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重新接种可诱导mTOR依赖性的对夏科-马里-图斯病神经元蛋白质合成的挽救。

Replating induces mTOR-dependent rescue of protein synthesis in Charcot-Marie-Tooth diseased neurons.

作者信息

Koenig Julianna, McGuire Alexys, Homedan Yara, Alberhasky Jessica, Summers Daniel W

机构信息

Interdisciplinary Graduate Program in Genetics, University of Iowa, Iowa City, IA 52242 USA.

Department of Biology, University of Iowa, Iowa City, IA 52242 USA.

出版信息

bioRxiv. 2025 Aug 31:2025.08.26.672367. doi: 10.1101/2025.08.26.672367.

Abstract

Charcot-Marie-Tooth disease (CMT) is an inherited peripheral neuropathy characterized by sensory dysfunction and muscle weakness, manifesting in the most distal limbs first and progressing more proximal. Over a hundred genes are currently linked to CMT with enrichment for activities in myelination, axon transport, and protein synthesis. Mutations in tRNA synthetases cause dominantly inherited forms of CMT and animal models with CMT-linked mutations in these enzymes display defects in neuronal protein synthesis. Rescuing protein synthesis in CMT mutant neurons could offer exciting therapeutic options beyond symptom management. To address this need, we expressed CMT-linked variants in tyrosyl tRNA synthetase (YARS-CMT) in primary sensory neurons and evaluated impacts on protein synthesis and cell viability. YARS-CMT expression reduced protein synthesis in these neurons prior to the onset of caspase-dependent axon degeneration and cell death. To determine how YARS-CMT expression affects axon outgrowth, we dissociated and replated these neurons to stimulate axon regeneration. To our surprise, axonal regrowth occurred normally in replated YARS-CMT neurons. Moreover, replating YARS-CMT neurons rescued protein synthesis. Inhibiting mTOR suppressed rescue of protein synthesis after replating, consistent with its significant role in protein synthesis during axon regeneration. These discoveries identify new avenues for augmenting protein synthesis in diseased neurons and restoring protein synthesis in CMT or other neurological disorders.

摘要

夏科-马里-图斯病(CMT)是一种遗传性周围神经病变,其特征为感觉功能障碍和肌肉无力,首先在四肢最远端出现症状,并向近端发展。目前有一百多种基因与CMT相关,这些基因在髓鞘形成、轴突运输和蛋白质合成活动中富集。tRNA合成酶的突变会导致显性遗传形式的CMT,在这些酶中具有CMT相关突变的动物模型显示出神经元蛋白质合成缺陷。挽救CMT突变神经元中的蛋白质合成可能会带来除症状管理之外令人兴奋的治疗选择。为满足这一需求,我们在初级感觉神经元中表达了酪氨酸tRNA合成酶(YARS-CMT)中的CMT相关变体,并评估了其对蛋白质合成和细胞活力的影响。在半胱天冬酶依赖性轴突退化和细胞死亡开始之前,YARS-CMT的表达降低了这些神经元中的蛋白质合成。为了确定YARS-CMT的表达如何影响轴突生长,我们将这些神经元解离并重新接种以刺激轴突再生。令我们惊讶的是,重新接种的YARS-CMT神经元中轴突正常再生。此外,重新接种YARS-CMT神经元挽救了蛋白质合成。抑制mTOR可抑制重新接种后蛋白质合成的挽救,这与其在轴突再生过程中蛋白质合成中的重要作用一致。这些发现为增加患病神经元中的蛋白质合成以及在CMT或其他神经疾病中恢复蛋白质合成确定了新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18ca/12407962/50ab9d43f875/nihpp-2025.08.26.672367v1-f0001.jpg

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