Frohman E M, Frohman T C, Gupta S, de Fougerolles A, van den Noort S
Department of Neurology, California College of Medicine, University of California, Irvine 92717.
J Neurol Sci. 1991 Nov;106(1):105-11. doi: 10.1016/0022-510x(91)90202-i.
In this study, 13 clinically and pathologically diagnosed cases of Alzheimer's disease were analyzed for the presence of intercellular adhesion molecule 1 (ICAM-1), ICAM-2, lymphocyte function associated antigen-1 (LFA-1), HLA-DR, LN-1, and LN-2. ICAM-1 was observed primarily on neuritic plaques and cerebrovascular endothelium. ICAM-1 was also shown to be present in brain tissue derived from 14 normal cases; however, the degree of immunoreactivity was quantitatively less compared to Alzheimer cases and was largely restricted to cerebrovascular endothelium. LFA-1 was shown to be present on microglial cells and leukocytes. Consistent with the findings of previous reports, HLA-DR was found to be expressed on microglial cells. In this study we failed to demonstrate dual immunolocalization for ICAM-1 and LFA-1, ICAM-1 and HLA-DR, or ICAM-1 and LN-2. As microglial cells express both HLA-DR and LFA-1, they may serve to mediate antigen presentation functions by interacting with lymphocyte ICAM-1. Alternately, the expression of these immune-associated glycoproteins on glial cells may be epiphenomenal occurring secondary to some aspect of the disease process. Finally, the presence of ICAM-1 within neuritic plaques raises the question as to whether adhesion may play some role in the process of neurite outgrowth and neurodegeneration.
在本研究中,对13例临床和病理诊断为阿尔茨海默病的病例进行了细胞间黏附分子1(ICAM-1)、ICAM-2、淋巴细胞功能相关抗原-1(LFA-1)、HLA-DR、LN-1和LN-2的检测。ICAM-1主要在神经炎性斑块和脑血管内皮上观察到。ICAM-1也存在于14例正常病例的脑组织中;然而,与阿尔茨海默病病例相比,其免疫反应程度在数量上较少,且主要局限于脑血管内皮。LFA-1在小胶质细胞和白细胞上被检测到。与先前报道的结果一致,HLA-DR在小胶质细胞上表达。在本研究中,我们未能证明ICAM-1与LFA-1、ICAM-1与HLA-DR或ICAM-1与LN-2的双重免疫定位。由于小胶质细胞同时表达HLA-DR和LFA-1,它们可能通过与淋巴细胞ICAM-1相互作用来介导抗原呈递功能。或者,这些免疫相关糖蛋白在胶质细胞上的表达可能是疾病过程某些方面继发的附带现象。最后,神经炎性斑块中ICAM-1的存在提出了一个问题,即黏附是否可能在神经突生长和神经退行性变过程中发挥某种作用。