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Andrey A. Komissarov

Researcher at University of Texas Health Science Center at Tyler

Publications -  43
Citations -  578

Andrey A. Komissarov is an academic researcher from University of Texas Health Science Center at Tyler. The author has contributed to research in topics: Plasminogen activator & Plasminogen activator inhibitor-1. The author has an hindex of 14, co-authored 34 publications receiving 466 citations. Previous affiliations of Andrey A. Komissarov include University of Texas System.

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Effects of extracellular DNA on plasminogen activation and fibrinolysis

TL;DR: Extracellular DNA at physiological concentrations may potentiate fibrinolysis by stimulating fibrin-independent plasminogen activation and increases enzyme susceptibility to serpins, and DNA is a macromolecular template that both potentiates and inhibits fibrinelysis.
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Plasminogen Activator Inhibitor-1 Deficiency Augments Visceral Mesothelial Organization, Intrapleural Coagulation, and Lung Restriction in Mice with Carbon Black/Bleomycin–Induced Pleural Injury

TL;DR: It is found that a C57Bl/6j mouse model of carbon black/bleomycin injury demonstrates pleural organization resulting in pleural rind formation and PAI-1 regulates CBB-induced pleural injury severity via unrestricted fibrinolysis and cross-talk with coagulation proteases.
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Intrapleural Adenoviral Delivery of Human Plasminogen Activator Inhibitor–1 Exacerbates Tetracycline-Induced Pleural Injury in Rabbits

TL;DR: Intrapleural fibrinolytic therapy (IPFT) with plasminogen activators was effective in both animals overexpressing hPAI-1 and control animals with tetracycline injury alone, and may be both a biomarker of pleural injury and a molecular target for its treatment.
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Targeting of plasminogen activator inhibitor 1 improves fibrinolytic therapy for tetracycline-induced pleural injury in rabbits

TL;DR: PAI-1-neutralizing mAbs improved IPFT by increasing the durability of intrapleural PA activity and suggesting a novel, well-tolerated IPFT strategy that is tractable for clinical development.
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Proteolytic regulation of epithelial sodium channels by urokinase plasminogen activator: cutting edge and cleavage sites

TL;DR: In this article, the authors demonstrate multifaceted mechanisms for uPA-mediated up-regulation of ENaC, which form the cellular and molecular rationale for the beneficial effects of urokinase in mitigating mortal pulmonary edema and pleural effusions.