Angiotensin II induction of AP-1 in neurons requires stimulation of PI3-K and JNK |
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Authors: | Fleegal Melissa A Sumners Colin |
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Affiliation: | Department of Physiology and Functional Genomics, University of Florida, Gainesville, FL 32610, USA. |
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Abstract: | Angiotensin II (Ang II) acts via its type 1 (AT(1)) receptor in neurons to regulate the activity of multiple intracellular signaling molecules, including intracellular Ca(2+), protein kinase C, phosphatidylinositol 3-kinase (PI3-K), and c-Jun NH(2)-terminal kinase (JNK). The present studies investigated the upstream signaling molecules involved in the Ang II stimulation of activator protein-1 (AP-1) DNA binding in neurons. Treatment of neurons cultured from neonatal rat hypothalamus and brainstem with Ang II (100 nM) showed a time-dependent increase in AP-1 DNA binding and this effect was inhibited by the AT(1) receptor antagonist, losartan (1 microM), the PI3-K inhibitor, LY294002 (10 microM), and the JNK inhibitor, JNK inhibitor II (100 nM). Furthermore, Ang II (100 nM) causes a time-dependent increase in JNK activity which was attenuated by PI3-K inhibition. These data establish, for the first time, a signaling cascade involved in the Ang II activation of AP-1 DNA binding in neurons. |
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Keywords: | Angiotensin II Activator protein-1 Phosphatidylinositol 3-kinase c-Jun NH2-terminal kinase Protein kinase C Neurons |
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