DOS in Biochemistry, University of Mysore, Manasagangotri, Mysuru 570 006, India.
Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore 560 012, India.
Biochim Biophys Acta Gen Subj. 2020 Jun;1864(6):129561. doi: 10.1016/j.bbagen.2020.129561. Epub 2020 Feb 15.
Neutrophils are the first line defense cells of the innate immunity. As a final defense, they discharge their de-condensed chromatin/DNA fibers, the NETs (Neutrophil Extracellular Traps), by a process called NETosis. Two types of NETosis have been currently described: the suicidal/delayed/classical-type, which is ROS dependent that results in the ejection of nuclear DNA, and the vital/rapid/early-type, which may or may not require ROS but, eject nuclear/mitochondrial DNA or both. Thus, Echis carinatus and Naja naja venoms are comparatively studied for their NET inducing property.
Formation of NETs, cell viability, ROS, and Ca levels are estimated. An in vivo toxicity study and possible cellular signaling have been addressed using immunoblots and pharmacological inhibitors.
E. carinatus and N. naja venoms respectively induce suicidal and vital NETosis. E. carinatus venom induces NETosis by activating NOX and PAD-4 enzymes in a ROS dependent manner via PKC/ERK/JNK signaling axis, while N. naja venom does it by activating PAD-4 enzyme, but independent of ROS requirement and as well as PKC/ERK/JNK activation.
For the first time our study demonstrates the distinct action of E. carinatus and N. naja venoms on the process of NETosis. NETosis being a newly explored area in snake venom pharmacodynamics, it is important to study its impact on the various pathophysiological properties induced by snake venoms.
Understanding the varied actions of snake venoms on neutrophils/blood cells and the role of DNase are likely to provide insights for better management of snakebite pathophysiology.
中性粒细胞是先天免疫系统的第一道防线细胞。作为最后的防御手段,它们通过一种称为 NETosis 的过程释放出浓缩的染色质/DNA 纤维,即 NET(中性粒细胞胞外陷阱)。目前已经描述了两种类型的 NETosis:自杀/延迟/经典型,它依赖于 ROS,导致核 DNA 的排出,以及重要/快速/早期型,它可能需要或不需要 ROS,但排出核/线粒体 DNA 或两者兼有。因此,比较研究了 Echis carinatus 和 Naja naja 毒液的诱导 NET 形成特性。
估计 NET 的形成、细胞活力、ROS 和 Ca 水平。使用免疫印迹和药理学抑制剂研究了体内毒性研究和可能的细胞信号转导。
E. carinatus 和 N. naja 毒液分别诱导自杀和重要的 NETosis。E. carinatus 毒液通过激活 NOX 和 PAD-4 酶,以 ROS 依赖的方式通过 PKC/ERK/JNK 信号轴诱导 NETosis,而 N. naja 毒液通过激活 PAD-4 酶,但不依赖于 ROS 需求以及 PKC/ERK/JNK 的激活。
我们的研究首次证明了 E. carinatus 和 N. naja 毒液在 NETosis 过程中的不同作用。NETosis 是蛇毒药理学中一个新探索的领域,研究它对蛇毒引起的各种病理生理特性的影响很重要。
了解蛇毒液对中性粒细胞/血细胞的不同作用以及 DNase 的作用可能为更好地管理蛇咬伤的病理生理学提供思路。