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dc.contributor.authorGiordo, Roberta
dc.contributor.authorThuan, Duong Thi Bich
dc.contributor.authorPosadino, Anna Maria
dc.contributor.authorCossu, Annalisa
dc.contributor.authorZinellu, Angelo
dc.contributor.authorErre, Gian Luca
dc.contributor.authorPintus, Gianfranco
dc.date.accessioned2024-12-25T11:59:37Z
dc.date.available2024-12-25T11:59:37Z
dc.date.issued2021-08-02
dc.identifier.urihttps://vinspace.edu.vn/handle/VIN/529
dc.description.abstractEndothelial cell injury is an early event in systemic sclerosis (SSc) pathogenesis and several studies indicate oxidative stress as the trigger of SSc-associated vasculopathy. Here, we show that circulating factors present in sera of SSc patients increased reactive oxygen species (ROS) production and collagen synthesis in human pulmonary microvascular endothelial cells (HPMECs). In addition, the possibility that iloprost, a drug commonly used in SSc therapy, might modulate the above-mentioned biological phenomena has been also investigated. In this regard, as compared to sera of SSc patients, sera of iloprost-treated SSc patients failed to increased ROS levels and collagen synthesis in HPMEC, suggesting a potential antioxidant mechanism of this drug.en_US
dc.language.isoenen_US
dc.subjectcollagen synthesisen_US
dc.subjectiloprosten_US
dc.subjectoxidative stressen_US
dc.subjectsystemic sclerosisen_US
dc.titleIloprost attenuates oxidative stress-dependent activation of collagen synthesis induced by sera from scleroderma patients in human pulmonary microvascular endothelial cellsen_US
dc.typeArticleen_US


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