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假性胰岛作为主要的胰岛替代物用于研究:在英国伦敦国王学院举行的研讨会报告。

Pseudoislets as primary islet replacements for research: report on a symposium at King's College London, London UK.

机构信息

King's College, London, UK.

出版信息

Islets. 2010 Jul-Aug;2(4):236-9. doi: 10.4161/isl.2.4.12557.

Abstract

Laboratory-based research aimed at understanding processes regulating insulin secretion and mechanisms underlying β-cell dysfunction and loss in diabetes often makes use of rodents, as these processes are in many respects similar between rats/mice and humans. Indeed, a rough calculation suggests that islets have been isolated from as many as 150,000 rodents to generate the data contained within papers published in 2009 and the first four months of 2010. Rodent use for islet isolation has been mitigated, to a certain extent, by the availability of a variety of insulin-secreting cell lines that are used by researchers world-wide. However, when maintained as monolayers the cell lines do not replicate the robust, sustained secretory responses of primary islets which limits their usefulness as islet surrogates. On the other hand, there have been several reports that configuration of MIN6 β-cells, derived from a mouse insulinoma, as three-dimensional cell clusters termed ‘pseudoislets’ largely recapitulates the function of primary islet β-cells. The Diabetes Research Group at King’s College London has been using the MIN6 pseudoislet model for over a decade and they hosted a symposium on “Pseudoislets as primary islet replacements for research”, which was funded by the UK National Centre for the Replacement, Refinement and Reduction of Animals in Research (NC3Rs), in London on 15th and 16th April 2010. This small, focused meeting was conceived as an opportunity to consolidate information on experiences of working with pseudoislets between different UK labs, and to introduce the theory and practice of pseudoislet culture to laboratories working with islets and/or β-cell lines but who do not currently use pseudoislets. This short review summarizes the background to the development of the cell line-derived pseudoislet model, the key messages arising from the symposium and emerging themes for future pseudoislet research.

摘要

基于实验室的研究旨在理解调节胰岛素分泌的过程和糖尿病中β细胞功能障碍和丧失的机制,通常利用啮齿动物,因为这些过程在许多方面与大鼠/小鼠和人类相似。事实上,粗略计算表明,为了生成 2009 年和 2010 年前四个月发表的论文中包含的数据,已经从多达 15 万只啮齿动物中分离出胰岛。通过使用世界各地研究人员使用的各种胰岛素分泌细胞系,在一定程度上减轻了用于胰岛分离的啮齿动物的使用。然而,当作为单层培养时,这些细胞系不能复制原代胰岛的强大、持续的分泌反应,这限制了它们作为胰岛替代物的有用性。另一方面,有几项报道称,源自小鼠胰岛素瘤的 MIN6 β细胞被配置为三维细胞簇,称为“拟胰岛”,在很大程度上再现了原代胰岛β细胞的功能。伦敦国王学院的糖尿病研究小组已经使用 MIN6 拟胰岛模型超过十年,他们于 2010 年 4 月 15 日和 16 日在伦敦举办了一次关于“拟胰岛作为研究用原代胰岛替代品”的专题讨论会,该会议由英国国家替代、改进和减少动物在研究中的使用中心(NC3Rs)资助。这个小型的、重点突出的会议是为了整合英国不同实验室在使用拟胰岛方面的经验信息,并向使用胰岛和/或β细胞系但目前不使用拟胰岛的实验室介绍拟胰岛培养的理论和实践而构想的。这篇简短的综述总结了细胞系衍生的拟胰岛模型的发展背景、专题讨论会上提出的关键信息以及未来拟胰岛研究的新兴主题。

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