Ulrich J, Haugh M, Anderton B H, Probst A, Lautenschlager C, His B
Acta Neuropathol. 1987;73(3):240-6. doi: 10.1007/BF00686617.
Sections of formaldehyde-fixed paraffin-embedded cortical and hippocampal brain tissue from five cases with senile dementia of Alzheimer type (SDAT) and five cases with Pick's disease (PD) were immunostained with the monoclonal antibodies (mabs) 147, RT 97, BF 10 and 8D8 with and without pretreatment with alkaline phosphatase (AP) or trypsin (Tr). The mabs 147, RT 97 and BF 10 had previously been demonstrated to bind exclusively to phosphorylated epitopes of neurofilament proteins, while mab 8D8 is shown in this report to bind mainly, but not exclusively, to phosphorylated neurofilament epitopes. The mabs RT 97, BF 10 and 8D8, but not 147 stain most, if not all, Pick bodies (PB) and Alzheimer neurofibrillary tangles (NFT). When sections are pretreated with AP or Tr the immunostaining with mab BF 10 is very resistent in both PB and NFT. This resistance of PB and NFT is in contrast to the reduced staining of axons and of swollen cells in PD by the same enzymatic pretreatment. Immunostaining with mab RT 97 of PB and NFT is reduced moderately by AP and considerably by Tr. Only when stained with mab 8D8 is there a discrepancy between PB and NFT in their reaction to the pretreatment with AP: NFT staining with mab 8D8 is not affected, while that of PB is abolished. Thus, in spite of their different ultrastructure, PB and NFT are very similar immunocytochemically and in the accessibility of their phosphorylated epitopes to enzymatic treatment.
取自5例阿尔茨海默型老年痴呆症(SDAT)患者和5例皮克病(PD)患者的甲醛固定石蜡包埋的皮质和海马脑组织切片,用单克隆抗体(mab)147、RT 97、BF 10和8D8进行免疫染色,染色时有的经过碱性磷酸酶(AP)或胰蛋白酶(Tr)预处理,有的没有经过预处理。之前已证实mab 147、RT 97和BF 10仅与神经丝蛋白的磷酸化表位结合,而本报告显示mab 8D8主要但并非仅与磷酸化神经丝表位结合。mab RT 97、BF 10和8D8能对大多数(如果不是全部的话)皮克小体(PB)和阿尔茨海默神经原纤维缠结(NFT)染色,但mab 147不能。当切片用AP或Tr预处理时,mab BF 10对PB和NFT的免疫染色非常稳定。PB和NFT的这种稳定性与相同酶预处理后PD中轴突和肿胀细胞染色减少形成对比。PB和NFT用mab RT 97免疫染色时,AP能使其适度减少,Tr能使其显著减少。仅在用mab 8D8染色时,PB和NFT对AP预处理的反应存在差异:用mab 8D8对NFT染色不受影响,而对PB的染色则被消除。因此,尽管PB和NFT的超微结构不同,但它们在免疫细胞化学以及其磷酸化表位对酶处理的可及性方面非常相似。