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Application of an Endothelialized Modular Construct for Islet Transplantation in Syngeneic and Allogeneic Immunosuppressed Rat Models

机译:内皮化模块化结构在胰岛移植在同基因和同种异体免疫抑制大鼠模型中的应用

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摘要

Modular tissue engineering is a novel approach to assemble tissues with an inherent vascularization. In this article, we evaluated whether endothelialized module-driven vascularization enhances islet engraftment in diabetic rats. Two thousand islets were transplanted in the omental pouch of syngeneic and allogeneic immunosuppressed diabetic recipients as free islets, islets in collagen modules, or islets in endothelialized modules. Transplantation of islets in endothelialized modules significantly increased the vessel density compared with controls. Donor green fluorescent protein-positive endothelial cells (ECs) formed vessels in proximity to transplanted islets; donor vessels connected to host vasculature as the vessels included erythrocytes in their lumens and were supported by host smooth muscle cells by 21 days. Transplantation of 2000 islets reversed diabetes in two of five of syngeneic recipients until 60 days, although there was no apparent benefit to islet function of adding ECs relative to collagen modules without EC. However, there was a trend toward increased viability when islets were implanted in endothelialized modules compared with collagen modules at 21 days. Meanwhile, 2000 islets in allogeneic immunosuppressed recipients lowered blood glucose levels short term, but there was graft failure within 1 week. This study explored the simultaneous transplantation of primary ECs with islets in diabetic recipients. The endothelialized modular approach increased vessel density around transplanted islets. Further modulation (i.e., acceleration) of vessel maturation, is presumed necessary to improve islet engraftment.
机译:模块化组织工程是一种具有固有血管形成的新颖组织组装方法。在本文中,我们评估了内皮化模块驱动的血管形成是否增强了糖尿病大鼠的胰岛植入。将两千个胰岛作为游离胰岛,胶原模块中的胰岛或内皮化模块中的胰岛移植到同基因和同种异体免疫抑制的糖尿病受体的网膜袋中。与对照组相比,将胰岛移植到内皮化模块中显着增加了血管密度。供体绿色荧光蛋白阳性内皮细胞(EC)在移植的胰岛附近形成血管。供体血管与宿主脉管系统相连,因为该血管的腔内包含红细胞,并在21天时得到宿主平滑肌细胞的支持。尽管没有EC的胶原蛋白模块对添加EC的胰岛功能没有明显的益处,但2000个胰岛的移植使5个同基因接受者中的2个糖尿病逆转至60天。然而,当将胰岛植入与胶原模块相比,在21天时,将胰岛植入到内皮模块中存在生存能力增加的趋势。同时,异体免疫抑制受体中的2000个胰岛在短期内降低了血糖水平,但在1周内出现了移植失败。这项研究探索了在糖尿病受体中原发性EC与胰岛的同时移植。内皮模块化方法增加了移植胰岛周围的血管密度。推测需要进一步调节(即加速)血管成熟以改善胰岛的植入。

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