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模拟人类糖尿病:浅析青年发病的成年型糖尿病。

Modelling human diabetes : a glance at maturity onset diabetes of the young.

机构信息

Department of Signaling, Radiobiology and Cancer, Institut Curie, Orsay, France.

INSERM U1021, Centre Universitaire, Orsay, France.

出版信息

Front Endocrinol (Lausanne). 2024 Sep 25;15:1427413. doi: 10.3389/fendo.2024.1427413. eCollection 2024.

DOI:10.3389/fendo.2024.1427413
PMID:39387055
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11461259/
Abstract

Diabetes is a complex metabolic disease which most commonly has a polygenic origin; however, in rare cases, diabetes may be monogenic. This is indeed the case in both Maturity Onset Diabetes of the Young (MODY) and neonatal diabetes. These disease subtypes are believed to be simpler than Type 1 (T1D) and Type 2 Diabetes (T2D), which allows for more precise modelling. During the three last decades, many studies have focused on rodent models. These investigations provided a wealth of knowledge on both pancreas development and beta cell function. In particular, they allowed the establishment of a hierarchy of the transcription factors and highlighted the role of microenvironmental factors in the control of progenitor cell proliferation and differentiation. Transgenic mice also offered the possibility to decipher the mechanisms that define the functional identity of the pancreatic beta cells. Despite such interest in transgenic mice, recent data have also indicated that important differences exist between mice and human. To overcome these limitations, new human models are necessary. In the present review, we describe these models, which are created using stem cells and organoids, and represent an important step toward islet cell therapy and drug discovery.

摘要

糖尿病是一种复杂的代谢疾病,通常具有多基因起源;然而,在极少数情况下,糖尿病可能是单基因的。这种情况确实存在于青年发病型成年糖尿病(MODY)和新生儿糖尿病中。这些疾病亚型被认为比 1 型糖尿病(T1D)和 2 型糖尿病(T2D)更简单,这使得建模更加精确。在过去的三十年中,许多研究都集中在啮齿动物模型上。这些研究为胰腺发育和β细胞功能提供了丰富的知识。特别是,它们确立了转录因子的层次结构,并强调了微环境因素在控制祖细胞增殖和分化中的作用。转基因小鼠还提供了一种可能性,可以揭示定义胰腺β细胞功能特征的机制。尽管对转基因小鼠有如此大的兴趣,但最近的数据也表明,老鼠和人类之间存在重要差异。为了克服这些局限性,需要新的人类模型。在本综述中,我们描述了这些使用干细胞和类器官创建的模型,它们是胰岛细胞治疗和药物发现的重要一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f5b/11461259/74af285a7e15/fendo-15-1427413-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f5b/11461259/74af285a7e15/fendo-15-1427413-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f5b/11461259/74af285a7e15/fendo-15-1427413-g001.jpg

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本文引用的文献

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EndoC-βH5 cells are storable and ready-to-use human pancreatic beta cells with physiological insulin secretion.EndoC-βH5 细胞是可储存的、即用型的人胰腺β细胞,具有生理性胰岛素分泌功能。
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Towards a better understanding of diabetes mellitus using organoid models.利用类器官模型深入了解糖尿病。
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Second MAFA Variant Causing a Phosphorylation Defect in the Transactivation Domain and Familial Insulinomatosis.
导致反式激活结构域磷酸化缺陷及家族性胰岛素瘤的第二种MAFA变体
Cancers (Basel). 2022 Apr 1;14(7):1798. doi: 10.3390/cancers14071798.
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HIF-1α inhibitor PX-478 preserves pancreatic β cell function in diabetes.HIF-1α 抑制剂 PX-478 可维持糖尿病中的胰岛β细胞功能。
Sci Transl Med. 2022 Mar 30;14(638):eaba9112. doi: 10.1126/scitranslmed.aba9112.
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An HNF1α truncation associated with maturity-onset diabetes of the young impairs pancreatic progenitor differentiation by antagonizing HNF1β function.一种与青年发病的成年型糖尿病相关的 HNF1α 截断突变通过拮抗 HNF1β 功能而损害胰腺祖细胞的分化。
Cell Rep. 2022 Mar 1;38(9):110425. doi: 10.1016/j.celrep.2022.110425.
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MAFA and MAFB regulate exocytosis-related genes in human β-cells.MAFA和MAFB调节人类β细胞中与胞吐作用相关的基因。
Acta Physiol (Oxf). 2022 Feb;234(2):e13761. doi: 10.1111/apha.13761. Epub 2022 Jan 11.
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