MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1073/pnas.0402178101

Медицинская библиотека · Proceedings of the National Academy of Sciences of the United States of America · 2004

The kinase Grk2 regulates Nedd4/Nedd4-2-dependent control of epithelial Na+ channels.

Dinudom Anuwat, Fotia Andrew B, Lefkowitz Robert J, Young John A, Kumar Sharad, Cook David I

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Epithelial Na(+) channels mediate the transport of Na across epithelia in the kidney, gut, and lungs and are required for blood pressure regulation. They are inhibited by ubiquitin protein ligases, such as Nedd4 and Nedd4-2, with loss of this inhibition leading to hypertension. Here, we report that these channels are maintained in the active state by the G protein-coupled receptor kinase, Grk2, which has been previously implicated in the development of essential hypertension. We also show that Grk2 phosphorylates the C terminus of the channel beta subunit and renders the channels insensitive to inhibition by Nedd4-2. This mechanism has not been previously reported to regulate epithelial Na(+) channels and provides a potential explanation for the observed association of Grk2 overactivity with hypertension. Here, we report a G protein-coupled receptor kinase regulating a membrane protein other than a receptor and provide a paradigm for understanding how the interaction between membrane proteins and ubiquitin protein ligases is controlled.

Для цитирования: Dinudom Anuwat, Fotia Andrew B, Lefkowitz Robert J, Young John A, Kumar Sharad, Cook David I. The kinase Grk2 regulates Nedd4/Nedd4-2-dependent control of epithelial Na+ channels.. Proceedings of the National Academy of Sciences of the United States of America. 2004. DOI: 10.1073/pnas.0402178101.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.