Synergizing stem cells with biomaterials for therapeutic angiogenesis in ischemic diseases.

IF 4.8 2区 医学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
STEM CELLS Pub Date : 2026-07-22 DOI:10.1093/stmcls/sxag018
Taiyan Ji, Jiajia Shi, Jing Yang
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引用次数: 0

Abstract

Therapeutic angiogenesis (TA) is a promising strategy for treating ischemic diseases, mainly by targeting the angiogenesis pathways and cells, particularly VEGF and endothelial progenitor cells. Although stem cell therapy has been extensively investigated, its clinical translation remains limited by challenges such as poor cell retention, low survival rates, and inefficient integration. In this review, we propose a mechanism-based framework of angiogenesis to discuss how biomaterials act synergistically with stem cells mainly through two distinct pathways: enhancing paracrine capacity and promoting direct differentiation of vascular lineage cells for vascular repair. Firstly, we go through the scientific literature and clinical studies, and summary the researches on biomaterials serve as artificial microenvironments to improve the retention and secretory function of mesenchymal stem cells (MSCs) and adipose-derived stem cells (ADSCs), thereby maximizing the release of angiogenic factors such as VEGF, bFGF, NGF, microRNA and so on. Secondly, we explore how functionalized biomaterials guide the in situ recruitment of endothelial progenitor cells (EPCs) and support the structural maturation of induced pluripotent stem cell (iPSC)-derived endothelial cells. By integrating these mechanism-driven approaches, we offer new perspectives on future directions for preclinical research and clinical translation of biomaterial-based therapies. Overall, this review has examined the role of individual stem cells and biomaterials, especially enhanced angiogenesis by stem cells focusing on their mechanisms of action and preclinical and clinical applications. We further discussed the challenges encountered by stem cell therapy in advancing to the stage of clinical transformation and considered future prospects.

干细胞与生物材料协同治疗缺血性疾病血管生成。
治疗性血管生成(TA)是治疗缺血性疾病的一种很有前途的策略,主要是针对血管生成途径和细胞,特别是VEGF和内皮祖细胞。尽管干细胞疗法已被广泛研究,但其临床转化仍然受到诸如细胞保留率低、存活率低和整合效率低等挑战的限制。在这篇综述中,我们提出了一个基于血管生成机制的框架,以讨论生物材料如何主要通过两种不同的途径与干细胞协同作用:增强旁分泌能力和促进血管谱系细胞的直接分化以进行血管修复。首先,我们通过科学文献和临床研究,总结了生物材料作为人工微环境改善间充质干细胞(MSCs)和脂肪源性干细胞(ADSCs)的保留和分泌功能,从而最大限度地释放VEGF、bFGF、NGF、microRNA等血管生成因子的研究。其次,我们探索功能化生物材料如何引导内皮祖细胞(EPCs)的原位募集,并支持诱导多能干细胞(iPSC)衍生的内皮细胞的结构成熟。通过整合这些机制驱动的方法,我们为基于生物材料的疗法的临床前研究和临床转化的未来方向提供了新的视角。总的来说,这篇综述研究了单个干细胞和生物材料的作用,特别是干细胞增强血管生成的作用,重点是它们的作用机制和临床前和临床应用。我们进一步讨论了干细胞治疗在进入临床转化阶段所遇到的挑战,并展望了未来的前景。
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
STEM CELLS
STEM CELLS 医学-生物工程与应用微生物
CiteScore
10.30
自引率
1.90%
发文量
104
审稿时长
3 months
期刊介绍: STEM CELLS, a peer reviewed journal published monthly, provides a forum for prompt publication of original investigative papers and concise reviews. STEM CELLS is read and written by clinical and basic scientists whose expertise encompasses the rapidly expanding fields of stem and progenitor cell biology. STEM CELLS covers: Cancer Stem Cells, Embryonic Stem Cells/Induced Pluripotent Stem (iPS) Cells, Regenerative Medicine, Stem Cell Technology: Epigenetics, Genomics, Proteomics, and Metabonomics, Tissue-Specific Stem Cells, Translational and Clinical Research.
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