具有血管化微囊结构的仿生人工胰岛模型可实现持久血糖控制

Jingbo Li, Yile Fang, Zhuhao Wu, Luoran Shang, Ling Li
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引用次数: 0

摘要

胰岛移植能重现内源性胰岛素分泌,并提供长期血糖控制,因此是一种很有前景的糖尿病治疗策略。用生物材料支架构建的胰岛模型能再现原生胰岛的生物学特性,是规避供体短缺和需要长期免疫抑制的窘境的可行方案。在此,我们利用微流体电喷策略开发了基于生物启发的人工微囊胰岛模型,该模型带有微血管,可用于血糖控制。微流体电喷可生成具有核壳结构的均匀水凝胶微囊,用于包裹胰岛细胞。装载细胞的微囊能有效运输营养物质、氧气和胰岛素,并与微血管结合,促进葡萄糖反应和分子交换。我们通过活体实验证明,胰岛微囊移植后,糖尿病小鼠模型的血糖、进食量和体重均有所下降,葡萄糖耐量也有所提高。我们还通过标准组织学和分子分析进一步证实了移植胰岛模型在胰岛素分泌、免疫逃逸和微循环方面的功能改善。这些结果表明,带微血管的微囊是一种很有前景的人工胰岛模型,对治疗糖尿病很有价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biomimetic artificial islet model with vascularized microcapsule structures for durable glycemic control
Islet transplantation is a promising strategy for diabetes mellitus treatment as it can recapitulate endogenous insulin secretion and provide long-term glycemic control. Islet models constructed in biomaterial scaffolds that reproduce biological characteristics of native islets is a feasible option to circumvent the dilemma of donor shortage and the requirement of chronic immunosuppression. Herein, we developed bioinspired artificial microcapsule-based islet models with microvessels for glycemic control using microfluidic electrospray strategy. Microfluidic electrospray can generate uniform hydrogel microcapsules with core-shell structure for encapsulating islet cells. The cell-laden microcapsules enabled the efficient transportation of nutrient, oxygen, and insulin; as well as the incorporation with microvessels for prompting glucose responsiveness and molecular exchange. We demonstrated by in vivo experiments that the blood glucose, food intake, and body weight of diabetic mouse models were alleviated, and the glucose tolerance was promoted after the engraftment of islet microcapsules. We further demonstrated the improved functionality of transplanted islet model in insulin secretion, immune escape, and microcirculation using standard histological and molecular analysis. These results indicated that the microcapsules with microvessels are promising artificial islet models and are valuable for treating diabetes.
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