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在缺乏GATA4或GATA6的情况下发育中的小肠的特征

Characterization of the developing small intestine in the absence of either GATA4 or GATA6.

作者信息

Walker Emily M, Thompson Cayla A, Kohlnhofer Bridget M, Faber Mary L, Battle Michele A

机构信息

Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USA.

出版信息

BMC Res Notes. 2014 Dec 11;7:902. doi: 10.1186/1756-0500-7-902.

Abstract

BACKGROUND

Studies of adult mice lacking either GATA4 or GATA6 in the small intestine demonstrate roles for these factors in small intestinal biology. Deletion of Gata4 in the adult mouse intestine revealed an essential role for GATA4 in jejunal function. Deletion of Gata6 in the adult mouse ileum alters epithelial cell types and ileal enterocyte gene expression. The effect of deletion of Gata4 or Gata6 alone during embryonic small intestinal development, however, has not been examined. We recently demonstrated that loss of both factors in double conditional knockout embryos causes severe defects in jejunal development. Therefore, the goal of this study is to provide phenotypic analysis of the small intestine of single Gata4 and Gata6 conditional knockout embryos.

RESULTS

Villin-Cre was used to delete Gata4 or Gata6 in the developing intestinal epithelium. Elimination of either GATA4 or GATA6 in the jejunum, where these factors are co-expressed, caused changes in enterocyte and enteroendocrine cell gene expression. Ectopic expression of markers of the ileal-specific bile acid metabolism pathway was induced in GATA4-deficient jejunum but not in GATA6-deficient jejunum. A subtle increase in goblet cells was also identified in jejunum of both mutants. In GATA6-deficient embryonic ileum, villus length was altered, and enterocyte gene expression was perturbed including ectopic expression of the colon marker Car1. Goblet cells were increased, and enteroendocrine cells were decreased.

CONCLUSIONS

Overall, we show that aspects of the phenotypes observed in the small intestine of adult Gata4 and Gata6 conditional knockout mice emerge during development. The effect of eliminating GATA6 from the developing ileum was greater than that of eliminating either GATA4 or GATA6 from the developing jejunum likely reflecting functional redundancy between these factors in the jejunum. Although GATA4 and GATA6 functions overlap, our data also suggest unique functions for GATA4 and GATA6 within the developing intestine. GATA4 likely operates independently of GATA6 within the jejunum to regulate jejunal versus ileal enterocyte identity and consequently jejunal physiology. GATA6 likely regulates enteroendocrine cell differentiation cell autonomously whereas GATA4 affects this population indirectly.

摘要

背景

对成年小鼠小肠中缺乏GATA4或GATA6的研究表明,这些因子在小肠生物学中发挥作用。成年小鼠肠道中Gata4的缺失揭示了GATA4在空肠功能中的重要作用。成年小鼠回肠中Gata6的缺失改变了上皮细胞类型和回肠肠上皮细胞基因表达。然而,在胚胎小肠发育过程中单独缺失Gata4或Gata6的影响尚未得到研究。我们最近证明,双条件敲除胚胎中这两种因子的缺失会导致空肠发育的严重缺陷。因此,本研究的目的是对单Gata4和Gata6条件敲除胚胎的小肠进行表型分析。

结果

使用Villin-Cre在发育中的肠上皮中删除Gata4或Gata6。在这些因子共同表达的空肠中,消除GATA4或GATA6会导致肠上皮细胞和肠内分泌细胞基因表达的变化。在GATA4缺陷的空肠中诱导了回肠特异性胆汁酸代谢途径标志物的异位表达,但在GATA6缺陷的空肠中未诱导。在两个突变体的空肠中也发现杯状细胞略有增加。在GATA6缺陷的胚胎回肠中,绒毛长度改变,肠上皮细胞基因表达受到干扰,包括结肠标志物Car1的异位表达。杯状细胞增加,肠内分泌细胞减少。

结论

总体而言,我们表明在成年Gata4和Gata6条件敲除小鼠小肠中观察到的表型特征在发育过程中就已出现。从发育中的回肠中消除GATA6的影响大于从发育中的空肠中消除GATA4或GATA6的影响,这可能反映了这些因子在空肠中的功能冗余。尽管GATA4和GATA6的功能重叠,但我们的数据也表明GATA4和GATA6在发育中的肠道内具有独特的功能。GATA4可能在空肠内独立于GATA6发挥作用,以调节空肠与回肠肠上皮细胞的特性,从而影响空肠生理功能。GATA6可能自主调节肠内分泌细胞的分化,而GATA4则间接影响这一群体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/130b/4307969/4509965721e8/13104_2014_3474_Fig1_HTML.jpg

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