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dc.contributor.authorGiordo, Roberta
dc.contributor.authorDuong, Thi Bich Thuan
dc.contributor.authorPosadino, Anna Maria
dc.contributor.authorCossu, Annalisa
dc.contributor.authorZinellu, Angelo
dc.contributor.authorErre, Gian Luca
dc.contributor.authorPintus, Gianfranco
dc.date.accessioned2024-08-21T16:10:46Z
dc.date.available2024-08-21T16:10:46Z
dc.date.issued2021-08-05
dc.identifier.urihttps://vinspace.edu.vn/handle/VIN/216
dc.description.abstractEndothelial cell injury is an early event in the pathogenesis of systemic sclerosis (SSc), with oxidative stress being a key trigger of SSc-associated vasculopathy. This study demonstrates that circulating factors in the sera of SSc patients significantly increase reactive oxygen species (ROS) production and collagen synthesis in human pulmonary microvascular endothelial cells (HPMECs). Additionally, we explored the impact of iloprost, a drug commonly used in SSc therapy, on these biological processes. Our results show that sera from SSc patients treated with iloprost do not elevate ROS levels or collagen synthesis in HPMECs compared to untreated SSc sera, suggesting that iloprost may exert its therapeutic effects through an antioxidant mechanism.en_US
dc.language.isoen_USen_US
dc.subjectsystemic sclerosisen_US
dc.subjectoxidative stressen_US
dc.subjectcollagen synthesisen_US
dc.subjectiloprosten_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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