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针对钠通道阻滞剂河豚毒素的单克隆抗体对神经毒性的保护作用。

Protection against nerve toxicity by monoclonal antibodies to the sodium channel blocker tetrodotoxin.

作者信息

Huot R I, Armstrong D L, Chanh T C

机构信息

Department of Virology, Southwest Foundation for Biomedical Research, San Antonio, Texas 78284.

出版信息

J Clin Invest. 1989 Jun;83(6):1821-6. doi: 10.1172/JCI114087.

Abstract

The sodium channel blocker, tetrodotoxin (TDT), was conjugated to keyhole limpet hemocyanin (KLH) and used to immunize BALB/c mice. Anti-TDT antibodies were detected in serum by ELISA and reached stable levels 4-5 wk after the first immunization. Spleens from immunized mice were fused with NS-1 mouse myeloma cells and approximately 9,329 resultant hybrids were screened by ELISA for reactivity to TDT. Two stable hybrids were isolated, subcloned, and characterized. These hybrids, termed TD13a1 and TD2C5, secreted specific anti-TDT antibodies that recognized TDT but not the related sodium channel blocker, saxitoxin (STX), as determined by competition ELISA. Both antibodies were of the IgG1k subclass with Ka's approaching 10(7) M-1. The inhibitory ability of these antibodies was tested by a competitive displacement assay for [3H]STX on rat brain membranes. Both antibodies strongly inhibited TDT binding to membranes. A nanomole of TD2C5 was able to bind approximately 1.8 nmol of TDT, whereas a comparable amount of TD13a1 bound half as much. Furthermore, TD2C5 was able to protect against TDT-induced reduction of peripheral nerve action potentials in rat tibial nerve when administered in situ. These antibodies thus represent potentially useful reagents for neurobiologic research, detection of toxin contamination and diagnosis of poisoning, and may provide protection against the toxicity of TDT in vivo.

摘要

将钠通道阻滞剂河豚毒素(TDT)与钥孔血蓝蛋白(KLH)偶联,用于免疫BALB/c小鼠。通过酶联免疫吸附测定(ELISA)在血清中检测到抗TDT抗体,首次免疫后4-5周达到稳定水平。将免疫小鼠的脾脏与NS-1小鼠骨髓瘤细胞融合,通过ELISA筛选约9329个产生的杂交细胞对TDT的反应性。分离出两个稳定的杂交细胞,进行亚克隆并鉴定。通过竞争ELISA测定,这些称为TD13a1和TD2C5的杂交细胞分泌特异性抗TDT抗体,该抗体识别TDT但不识别相关的钠通道阻滞剂石房蛤毒素(STX)。两种抗体均为IgG1k亚类,亲和常数接近10⁷ M⁻¹。通过对大鼠脑膜上的[³H]STX进行竞争置换试验,测试了这些抗体的抑制能力。两种抗体均强烈抑制TDT与膜的结合。一纳摩尔的TD2C5能够结合约1.8纳摩尔的TDT,而等量的TD13a1的结合量仅为其一半。此外,原位给药时,TD2C5能够保护大鼠胫神经免受TDT诱导的外周神经动作电位降低的影响。因此,这些抗体是神经生物学研究、毒素污染检测和中毒诊断中潜在有用的试剂,并且可能在体内提供针对TDT毒性的保护作用。

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Nonprotein neurotoxins.非蛋白质神经毒素
Clin Toxicol. 1981 Jul;18(7):813-63. doi: 10.3109/15563658108990310.

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