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本文引用的文献

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Hippo Signaling Pathway in Pancreas Development.胰腺发育中的河马信号通路。
Front Cell Dev Biol. 2021 May 17;9:663906. doi: 10.3389/fcell.2021.663906. eCollection 2021.
2
The epithelial-mesenchymal transition and the cytoskeleton in bioengineered systems.生物工程系统中的上皮-间充质转化和细胞骨架。
Cell Commun Signal. 2021 Mar 10;19(1):32. doi: 10.1186/s12964-021-00713-2.
3
The promise of stem cell-derived islet replacement therapy.干细胞衍生胰岛替代治疗的前景。
Diabetologia. 2021 May;64(5):1030-1036. doi: 10.1007/s00125-020-05367-2. Epub 2021 Jan 16.
4
A Specialized Niche in the Pancreatic Microenvironment Promotes Endocrine Differentiation.胰腺微环境中的特定龛位促进内分泌分化。
Dev Cell. 2020 Oct 26;55(2):150-162.e6. doi: 10.1016/j.devcel.2020.08.003. Epub 2020 Aug 27.
5
Apical Restriction of the Planar Cell Polarity Component VANGL in Pancreatic Ducts Is Required to Maintain Epithelial Integrity.平面细胞极性组分 VANGL 在胰腺导管中的顶端限制对于维持上皮完整性是必需的。
Cell Rep. 2020 May 26;31(8):107677. doi: 10.1016/j.celrep.2020.107677.
6
Hippo Signaling-Mediated Mechanotransduction in Cell Movement and Cancer Metastasis.细胞运动和癌症转移中河马信号介导的机械转导
Front Mol Biosci. 2020 Jan 31;6:157. doi: 10.3389/fmolb.2019.00157. eCollection 2019.
7
Stem Cell Therapy for Diabetes: Beta Cells versus Pancreatic Progenitors.干细胞治疗糖尿病:β细胞与胰腺祖细胞。
Cells. 2020 Jan 23;9(2):283. doi: 10.3390/cells9020283.
8
New insights into apical-basal polarization in epithelia.上皮细胞顶底极性的新见解。
Curr Opin Cell Biol. 2020 Feb;62:1-8. doi: 10.1016/j.ceb.2019.07.017. Epub 2019 Sep 7.
9
LATS1/2 suppress NFκB and aberrant EMT initiation to permit pancreatic progenitor differentiation.LATS1/2 抑制 NFκB 和异常 EMT 起始,从而允许胰腺祖细胞分化。
PLoS Biol. 2019 Jul 19;17(7):e3000382. doi: 10.1371/journal.pbio.3000382. eCollection 2019 Jul.
10
Switching states: dynamic remodelling of polarity complexes as a toolkit for cell polarization.切换状态:极性复合物的动态重塑作为细胞极化的工具包。
Curr Opin Cell Biol. 2019 Oct;60:121-130. doi: 10.1016/j.ceb.2019.05.002. Epub 2019 Jul 9.

细胞皮层作为胰腺上皮发育和内分泌分化的中介。

The cell cortex as mediator of pancreatic epithelial development and endocrine differentiation.

机构信息

Department of Molecular Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390, USA.

Department of Molecular Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390, USA.

出版信息

Curr Opin Genet Dev. 2022 Feb;72:118-127. doi: 10.1016/j.gde.2021.11.004. Epub 2021 Dec 17.

DOI:10.1016/j.gde.2021.11.004
PMID:34929610
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8915777/
Abstract

Organogenesis is the complex process of cells coordinating their own proliferation with changes to their shape, cell migration and cell-cell signaling, so that they transform into a three dimensional functional tissue, with its own custom range of differentiated cell types. Understanding when and where critical signals emanate from, and how those signals are transduced and interpreted, is the fundamental challenge of developmental biology. Here, we review recent findings regarding how progenitor cells interpret cues during pancreatic morphogenesis and how they coordinate cell fate determination. Recent evidence suggests that molecules located in the cell cortex play a crticial role in determining cellular behavior during pancreatic morphogenesis. Specifically, we find that control of cell adhesion, polarity, and constriction are all integral to both initiation of epithelial development and to later cell differentiation. Here, we review key molecules that coordinate these processes and suggest that the cell cortex acts as a signaling center that relays cues during pancreas development.

摘要

器官发生是细胞通过自身增殖与形态变化、细胞迁移和细胞间信号传递的协调,将自身转化为具有三维功能的组织,并具有自身特定分化细胞类型的复杂过程。了解关键信号何时何地发出,以及这些信号如何转导和解释,是发育生物学的基本挑战。在这里,我们回顾了最近关于祖细胞如何在胰腺形态发生过程中解读线索以及它们如何协调细胞命运决定的发现。最近的证据表明,位于细胞皮质的分子在决定胰腺形态发生过程中的细胞行为方面起着关键作用。具体来说,我们发现细胞黏附、极性和收缩的控制对于上皮发育的开始和后来的细胞分化都是必不可少的。在这里,我们回顾了协调这些过程的关键分子,并提出细胞皮质作为信号中心,在胰腺发育过程中传递线索。