GPER Acts Through the cAMP/Epac/JNK/AP-1 Pathway to Induce Transcription of Alpha 2C Adrenoceptor in Human Microvascular Smooth Muscle Cells

dc.contributor.authorFardoun, Manal Muin
dc.contributor.authorNasser, Suzanne A.
dc.contributor.authorEl-Yazbi, Ahmed F.
dc.contributor.authorEid, Ali H.
dc.contributor.departmentPharmacology and Toxicology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:40:03Z
dc.date.available2025-01-24T11:40:03Z
dc.date.issued2023
dc.description.abstractRaynaud'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.
dc.identifier.doihttps://doi.org/10.1097/FJC.0000000000001489
dc.identifier.eid2-s2.0-85179007460
dc.identifier.pmid37773889
dc.identifier.urihttp://hdl.handle.net/10938/29422
dc.language.isoen
dc.publisherLippincott Williams and Wilkins
dc.relation.ispartofJournal of Cardiovascular Pharmacology
dc.sourceScopus
dc.subjectAlpha 2c adrenoceptor
dc.subjectEstrogen
dc.subjectG-protein estrogen receptor
dc.subjectPeripheral vascular disease
dc.subjectRaynaud's phenomenon
dc.subjectVascular smooth muscle
dc.subjectCells, cultured
dc.subjectCyclic amp
dc.subjectEstrogens
dc.subjectFemale
dc.subjectGuanine nucleotide exchange factors
dc.subjectHumans
dc.subjectMale
dc.subjectMyocytes, smooth muscle
dc.subjectSignal transduction
dc.subjectTranscription factor ap-1
dc.subjectAlpha 2c adrenergic receptor
dc.subjectAnthra[1,9 cd]pyrazol 6(2h) one
dc.subjectBovine serum albumin
dc.subjectEstradiol
dc.subjectG protein coupled receptor 30
dc.subjectGuanine nucleotide binding protein
dc.subjectProtein
dc.subjectProtein epac dominant negative mutant
dc.subjectStress activated protein kinase
dc.subjectTranscription factor ap 1
dc.subjectUnclassified drug
dc.subjectGuanine nucleotide exchange factor
dc.subjectArticle
dc.subjectBinding site
dc.subjectCamp signaling
dc.subjectControlled study
dc.subjectEnzyme activity
dc.subjectEnzyme linked immunosorbent assay
dc.subjectGenetic transcription
dc.subjectHuman
dc.subjectHuman cell
dc.subjectJnk signaling
dc.subjectLuciferase assay
dc.subjectPka
dc.subjectPlasmid
dc.subjectPromoter region
dc.subjectProtein expression
dc.subjectProtein expression level
dc.subjectProtein function
dc.subjectProtein phosphorylation
dc.subjectReporter gene
dc.subjectTransient transfection
dc.subjectUpregulation
dc.subjectVascular smooth muscle cell
dc.subjectVasoconstriction
dc.subjectCell culture
dc.subjectGenetics
dc.subjectMetabolism
dc.subjectSmooth muscle cell
dc.titleGPER Acts Through the cAMP/Epac/JNK/AP-1 Pathway to Induce Transcription of Alpha 2C Adrenoceptor in Human Microvascular Smooth Muscle Cells
dc.typeArticle

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