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Biochemical increase in phosphorylated alpha-synuclein precedes histopathology of lewy-type synucleinopathies

机译:磷酸化α-突触核蛋白的生化增加先于路易型突触核蛋白病的组织病理学

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摘要

A key component in Lewy body (LB) pathology in LB disorders is α-synuclein phosphorylated at serine 129 (pαsyn). However, it is not known if increase in the level of biochemically measurable pαsyn precedes the presence of histologically identified Lewy-type synucleinopathy (LTS). To gain sights into possible temporal sequence, we measured levels of pαsyn in cingulate and temporal cortices that develop LTS pathology at later stages of LB disorders. Brain homogenates from 128 autopsy cases including normal controls and subjects classified by Unified LTS histopathology staging system were studied. We found that biochemically measurable pαsyn levels in cingulate and temporal cortices were significantly increased at Unified stages III and IV. When pαsyn levels were compared between LTS density scores instead of Unified stages, significant increases were detected even as LTS density scores increased from 0 to 1 in olfactory bulb and substantia nigra. Therefore, our findings demonstrated that changes of pαsyn levels in cingulate and temporal cortices coincided with the early appearance of the LTS pathology in olfactory bulb and substantia nigra, even though histologically demonstrable LTS was lacking in the cortical region. Therefore, identifying the underlying mechanisms driving these changes could be crucial to understanding the pathogenesis of LB disorders.
机译:LB疾病的路易体(LB)病理学的关键成分是在丝氨酸129(pαsyn)磷酸化的α-突触核蛋白。然而,尚不知道在生物化学上可测量的pαsyn水平的增加是否先于组织学上确定的路易型突触核蛋白病(LTS)的出现。为了了解可能的时间序列,我们测量了扣带状和颞叶皮层中pαsyn的水平,这些皮层在LB疾病的后期发展为LTS病理。研究了128例尸检病例的脑匀浆,包括正常对照和通过统一LTS组织病理学分期系统分类的受试者。我们发现,在统一阶段III和IV中,扣带回和颞皮质的生化可测量pαsyn水平显着增加。当在LTS密度评分而非统一阶段之间比较pαsyn水平时,即使嗅球和黑质中LTS密度评分从0增加到1,也检测到显着增加。因此,我们的发现表明,即使在皮质区域缺乏组织学上可证实的LTS,在扣叶和颞皮质的pαsyn水平的变化与嗅球和黑质中LTS病理的早期出现相吻合。因此,确定驱动这些变化的潜在机制对于了解LB疾病的发病机制可能至关重要。

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