期刊
TOXINS
卷 13, 期 12, 页码 -出版社
MDPI
DOI: 10.3390/toxins13120868
关键词
Bothrops phospholipases A(2); inflammation; lipid mediators; signaling pathways
资金
- Fundacao Butantan, Sao Paulo, Brazil
- Coordenacao de Aperfeiccoamento de Pessoal de Nivel Superior (CAPES)
- Conselho Nacional de Desenvolvimento Cientifico e Tecnologico fellowship (PQ-CNPq) [310930/201.7]
- Fundacao Butantan [FB 001/0708/003.434/2021]
Snake venom PLA(2)s play a significant role in viperid and crotalid snake venoms, exhibiting remarkable functional diversity and proinflammatory properties. Research on these enzymes is crucial for better understanding the pathophysiology of snake envenomation and for the development of new therapeutic agents.
Phospholipases A(2)s (PLA(2)s) constitute one of the major protein groups present in the venoms of viperid and crotalid snakes. Snake venom PLA(2)s (svPLA(2)s) exhibit a remarkable functional diversity, as they have been described to induce a myriad of toxic effects. Local inflammation is an important characteristic of snakebite envenomation inflicted by viperid and crotalid species and diverse svPLA(2)s have been studied for their proinflammatory properties. Moreover, based on their molecular, structural, and functional properties, the viperid svPLA(2)s are classified into the group IIA secreted PLA(2)s, which encompasses mammalian inflammatory sPLA(2)s. Thus, research on svPLA(2)s has attained paramount importance for better understanding the role of this class of enzymes in snake envenomation and the participation of GIIA sPLA(2)s in pathophysiological conditions and for the development of new therapeutic agents. In this review, we highlight studies that have identified the inflammatory activities of svPLA(2)s, in particular, those from Bothrops genus snakes, which are major medically important snakes in Latin America, and we describe recent advances in our collective understanding of the mechanisms underlying their inflammatory effects. We also discuss studies that dissect the action of these venom enzymes in inflammatory cells focusing on molecular mechanisms and signaling pathways involved in the biosynthesis of lipid mediators and lipid accumulation in immunocompetent cells.
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