Pillai S, Wright D, Gupta A, Zhou G, Hull G, Jiang H, Zhang H
Department of Obstetrics and Gynecology, Medical University of South Carolina, Charleston 29425-2233, USA.
J Urol. 1996 Jun;155(6):1928-33.
We determined the molecular weights and isoelectric points of antigens in the uncapacitated and capacitated spermatozoa of fertile men binding to the serum immunoglobulin G (IgG) from 8 autoimmune infertile men and 8 fertile nonautoimmune men.
We used double fluorochrome cytotoxicity and immunobead binding assays to determine the sperm antibody status of the study subjects. 2-Dimensional gel electrophoresis and Western blot analysis were used to determine the molecular weights and isoelectric points of sperm antigens binding to serum IgG from these men. Amino acid sequencing of the digested peptides of chosen proteins was accomplished. Immune reactivity to the proteins in autoimmune infertile men was further verified.
Serum IgG from fertile men failed to react significantly. Serum IgG from all autoimmune men (100%) showed significant binding to proteins with a molecular weight of 92 kDa. and isoelectric points of 3.5 to 4.0 in the capacitated spermatozoa. Six of 8 infertile men (75%) had serum IgG binding to capacitated sperm antigens with a molecular weight of 18 kDa. and isoelectric points of 4.5 to 5.2. Amino acid sequencing of peptides of the 92 kDa. protein matched complement component 1 (C1) inhibitor, with noted differences in the amino acid sequencing from the latter. The 18 kDa. protein matched calmodulin. We verified that serum IgG from autoimmune infertile men bound with C1 inhibitor and ascertained that the 92 kDa. protein in the spermatozoa was C1 inhibitor-like protein.
Significant antibody responses to C1 inhibitor-like protein and calmodulin were noted in autoimmune men. Both of these proteins may be of testicular origin and these autoimmune responses may be highly relevant to infertility.
我们测定了可育男性未获能和获能精子中与8名自身免疫性不育男性及8名可育非自身免疫性男性血清免疫球蛋白G(IgG)结合的抗原的分子量和等电点。
我们使用双荧光染料细胞毒性和免疫珠结合试验来确定研究对象的精子抗体状态。二维凝胶电泳和蛋白质印迹分析用于确定与这些男性血清IgG结合的精子抗原的分子量和等电点。完成了所选蛋白质消化肽段的氨基酸测序。进一步验证了自身免疫性不育男性对这些蛋白质的免疫反应性。
可育男性的血清IgG未显示出明显反应。所有自身免疫性男性(100%)的血清IgG与获能精子中分子量为92 kDa、等电点为3.5至4.0的蛋白质有显著结合。8名不育男性中有6名(75%)的血清IgG与分子量为18 kDa、等电点为4.5至5.2的获能精子抗原结合。92 kDa蛋白质肽段的氨基酸测序与补体成分1(C1)抑制剂匹配,但与后者的氨基酸测序存在显著差异。18 kDa蛋白质与钙调蛋白匹配。我们证实自身免疫性不育男性的血清IgG与C1抑制剂结合,并确定精子中的92 kDa蛋白质为C1抑制剂样蛋白。
在自身免疫性男性中观察到对C1抑制剂样蛋白和钙调蛋白的显著抗体反应。这两种蛋白质可能都起源于睾丸,这些自身免疫反应可能与不育高度相关。