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胰岛形态的维持有利于糖尿病小鼠的移植效果。

Maintenance of islet morphology is beneficial for transplantation outcome in diabetic mice.

机构信息

Diabetes Research Group, Division of Diabetes and Nutritional Sciences, School of Medicine, King's College London, London, United Kingdom.

出版信息

PLoS One. 2013;8(2):e57844. doi: 10.1371/journal.pone.0057844. Epub 2013 Feb 25.

DOI:10.1371/journal.pone.0057844
PMID:23451276
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3581500/
Abstract

We have previously shown that co-transplantation of islets and Mesenchymal Stem Cells (MSCs) improves islet graft function and revascularisation, which was associated with the maintenance of normal islet morphology. The aim of the current study was to determine whether maintaining islet morphology in the absence of additional islet-helper cells would improve transplantation outcome in diabetic mice. Islets were isolated from C57BL/6 mice. Recipient streptozotocin-diabetic C57BL/6 mice were transplanted with a minimal mass of 150 islets as a single pellet or islets that were either manually dispersed or dispersed within a matrigel plug beneath the kidney capsule. Blood glucose concentrations were monitored for one month. Islet graft morphology and vascularisation were analysed by histology. Islets dispersed either alone or within matrigel plugs maintained near normal morphology, in contrast to pelleted islets, where individual islets fused to form large endocrine aggregates. The vascularisation of manually dispersed islets and islets dispersed within matrigel plugs was increased relative to respective control pelleted islet grafts. After one month 1/6 mice transplanted with pelleted islets cured compared to 5/6 mice transplanted with manually dispersed islets. The curative capacity of islets dispersed in matrigel was also better than that of pelleted islets (5/8 islet-matrigel implanted mice vs. 1/7 mice transplanted with pelleted islets cured by one month). Therefore, this study demonstrates that the maintenance of islet morphology is associated with improved graft function and revascularisation in diabetic mice.

摘要

我们之前的研究表明,胰岛和间充质干细胞(MSCs)的共移植可以改善胰岛移植物的功能和血管生成,这与维持正常的胰岛形态有关。本研究的目的是确定在没有额外胰岛辅助细胞的情况下,维持胰岛形态是否会改善糖尿病小鼠的移植效果。从 C57BL/6 小鼠中分离胰岛。受体链脲佐菌素诱导糖尿病 C57BL/6 小鼠接受作为单个微球的最小质量为 150 个胰岛的移植,或接受手动分散或分散在肾包膜下基质胶塞内的胰岛。监测血糖浓度一个月。通过组织学分析胰岛移植物的形态和血管生成。单独分散或在基质胶塞内分散的胰岛保持接近正常的形态,而作为微球的胰岛,其中单个胰岛融合形成大的内分泌聚集体。与各自的对照胰岛微球移植物相比,手动分散的胰岛和分散在基质胶塞内的胰岛的血管化增加。一个月后,与接受胰岛微球移植的 1/6 只小鼠相比,有 5/6 只接受手动分散胰岛移植的小鼠被治愈。在基质胶中分散的胰岛的治愈能力也优于胰岛微球(5/8 个胰岛-基质胶植入小鼠与 1/7 个接受胰岛微球移植并在一个月内被治愈的小鼠相比)。因此,这项研究表明,维持胰岛形态与改善糖尿病小鼠的移植物功能和血管生成有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f6d/3581500/c48dac4cd0df/pone.0057844.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f6d/3581500/1b962e0cec89/pone.0057844.g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f6d/3581500/90d4adb943f6/pone.0057844.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f6d/3581500/34e694ead8b9/pone.0057844.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f6d/3581500/68c6f2a68612/pone.0057844.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f6d/3581500/c48dac4cd0df/pone.0057844.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f6d/3581500/1b962e0cec89/pone.0057844.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f6d/3581500/2b85d45ae936/pone.0057844.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f6d/3581500/ad5a47d39642/pone.0057844.g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f6d/3581500/68c6f2a68612/pone.0057844.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f6d/3581500/c48dac4cd0df/pone.0057844.g007.jpg

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