Activation of ERK, JNK, Akt, and G-protein coupled signaling by hybrid angiotensin II AT1/bradykinin B2 receptors expressed in HEK-293 cells

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Standard

Activation of ERK, JNK, Akt, and G-protein coupled signaling by hybrid angiotensin II AT1/bradykinin B2 receptors expressed in HEK-293 cells. / Yu, Jun; Lubinsky, David; Tsomaia, Natia; Huang, Zhenhua; Taylor, Linda; Mierke, Dale; Navarro, Javier; Mirza, Osman Asghar; Polgar, Peter.

I: Journal of Cellular Biochemistry, Bind 101, Nr. 1, 2007, s. 192-204.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Yu, J, Lubinsky, D, Tsomaia, N, Huang, Z, Taylor, L, Mierke, D, Navarro, J, Mirza, OA & Polgar, P 2007, 'Activation of ERK, JNK, Akt, and G-protein coupled signaling by hybrid angiotensin II AT1/bradykinin B2 receptors expressed in HEK-293 cells', Journal of Cellular Biochemistry, bind 101, nr. 1, s. 192-204. https://doi.org/10.1002/jcb.21161

APA

Yu, J., Lubinsky, D., Tsomaia, N., Huang, Z., Taylor, L., Mierke, D., Navarro, J., Mirza, O. A., & Polgar, P. (2007). Activation of ERK, JNK, Akt, and G-protein coupled signaling by hybrid angiotensin II AT1/bradykinin B2 receptors expressed in HEK-293 cells. Journal of Cellular Biochemistry, 101(1), 192-204. https://doi.org/10.1002/jcb.21161

Vancouver

Yu J, Lubinsky D, Tsomaia N, Huang Z, Taylor L, Mierke D o.a. Activation of ERK, JNK, Akt, and G-protein coupled signaling by hybrid angiotensin II AT1/bradykinin B2 receptors expressed in HEK-293 cells. Journal of Cellular Biochemistry. 2007;101(1):192-204. https://doi.org/10.1002/jcb.21161

Author

Yu, Jun ; Lubinsky, David ; Tsomaia, Natia ; Huang, Zhenhua ; Taylor, Linda ; Mierke, Dale ; Navarro, Javier ; Mirza, Osman Asghar ; Polgar, Peter. / Activation of ERK, JNK, Akt, and G-protein coupled signaling by hybrid angiotensin II AT1/bradykinin B2 receptors expressed in HEK-293 cells. I: Journal of Cellular Biochemistry. 2007 ; Bind 101, Nr. 1. s. 192-204.

Bibtex

@article{32dfb5501d0411deb43e000ea68e967b,
title = "Activation of ERK, JNK, Akt, and G-protein coupled signaling by hybrid angiotensin II AT1/bradykinin B2 receptors expressed in HEK-293 cells",
abstract = "Bradykinin (BK) and angiotensin II (AngII) often have opposite roles in cardiovascular diseases. Our aim here was to construct hybrid receptors which bind AngII but signal as BK. Various sequences of the intracellular face of the AngII type I receptor, AT1R, were replaced with corresponding sequences from the bradykinin B2 receptor (BKB2R). The hybrids demonstrated a number of signaling characteristics of the BKB2R. For example, the hybrids demonstrated BK as opposed to AngII like phosphorylation of Akt and JNK. The hybrids containing the BKB2R intracellular loop 2 (IC2) displayed minimal G-protein, Galphai/Galphaq, linked signaling. Computer based molecular models suggested that Ser-Met-Gly from the IC2 of the BKB2R is detrimental for the Galphai/Galphaq coupled functions of this hybrid. The return of Lys-Ser-Arg of the AT1R to this hybrid led to almost full recovery of Galphai and Galphaq activation. The design and production of AT1/BKB2 hybrid receptors is a potential approach in the treatment of hypertension related diseases where the presence of AngII, its AT1 receptor and the consequent signal transduction has proven detrimental.",
keywords = "Former Faculty of Pharmaceutical Sciences",
author = "Jun Yu and David Lubinsky and Natia Tsomaia and Zhenhua Huang and Linda Taylor and Dale Mierke and Javier Navarro and Mirza, {Osman Asghar} and Peter Polgar",
note = "Keywords: Amino Acid Sequence; Arachidonic Acid; Calcium; Cell Line; Enzyme Activation; Extracellular Signal-Regulated MAP Kinases; GTP-Binding Proteins; Humans; Kinetics; Ligands; MAP Kinase Kinase 4; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Phosphatidylinositols; Phosphorylation; Protein Binding; Protein Structure, Secondary; Protein Structure, Tertiary; Proto-Oncogene Proteins c-akt; Receptor, Angiotensin, Type 1; Receptor, Bradykinin B2; Sequence Analysis, DNA; Signal Transduction; Transfection",
year = "2007",
doi = "10.1002/jcb.21161",
language = "English",
volume = "101",
pages = "192--204",
journal = "Journal of cellular biochemistry. Supplement",
issn = "0733-1959",
publisher = "JohnWiley & Sons, Inc.",
number = "1",

}

RIS

TY - JOUR

T1 - Activation of ERK, JNK, Akt, and G-protein coupled signaling by hybrid angiotensin II AT1/bradykinin B2 receptors expressed in HEK-293 cells

AU - Yu, Jun

AU - Lubinsky, David

AU - Tsomaia, Natia

AU - Huang, Zhenhua

AU - Taylor, Linda

AU - Mierke, Dale

AU - Navarro, Javier

AU - Mirza, Osman Asghar

AU - Polgar, Peter

N1 - Keywords: Amino Acid Sequence; Arachidonic Acid; Calcium; Cell Line; Enzyme Activation; Extracellular Signal-Regulated MAP Kinases; GTP-Binding Proteins; Humans; Kinetics; Ligands; MAP Kinase Kinase 4; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Phosphatidylinositols; Phosphorylation; Protein Binding; Protein Structure, Secondary; Protein Structure, Tertiary; Proto-Oncogene Proteins c-akt; Receptor, Angiotensin, Type 1; Receptor, Bradykinin B2; Sequence Analysis, DNA; Signal Transduction; Transfection

PY - 2007

Y1 - 2007

N2 - Bradykinin (BK) and angiotensin II (AngII) often have opposite roles in cardiovascular diseases. Our aim here was to construct hybrid receptors which bind AngII but signal as BK. Various sequences of the intracellular face of the AngII type I receptor, AT1R, were replaced with corresponding sequences from the bradykinin B2 receptor (BKB2R). The hybrids demonstrated a number of signaling characteristics of the BKB2R. For example, the hybrids demonstrated BK as opposed to AngII like phosphorylation of Akt and JNK. The hybrids containing the BKB2R intracellular loop 2 (IC2) displayed minimal G-protein, Galphai/Galphaq, linked signaling. Computer based molecular models suggested that Ser-Met-Gly from the IC2 of the BKB2R is detrimental for the Galphai/Galphaq coupled functions of this hybrid. The return of Lys-Ser-Arg of the AT1R to this hybrid led to almost full recovery of Galphai and Galphaq activation. The design and production of AT1/BKB2 hybrid receptors is a potential approach in the treatment of hypertension related diseases where the presence of AngII, its AT1 receptor and the consequent signal transduction has proven detrimental.

AB - Bradykinin (BK) and angiotensin II (AngII) often have opposite roles in cardiovascular diseases. Our aim here was to construct hybrid receptors which bind AngII but signal as BK. Various sequences of the intracellular face of the AngII type I receptor, AT1R, were replaced with corresponding sequences from the bradykinin B2 receptor (BKB2R). The hybrids demonstrated a number of signaling characteristics of the BKB2R. For example, the hybrids demonstrated BK as opposed to AngII like phosphorylation of Akt and JNK. The hybrids containing the BKB2R intracellular loop 2 (IC2) displayed minimal G-protein, Galphai/Galphaq, linked signaling. Computer based molecular models suggested that Ser-Met-Gly from the IC2 of the BKB2R is detrimental for the Galphai/Galphaq coupled functions of this hybrid. The return of Lys-Ser-Arg of the AT1R to this hybrid led to almost full recovery of Galphai and Galphaq activation. The design and production of AT1/BKB2 hybrid receptors is a potential approach in the treatment of hypertension related diseases where the presence of AngII, its AT1 receptor and the consequent signal transduction has proven detrimental.

KW - Former Faculty of Pharmaceutical Sciences

U2 - 10.1002/jcb.21161

DO - 10.1002/jcb.21161

M3 - Journal article

C2 - 17212359

VL - 101

SP - 192

EP - 204

JO - Journal of cellular biochemistry. Supplement

JF - Journal of cellular biochemistry. Supplement

SN - 0733-1959

IS - 1

ER -

ID: 11638879