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(Hypertension. 2003;41:781.)
© 2003 American Heart Association, Inc.

Scientific Contributions

Role of EGFR Transactivation in Angiotensin II Signaling to Extracellular Regulated Kinase in Preglomerular Smooth Muscle Cells

Bradley T. Andresen; Jenny J. Linnoila; Edwin K. Jackson; Guillermo G. Romero

From the Department of Pharmacology (B.T.A., E.K.J., G.G.R.), Department of Medicine (J.J.L.), and Center for Clinical Pharmacology (B.T.A., E.K.J.), University of Pittsburgh, Penn. Dr. Andresen is now at Oral and Pharyngeal Cancer Branch, NIDCR, National Institutes of Health, Bethesda, Md.

Correspondence to Guillermo G. Romero, PhD, W1345 Biological Science Tower, Department of Pharmacology, University of Pittsburgh, Pittsburgh, PA 15261. E-mail ggr{at}pitt.edu

Angiotensin (Ang) II promotes the phosphorylation of extracellular regulated kinase (ERK); however, the mechanisms leading to Ang II-induced ERK phosphorylation are debated. The currently accepted theory involves transactivation of epidermal growth factor receptor (EGFR). We have shown that generation of phosphatidic acid (PA) is required for the recruitment of Raf to membranes and the activation of ERK by multiple agonists, including Ang II. In the present report, we confirm that phospholipase D-dependent generation of PA is required for Ang II-mediated phosphorylation of ERK in Wistar-Kyoto and spontaneously hypertensive rat preglomerular smooth muscle cells (PGSMCs). However, EGF stimulation does not activate phospholipase D or generate PA. These observations indicate that EGF recruits Raf to membranes via a mechanism that does not involve PA, and thus, Ang II-mediated phosphorylation of ERK is partially independent of EGFR-mediated signaling cascades. We hypothesized that phosphoinositide-3-kinase (PI3K) can also act to recruit Raf to membranes; therefore, inhibition of PI3K should inhibit EGF signaling to ERK. Wortmannin, a PI3K inhibitor, inhibited EGF-mediated phosphorylation of ERK (IC₅₀, 14 nmol/L). To examine the role of the EGFR in Ang II-mediated phosphorylation of ERK we utilized 100 nmol/L wortmannin to inhibit EGFR signaling to ERK and T19N RhoA to block Ang II-mediated ERK phosphorylation. Wortmannin treatment inhibited EGF-mediated but not Ang II-mediated phosphorylation of ERK. Furthermore, T19N RhoA inhibited Ang II-mediated ERK phosphorylation, whereas T19N RhoA had significantly less effect on EGF-mediated ERK phosphorylation. We conclude that transactivation of the EGFR is not primarily responsible for Ang II-mediated activation of ERK in PGSMCs.

Key Words: angiotensin II • epidermal growth factors • extracellular regulated kinase • phospholipase D • phosphoinositide-3-kinase • transactivation

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