Matching model with mechanism: Appropriate rodent models for studying various aspects of diabetes pathophysiology.

4区 生物学 Q4 Biochemistry, Genetics and Molecular Biology
Methods in cell biology Pub Date : 2025-01-01 Epub Date: 2024-06-19 DOI:10.1016/bs.mcb.2024.05.003
Lydia F Daniels Gatward, Aileen J F King
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引用次数: 0

Abstract

Many rodent models are available for preclinical diabetes research making it a challenge for researchers to choose the most appropriate one for their experimental question. To aid in this, models have classically been categorized according to which type of diabetes they represent, and further into whether the model is induced, spontaneous or the result of genetic manipulation. This fails to capture the complexity of pathogenesis seen in diabetes in humans. This includes pathogenesis specifically involving the beta cell, which is no longer considered to be innocuous in the development and progression of diabetes. In this chapter we explore rodent models that incorporate the initiating factors believed to be involved in type 1 diabetes (autoimmunity) and type 2 diabetes (insulin resistance), before further discussing rodents that can be used to model specific mechanisms involved in a failure of functional beta cell mass (impaired beta cell function and beta cell apoptosis). We segregate models of beta cell pathogenesis based on the beta cell stressor predominantly associated with phenotype, but it is important to consider that most rodent models will exhibit more than one beta cell stressor. Similarly, many models exhibit more than one pathogenic mechanism, for example the same model may show insulin resistance, impaired beta cell function as well as beta cell loss. This can complicate interpretation of results and should be considered, and the model thoroughly researched, during the experimental planning stage.

与机制匹配的模型:适合研究糖尿病病理生理各方面的啮齿动物模型。
许多啮齿动物模型可用于临床前糖尿病研究,这对研究人员来说是一个挑战,为他们的实验问题选择最合适的模型。为了做到这一点,模型通常根据它们所代表的糖尿病类型进行分类,并进一步分为模型是诱导的、自发的还是基因操纵的结果。这未能捕捉到人类糖尿病发病机制的复杂性。这包括特别涉及β细胞的发病机制,β细胞在糖尿病的发生和进展中不再被认为是无害的。在本章中,我们探讨了包含被认为与1型糖尿病(自身免疫)和2型糖尿病(胰岛素抵抗)相关的启动因子的啮齿动物模型,然后进一步讨论了可用于模拟与功能性β细胞质量失败(β细胞功能受损和β细胞凋亡)相关的特定机制的啮齿动物模型。我们根据主要与表型相关的β细胞应激源分离β细胞发病机制模型,但重要的是要考虑到大多数啮齿动物模型将表现出多个β细胞应激源。同样,许多模型表现出不止一种致病机制,例如,同一模型可能表现出胰岛素抵抗、β细胞功能受损以及β细胞损失。这可能会使结果的解释复杂化,在实验计划阶段应该考虑到这一点,并对模型进行深入研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Methods in cell biology
Methods in cell biology 生物-细胞生物学
CiteScore
3.10
自引率
0.00%
发文量
125
审稿时长
3 months
期刊介绍: For over fifty years, Methods in Cell Biology has helped researchers answer the question "What method should I use to study this cell biology problem?" Edited by leaders in the field, each thematic volume provides proven, state-of-art techniques, along with relevant historical background and theory, to aid researchers in efficient design and effective implementation of experimental methodologies. Over its many years of publication, Methods in Cell Biology has built up a deep library of biological methods to study model developmental organisms, organelles and cell systems, as well as comprehensive coverage of microscopy and other analytical approaches.
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