The Journal of biological chemistry · 2004
Cathepsin V, a novel and potent elastolytic activity expressed in activated macrophages.
СтатьяПоддержка службы здравоохранения СШАНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
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.
Yasuda Yoshiyuki, Li Zhenqiang, Greenbaum Doron, Bogyo Matthew, Weber Ekkehard, Brömme Dieter
Аннотация
Atherosclerosis is characterized by a thickening and loss of elasticity of the arterial wall. Loss of elasticity has been attributed to the degradation of the arterial elastin matrix. Cathepsins K and S are papain-like cysteine proteases with known elastolytic activities, and both enzymes have been identified in macrophages present in plaque areas of diseased blood vessels. Here we demonstrate that macrophages express a third elastolytic cysteine protease, cathepsin V, which exhibits the most potent elastase activity yet described among human proteases and that cathepsin V is present in atherosclerotic plaque specimens. Approximately 60% of the total elastolytic activity of macrophages can be attributed to cysteine proteases with cathepsins V, K, and S contributing equally. From this 60%, two-thirds occur extracellularly and one-third intracellularly with the latter credited to cathepsin V. Ubiquitously expressed glycosaminoglycans (GAGs) such as chondroitin sulfate specifically inhibit the elastolytic activities of cathepsins V and K via the formation of specific cathepsin-GAG complexes. In contrast, cathepsin S, which does not form complexes with chondroitin sulfate is not inhibited; thus suggesting a specific regulation of elastolytic activities of cathepsins by GAGs. Because the GAG content is reduced in atherosclerotic plaques, an increase of cathepsins V and K activities may accelerate the destruction of the elastin matrix in diseased arteries.
Предметные рубрики MeSH
AnimalsArteriesBinding SitesBinding, CompetitiveBlotting, WesternCatalytic DomainCathepsin KCathepsin LCathepsinsCell DifferentiationCells, CulturedChondroitin SulfatesCongo RedCysteine EndopeptidasesDose-Response Relationship, DrugElastinElectrophoresis, Polyacrylamide GelGlycosaminoglycansHumansKineticsLeukocytes, MononuclearMacrophagesMatrix Metalloproteinase 2MiceMicroscopy, FluorescenceNIH 3T3 CellsPapainProtein BindingRNA, MessengerRecombinant ProteinsReverse Transcriptase Polymerase Chain ReactionSodium ChlorideTime Factors