Cellular localization of the microsomal antigen and the thyroid peroxidase antigen.

A Pinchera, S Mariotti, L Chiovato, P Vitti, G Lopez, A Lombardi, S Anelli, R Bechi, P Carayon
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引用次数: 8

Abstract

Evidence has been accumulated that human thyroid microsomal/microvillar autoantigen (M) is expressed both in the cytoplasm and on the surface of thyroid follicular cells. The availability of this autoantigen to the immune system, possibly associated with abnormally expressed HLA-DR antigens may be relevant both to the triggering and to maintenance of thyroid autoimmune reactions. Preliminary biochemical characterization of M suggested that it was a glycoprotein with a mol. wt. of about 100-110 kD. recent studies carried out in our laboratories taking advantage of monoclonal antibodies provided evidence that the structure presently referred as M-Ag is represented by thyroid peroxidase (TPO). The identity between TPO and M is further supported by four-layer immunofluorescence analysis showing a complete overlap of the two antigens both in the surface and in the cytoplasm of thyroid cells and by the observation that the expression of M and TPO is similarly modulated by TSH, possibly through a cAMP-dependent mechanism.

微粒体抗原和甲状腺过氧化物酶抗原的细胞定位。
已积累的证据表明,人甲状腺微粒体/微绒毛自身抗原(M)在细胞质和甲状腺滤泡细胞表面均有表达。这种自身抗原对免疫系统的可用性,可能与异常表达的HLA-DR抗原有关,可能与甲状腺自身免疫反应的触发和维持有关。初步的生化鉴定表明,M是一种分子量约为100-110 kD的糖蛋白。最近在我们实验室利用单克隆抗体进行的研究提供了证据,目前被称为M-Ag的结构是由甲状腺过氧化物酶(TPO)代表的。四层免疫荧光分析进一步支持了TPO和M之间的一致性,显示两种抗原在甲状腺细胞的表面和细胞质中完全重叠,并且观察到M和TPO的表达类似地受到TSH的调节,可能通过camp依赖机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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