Angiotensin metabolites can stimulate receptors of the Mas-related genes family

被引:72
作者
Gembardt, Florian [2 ,3 ]
Grajewski, Sonja [2 ]
Vahl, Martin [2 ]
Schultheiss, Heinz-Peter [2 ]
Walther, Thomas [1 ,2 ]
机构
[1] Univ Hull, Hull York Med Sch, Dept Biomed Sci, Kingston Upon Hull HU6 7LX, N Humberside, England
[2] Charite Univ Med Berlin, Dept Cardiol, Berlin, Germany
[3] Erasmus MC, Dept Pharmacol, Rotterdam, Netherlands
关键词
Renin-angiotensin system; Mas-related genes; G protein-coupled receptor; Angiotensin; Arachidonic acid; Serum response factor;
D O I
10.1007/s11010-008-9884-4
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Mas protooncogene encodes a G protein-coupled receptor, we identified, also by using the specific angiotensin-(1-7) antagonist A-779, to be associated with intracellular signaling of the angiotensin (Ang) II metabolite Ang-(1-7). Recently, Mas-related genes (Mrg) have been identified coding for the Mrg-receptor family. All family members share high sequence homology to Mas. Most of them are orphan receptors. To proof whether structure similarities of the Mrg receptors with Mas turn them into potential receptors for Ang-(1-7) or other Ang metabolites, we transfected COS or HEK293 cells with an assortment of Mrg receptors and investigated arachidonic acid (AA) release and transcriptional activation by recording serum response factor (SRF) activation after stimulation with Ang II, Ang III, Ang IV, and Ang-(1-7). None of the investigated receptors activated transcription via SRF. Ang-(1-7) stimulated AA release already in control vector-transfected COS cells, indicating the existence of an endogenous receptor (A-779 sensitive). Though less pronounced than for Mas, two of the six studied receptors (MrgD, MRG) initiated significant AA release after stimulation with Ang-(1-7). Interestingly, Mas, MrgD, and MRG mediated Ang IV-stimulated AA release that was highest for Mas. While Ang III activated Mas and MrgX2, Ang II stimulated AA release via Mas and MRG. Thus, we identified other receptors of the Mrg family to respond on Ang-(1-7) stimulation. Furthermore, we describe first an AT(1)-independent direct Ang IV signaling and show that Ang II and Ang III mediate signaling independent of their specific receptors AT(1) and AT(2), whereby the receptor specificity differs.
引用
收藏
页码:115 / 123
页数:9
相关论文
共 36 条
  • [31] Angiotensin-(1-7): Pharmacology and new perspectives in cardiovascular treatments
    Trask, Aaron J.
    Ferrario, Carlos M.
    [J]. CARDIOVASCULAR DRUG REVIEWS, 2007, 25 (02): : 162 - 174
  • [32] A COMPARISON OF THE PROPERTIES AND ENZYMATIC-ACTIVITIES OF 3 ANGIOTENSIN PROCESSING ENZYMES - ANGIOTENSIN-CONVERTING ENZYME, PROLYL ENDOPEPTIDASE AND NEUTRAL ENDOPEPTIDASE 24.11
    WELCHES, WR
    BROSNIHAN, KB
    FERRARIO, CM
    [J]. LIFE SCIENCES, 1993, 52 (18) : 1461 - 1480
  • [33] Angiotensin and cytoskeletal proteins: Role in vascular remodeling
    Wesselman, JPM
    De Mey, JGR
    [J]. CURRENT HYPERTENSION REPORTS, 2002, 4 (01) : 63 - 70
  • [34] An expressed sequence tag (EST) data mining strategy succeeding in the discovery of new G-protein coupled receptors
    Wittenberger, T
    Schaller, HC
    Hellebrand, S
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2001, 307 (03) : 799 - 813
  • [35] Angiotensin II stimulates protein kinase D-dependent histone deacetylase 5 phosphorylation and nuclear export leading to vascular smooth muscle cell hypertrophy
    Xu, Xiangbin
    Ha, Chang-Hoon
    Wong, Chelsea
    Wang, Weiye
    Hausser, Angelika
    Pfizenmaier, Klaus
    Olson, Eric N.
    McKinsey, Timothy A.
    Jin, Zheng-Gen
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2007, 27 (11) : 2355 - 2362
  • [36] ISOLATION AND CHARACTERIZATION OF A NEW CELLULAR ONCOGENE ENCODING A PROTEIN WITH MULTIPLE POTENTIAL TRANSMEMBRANE DOMAINS
    YOUNG, D
    WAITCHES, G
    BIRCHMEIER, C
    FASANO, O
    WIGLER, M
    [J]. CELL, 1986, 45 (05) : 711 - 719