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Titlebook: Biochemistry, Molecular Biology, and Physiology of Phospholipase A2 and Its Regulatory Factors; Anil B. Mukherjee Book 1990 The Editor(s)

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期刊全称Biochemistry, Molecular Biology, and Physiology of Phospholipase A2 and Its Regulatory Factors
影响因子2023Anil B. Mukherjee
视频video
学科分类Advances in Experimental Medicine and Biology
图书封面Titlebook: Biochemistry, Molecular Biology, and Physiology of Phospholipase A2 and Its Regulatory Factors;  Anil B. Mukherjee Book 1990 The Editor(s)
影响因子During the past decade there has been a dramatic expansion of our knowledge on phospholipases in general, and phospholipase A2 (PLA2) in particular. Progress in this field has been evident on many fronts, with novel information rapidly accumulating in the literature regarding the chemistry and molecular biology of this enzyme and its role in many important physiological processes. These include cellular signal transduction via the G-protein cycle, and in the generation of many cellular mediators, such as the platelet activating factor (PAF) and the eicosanoids that participate in the initiation and propagation of inflammation, to mention a few. This symposium was organized to obtain an overview of current investigations on this enzyme from the standpoint of its chemistry, molecular biology and physiology. Another important focus of this symposium concerns the regulation of PLA2, including endogenous and synthetic inhibitors and activators of this enzyme. To review these important areas in PLA2 research we invited scientists who made significant contributions in this field. The papers in this volume are organized to emphasize the recent advances in several areas of investigation, in
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Stimulation of Phospholipases A2 by Transglutaminases,m the enzymological point of view (1–4). Nevertheless, the physiological role(s) of these enzymes, particularly the intracellular TGs, are still poorly understood. TGs are a class of enzymes which catalyze a Ca.-dependent acyl-transfer reaction in which the γ-carboxamide group of a peptide-bound glu
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Functional Consequences of Phospholipase A2 Activation in Human Monocytes,etradecanoate phorbol-13-acetate, TPA), calcium ionophores (ionomycin), serum-treated zymosan (STZ) concanavalin A (Con A), and, to a minor degree, lipopolysaccharides (LPS). Protein Kinase C activation or increased intracellular Ca. are common features of the actions of most, if not all, of these s
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Antiflammins Inhibit Synthesis of Platelet-Activating Factor and Intradermal Inflammatory Reactions. Lipocortins inhibit phospholipase A. (PLA.) activity in vitro with a mechanism still unclear (Davidson et al., 1987; Haigier et al., 1987). Furthermore, recombinant lipocortin I inhibits eicosanoid synthesis in vivo in perfused lungs (Cirino at al., 1987). Another steroid-induced protein with PLA.
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