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基底膜聚糖:一种具有保护性抗炎特性的胰岛基底膜蛋白。

Perlecan: An Islet Basement Membrane Protein with Protective Anti-Inflammatory Characteristics.

作者信息

Brandhorst Daniel, Brandhorst Heide, Acreman Samuel, Johnson Paul R V

机构信息

Islet Transplant Research Group, Nuffield Department of Surgical Sciences, University of Oxford, Oxford OX3 9DU, UK.

Oxford Consortium for Islet Transplantation, Oxford Centre for Diabetes, Endocrinology, and Metabolism (OCDEM), Churchill Hospital, University of Oxford, Oxford OX3 7LE, UK.

出版信息

Bioengineering (Basel). 2024 Aug 13;11(8):828. doi: 10.3390/bioengineering11080828.

Abstract

Throughout the isolation process, human islets are subjected to destruction of the islet basement membrane (BM) and reduced oxygen supply. Reconstruction of the BM represents an option to improve islet function and survival post-transplant and may particularly be relevant for islet encapsulation devices and scaffolds. In the present study, we assessed whether Perlecan, used alone or combined with the BM proteins (BMPs) Collagen-IV and Laminin-521, has the ability to protect isolated human islets from hypoxia-induced damage. Islets isolated from the pancreas of seven different organ donors were cultured for 4-5 days at 2% oxygen in plain CMRL (sham-treated controls) or in CMRL supplemented with BMPs used either alone or in combination. Postculture, islets were characterized regarding survival, in vitro function and production of chemokines and reactive oxygen species (ROS). Individually added BMPs significantly doubled islet survival and increased in vitro function. Combining BMPs did not provide a synergistic effect. Among the tested BMPs, Perlecan demonstrated the significantly strongest inhibitory effect on chemokine and ROS production when compared with sham-treatment ( < 0.001). Perlecan may be useful to improve islet survival prior to and after transplantation. Its anti-inflammatory potency should be considered to optimise encapsulation and scaffolds to protect isolated human islets post-transplant.

摘要

在整个分离过程中,人胰岛会受到胰岛基底膜(BM)的破坏和氧气供应减少的影响。重建基底膜是改善移植后胰岛功能和存活率的一种选择,对于胰岛封装装置和支架可能尤为重要。在本研究中,我们评估了单独使用硫酸乙酰肝素蛋白聚糖或与基底膜蛋白(BMPs)Ⅳ型胶原蛋白和层粘连蛋白-521联合使用时,是否有能力保护分离的人胰岛免受缺氧诱导的损伤。从7名不同器官供体的胰腺中分离出的胰岛,在普通CMRL培养基(假处理对照)中或添加了单独或联合使用的BMPs的CMRL培养基中,于2%氧气条件下培养4-5天。培养后,对胰岛的存活率、体外功能以及趋化因子和活性氧(ROS)的产生进行了表征。单独添加的BMPs使胰岛存活率显著提高一倍,并增强了体外功能。联合使用BMPs未产生协同效应。在测试的BMPs中,与假处理相比,硫酸乙酰肝素蛋白聚糖对趋化因子和ROS产生的抑制作用最为显著(<0.001)。硫酸乙酰肝素蛋白聚糖可能有助于提高移植前后胰岛的存活率。在优化封装和支架以保护移植后的分离人胰岛时,应考虑其抗炎效力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed79/11351669/b1c34307fa6d/bioengineering-11-00828-g001.jpg

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