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细胞间接触丧失会抑制α-连环蛋白敲除的P19胚胎癌细胞的细胞分化及其向发育中的小鼠胚胎的定植。

Loss of Cell-Cell Contact Inhibits Cellular Differentiation of α-Catenin Knock Out P19 Embryonal Carcinoma Cells and Their Colonization into the Developing Mouse Embryos.

作者信息

Sato Masahiro, Inada Emi, Kubota Naoko, Ozawa Masayuki

机构信息

Section of Gene Expression Regulation, Frontier Science Research Center, Kagoshima University, Kagoshima 890-8544, Japan.

Department of Pediatric Dentistry, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima 890-8544, Japan.

出版信息

BioTech (Basel). 2024 Oct 3;13(4):41. doi: 10.3390/biotech13040041.

Abstract

Cadherin-catenin cell-cell adhesion complexes, composed of cadherin, β-catenin or plakoglobin, and α-catenin (α-cat) molecules, are crucial for maintaining cell-cell contact and are commonly referred to as "adherens junctions (AJs)." Inactivating this system leads to loss of cell-cell contact and developmental arrest in early embryos. However, it remains unclear whether the loss of cell-cell contact affects the differentiation of embryonic cells. In this study, we explored the use of a murine embryonal carcinoma cell line, P19, as an in vitro model for early embryogenesis. P19 cells easily form embryoid bodies (EBs) and are susceptible to cellular differentiation in response to retinoic acid (RA) and teratoma formation. Using CRISPR/Cas9 technology to disrupt the endogenous gene in P19 cells, we generated knockout (KO) cells that exhibited a loss of cell-cell contact. When cultivated on non-coated dishes, these KO cells formed EBs, but their structures were labile. In the RA-containing medium, the KO EBs failed to produce differentiated cells on their outer layer and continued to express SSEA-1, an antigen specific to pluripotent cells. Teratoma formation assays revealed an absence of overt differentiated cells in tumors derived from KO P19 cells. Aggregation assays revealed the inability of the KO cells to colonize into the zona pellucida-denuded 8-cell embryos. These findings suggest that the AJs are essential for promoting the early stages of cellular differentiation and for the colonization of early-developing embryos.

摘要

钙黏蛋白 - 连环蛋白细胞间黏附复合体由钙黏蛋白、β - 连环蛋白或桥粒斑珠蛋白以及α - 连环蛋白(α - cat)分子组成,对于维持细胞间接触至关重要,通常被称为“黏着连接(AJs)”。使该系统失活会导致细胞间接触丧失以及早期胚胎发育停滞。然而,细胞间接触丧失是否影响胚胎细胞分化仍不清楚。在本研究中,我们探索了使用小鼠胚胎癌细胞系P19作为早期胚胎发生的体外模型。P19细胞容易形成胚状体(EBs),并且易受视黄酸(RA)诱导的细胞分化和畸胎瘤形成的影响。利用CRISPR/Cas9技术破坏P19细胞中的内源性基因,我们产生了表现出细胞间接触丧失的基因敲除(KO)细胞。当在未包被的培养皿上培养时,这些KO细胞形成了EBs,但它们的结构不稳定。在含RA的培养基中,KO EBs未能在其外层产生分化细胞,并继续表达多能细胞特有的抗原SSEA - 1。畸胎瘤形成试验显示,源自KO P19细胞的肿瘤中没有明显的分化细胞。聚集试验显示,KO细胞无法定殖到去除透明带的8细胞胚胎中。这些发现表明,黏着连接对于促进细胞分化的早期阶段以及早期发育胚胎的定殖至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a13/12456414/71c7745629a8/biotech-13-00041-g001.jpg

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