Christie K N, Stoward P J
Histochem J. 1978 Jul;10(4):425-33. doi: 10.1007/BF01003006.
Hamster mast cells have been found to give strong peroxidatic reactions at pH 5, 7.5 and 10 when sections of skeletal muscle are incubated for 2.5 h in the dark at room temperature on semipermeable membranes covering a gelled incubation medium consisting of 0.01% hydrogen peroxide, 5.5mM diaminobenzidine and 1.36% agar dissolved in Universal buffer. The technique is very efficient: with it, all mast cells react in marked contrast to the negative reaction they usually give with conventional techniques. The peroxidatic reactions are abolished if tissues are perfused beforehand with either aminotriazole or KCN but not if these inhibitors are incorporated in the gelled incubation medium. This and other evidence suggests that the mast cell reactions are not due to either catalase or haemoglobin adsorbed onto mast cell granules from lysed red blood cells. Skeletal muscle fibres do not exhibit any visible peroxidase activity with the membrane technique.
已发现,当骨骼肌切片在室温下于黑暗中在覆盖由0.01%过氧化氢、5.5mM二氨基联苯胺和溶解于通用缓冲液中的1.36%琼脂组成的凝胶化孵育培养基的半透膜上孵育2.5小时时,仓鼠肥大细胞在pH 5、7.5和10时会产生强烈的过氧化物酶反应。该技术非常有效:使用它时,所有肥大细胞都会发生反应,这与它们通常用传统技术产生的阴性反应形成明显对比。如果预先用氨基三唑或KCN灌注组织,过氧化物酶反应就会消失,但如果将这些抑制剂加入凝胶化孵育培养基中则不会。这一证据以及其他证据表明,肥大细胞反应并非由于过氧化氢酶或从裂解的红细胞吸附到肥大细胞颗粒上的血红蛋白所致。骨骼肌纤维用膜技术未表现出任何可见的过氧化物酶活性。