Levels of Synaptic Proteins in Brain and Neurofilament Light Chain in Cerebrospinal Fluid and Plasma of OVT73 Huntington's Disease Sheep Support a Prodromal Disease State.

IF 2.1 Q3 NEUROSCIENCES
Ellen Sapp, Adel Boudi, Suzanne J Reid, Bianca A Trombetta, Pia Kivisäkk, Toloo Taghian, Steven E Arnold, David Howland, Heather Gray-Edwards, Kimberly B Kegel-Gleason, Marian DiFiglia
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Abstract

Background: Synaptic changes occur early in patients with Huntington's disease (HD) and in mouse models of HD. An analysis of synaptic changes in HD transgenic sheep (OVT73) is fitting since they have been shown to have some phenotypes. They also have larger brains, longer lifespan, and greater motor and cognitive capacities more aligned with humans, and can provide abundant biofluids for in vivo monitoring of therapeutic interventions.

Objective: The objective of this study was to determine if there were differences between 5- and 10-year-old OVT73 and wild-type (WT) sheep in levels of synaptic proteins in brain and in neurofilament light chain (NfL) in cerebrospinal fluid (CSF) and plasma.

Methods: Mutant huntingtin (mHTT) and other proteins were measured by western blot assay in synaptosomes prepared from caudate, motor, and piriform cortex in 5-year-old and caudate, putamen, motor; and piriform cortex in 10-year-old WT and OVT73 sheep. Levels of NfL, a biomarker for neuronal damage increased in many neurological disorders including HD, were examined in CSF and plasma samples from 10-year-old WT and OVT73 sheep using the Simoa NfL Advantage kit.

Results: Western blot analysis showed mHTT protein expression in synaptosomes from OVT73 sheep was  23% of endogenous sheep HTT levels at both ages. Significant changes were detected in brain levels of PDE10A, SCN4B, DARPP32, calmodulin, SNAP25, PSD95, VGLUT 1, VAMP1, and Na+/K+-ATPase, which depended on age and brain region. There was no difference in NfL levels in CSF and plasma in OVT73 sheep compared to age-matched WT sheep.

Conclusions: These results show that synaptic changes occur in brain of 5- and 10-year-old OVT73 sheep, but levels of NfL in biofluids are unaffected. Altogether, the data support a prodromal disease state in OVT73 sheep that involves the caudate, putamen and cortex.

OVT73亨廷顿舞蹈症绵羊脑中突触蛋白和脑脊液和血浆中神经丝轻链的水平支持前驱疾病状态。
背景:亨廷顿舞蹈症(HD)患者和HD小鼠模型早期发生突触变化。对HD转基因绵羊(OVT73)突触变化的分析是合适的,因为它们已经被证明具有一些表型。它们还具有更大的大脑、更长的寿命、更大的运动和认知能力,与人类更为一致,并可以为治疗干预的体内监测提供丰富的生物流体。目的:本研究的目的是确定5岁和10岁OVT73与野生型(WT)绵羊在脑突触蛋白水平以及脑脊液(CSF)和血浆中神经丝轻链(NfL)水平是否存在差异。方法:用蛋白质印迹法测定5岁儿童尾状、运动、梨状皮质和尾状、壳核、运动突触体中突变亨廷顿蛋白(mHTT)等蛋白的含量;以及10岁WT和OVT73绵羊的梨状皮层。使用Simoa NfL Advantage试剂盒在10岁WT和OVT73绵羊的CSF和血浆样本中检测了NfL水平,NfL是包括HD在内的许多神经系统疾病中神经元损伤增加的生物标志物。结果:Western印迹分析显示,在两个年龄段,OVT73绵羊突触体中mHTT蛋白的表达均为内源性绵羊HTT水平的23%。脑内PDE10A、SCN4B、DARPP32、钙调素、SNAP25、PSD95、VGLUT1、VAMP1和Na+/K+-ATP酶的水平发生了显著变化,这取决于年龄和脑区。与年龄匹配的野生型绵羊相比,OVT73绵羊的CSF和血浆中NfL水平没有差异。结论:这些结果表明,5岁和10岁OVT73绵羊的大脑发生突触变化,但生物流体中的NfL水平不受影响。总之,这些数据支持OVT73绵羊的前驱疾病状态,包括尾状核、壳核和皮层。
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来源期刊
CiteScore
4.80
自引率
9.70%
发文量
60
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