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靶向软骨素酶 ABC 至轴突可增强软骨素酶促进神经突生长和发芽的能力。

Targeting chondroitinase ABC to axons enhances the ability of chondroitinase to promote neurite outgrowth and sprouting.

机构信息

Department of Physiology Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.

John Van Geest Centre for Brain Repair, University of Cambridge, Cambridge, United Kingdom.

出版信息

PLoS One. 2020 Jan 21;15(1):e0221851. doi: 10.1371/journal.pone.0221851. eCollection 2020.

Abstract

BACKGROUND

There is currently no effective treatment for promoting regeneration of injured nerves in patients who have sustained injury to the central nervous system such as spinal cord injury. Chondroitinase ABC is an enzyme, which promotes neurite outgrowth and regeneration. It has shown considerable promise as a therapy for these conditions. The aim of the study is to determine if targeting chondroitinase ABC expression to the neuronal axon can further enhance its ability to promote axon outgrowth. Long-distance axon regeneration has not yet been achieved, and would be a significant step in attaining functional recovery following spinal cord injury.

METHODOLOGY/PRINCIPAL FINDINGS: To investigate this, neuronal cultures were transfected with constructs encoding axon-targeted chondroitinase, non-targeted chondroitinase or GFP, and the effects on neuron outgrowth and sprouting determined on substrates either permissive or inhibitory to neuron regeneration. The mechanisms underlying the observed effects were also explored. Targeting chondroitinase to the neuronal axon markedly enhances its ability to promote neurite outgrowth. The increase in neurite length is associated with an upregulation of β-integrin staining at the axonal cell surface. Staining for phosphofocal adhesion kinase, is also increased, indicating that the β-integrins are in an activated state. Expression of chondroitinase within the neurons also resulted in a decrease in expression of PTEN and RhoA, molecules which present a block to neurite outgrowth, thus identifying two of the pathways by which ChABC promotes neurite outgrowth.

CONCLUSIONS / SIGNIFICANCE: The novel finding that targeting ChABC to the axon significantly enhances its ability to promote neurite extension, suggests that this may be an effective way of promoting long-distance axon regeneration following spinal cord injury. It could also potentially improve its efficacy in the treatment of other pathologies, where it has been shown to promote recovery, such as myocardial infarction, stroke and Parkinson's disease.

摘要

背景

目前对于因脊髓损伤等中枢神经系统损伤而导致的受损神经,尚无有效的再生促进治疗方法。软骨素酶 ABC 是一种酶,可促进神经突生长和再生。它在这些疾病的治疗中显示出很大的潜力。本研究旨在确定将软骨素酶 ABC 靶向神经元轴突是否可以进一步增强其促进轴突生长的能力。目前尚未实现长距离轴突再生,如果能够实现,将是脊髓损伤后实现功能恢复的重要一步。

方法/主要发现:为了研究这一点,用编码靶向轴突的软骨素酶、非靶向软骨素酶或 GFP 的构建体转染神经元培养物,并在允许或抑制神经元再生的基质上确定其对神经元突起生长和发芽的影响。还探讨了观察到的效应的潜在机制。将软骨素酶靶向神经元轴突可显著增强其促进神经突生长的能力。神经突长度的增加与轴突细胞表面β-整合素染色的上调有关。磷酸化粘着斑激酶的染色也增加,表明β-整合素处于激活状态。神经元内软骨素酶的表达也导致 PTEN 和 RhoA 的表达减少,这两种分子会阻碍神经突生长,从而确定了 ChABC 促进神经突生长的两种途径。

结论/意义:将 ChABC 靶向轴突可显著增强其促进神经突延伸的能力,这一新颖的发现表明,这可能是促进脊髓损伤后长距离轴突再生的有效方法。它还可能潜在地提高其在治疗其他疾病中的疗效,例如心肌梗死、中风和帕金森病,在这些疾病中已显示出其促进恢复的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/016c/6974052/48ffaf34af29/pone.0221851.g001.jpg

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