دورية أكاديمية

Arginase II activity regulates cytosolic Ca2+ level in a p32-dependent manner that contributes to Ca2+-dependent vasoconstriction in native low-density lipoprotein-stimulated vascular smooth muscle cells

التفاصيل البيبلوغرافية
العنوان: Arginase II activity regulates cytosolic Ca2+ level in a p32-dependent manner that contributes to Ca2+-dependent vasoconstriction in native low-density lipoprotein-stimulated vascular smooth muscle cells
المؤلفون: Bon-hyeock Koo, Dongeui Hong, Hyeon Don Hong, Hyun Kyo Lim, Kwang Lae Hoe, Moo-Ho Won, Young Myeong Kim, Dan E. Berkowitz, Sungwoo Ryoo
المصدر: Experimental and Molecular Medicine, Vol 51, Iss 6, Pp 1-12 (2019)
بيانات النشر: Nature Publishing Group, 2019.
سنة النشر: 2019
المجموعة: LCC:Medicine
LCC:Biochemistry
مصطلحات موضوعية: Medicine, Biochemistry, QD415-436
الوصف: Vascular disease: Controlling arterial constriction Researchers have illuminated how a protein, arginase II (ArgII), is involved in development of vascular diseases such as atherosclerosis, or narrowing of the arteries by plaque deposits. Blood vessel diameter is regulated by layers of muscle; the balance between constriction and relaxation is critical for blood flow and vascular health. Increased ArgII is known to be a factor in arterial disease; however, the details of regulation, and how they relate to plaque deposition, remain poorly understood. Sungwoo Ryoo at Kangwon National University, Chuncheon, South Korea and co-workers investigated how ArgII levels affect arterial constriction and relaxation in mice. Decreasing ArgII restored the muscle cells’ contraction response by preventing excessive calcium accumulation in the cellular powerhouse, mitochondria. These results may aid in developing treatments for one of the leading causes of death worldwide.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1226-3613
2092-6413
Relation: https://doaj.org/toc/1226-3613; https://doaj.org/toc/2092-6413
DOI: 10.1038/s12276-019-0262-y
URL الوصول: https://doaj.org/article/9abe9aa87a9c496e8d460058ef7359bc
رقم الأكسشن: edsdoj.9abe9aa87a9c496e8d460058ef7359bc
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:12263613
20926413
DOI:10.1038/s12276-019-0262-y