Chitooligosaccharides accelarate myelin clearance by Wipi1 mediated Schwann cell autophagy promoting peripheral nerve regeneration.

IF 8.1 1区 医学 Q1 MATERIALS SCIENCE, BIOMATERIALS
Regenerative Biomaterials Pub Date : 2025-05-19 eCollection Date: 2025-01-01 DOI:10.1093/rb/rbaf044
Hongkui Wang, Miao Zhang, Mengke Liu, Jina Liu, Jiahuan Gong, Long Yin, Yumin Yang, Yahong Zhao
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引用次数: 0

Abstract

As the most feasible method to reconstruct long-distance peripheral nerve injuries, tissue-engineered nerves rely on biomaterials as a key driving factor. Chitooligosaccharides, intermediate products of chitosan degradation, have the ability to positively regulate nerve regeneration microenvironments. However, the impact of chitooligosaccharides on clearance of myelin debris during Wallerian degeneration is unrevealed. The focus is on exploring the role of chitooligosaccharides in myelin clearance, which is a crucial preparation stage for nerve regeneration. The effects of chitooligosaccharides on nerve regeneration were demonstrated through the morphological and functional evaluations. Then, the myelin lipids and proteins were analyzed using the morphological staining, and molecular and protein detection. The microstructure and ultrastructure observations of lysosomes and autophagosomes were performed. In addition, the proteomics and bioinformatics analysis of injured nerves treated with chitooligosaccharides. The interacting molecules and the regulatory network of Wipi1 were further predicted. On the basis of positive roles on peripheral nerve regeneration, it was illustrated that chitooligosaccharides accelerated the clearance of myelin. Furthermore chitooligosaccharides could regulate lysosomal and autophagic functions, and its role in promoting myelin clearance was mainly related to the enhanced autophagy of Schwann cells rather than macrophages. The big data analysis revealed that Wipi1 was notably upregulated in Schwann cells, mediating chitooligosaccharides to promote autophagy and myelin clearance. Meanwhile, as a potential therapeutic target, Wipi1 significantly accelerated myelin clearance and lipid metabolism after peripheral nerve injury. Our research deepens the comprehensive understanding of the positive regulatory role of chitosan and chitooligosaccharides; and it expands new content and ideas for designing and constructing better tissue-engineered nerves from the perspective of mutual communication and response between biomaterials and body tissues.

壳寡糖通过Wipi1介导的雪旺细胞自噬加速髓磷脂清除,促进周围神经再生。
组织工程神经作为长距离周围神经损伤重建最可行的方法,其关键驱动因素是生物材料。壳寡糖是壳聚糖降解的中间产物,具有正向调节神经再生微环境的能力。然而,壳寡糖对Wallerian变性过程中髓鞘碎片清除的影响尚不清楚。重点是探索壳寡糖在髓鞘清除中的作用,髓鞘清除是神经再生的关键准备阶段。通过形态学和功能评价证实了壳寡糖对神经再生的影响。利用形态学染色、分子和蛋白检测对髓磷脂脂质和蛋白进行分析。观察溶酶体和自噬体的微观结构和超微结构。此外,壳寡糖处理损伤神经的蛋白质组学和生物信息学分析。进一步预测了Wipi1的相互作用分子和调控网络。基于壳寡糖对周围神经再生的积极作用,说明壳寡糖能加速髓磷脂的清除。此外,壳寡糖还能调节溶酶体和自噬功能,其促进髓磷脂清除的作用主要与增强雪旺细胞的自噬有关,而与巨噬细胞无关。大数据分析显示,Wipi1在雪旺细胞中显著上调,通过介导壳寡糖促进自噬和髓磷脂清除。同时,作为潜在的治疗靶点,Wipi1可显著加速周围神经损伤后髓磷脂清除和脂质代谢。我们的研究加深了对壳聚糖和壳寡糖正调控作用的全面认识;从生物材料与机体组织的相互交流和反应的角度出发,为设计和构建更好的组织工程神经拓展了新的内容和思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Regenerative Biomaterials
Regenerative Biomaterials Materials Science-Biomaterials
CiteScore
7.90
自引率
16.40%
发文量
92
审稿时长
10 weeks
期刊介绍: Regenerative Biomaterials is an international, interdisciplinary, peer-reviewed journal publishing the latest advances in biomaterials and regenerative medicine. The journal provides a forum for the publication of original research papers, reviews, clinical case reports, and commentaries on the topics relevant to the development of advanced regenerative biomaterials concerning novel regenerative technologies and therapeutic approaches for the regeneration and repair of damaged tissues and organs. The interactions of biomaterials with cells and tissue, especially with stem cells, will be of particular focus.
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