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.author | Fardoun, Manal Muin | |
| dc.contributor.author | Nasser, Suzanne A. | |
| dc.contributor.author | El-Yazbi, Ahmed F. | |
| dc.contributor.author | Eid, Ali H. | |
| dc.contributor.department | Pharmacology and Toxicology | |
| dc.contributor.faculty | Faculty of Medicine (FM) | |
| dc.contributor.institution | American University of Beirut | |
| dc.date.accessioned | 2025-01-24T11:40:03Z | |
| dc.date.available | 2025-01-24T11:40:03Z | |
| dc.date.issued | 2023 | |
| dc.description.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. | |
| dc.identifier.doi | https://doi.org/10.1097/FJC.0000000000001489 | |
| dc.identifier.eid | 2-s2.0-85179007460 | |
| dc.identifier.pmid | 37773889 | |
| dc.identifier.uri | http://hdl.handle.net/10938/29422 | |
| dc.language.iso | en | |
| dc.publisher | Lippincott Williams and Wilkins | |
| dc.relation.ispartof | Journal of Cardiovascular Pharmacology | |
| dc.source | Scopus | |
| dc.subject | Alpha 2c adrenoceptor | |
| dc.subject | Estrogen | |
| dc.subject | G-protein estrogen receptor | |
| dc.subject | Peripheral vascular disease | |
| dc.subject | Raynaud's phenomenon | |
| dc.subject | Vascular smooth muscle | |
| dc.subject | Cells, cultured | |
| dc.subject | Cyclic amp | |
| dc.subject | Estrogens | |
| dc.subject | Female | |
| dc.subject | Guanine nucleotide exchange factors | |
| dc.subject | Humans | |
| dc.subject | Male | |
| dc.subject | Myocytes, smooth muscle | |
| dc.subject | Signal transduction | |
| dc.subject | Transcription factor ap-1 | |
| dc.subject | Alpha 2c adrenergic receptor | |
| dc.subject | Anthra[1,9 cd]pyrazol 6(2h) one | |
| dc.subject | Bovine serum albumin | |
| dc.subject | Estradiol | |
| dc.subject | G protein coupled receptor 30 | |
| dc.subject | Guanine nucleotide binding protein | |
| dc.subject | Protein | |
| dc.subject | Protein epac dominant negative mutant | |
| dc.subject | Stress activated protein kinase | |
| dc.subject | Transcription factor ap 1 | |
| dc.subject | Unclassified drug | |
| dc.subject | Guanine nucleotide exchange factor | |
| dc.subject | Article | |
| dc.subject | Binding site | |
| dc.subject | Camp signaling | |
| dc.subject | Controlled study | |
| dc.subject | Enzyme activity | |
| dc.subject | Enzyme linked immunosorbent assay | |
| dc.subject | Genetic transcription | |
| dc.subject | Human | |
| dc.subject | Human cell | |
| dc.subject | Jnk signaling | |
| dc.subject | Luciferase assay | |
| dc.subject | Pka | |
| dc.subject | Plasmid | |
| dc.subject | Promoter region | |
| dc.subject | Protein expression | |
| dc.subject | Protein expression level | |
| dc.subject | Protein function | |
| dc.subject | Protein phosphorylation | |
| dc.subject | Reporter gene | |
| dc.subject | Transient transfection | |
| dc.subject | Upregulation | |
| dc.subject | Vascular smooth muscle cell | |
| dc.subject | Vasoconstriction | |
| dc.subject | Cell culture | |
| dc.subject | Genetics | |
| dc.subject | Metabolism | |
| dc.subject | Smooth muscle cell | |
| dc.title | GPER Acts Through the cAMP/Epac/JNK/AP-1 Pathway to Induce Transcription of Alpha 2C Adrenoceptor in Human Microvascular Smooth Muscle Cells | |
| dc.type | Article |
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