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[细胞因子IL-1α和S100β在阿尔茨海默病不同类型斑块中的表达]

[Expression of cytokine IL-1α and S100β in different types of plaques in Alzheimer's disease].

作者信息

Yao Jing-jing, He Shu-rong, Chen Lan, Yang Li, Qiao Xu-bai, Zhang Wei, Du Jun, Liu Dong-ge

机构信息

Department of Pathology, Beijing Hospital, Beijing 100730, China.

出版信息

Zhonghua Bing Li Xue Za Zhi. 2011 Sep;40(9):581-4.

PMID:22177239
Abstract

OBJECTIVE

To study the significance of cytokine IL-1α and S100β expression in formation and evolution of different types of plaques in Alzheimer's disease.

METHODS

Thirty-four autopsy cases of Alzheimer's disease encountered during the period from 1982 to 2008 were retrieved from the archival files of Department of Pathology, Beijing Hospital. Tissue blocks were taken from hippocampus for dual immunostaining for IL-1α/Aβ and S100β/Aβ.

RESULTS

Immunohistochemical studied for IL-1α/Aβ and S100β/Aβ delineated four different types of senile plaques: diffuse non-neuritic plaques, diffuse neuritic plaques, dense-core neuritic plaques and dense-core non-neuritic plaques. The numbers of IL-1α-positive microglias and S100β-positive astrocytes associated with diffuse neuritic plaques were (7.29 ± 3.04) per mm(2) and (6.49 ± 2.20) per mm(2), respectively. In contrast, the numbers of IL-1α-positive microglias and S100β-positive astrocytes associated with diffuse non-neuritic plaques, dense-core neuritic plaques and dense-core non-neuritic plaques were (3.24 ± 1.53) per mm(2) and (4.14 ± 1.77) per mm(2), (2.09 ± 1.37) per mm(2) and (2.25 ± 0.83) per mm(2), and (1.38 ± 0.90) per mm(2) and (0.58 ± 0.36) per mm(2), respectively. The numbers of IL-1α-positive microglias and S100β-positive astrocytes associated with diffuse neuritic plaques were significantly higher than those of the other three types of plaques (P < 0.05).

CONCLUSION

The IL-1α-positive microglias and S100β-positive astrocytes may be of certain significance in transformation of diffuse non-neuritic plaques to diffuse neuritic plaques in Alzheimer's disease.

摘要

目的

研究细胞因子白细胞介素-1α(IL-1α)和S100β在阿尔茨海默病不同类型斑块形成和演变中的意义。

方法

从北京医院病理科档案中检索1982年至2008年期间遇到的34例阿尔茨海默病尸检病例。从海马体取材制作组织块,进行IL-1α/Aβ和S100β/Aβ双重免疫染色。

结果

对IL-1α/Aβ和S100β/Aβ进行免疫组织化学研究,划分出四种不同类型的老年斑:弥漫性无神经炎性斑块、弥漫性神经炎性斑块、致密核心神经炎性斑块和致密核心无神经炎性斑块。与弥漫性神经炎性斑块相关的IL-1α阳性小胶质细胞和S100β阳性星形胶质细胞数量分别为每平方毫米(7.29±3.04)个和每平方毫米(6.49±2.20)个。相比之下,与弥漫性无神经炎性斑块、致密核心神经炎性斑块和致密核心无神经炎性斑块相关的IL-1α阳性小胶质细胞和S100β阳性星形胶质细胞数量分别为每平方毫米(3.24±1.53)个和每平方毫米(4.14±1.77)个、每平方毫米(2.09±1.37)个和每平方毫米(2.25±0.83)个、每平方毫米(1.38±0.90)个和每平方毫米(0.58±0.36)个。与弥漫性神经炎性斑块相关的IL-1α阳性小胶质细胞和S100β阳性星形胶质细胞数量显著高于其他三种类型的斑块(P<0.05)。

结论

IL-1α阳性小胶质细胞和S100β阳性星形胶质细胞在阿尔茨海默病弥漫性无神经炎性斑块向弥漫性神经炎性斑块的转变中可能具有一定意义。

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