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阿尔茨海默病淀粉样蛋白和炎症特征的进化观点。

Evolutionary perspectives on amyloid and inflammatory features of Alzheimer disease.

作者信息

Finch C E, Marchalonis J J

机构信息

Andrus Gerontology Center, University of Southern California, Los Angeles 90089, USA.

出版信息

Neurobiol Aging. 1996 Sep-Oct;17(5):809-15. doi: 10.1016/0197-4580(96)00119-4.

Abstract

We propose that the amyloid deposits in senile plaques of Alzheimer's Disease (AD) result from ancient mechanisms in wound-healing and inflammatory processes that preceded the evolution of the inducible combinatorial immune responses characteristic of jawed vertebrates. AD plaques are unlike active plaques in MS, because antibodies, T-cells and, B cells are not conspicuous components of senile plaques or other loci of degeneration. However, senile plaques contain amyloids and other inflammatory proteins of ancient origin that appear to be made by local brain cells, including neurons, astrocytes, and microglia. We describe a highly conserved 16-mer found in pentrakins from mammals and from the horseshoe crab. The senile plaque thus provides a novel opportunity to study primitive features of complement-mediated inflammatory responses in the absence of immunoglobulins.

摘要

我们提出,阿尔茨海默病(AD)老年斑中的淀粉样沉积物源于伤口愈合和炎症过程中的古老机制,这些机制早于有颌脊椎动物特有的诱导性组合免疫反应的进化。AD斑块与多发性硬化症中的活性斑块不同,因为抗体、T细胞和B细胞不是老年斑或其他退化部位的显著成分。然而,老年斑含有古老起源的淀粉样蛋白和其他炎症蛋白,这些蛋白似乎是由局部脑细胞产生的,包括神经元、星形胶质细胞和小胶质细胞。我们描述了一种在哺乳动物和鲎的五聚蛋白中发现的高度保守的16聚体。因此,老年斑为在没有免疫球蛋白的情况下研究补体介导的炎症反应的原始特征提供了一个新的机会。

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