دورية أكاديمية

Lysophosphatidic acid metabolism and signaling in heart disease.

التفاصيل البيبلوغرافية
العنوان: Lysophosphatidic acid metabolism and signaling in heart disease.
المؤلفون: Jose A; Department of Biochemistry and Molecular Biology, Dalhousie University, Dalhousie Medicine New Brunswick, Saint John, NB, Canada., Fernando JJ; Department of Biochemistry and Molecular Biology, Dalhousie University, Dalhousie Medicine New Brunswick, Saint John, NB, Canada., Kienesberger PC; Department of Biochemistry and Molecular Biology, Dalhousie University, Dalhousie Medicine New Brunswick, Saint John, NB, Canada.
المصدر: Canadian journal of physiology and pharmacology [Can J Physiol Pharmacol] 2024 Jul 05. Date of Electronic Publication: 2024 Jul 05.
Publication Model: Ahead of Print
نوع المنشور: Journal Article; Review
اللغة: English
بيانات الدورية: Publisher: Canadian Science Publishing Country of Publication: Canada NLM ID: 0372712 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1205-7541 (Electronic) Linking ISSN: 00084212 NLM ISO Abbreviation: Can J Physiol Pharmacol Subsets: MEDLINE
أسماء مطبوعة: Publication: 2011- : Ottawa, ON : Canadian Science Publishing
Original Publication: Ottawa, National Research Council of Canada.
مستخلص: Lysophosphatidic acid (LPA) is a bioactive lipid that is mainly produced by the secreted lysophospholipase D, autotaxin (ATX), and signals through at least six G protein-coupled receptors (LPA1-6). Extracellular LPA is degraded through lipid phosphate phosphatases (LPP1, LPP2, and LPP3) at the plasmamembrane, terminating LPA receptor signaling. The ATX-LPA-LPP3 pathway is critically involved in a wide range of physiological processes, including cell survival, migration, proliferation, angiogenesis, and organismal development. Similarly, dysregulation of this pathway has been linked to many pathological processes, including cardiovascular disease. This review summarizes and interprets current literature examining the regulation and role of the ATX-LPA-LPP3 axis in heart disease. Specifically, the contribution of altered LPA metabolism via ATX and LPP3 and resulting changes to LPA receptor signaling in obesity cardiomyopathy, cardiac mitochondrial dysfunction, myocardial infarction/ischemia-reperfusion injury, hypertrophic cardiomyopathy, and aortic valve stenosis is discussed.
Competing Interests: The authors declare there are no competing interests.
فهرسة مساهمة: Keywords: autotaxin; cardiomyopathy; heart disease; lipid phosphate phosphatase; lysophosphatidic acid
تواريخ الأحداث: Date Created: 20240705 Latest Revision: 20240826
رمز التحديث: 20240826
DOI: 10.1139/cjpp-2024-0077
PMID: 38968609
قاعدة البيانات: MEDLINE
الوصف
تدمد:1205-7541
DOI:10.1139/cjpp-2024-0077