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特异性自身抗体(抗-T)和补体在体外诱导豚鼠精子产生的超微结构损伤。

Ultrastructural lesions induced in vitro in guinea-pig spermatozoa by a specific autoantibody (anti-T) and complement.

作者信息

Le Bouteiller P, Toullet F, Voisin G A

出版信息

Immunology. 1975 May;28(5):983-99.

Abstract

A quantitative ultrastructural study has been carried out on the lesions that are induced in vitro in guinea-pig spermatozoa by the action of auto-antispermatozoa antibodies and complement. The responsibility of three-independent autoantigen-autoantibody systems (S, P and T) has been explored. The only anti-T antibody known to fix complement and to be spermotoxic (T is a membrane-linked autoantigen), caused significant and important lesions, the immunologically specific origin of which was demonstrated. These lesions began a few seconds after complement had been added. The cytoplasmic membrane is first involved, then the acrosomal membranes, and then the acrosomal contents are lysed. The remarkable rapidity of action of complement on the antibody-sensitized target is emphasized. A typical dose-effect curve is obtained with dilutions of anti-T immune sera. Non-C1-fixing anti-S as well as C1-fixing anti-P antibodies (P has been shown to be intra-acrosomal) do not provoke any significant lesions, even in the presence fo complement, as compared to normal and various controls. However, anti-P serum, when added to non-damaging dilutions of anti-T in the presence of complement, was able to provoke significant lesions in the acrosomes. The bearing of these findings on the mechanisms of in vivo lesions is discussed.

摘要

已对自身抗精子抗体和补体在体外诱导豚鼠精子产生的病变进行了定量超微结构研究。研究了三种独立的自身抗原-自身抗体系统(S、P和T)的作用。已知唯一能固定补体并具有精子毒性的抗T抗体(T是一种膜相关自身抗原)会引起显著且重要的病变,其免疫特异性起源已得到证实。这些病变在添加补体后几秒内就开始出现。首先涉及细胞质膜,然后是顶体膜,接着顶体内容物被溶解。强调了补体对抗体致敏靶标的显著快速作用。用抗T免疫血清的稀释液可得到典型的剂量-效应曲线。与正常及各种对照相比,不固定C1的抗S抗体以及固定C1的抗P抗体(已证明P存在于顶体内)即使在有补体存在的情况下也不会引发任何显著病变。然而,在有补体存在的情况下,当将抗P血清添加到抗T的无损伤稀释液中时,能够在顶体中引发显著病变。讨论了这些发现对体内病变机制的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b6d/1445919/17491d62554a/immunology00316-0184-a.jpg

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