Plasma Proteomic Signature of Mucolipidosis Type IV

B. Tobin, A. Misko, V. Miller-Browne, M. Sangster, Y. Grishchuk, L. B. Wood
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Abstract

Mucolipidosis IV (MLIV) is an autosomal-recessive pediatric disease that leads to motor and cognitive deficits and loss of vision. It is caused by the loss of function of the lysosomal channel transient receptor potential mucolipin-1, TRPML1, and is associated with an early brain phenotype consisting of glial reactivity, hypomyelination, lysosomal abnormalities, and increased cytokine expression. Although the field is approaching the first translationally relevant therapy, we currently lack a molecular signature of disease that can be used to detect therapeutic efficacy. In the current study, we analyzed 7,322 proteins in the plasma proteome and compare protein profiles with clinical measures of disease severity (motor function, muscle tone, and age). To do so, we used aptamer-based protein profiling on plasma isolated from 18 MLIV patients and 37 aged-matched controls from a biorepository. We identified a total of 1,961 differentially expressed proteins between MLIV and control subjects, with functions spanning many major hallmarks of MLIV. Our analysis revealed a decrease in the abundance of neuronal proteins and an increase in muscle proteins, consistent with the neuronal dysfunction and muscle pathology observed in patients. In particular, lower levels of synaptic proteins (e.g., GABARAP) best correlated with disease severity. Next, we compared the plasma proteome of patients to the brain proteome from the mouse model of MLIV and identified shared alterations in 45 proteins. The up-regulated overlapping proteins were largely related to lysosomal function (e.g., ACTN2, GLB1), while the down-regulated proteins were largely related to myelination (e.g. TPPP3, CNTN2). Both signatures are consistent with our understanding of key disease hallmarks: impaired myelination and modified lysosomal function. Collectively, these data indicate that peripheral blood plasma protein signatures mirror changes found in the MLIV brain and suggest candidate markers relevant to MLIV pathology to be validated in future studies.
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Ⅳ型黏脂病的血浆蛋白质组特征
粘脂病 IV(MLIV)是一种常染色体隐性遗传的儿科疾病,会导致运动和认知障碍以及视力丧失。它是由溶酶体通道瞬时受体电位粘脂-1(TRPML1)功能缺失引起的,与早期脑表型有关,包括神经胶质反应性、髓鞘化不足、溶酶体异常和细胞因子表达增加。尽管该领域正在接近第一种可转化的相关疗法,但我们目前还缺乏一种可用于检测疗效的疾病分子特征。在目前的研究中,我们分析了血浆蛋白质组中的 7,322 种蛋白质,并将蛋白质特征与疾病严重程度的临床指标(运动功能、肌张力和年龄)进行了比较。为此,我们对从生物库中分离的 18 名 MLIV 患者和 37 名年龄匹配的对照者的血浆进行了基于适配体的蛋白质分析。我们在 MLIV 和对照组受试者之间共发现了 1,961 个表达不同的蛋白质,其功能涵盖了 MLIV 的许多主要特征。我们的分析表明,神经元蛋白的丰度降低了,而肌肉蛋白的丰度增加了,这与在患者身上观察到的神经元功能障碍和肌肉病理变化是一致的。特别是,突触蛋白(如 GABARAP)水平较低与疾病严重程度的相关性最佳。接下来,我们将患者的血浆蛋白质组与 MLIV 小鼠模型的脑蛋白质组进行了比较,发现了 45 种蛋白质的共同改变。上调的重叠蛋白主要与溶酶体功能有关(如 ACTN2、GLB1),而下调的蛋白主要与髓鞘化有关(如 TPPP3、CNTN2)。这两种特征都符合我们对疾病关键特征的理解:髓鞘化受损和溶酶体功能改变。总之,这些数据表明,外周血血浆蛋白特征反映了在 MLIV 大脑中发现的变化,并提出了与 MLIV 病理学相关的候选标记物,有待在今后的研究中加以验证。
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