Department of Signaling, Radiobiology and Cancer, Institut Curie, Orsay, France.
INSERM U1021, Centre Universitaire, Orsay, France.
Front Endocrinol (Lausanne). 2024 Sep 25;15:1427413. doi: 10.3389/fendo.2024.1427413. eCollection 2024.
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.
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。