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المؤلفWehbe, Nadine
المؤلفNasser, Suzanne A.
المؤلفAl-Dhaheri, Yusra
المؤلفIratni, Rabah
المؤلفBitto, Alessandra
المؤلفEl-Yazbi, Ahmed F.
المؤلفBadran, Adnan
المؤلفKobeissy, Firas
المؤلفBaydoun, Elias
المؤلفEid, Ali H.
تاريخ الإتاحة2023-09-25T10:26:16Z
تاريخ النشر2020
اسم المنشورInternational Journal of Molecular Sciences
المصدرScopus
معرّف المصادر الموحدhttp://dx.doi.org/10.3390/ijms21145160
معرّف المصادر الموحدhttp://hdl.handle.net/10576/47946
الملخصVascular smooth muscle cells (VSMCs) are major components of blood vessels. They regulate physiological functions, such as vascular tone and blood flow. Under pathological conditions, VSMCs undergo a remodeling process known as phenotypic switching. During this process, VSMCs lose their contractility and acquire a synthetic phenotype, where they over-proliferate and migrate from the tunica media to the tunica interna, contributing to the occlusion of blood vessels. Since their discovery as effector proteins of cyclic adenosine 3′,5′-monophosphate (cAMP), exchange proteins activated by cAMP (EPACs) have been shown to play vital roles in a plethora of pathways in different cell systems. While extensive research to identify the role of EPAC in the vasculature has been conducted, much remains to be explored to resolve the reported discordance in EPAC’s effects. In this paper, we review the role of EPAC in VSMCs, namely its regulation of the vascular tone and phenotypic switching, with the likely involvement of reactive oxygen species (ROS) in the interplay between EPAC and its targets/effectors.
راعي المشروعrepresent a potential target for drugs designed to treat atherosclerosis and hypertension. It is, therefore, important that future studies identify other downstream effectors that mediate Rap1-independent EPAC signaling to facilitate the development of new therapeutics that may target this family of cAMP effectors. Extensive research is also required to resolve the discrepancies in the role of EPAC in the vasculature and to translate in vitro and in vivo studies into clinical trials. Author Contributions: N.W., S.A.N., Y.A.-D., R.I., A.B. (Alessandra Bitto), A.F.E.-Y., A.B. (Adnan Badran), F.K., E.B. and A.H.E. contributed to writing the manuscript. N.W., S.A.N. and A.H.E. led the writing of the first draft. Author Contributions: All authors contributed to writing the manuscript. N.W., S.A.N. and A.H.E. led the A.H.E. conceived, edited, and finalized the manuscript. All authors have read and agreed to the published version writing of the first draft. A.H.E. conceived, edited, and finalized the manuscript. of the manuscript. Funding: This work was supported by the American University of Beirut (Grant: MPP 320133 and Farouk Jabre Awarrdtto Allii Eiidd)),, and United Arab Emirates University (Grant #: 31S398--UPAR to Yusraa Al-Dhaheri).
اللغةen
الناشرMDPI
الموضوعCAMP
Cardiovascular disease
EPAC
Phenotypic switch
ROS
Vascular smooth muscle cells
العنوانEpac in vascular smooth muscle cells
النوعArticle Review
الصفحات1-14
رقم العدد14
رقم المجلد21
dc.accessType Open Access


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