Smith C I, Hammarström L
Department of Immunobiology, Karolinska Institute, Stockholm, Sweden.
Scand J Immunol. 1980;11(1):79-84. doi: 10.1111/j.1365-3083.1980.tb00211.x.
Using a modification of the protein A plaque assay, muramidase (lysozyme)-producing leucocytes were detected as plaque-forming cells. In the presence of anti-muramidase Ig and complement the secreted lysozyme resulted in lysis of protein-A-coated target erythrocytes. By the use of a monolayer technique individual plaque-forming cells could be identified by staining procedures. Granulocytes as well as monocytes were found to produce muramidase and thus to form plaques. This method could serve as a useful tool when studying lysozyme secretion. Furthermore, by the use of appropriate antisera, this method could be employed for the study of any cell type (any secretion), provided enough molecules are being secreted.
采用蛋白A蚀斑检测法的一种改良方法,将产生溶菌酶的白细胞检测为蚀斑形成细胞。在抗溶菌酶Ig和补体存在的情况下,分泌的溶菌酶导致包被蛋白A的靶红细胞裂解。通过使用单层技术,单个蚀斑形成细胞可通过染色程序进行鉴定。发现粒细胞和单核细胞均产生溶菌酶并因此形成蚀斑。该方法可作为研究溶菌酶分泌的有用工具。此外,通过使用合适的抗血清,只要有足够的分子被分泌,该方法可用于研究任何细胞类型(任何分泌物)。