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验证人胰腺发育过程中β细胞成熟相关基因的表达

Validating expression of beta cell maturation-associated genes in human pancreas development.

作者信息

Tremmel Daniel M, Mikat Anna E, Gupta Sakar, Mitchell Samantha A, Curran Andrew M, Menadue Jenna A, Odorico Jon S, Sackett Sara Dutton

机构信息

University of Wisconsin-Madison, Department of Surgery, Transplantation Division, Madison, WI, United States.

出版信息

Front Cell Dev Biol. 2023 Feb 1;11:1103719. doi: 10.3389/fcell.2023.1103719. eCollection 2023.

DOI:10.3389/fcell.2023.1103719
PMID:36846594
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9945361/
Abstract

The identification of genes associated with human pancreatic beta cell maturation could stimulate a better understanding of normal human islet development and function, be informative for improving stem cell-derived islet (SC-islet) differentiation, and facilitate the sorting of more mature beta cells from a pool of differentiated cells. While several candidate factors to mark beta cell maturation have been identified, much of the data supporting these markers come from animal models or differentiated SC-islets. One such marker is Urocortin-3 (UCN3). In this study, we provide evidence that is expressed in human fetal islets well before the acquisition of functional maturation. When SC-islets expressing significant levels of were generated, the cells did not exhibit glucose-stimulated insulin secretion, indicating that expression is not correlated with functional maturation in these cells. We utilized our tissue bank and SC-islet resources to test an array of other candidate maturation-associated genes, and identified CHGB, G6PC2, FAM159B, GLUT1, IAPP and ENTPD3 as markers with expression patterns that correlate developmentally with the onset of functional maturation in human beta cells. We also find that human beta cell expression of ERO1LB, HDAC9, KLF9, and ZNT8 does not change between fetal and adult stages.

摘要

鉴定与人类胰腺β细胞成熟相关的基因,有助于更好地理解正常人类胰岛的发育和功能,为改善干细胞来源的胰岛(SC-胰岛)分化提供信息,并促进从分化细胞池中筛选出更成熟的β细胞。虽然已经鉴定出了几种标记β细胞成熟的候选因子,但支持这些标记的许多数据都来自动物模型或分化的SC-胰岛。其中一种标记是尿皮质素-3(UCN3)。在本研究中,我们提供证据表明,在获得功能成熟之前,其就在人类胎儿胰岛中表达。当产生表达显著水平的SC-胰岛时,细胞并未表现出葡萄糖刺激的胰岛素分泌,这表明在这些细胞中,其表达与功能成熟不相关。我们利用我们的组织库和SC-胰岛资源,测试了一系列其他与成熟相关的候选基因,并确定嗜铬粒蛋白B(CHGB)、葡萄糖-6-磷酸酶催化亚基2(G6PC2)、家族性159B(FAM159B)、葡萄糖转运蛋白1(GLUT1)、胰岛淀粉样多肽(IAPP)和外核苷酸焦磷酸酶/磷酸二酯酶3(ENTPD3)作为标记,其表达模式在发育上与人类β细胞功能成熟的开始相关。我们还发现,内质网氧化还原酶1β(ERO1LB)、组蛋白去乙酰化酶9(HDAC9)、 Kruppel样因子9(KLF9)和锌转运体8(ZNT8)在人类β细胞中的表达在胎儿期和成年期之间没有变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d95/9945361/c2659c41b822/fcell-11-1103719-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d95/9945361/3c945912746e/fcell-11-1103719-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d95/9945361/45a0b50c9efb/fcell-11-1103719-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d95/9945361/211e78de388f/fcell-11-1103719-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d95/9945361/ac73a7814615/fcell-11-1103719-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d95/9945361/6da5b8a4e9e1/fcell-11-1103719-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d95/9945361/c2659c41b822/fcell-11-1103719-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d95/9945361/3c945912746e/fcell-11-1103719-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d95/9945361/45a0b50c9efb/fcell-11-1103719-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d95/9945361/211e78de388f/fcell-11-1103719-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d95/9945361/ac73a7814615/fcell-11-1103719-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d95/9945361/6da5b8a4e9e1/fcell-11-1103719-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d95/9945361/c2659c41b822/fcell-11-1103719-g006.jpg

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