Intracellular angiotensin II fusion protein alters AT1 receptor fusion protein distribution and activates CREB

被引:46
作者
Cook, JL [1 ]
Re, R [1 ]
Alam, J [1 ]
Hart, M [1 ]
Zhang, Z [1 ]
机构
[1] Ochsner Clin Fdn, Div Res, New Orleans, LA 70121 USA
关键词
angiotensin II; intracrine; enhanced green fluorescent protein; CREB;
D O I
10.1016/j.yjmcc.2003.09.021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In recently published studies, we show that angiotensin II (AII) generated from an engineered rat angiotensinogen cDNA, and maintained intracellularly, is growth stimulatory for a rat hepatoma cell line. In the present study, we report that co-expression of AII fused to cyan fluorescent protein (ECFP/AII) and angiotensin type I receptor fused to yellow fluorescent protein (AT(1)R/EYFP) enhances proliferation of COS-7 and CHO-K1 cells by 59% and 64%, respectively, compared to cells expressing the corresponding independent proteins (P < 0.001 for both). This effect is inhibited by losartan, suggesting (as in our previous published studies) that losartan is internalized by the cells, via receptor-mediated endocytosis, and thus inhibits intracellular receptor-ligand interaction. The growth effect is independent of anti-All antibodies suggesting that it does not reflect All secretion into the culture media; All is also undetectable in the media. Expression of AT(1)R/EYFP with ECFP/AII(C) (control scrambled sequence AII fused to ECFP) has no effect upon cell proliferation. ECFP/AII also alters the cellular localization of AT(1)R/EYFP. ECFP/AII is concentrated in the nucleus, but shows diffuse cytoplasmic fluorescence as well. AT(1)R/EYFP, expressed independently, is visible in the endoplasmic reticulum and Golgi apparatus of COS-7 and CHO-K1 cells as early as 24-h post-transfection. At 72 h, it is visibly associated with the plasma membrane. By 144 h, 85% of the cells show detectable circumferential fluorescence. In contrast, in cells that express AT(1)R/EYFP and ECFP/AII, both proteins accumulate in the nucleus and only 13% of the cells show visible plasma membrane-associated yellow fluorescence at 144 h (P < 0.001). Furthermore, co-expression of ECFP/AII with AT(1)R/EYFP stimulates cAMP response element-binding protein (CREB) activity in CHO-K1 and COS-7 cells. Exogenous AII similarly significantly increases CREB activation in AT(1)R/EYFP-stably transfected CHO-K1 and COS-7 cells. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:75 / 90
页数:16
相关论文
共 54 条
[1]   INTRACELLULAR-LOCALIZATION OF THE P21(RHO) PROTEINS [J].
ADAMSON, P ;
PATERSON, HF ;
HALL, A .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :617-627
[2]  
Alam J, 2000, J BIOL CHEM, V275, P27694
[3]   Characterization of the sequences of the human cytomegalovirus enhancer that mediate differential regulation by natural and synthetic retinoids [J].
Angulo, A ;
Suto, C ;
Heyman, RA ;
Ghazal, P .
MOLECULAR ENDOCRINOLOGY, 1996, 10 (07) :781-793
[4]   MEMBRANE TARGETING OF THE NUCLEOTIDE EXCHANGE FACTOR SOS IS SUFFICIENT FOR ACTIVATING THE RAS SIGNALING PATHWAY [J].
ARONHEIM, A ;
ENGELBERG, D ;
LI, NX ;
ALALAWI, N ;
SCHLESSINGER, J ;
KARIN, M .
CELL, 1994, 78 (06) :949-961
[5]   Canine ventricular myocytes possess a renin-angiotensin system that is upregulated with heart failure [J].
Barlucchi, L ;
Leri, A ;
Dostal, DE ;
Fiordaliso, F ;
Tada, H ;
Hintze, TH ;
Kajstura, J ;
Nadal-Ginard, B ;
Anversa, P .
CIRCULATION RESEARCH, 2001, 88 (03) :298-304
[6]   Angiotensin II AT1 receptor internalization, translocation and de novo synthesis modulate cytosolic and nuclear calcium in human vascular smooth muscle cells [J].
Bkaily, G ;
Sleiman, S ;
Stephan, J ;
Asselin, C ;
Choufani, S ;
Kamal, M ;
Jacques, D ;
Gobeil, F ;
D'Orléans-Juste, P .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 2003, 81 (03) :274-287
[7]   Angiotensin II promotes the phosphorylation of cyclic AMP-responsive element binding protein (CREB) at Ser133 through an ERK1/2-dependent mechanism [J].
Cammarota, M ;
Bevilaqua, LRM ;
Dunkley, PR ;
Rostas, JAP .
JOURNAL OF NEUROCHEMISTRY, 2001, 79 (06) :1122-1128
[8]   A functional angiotensin II receptor-GFP fusion protein: evidence for agonist-dependent nuclear translocation [J].
Chen, R ;
Mukhin, YV ;
Garnovskaya, MN ;
Thielen, TE ;
Iijima, Y ;
Huang, C ;
Raymond, JR ;
Ullian, ME ;
Paul, RV .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2000, 279 (03) :F440-F448
[9]   Pollycation gene delivery systems: escape from endosomes to cytosol [J].
Cho, YW ;
Kim, JD ;
Park, K .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2003, 55 (06) :721-734
[10]   An alternative transcript of the rat renin gene can result in a truncated prorenin that is transported into adrenal mitochondria [J].
Clausmeyer, S ;
Stürzebecher, R ;
Peters, J .
CIRCULATION RESEARCH, 1999, 84 (03) :337-344