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肉鸡卵黄囊和小肠中 PepT1 mRNA 的空间转录组谱。

Spatial transcriptional profile of PepT1 mRNA in the yolk sac and small intestine in broiler chickens.

出版信息

Poult Sci. 2017 Aug 1;96(8):2871-2876. doi: 10.3382/ps/pex056.

DOI:10.3382/ps/pex056
PMID:28482069
Abstract

The yolk sac and small intestine are 2 important organs responsible for the digestion and absorption of nutrients in chickens during the embryonic and posthatch periods, respectively. The peptide transporter PepT1 is expressed in both the yolk sac and small intestine and plays an important role in the transport of amino acids as short peptides. The objective of this study was to profile the spatial transcriptional patterns of PepT1 mRNA in the yolk sac and small intestine from embryonic and posthatch broilers. The distribution of PepT1 mRNA was investigated by in situ hybridization at embryonic (e) d 11, 13, 15, 17, 19 and day of hatch (doh) in the yolk sac and at e19, doh, and d 1, d 4, and d 7 posthatch in the small intestine. PepT1 mRNA was expressed in the endodermal cells of the yolk sac. PepT1 mRNA was barely detectable at e11, increased from e11 to e13, e15, and e17, and then gradually decreased from e19 to doh. In the small intestine, there was a rapid increase in expression of PepT1 mRNA in the enterocytes from e19 to doh, with expression relatively constant from d 1 to d 7. In addition, there was a differential increase in the heights of the villi in different parts of the small intestine from d 1 to 7, which may partially explain the temporal increase in PepT1 mRNA detected by qPCR. The villi in the duodenum showed the earliest increase in villus height and ultimately resulted in the highest villi at d 7. These results demonstrate that there are temporal changes in PepT1 mRNA expression in the yolk sac and the small intestine, which correspond with their expected role in nutrient uptake during the embryonic and posthatch periods.

摘要

卵黄囊和小肠是鸡胚胎期和出壳后分别负责消化和吸收营养的两个重要器官。肽转运蛋白 PepT1 在卵黄囊和小肠中均有表达,在氨基酸作为短肽的转运中发挥重要作用。本研究旨在描绘胚胎期和出壳后肉鸡卵黄囊和小肠中 PepT1 mRNA 的空间转录模式。通过原位杂交技术在卵黄囊中的 e 天 11、13、15、17 和 19 以及出壳日(doh)以及小肠中的 e 天 19、doh、d 1、d 4 和 d 7 检测 PepT1 mRNA 的分布。PepT1 mRNA 表达在卵黄囊的内胚层细胞中。e11 时 PepT1 mRNA 几乎检测不到,从 e11 到 e13、e15 和 e17 逐渐增加,然后从 e19 到 doh 逐渐减少。在小肠中,从 e19 到 doh,肠细胞中 PepT1 mRNA 的表达迅速增加,从 d 1 到 d 7 表达相对稳定。此外,从 d 1 到 7,不同部位小肠的绒毛高度呈差异增加,这可能部分解释了 qPCR 检测到的 PepT1 mRNA 的时间增加。十二指肠的绒毛最早增加绒毛高度,最终导致 d 7 时绒毛最高。这些结果表明,卵黄囊和小肠中 PepT1 mRNA 的表达存在时间变化,与它们在胚胎期和出壳后期间吸收营养的预期作用相对应。

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