A Brief Overview of the Toxic Sphingomyelinase Ds of Brown Recluse Spider Venom and Other Organisms and Simple Methods To Detect Production of Its Signature Cyclic Ceramide Phosphate.

IF 3.2 3区 医学 Q2 PHARMACOLOGY & PHARMACY Molecular Pharmacology Pub Date : 2024-02-15 DOI:10.1124/molpharm.123.000709
Hannah Lachmayr, Alfred H Merrill
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Abstract

A special category of phospholipase D (PLD) in the venom of the brown recluse spider (Loxosceles reclusa) and several other sicariid spiders accounts for the dermonecrosis and many of the other clinical symptoms of envenomation. Related proteins are produced by other organisms, including fungi and bacteria. These PLDs are often referred to as sphingomyelinase Ds (SMase Ds) because they cleave sphingomyelin (SM) to choline and "ceramide phosphate." The lipid product has actually been found to be a novel sphingolipid: ceramide 1,3-cyclic phosphate (Cer1,3P). Since there are no effective treatments for the injury induced by the bites of these spiders, SMase D/PLDs are attractive targets for therapeutic intervention, and some of their features will be described in this minireview. In addition, two simple methods are described for detecting the characteristic SMase D activity using a fluorescent SM analog, (N-[12-[(7-nitro-2-1,3-benzoxadiazol-4-yl)amino]dodecanoyl]-SM (C12-NBD-SM), that is cleaved to C12-NBD-Cer1,3P, which is easily separated from other potential metabolites by thin-layer chromatography and visualized under UV light. Besides confirming that C12-NBD-Cer1,3P is the only product detected upon incubation of C12-NBD-SM with brown recluse spider venom, the method was also able to detect for the first time very low levels of activity in venom from another spider, Kukulcania hibernalis The simplicity of the methods makes it relatively easy to determine this signature activity of SMase D/PLD. SIGNIFICANCE STATEMENT: The sphingomyelinase D/phospholipase D that are present in the venom of the brown recluse spider and other sources cause considerable human injury, but detection of the novel sphingolipid product, ceramide 1,3-cyclic phosphate, is not easy by previously published methods. This minireview describes simple methods for detection of this activity that will be useful for studies of its occurrence in spider venoms and other biological samples, perhaps including lesions from suspected spider bites and infections.

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简要概述了褐隐蛛毒液和其他生物的毒性鞘磷脂酶Ds,以及检测其标志性环状神经酰胺磷酸盐产生的简单方法。
棕色隐遁蛛(Loxosceles隐士)和其他几种西西里蜘蛛毒液中的一种特殊类型的磷脂酶D(PLD)导致了皮肤病和许多其他临床症状。相关蛋白质由包括真菌和细菌在内的其他生物体产生。这些PLD通常被称为鞘磷脂酶Ds(SMase D),因为它们将鞘磷脂(SM)切割成胆碱和“神经酰胺磷酸盐”。实际上,已经发现脂质产物是一种新型鞘脂:神经酰胺1,3-环磷酸盐(Cer1,3P)。由于没有有效的治疗方法来治疗这些蜘蛛叮咬引起的损伤,SMase D/PLD是治疗干预的有吸引力的靶点,它们的一些特征将在本小综述中描述。此外,描述了使用荧光SM类似物(N-[12-[(7-硝基-2-1,3-苯并恶二唑-4-基)氨基]十二烷酰基]-SM(C12-NBD-SM)检测特征性SMase D活性的两种简单方法,其被切割成C12-NBD-Cer1,3P,其通过薄层色谱法容易地与其他潜在代谢产物分离并在紫外光下显现。除了证实C12-NBD-Cer1,3P是C12-NBD-SM与棕色隐世蜘蛛毒液孵育时检测到的唯一产物外,该方法还能够首次检测到另一种蜘蛛Kukulcania hibernalis毒液中极低水平的活性。该方法的简单性使确定SMase D/PLD的这种标志性活性相对容易。意义声明存在于褐隐蛛毒液和其他来源中的鞘磷脂酶D/PLD会对人类造成相当大的伤害,但通过以前发表的方法检测新的鞘脂产物1,3-环磷酸神经酰胺并不容易。这篇小型综述描述了一种检测这种活性的简单方法,该方法将有助于研究其在蜘蛛毒液和其他生物样本中的发生,可能包括疑似蜘蛛咬伤和感染引起的病变。
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来源期刊
Molecular Pharmacology
Molecular Pharmacology 医学-药学
CiteScore
7.20
自引率
2.80%
发文量
50
审稿时长
3-6 weeks
期刊介绍: Molecular Pharmacology publishes findings derived from the application of innovative structural biology, biochemistry, biophysics, physiology, genetics, and molecular biology to basic pharmacological problems that provide mechanistic insights that are broadly important for the fields of pharmacology and toxicology. Relevant topics include: Molecular Signaling / Mechanism of Drug Action Chemical Biology / Drug Discovery Structure of Drug-Receptor Complex Systems Analysis of Drug Action Drug Transport / Metabolism
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