干细胞表面增强内皮相互作用的离体肽修饰策略。

IF 5.1 2区 医学 Q2 CELL & TISSUE ENGINEERING
Tissue Engineering. Part B, Reviews Pub Date : 2024-06-01 Epub Date: 2023-11-15 DOI:10.1089/ten.TEB.2023.0210
Hee Won Park, Chae Eun Lee, Sungjun Kim, Woo-Jin Jeong, Kyobum Kim
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引用次数: 0

摘要

缺血性血管疾病(IVD)仍然是导致残疾和死亡的主要原因。尽管已经尝试了各种临床治疗方法,但再灌注损伤是主要问题,发生在血液在受损病变处再循环时。作为一种替代方法,基于细胞的治疗已经出现。间充质干细胞(MSC)由于其治疗能力,包括分化、安全性、血管生成和组织修复,是有吸引力的候选细胞。然而,低水平的受体/配体限制了干细胞的靶向迁移。因此,提高移植MSCs对受损内皮的归巢效率是非常重要的。在各种MSC调节中,离体细胞表面工程可以通过用替代受体/配体修饰MSC表面来有效提高归巢效率,从而促进细胞间与内皮的相互作用。特别是,肽在干细胞表面的外源修饰可以提供适当的功能信号部分来实现足够的MSC归巢。基于其蛋白质样功能、分子设计的高模块性以及对靶受体的高特异性亲和力和多价性,肽可能是具有代表性的表面可呈现部分。此外,肽具有温和的合成过程,能够精确控制氨基酸组成和序列。这种离体干细胞表面工程可以主要通过与肽缀合的锚定模块的细胞双层中的疏水相互作用以及通过肽和膜可用区室之间的共价缀合来实现。为此,本文综述了目前可用的肽介导的离体干细胞表面工程策略,通过促进与内皮细胞的相互作用来提高MSC归巢效率。使用基于肽的生物偶联物的干细胞表面工程技术有可能彻底改变当前的血管疾病治疗,同时解决其技术局限性。关键词:肽,表面修饰,离体细胞表面工程,干细胞,归巢,靶向递送影响声明:缺血性血管疾病是全球健康问题。尽管干细胞显示出治疗的前景,但低归巢能力是限制其有效性的一个限制。为了解决这个缺点,将归巢肽修饰到干细胞表面可以增强细胞迁移、归巢和组织修复。本文综述了目前开发的利用肽增强归巢治疗缺血性血管疾病的离体干细胞表面工程技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ex Vivo Peptide Decoration Strategies on Stem Cell Surfaces for Augmenting Endothelium Interaction.

Ischemic vascular diseases remain leading causes of disability and death. Although various clinical therapies have been tried, reperfusion injury is a major issue, occurring when blood recirculates at the damaged lesion. As an alternative approach, cell-based therapy has emerged. Mesenchymal stem cells (MSCs) are attractive cellular candidates due to their therapeutic capacities, including differentiation, safety, angiogenesis, and tissue repair. However, low levels of receptors/ligands limit targeted migration of stem cells. Thus, it is important to improve homing efficacy of transplanted MSCs toward damaged endothelium. Among various MSC modulations, ex vivo cell surface engineering could effectively augment homing efficiency by decorating MSC surfaces with alternative receptors/ligands, thereby facilitating intercellular interactions with the endothelium. Especially, exogenous decoration of peptides onto stem cell surfaces could provide appropriate functional signaling moieties to achieve sufficient MSC homing. Based on their protein-like functionalities, high modularity in molecular design, and high specific affinities and multivalency to target receptors, peptides could be representative surface-presentable moieties. Moreover, peptides feature a mild synthetic process, enabling precise control of amino acid composition and sequence. Such ex vivo stem cell surface engineering could be achieved primarily by hydrophobic interactions of the cellular bilayer with peptide-conjugated anchor modules and by covalent conjugation between peptides and available compartments in membranes. To this end, this review provides an overview of currently available peptide-mediated, ex vivo stem cell surface engineering strategies for enhancing MSC homing efficiency by facilitating interactions with endothelial cells. Stem cell surface engineering techniques using peptide-based bioconjugates have the potential to revolutionize current vascular disease treatments while addressing their technical limitations.

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来源期刊
Tissue Engineering. Part B, Reviews
Tissue Engineering. Part B, Reviews Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
12.80
自引率
1.60%
发文量
150
期刊介绍: Tissue Engineering Reviews (Part B) meets the urgent need for high-quality review articles by presenting critical literature overviews and systematic summaries of research within the field to assess the current standing and future directions within relevant areas and technologies. Part B publishes bi-monthly.
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