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用于研究小肠上皮细胞分化和迁移的肠道培养。

gut culture for studying differentiation and migration of small intestinal epithelial cells.

机构信息

School of Food Science, Washington State University, Pullman, WA 99164, USA.

School of Food Science, University of Idaho, Moscow, ID 83844, USA.

出版信息

Open Biol. 2018 Apr;8(4). doi: 10.1098/rsob.170256.

Abstract

Epithelial cultures are commonly used for studying gut health. However, due to the absence of mesenchymal cells and gut structure, epithelial culture systems including recently developed three-dimensional organoid culture cannot accurately represent gut development, which requires intense cross-regulation of the epithelial layer with the underlying mesenchymal tissue. In addition, organoid culture is costly. To overcome this, a new culture system was developed using mouse embryonic small intestine. Cultured intestine showed spontaneous peristalsis, indicating the maintenance of the normal gut physiological structure. During 10 days of culture, epithelial cells moved along the gut surface and differentiated into different epithelial cell types, including enterocytes, Paneth cells, goblet cells and enteroendocrine cells. We further used the established system to examine the role of AMP-activated protein kinase (AMPK) on gut epithelial health. Tamoxifen-induced AMPK1 knockout vastly impaired epithelial migration and differentiation of the developing gut, showing the crucial regulatory function of AMPK 1 in intestinal health.

摘要

上皮细胞培养常用于研究肠道健康。然而,由于缺乏间充质细胞和肠道结构,包括最近开发的三维类器官培养在内的上皮细胞培养系统并不能准确地代表肠道发育,肠道发育需要上皮层与底层间充质组织的强烈相互调节。此外,类器官培养成本高昂。为了克服这一问题,我们使用小鼠胚胎小肠开发了一种新的培养系统。培养的肠道表现出自发性蠕动,表明维持了正常的肠道生理结构。在 10 天的培养过程中,上皮细胞沿着肠道表面移动并分化为不同的上皮细胞类型,包括肠细胞、潘氏细胞、杯状细胞和肠内分泌细胞。我们进一步利用该系统研究了 AMP 激活蛋白激酶 (AMPK) 在肠道上皮健康中的作用。他莫昔芬诱导的 AMPK1 基因敲除极大地损害了正在发育的肠道上皮细胞的迁移和分化,表明 AMPK1 在肠道健康中具有关键的调节功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5308/5936714/c50ab79c3838/rsob-8-170256-g2.jpg

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