Berg Martin J, Rosa Corrinne M, Kumar Asok, Mohan Panaiyur S, Stavrides Philip, Marchionini Deanna M, Yang Dun-Sheng, Nixon Ralph A
bioRxiv. 2024 May 30:2024.05.29.596470. doi: 10.1101/2024.05.29.596470.
Accumulated levels of mutant huntingtin protein (mHTT) and its fragments are considered contributors to the pathogenesis of Huntington's disease (HD). Although lowering mHTT by stimulating autophagy has been considered a possible therapeutic strategy, the role and competence of autophagy-lysosomal pathway (ALP) during HD progression in the human disease remains largely unknown. Here, we used multiplex confocal and ultrastructural immunocytochemical analyses of ALP functional markers in relation to mHTT aggresome pathology in striatum and the less affected cortex of HD brains staged from HD2 to HD4 by Vonsattel neuropathological criteria compared to controls. Immunolabeling revealed the localization of HTT/mHTT in ALP vesicular compartments labeled by autophagy-related adaptor proteins p62/SQSTM1 and ubiquitin, and cathepsin D (CTSD) as well as HTT-positive inclusions. Although comparatively normal at HD2, neurons at later HD stages exhibited progressive enlargement and clustering of CTSD-immunoreactive autolysosomes/lysosomes and, ultrastructurally, autophagic vacuole/lipofuscin granules accumulated progressively, more prominently in striatum than cortex. These changes were accompanied by rises in levels of HTT/mHTT and p62/SQSTM1, particularly their fragments, in striatum but not in the cortex, and by increases of LAMP1 and LAMP2 RNA and LAMP1 protein. Importantly, no blockage in autophagosome formation and autophagosome-lysosome fusion was detected, thus pinpointing autophagy substrate clearance deficits as a basis for autophagic flux declines. The findings collectively suggest that upregulated lysosomal biogenesis and preserved proteolysis maintain autophagic clearance in early-stage HD, but failure at advanced stages contributes to progressive HTT build-up and potential neurotoxicity. These findings support the prospect that ALP stimulation applied at early disease stages, when clearance machinery is fully competent, may have therapeutic benefits in HD patients.
突变型亨廷顿蛋白(mHTT)及其片段的累积水平被认为是导致亨廷顿舞蹈症(HD)发病机制的因素。尽管通过刺激自噬来降低mHTT被认为是一种可能的治疗策略,但在人类疾病HD进展过程中自噬-溶酶体途径(ALP)的作用和能力仍 largely未知。在这里,我们使用多重共聚焦和超微结构免疫细胞化学分析ALP功能标记物,这些标记物与HD大脑纹状体和受影响较小的皮质中mHTT聚集体病理学相关,HD大脑根据冯·萨特尔神经病理学标准从HD2分期到HD4,与对照组相比。免疫标记揭示了HTT/mHTT在由自噬相关衔接蛋白p62/SQSTM1、泛素和组织蛋白酶D(CTSD)标记的ALP囊泡区室中的定位,以及HTT阳性包涵体。尽管在HD2阶段相对正常,但在HD后期阶段的神经元表现出CTSD免疫反应性自溶酶体/溶酶体的逐渐增大和聚集,并且在超微结构上,自噬泡/脂褐素颗粒逐渐积累,在纹状体中比皮质中更明显。这些变化伴随着纹状体中HTT/mHTT和p62/SQSTM1水平的升高,特别是它们的片段,但在皮质中没有,并且伴随着LAMP1和LAMP2 RNA以及LAMP1蛋白的增加。重要的是,未检测到自噬体形成和自噬体-溶酶体融合的阻滞,因此确定自噬底物清除缺陷是自噬通量下降的基础。这些发现共同表明,溶酶体生物合成上调和蛋白水解保留在HD早期维持自噬清除,但在晚期失败导致HTT逐渐积累和潜在的神经毒性。这些发现支持了这样一种前景,即在疾病早期阶段,当清除机制完全有能力时,应用ALP刺激可能对HD患者有治疗益处。