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原发性胆汁性肝硬化中的血清Fcγ受体样分子:一种可能的免疫调节机制。

Serum Fc gamma-receptor-like molecules in primary biliary cirrhosis: a possible immunoregulatory mechanism.

作者信息

MacLean C A, Goudie B M, MacSween R N, Sandilands G P

出版信息

Immunology. 1984 Oct;53(2):315-24.

Abstract

Functionally active Fc gamma-receptor-like molecules were isolated from normal human serum by affinity chromatography and shown to have an apparent molecular weight (MW) of approximately 60,000 as assessed by SDS-polyacrylamide gel electrophoresis. These low MW Fc gamma-receptor-like molecules were found to be significantly reduced in whole serum, and in all of six serum fractions, obtained from patients with primary biliary cirrhosis (PBC). A high MW IgG-binding factor, with partial Fc gamma-receptor-like activity, was also found in PBC serum. This factor was also observed to a lesser extent in normal serum. Detailed analysis of this factor suggests that it is a large macromolecule consisting of antigen (unknown). IgG class antibody and 60K Fc gamma-receptor-like molecules. Binding of serum Fc gamma R-like molecules to immune complexes may account for the apparent reduction in Fc gamma-receptor-like activity observed in whole PBC serum. These macromolecules may play an important role in immunoregulation.

摘要

通过亲和层析从正常人血清中分离出具有功能活性的Fcγ受体样分子,经十二烷基硫酸钠-聚丙烯酰胺凝胶电泳评估,其表观分子量(MW)约为60,000。发现这些低分子量的Fcγ受体样分子在原发性胆汁性肝硬化(PBC)患者的全血清以及六个血清组分中均显著减少。在PBC血清中还发现了一种具有部分Fcγ受体样活性的高分子量IgG结合因子。在正常血清中也能观察到这种因子,但程度较轻。对该因子的详细分析表明,它是一种由抗原(未知)、IgG类抗体和60K Fcγ受体样分子组成的大分子。血清FcγR样分子与免疫复合物的结合可能解释了在PBC全血清中观察到的Fcγ受体样活性明显降低的现象。这些大分子可能在免疫调节中起重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dba5/1454830/f6a3f6b6853f/immunology00199-0127-a.jpg

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