老年斑
疾病
病理
病因学
脑脊液
病态的
炎症
淀粉样变性
医学
多发性硬化
发病机制
阿尔茨海默病
免疫学
作者
Laure Duplan,Bernard Michel,José Boucraut,Sandrine Barthellémy,Sophie Desplat‐Jégo,Valérie Marin,D. Gambarelli,Dominique Bernard,P. Berthézène,Béatrice Alescio-Lautier,Jean‐Michel Verdier
标识
DOI:10.1016/s0197-4580(00)00182-2
摘要
According to one of the theories formulated to explain the etiology of Alzheimer's disease (AD), amylosis may reflect a specific inflammatory response. Two inflammatory proteins, lithostathine and PAP, were evidenced by immunohistochemistry in senile plaques and neurofibrillary tangles of patients with AD. In addition, lithostathine and PAP were significantly increased in the cerebrospinal fluid of patients with AD when compared to patients with multiple sclerosis, another inflammatory disease, and to normal control subjects. However, no correlation was observed with age of occurrence. Furthermore, lithostathine and PAP were increased even at the very early stages of AD, and their level remained elevated during the course of the AD unlike TNFalpha whose level, very high at very early stages, regularly decreased. Finally, if part of lithostathine and PAP are synthesized in the brain, a large part comes from serum by passage over the blood-brain barrier. These results indicate (i) the existence of an acute phase response followed by a chronic inflammation in AD, and (ii) that lithostathine and PAP are involved even at the first pre-clinical biochemical events of AD. In addition, because lithostathine undergoes an autolytic cleavage leading to its precipitation and the formation of fibrils, we believe that it may be involved in amyloidosis and tangles by allowing heterogeneous precipitation of other proteins.
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