不同采食量对仔猪肠道形态和上皮细胞分化的影响

IF 2.7 2区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Xin Wang, Lanmei Yin, Chunchun Geng, Jiaqi Zhang, Jianzhong Li, Pengfei Huang, Yali Li, Qiye Wang, Huansheng Yang
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引用次数: 0

摘要

本研究旨在探讨采食量对仔猪肠道形态发育和上皮细胞分化的影响。将 64 头 35 日龄健康断奶仔猪([大白×陆地赛] × 杜洛克)随机分为四组(采食量为 100%、80%、40% 和 20%),每组两个重复,共八个重复。在第 3 天和第 7 天采集样品。结果表明,随着限饲程度和时间的增加,仔猪的体重和器官指数显著下降,十二指肠、空肠和回肠的绒毛高度和隐窝深度也呈线性下降(P < 0.05)。限饲三天后,空肠ki67、内分泌细胞、鹅口疮细胞和绒毛内分泌/绒毛高度均呈线性下降,但绒毛杯/绒毛高度比呈线性上升,且40%和20%的绒毛杯/绒毛高度比明显高于100%和80%的绒毛杯/绒毛高度比(P<0.05)。限食 7 天的仔猪空肠 ki67、内分泌细胞、绒毛细胞和绒毛内分泌/绒毛高度也呈线性下降;但 20% 组的绒毛鹅口疮细胞/绒毛高度比明显高于 40% 组,与 80% 组相比无差异(P < 0.05)。在限饲三天期间,空肠分化标记基因的表达呈线性下降趋势(P < 0.05),但在限饲七天后呈线性上升趋势。白细胞介素17(IL-17)和IL-22的表达水平也呈线性上升趋势(P < 0.05)。KEGG和GSEA分析表明,PPAR信号通路、ECM-受体相互作用以及Th1、Th2和Th17细胞分化在这些过程中显著富集。RT-QPCR 显示,在七天的限饲期间,PPAR 和 ECM-受体相互作用都被明显激活(P < 0.05)。结果表明,随着限饲强度和时间的增加,肠道形态和上皮细胞的增殖和分化明显减少,但小管细胞除外。这一现象与Th细胞分泌的IL-17和IL-22调节肠道分化有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of different feed intake levels on intestinal morphology and epithelial cell differentiation in piglets.

This study aimed to investigate the effect of feed intake levels on the development of intestinal morphology and epithelial cell differentiation in piglets. Sixty-four 35-d-old healthy weaned piglets ([Large White × Landrace] × Duroc) with an initial weight (6.93 ± 0.12 kg) were randomly divided into 4 groups (100%, 80%, 40%, and 20% feed intake) with 8 replicates of 2 pigs each. Samples were collected on days 3 and 7. The results revealed that with an increase in feed restriction degree and time, the body weight and organ index of piglets significantly decreased, and the villus height (VH) and crypt depth of the duodenum, jejunum, and ileum also decreased linearly (P < 0.05). After 3 d of feed restriction, jejunal ki67, endocrine cells, goblet cells, and villus endocrine/VH all decreased linearly, but the villus cup/VH ratio increased linearly, and the 40% and 20% were significantly higher than those of the 100% and 80% (P < 0.05). There was also a linear decrease in jejunal ki67, endocrine cells, goblet cells, and villous endocrine/VH in piglets fed 7 d of food restriction; however, the villus goblet cells/VH ratio in the 20% was significantly higher than that in the 40% group and was not different from that in the 80% (P < 0.05). During 3 d of feed restriction, the expression of jejunal differentiation marker genes showed a linear decreasing trend (P < 0.05) but increased linearly after 7 d of feed restriction. The expression levels of interleukin17 (IL-17) and IL-22 also increased linearly (P < 0.05). Kyoto Encyclopedia of Genes and Genomes and gene set enrichment analysis analyses indicated that the PPAR signaling pathway, ECM-receptor interaction, and Th1, Th2, and Th17 cell differentiation were significantly enriched in these processes. real-time quantitative polymerase chain reaction demonstrated that both PPAR and ECM-receptor interactions were significantly activated during 7 d of feeding restriction (P < 0.05). The results showed that with an increase in feed restriction intensity and time, the intestinal morphology and epithelial cell proliferation and differentiation were significantly reduced, except for the goblet cells. This phenomenon is related to the regulation of intestinal differentiation by IL-17 and IL-22 secreted by the Th cells.

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来源期刊
Journal of animal science
Journal of animal science 农林科学-奶制品与动物科学
CiteScore
4.80
自引率
12.10%
发文量
1589
审稿时长
3 months
期刊介绍: The Journal of Animal Science (JAS) is the premier journal for animal science and serves as the leading source of new knowledge and perspective in this area. JAS publishes more than 500 fully reviewed research articles, invited reviews, technical notes, and letters to the editor each year. Articles published in JAS encompass a broad range of research topics in animal production and fundamental aspects of genetics, nutrition, physiology, and preparation and utilization of animal products. Articles typically report research with beef cattle, companion animals, goats, horses, pigs, and sheep; however, studies involving other farm animals, aquatic and wildlife species, and laboratory animal species that address fundamental questions related to livestock and companion animal biology will be considered for publication.
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