THAT IS PRESENT IN PROXIMAL TUBULE EPITHELIUM [J].
BURNS, KD ;
INAGAMI, T ;
HARRIS, RC .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (04) :F645-F654
[8]   ANGIOTENSIN-II STIMULATION OF NA-H ANTIPORTER ACTIVITY IS CAMP-INDEPENDENT IN OKP CELLS [J].
CANO, A ;
MILLER, RT ;
ALPERN, RJ ;
PREISIG, PA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (06) :C1603-C1608
[9]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[10]   INTRACELLULAR MESSENGER FOR ACTION OF ANGIOTENSIN-II ON FLUID TRANSPORT IN RABBIT PROXIMAL TUBULE [J].
DOMINGUEZ, JH ;
SNOWDOWNE, KW ;
FREUDENRICH, CC ;
BROWN, T ;
BORLE, AB .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 252 (03) :F423-F428