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SDF-1 结合肝素纳米颗粒招募祖细胞,促进卒中后分化和血管生成。

SDF-1 Bound Heparin Nanoparticles Recruit Progenitor Cells for Their Differentiation and Promotion of Angiogenesis after Stroke.

机构信息

Department of Biomedical Engineering, Duke University, Durham, NC, 27708-0281, USA.

Department of Chemical and Biomolecular Engineering, University of California Los Angeles, Los Angeles, CA, 90095, USA.

出版信息

Adv Healthc Mater. 2024 Oct;13(25):e2302081. doi: 10.1002/adhm.202302081. Epub 2023 Dec 20.

Abstract

Angiogenesis after stroke is correlated with enhanced tissue repair and functional outcomes. The existing body of research in biomaterials for stroke focuses on hydrogels for the delivery of stem cells, growth factors, or small molecules or drugs. Despite the ability of hydrogels to enhance all these delivery methods, no material has significantly regrown vasculature within the translatable timeline of days to weeks after stroke. Here, two novel biomaterial formulations of granular hydrogels are developed for tissue regeneration after stroke: highly porous microgels (i.e., Cryo microgels) and microgels bound with heparin-norbornene nanoparticles with covalently bound SDF-1α. The combination of these materials results in perfused vessels throughout the stroke core in only 10 days, in addition to increased neural progenitor cell recruitment, maintenance, and increased neuronal differentiation.

摘要

中风后的血管生成与增强的组织修复和功能结果相关。目前针对中风的生物材料的研究主要集中在水凝胶上,用于输送干细胞、生长因子或小分子或药物。尽管水凝胶能够增强所有这些输送方法,但在中风后几天到几周的可转化时间内,没有一种材料能显著再生血管。在这里,开发了两种用于中风后组织再生的新型生物材料颗粒水凝胶配方:高多孔微凝胶(即 Cryo 微凝胶)和与肝素-降冰片烯纳米粒子结合的微凝胶,其共价结合了 SDF-1α。这些材料的组合仅在 10 天内即可在中风核心区形成灌注血管,此外还增加了神经祖细胞的募集、维持和增加神经元分化。

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