Hajdu I
Cell Immunol. 1983 Jul 1;79(1):157-63. doi: 10.1016/0008-8749(83)90058-8.
The immunohistochemical detection of J chain in histological sections of tonsils was compared to that of immunoglobulin IgG, IgM, and IgA. Pretreatment of tissue sections with detergents (saponin and Triton X-100) and with proteolytic enzyme (trypsin) at different experimental conditions has shown (i) 0.1% trypsin digestion for 1 hr at room temperature increased dramatically both the number of J-chain-positive cells detected, and the intensity of the color reaction, while the detergents had no noticeable effect; (ii) under the same conditions, trypsin also improved the detection of immunoglobulins, but quantitatively and qualitatively far less effectively than for J chain. The effect of trypsin occurred after 30 min. These results indicate that in tissue sections, the antigenic determinants of J chain are "masked" in the molecule of immunoglobulin in such a manner that the use of trypsin hydrolysis may be important for its successful detection at the light microscopic level. In the case of intact immunoglobulins, this is less important.
将扁桃体组织切片中J链的免疫组织化学检测结果与免疫球蛋白IgG、IgM和IgA的检测结果进行了比较。在不同实验条件下,用去污剂(皂苷和曲拉通X-100)和蛋白水解酶(胰蛋白酶)对组织切片进行预处理,结果显示:(i)室温下用0.1%胰蛋白酶消化1小时,检测到的J链阳性细胞数量和显色反应强度均显著增加,而去污剂没有明显效果;(ii)在相同条件下,胰蛋白酶也改善了免疫球蛋白的检测,但在数量和质量上,其效果远不如对J链的检测。胰蛋白酶的作用在30分钟后出现。这些结果表明,在组织切片中,J链的抗原决定簇在免疫球蛋白分子中被“掩盖”,以至于在光学显微镜水平上,使用胰蛋白酶水解对成功检测J链可能很重要。对于完整的免疫球蛋白来说,这一点不太重要。