Tppp3 is a novel molecule for retinal ganglion cell identification and optic nerve regeneration.

IF 6.2 2区 医学 Q1 NEUROSCIENCES
Mishal Rao, Ziming Luo, Chia-Chun Liu, Chi-Yu Chen, Shining Wang, Michael Nahmou, Bogdan Tanasa, Aman Virmani, Leah Byrne, Jeffrey L Goldberg, José-Alain Sahel, Kun-Che Chang
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Abstract

Mammalian central nervous system (CNS) axons cannot spontaneously regenerate after injury, creating an unmet need to identify molecular regulators to promote axon regeneration and reduce the lasting impact of CNS injuries. While tubulin polymerization promoting protein family member 3 (Tppp3) is known to promote axon outgrowth in amphibians, its role in mammalian axon regeneration remains unknown. Here we investigated Tppp3 in retinal ganglion cells (RGCs) neuroprotection and axonal regeneration using an optic nerve crush (ONC) model in the rodent. Single-cell RNA sequencing identified the expression of Tppp3 in RGCs of mice, macaques, and humans. Tppp3 overexpression enhanced neurite outgrowth in mouse primary RGCs in vitro, promoted axon regeneration, and improved RGC survival after ONC. Bulk RNA sequencing indicated that Tppp3 overexpression upregulates axon regeneration genes such as Bmp4 and neuroinflammatory pathways. Our findings advance regenerative medicine by developing a new therapeutic strategy for RGC neuroprotection and axon regeneration.

Tppp3是一种用于视网膜神经节细胞识别和视神经再生的新分子。
哺乳动物的中枢神经系统(CNS)轴突在损伤后不能自发再生,因此需要确定分子调控因子来促进轴突再生,减轻中枢神经系统损伤的持久影响。虽然已知管蛋白聚合促进蛋白家族成员3(Tppp3)能促进两栖动物的轴突生长,但它在哺乳动物轴突再生中的作用仍然未知。在这里,我们利用啮齿动物视神经压碎(ONC)模型研究了Tppp3在视网膜神经节细胞(RGC)神经保护和轴突再生中的作用。单细胞 RNA 测序确定了 Tppp3 在小鼠、猕猴和人的 RGC 中的表达。Tppp3的过表达增强了小鼠原代RGC体外神经元的生长,促进了轴突再生,并提高了ONC后RGC的存活率。大量RNA测序表明,Tppp3过表达能上调轴突再生基因,如Bmp4和神经炎症通路。我们的研究结果为RGC神经保护和轴突再生开发了一种新的治疗策略,从而推动了再生医学的发展。
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来源期刊
Acta Neuropathologica Communications
Acta Neuropathologica Communications Medicine-Pathology and Forensic Medicine
CiteScore
11.20
自引率
2.80%
发文量
162
审稿时长
8 weeks
期刊介绍: "Acta Neuropathologica Communications (ANC)" is a peer-reviewed journal that specializes in the rapid publication of research articles focused on the mechanisms underlying neurological diseases. The journal emphasizes the use of molecular, cellular, and morphological techniques applied to experimental or human tissues to investigate the pathogenesis of neurological disorders. ANC is committed to a fast-track publication process, aiming to publish accepted manuscripts within two months of submission. This expedited timeline is designed to ensure that the latest findings in neuroscience and pathology are disseminated quickly to the scientific community, fostering rapid advancements in the field of neurology and neuroscience. The journal's focus on cutting-edge research and its swift publication schedule make it a valuable resource for researchers, clinicians, and other professionals interested in the study and treatment of neurological conditions.
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