人类脑脊液和血清有丝分裂生物标志物在阿尔茨海默病持续发展过程中的变化。

Autophagy Pub Date : 2024-08-01 Epub Date: 2024-05-02 DOI:10.1080/15548627.2024.2340408
Kateřina Veverová, Jan Laczó, Alžběta Katonová, Hana Horáková, Veronika Matušková, Francesco Angelucci, Martina Laczó, Zuzana Nedelská, Jakub Hort, He-Ling Wang, Jianying Zhang, Liu Shi, Evandro Fei Fang, Martin Vyhnálek
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引用次数: 0

摘要

在阿尔茨海默病(AD)患者的死后大脑和 iPSC 衍生神经元中,始终存在有丝分裂缺陷。然而,目前还缺乏对血清或脑脊液(CSF)中有丝分裂状态的广泛检查,有丝分裂生物标志物的临床潜力也尚未得到检验。我们对从捷克脑老化研究(Czech Brain Aging Study)中招募的246人的脑脊液和血清中的有丝分裂/自噬和溶酶体降解(PINK1、BNIP3L和TFEB)生物标志物进行了量化,这些人包括AD导致的轻度认知障碍(MCI-AD,n = 100)、AD导致的痴呆(AD-dementia,n = 100)和认知功能无障碍的人(CU,n = 46)。此外,还对认知功能和脑萎缩进行了评估。我们的数据显示,与相应的 CU 患者相比,AD 患者的血清和 CSF PINK1 以及血清 BNIP3L 含量较高,而血清 TFEB 含量较低。此外,有丝分裂障碍的程度与AD患者临床指标的严重程度相关。具体来说,PINK1的水平与脑脊液中磷酸化(p)-MAPT/tau(181)、总(t)-MAPT/tau、NEFL(神经丝轻链)和NRGN(神经粒蛋白)的水平呈正相关,而与记忆、执行功能和语言领域呈负相关。血清 TFEB 水平与 NEFL 呈负相关,与执行功能和语言呈正相关。这项研究揭示了反映在 AD 患者生物流体生物标志物中的有丝分裂障碍,并与更晚期的 AD 病理学相关:缩写:Aβ:淀粉样 beta;AD:阿兹海默病;AVs:有丝分裂:缩写:Aβ:淀粉样β蛋白;AD:阿尔茨海默病;AVs:自噬空泡;BNIP3L:BCL2互作蛋白3样;CU:认知功能未受损;CSF:脑脊液;LAMP1:溶酶体相关膜蛋白1;MAP1LC3/LC3:微管相关蛋白1轻链3;MCI:轻度认知功能障碍;NRGG:淀粉样β蛋白:NRGN:神经粒蛋白;NEFL:神经丝轻链;p-MAPT/tau:磷酸化微管相关蛋白 tau;PINK1:PTEN 诱导激酶 1;t-MAPT/tau:总微管相关蛋白 tau;TFEB:转录因子 EB;TMT:寻迹测试。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alterations of human CSF and serum-based mitophagy biomarkers in the continuum of Alzheimer disease.

Defective mitophagy is consistently found in postmortem brain and iPSC-derived neurons from Alzheimer disease (AD) patients. However, there is a lack of extensive examination of mitophagy status in serum or cerebrospinal fluid (CSF), and the clinical potential of mitophagy biomarkers has not been tested. We quantified biomarkers of mitophagy/autophagy and lysosomal degradation (PINK1, BNIP3L and TFEB) in CSF and serum from 246 individuals, covering mild cognitive impairment due to AD (MCI-AD, n = 100), dementia due to AD (AD-dementia, n = 100), and cognitively unimpaired individuals (CU, n = 46), recruited from the Czech Brain Aging Study. Cognitive function and brain atrophy were also assessed. Our data show that serum and CSF PINK1 and serum BNIP3L were higher, and serum TFEB was lower in individuals with AD than in corresponding CU individuals. Additionally, the magnitude of mitophagy impairment correlated with the severity of clinical indicators in AD patients. Specifically, levels of PINK1 positively correlated with phosphorylated (p)-MAPT/tau (181), total (t)-MAPT/tau, NEFL (neurofilament light chain), and NRGN (neurogranin) levels in CSF and negatively with memory, executive function, and language domain. Serum TFEB levels negatively correlated with NEFL and positively with executive function and language. This study reveals mitophagy impairment reflected in biofluid biomarkers of individuals with AD and associated with more advanced AD pathology.Abbreviation: Aβ: amyloid beta; AD: Alzheimer disease; AVs: autophagic vacuoles; BNIP3L: BCL2 interacting protein 3 like; CU: cognitively unimpaired; CSF: cerebrospinal fluid; LAMP1: lysosomal-associated membrane protein 1; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; MCI: mild cognitive impairment; NRGN: neurogranin; NEFL: neurofilament light chain; p-MAPT/tau: phosphorylated microtubule associated protein tau; PINK1: PTEN induced kinase 1; t-MAPT/tau: total microtubule associated protein tau; TFEB: transcription factor EB; TMT: Trail Making Test.

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