GPER Acts Through the cAMP/Epac/JNK/AP-1 Pathway to Induce Transcription of Alpha 2C Adrenoceptor in Human Microvascular Smooth Muscle Cells
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Lippincott Williams and Wilkins
Abstract
Raynaud's phenomenon, which results from exaggerated cold-induced vasoconstriction, is more prevalent in females than males. We previously showed that estrogen increases the expression of alpha 2C-adrenoceptors (α2C-AR), the sole mediator of cold-induced vasoconstriction. This effect of estrogen is reproduced by the cell-impermeable form of the hormone (E2:bovine serum albumin [BSA]), suggesting a role of the membrane estrogen receptor, G-protein-coupled estrogen receptor [GPER], in E2-induced α2C-AR expression. We also previously reported that E2upregulates α2C-AR in microvascular smooth muscle cells (VSMCs) via the cAMP/Epac/Rap/JNK/AP-1 pathway, and that E2:BSA elevates cAMP levels. We, therefore, hypothesized that E2uses GPER to upregulate α2C-AR through the cAMP/Epac/JNK/AP-1 pathway. Our results show that G15, a selective GPER antagonist, attenuates the E2-induced increase in α2C-AR transcription. G-1, a selective GPER agonist, induced α2C-AR transcription, which was concomitant with elevated cAMP levels and JNK activation. Pretreatment with ESI09, an Epac inhibitor, abolished G-1-induced α2C-AR upregulation and JNK activation. Moreover, pretreatment with SP600125, a JNK-specific inhibitor, but not H89, a PKA-specific inhibitor, abolished G-1-induced α2C-AR upregulation. In addition, transient transfection of an Epac dominant negative mutant (Epac-DN) attenuated G-1-induced activation of the α2C-AR promoter. This inhibitory effect of Epac-DN on the α2C-AR promoter was overridden by the cotransfection of constitutively active JNK mutant. Furthermore, mutation of AP-1 site in the α2C-AR promoter abrogated G1-induced expression. Collectively, these results indicate that GPER upregulates α2C-AR through the cAMP/EPAC/JNK/AP-1 pathway. These findings unravel GPER as a new mediator of cold-induced vasoconstriction, and present it as a potential target for treating Raynaud's phenomenon in estrogen-replete females. © 2023 Lippincott Williams and Wilkins. All rights reserved.
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Alpha 2c adrenoceptor, Estrogen, G-protein estrogen receptor, Peripheral vascular disease, Raynaud's phenomenon, Vascular smooth muscle, Cells, cultured, Cyclic amp, Estrogens, Female, Guanine nucleotide exchange factors, Humans, Male, Myocytes, smooth muscle, Signal transduction, Transcription factor ap-1, Alpha 2c adrenergic receptor, Anthra[1,9 cd]pyrazol 6(2h) one, Bovine serum albumin, Estradiol, G protein coupled receptor 30, Guanine nucleotide binding protein, Protein, Protein epac dominant negative mutant, Stress activated protein kinase, Transcription factor ap 1, Unclassified drug, Guanine nucleotide exchange factor, Article, Binding site, Camp signaling, Controlled study, Enzyme activity, Enzyme linked immunosorbent assay, Genetic transcription, Human, Human cell, Jnk signaling, Luciferase assay, Pka, Plasmid, Promoter region, Protein expression, Protein expression level, Protein function, Protein phosphorylation, Reporter gene, Transient transfection, Upregulation, Vascular smooth muscle cell, Vasoconstriction, Cell culture, Genetics, Metabolism, Smooth muscle cell