Tianxi Zhang, Zhiyuan Ma, Fei Li, Fenja Klevenhusen, Long Guo, Li Wang, Zhian Zhang, Shuai Jiao, Fang Luo, Tao Guo, Xinji Wang, Kaidong Li, Baocang Liu
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引用次数: 0
Abstract
High-grain diets can reduce rumen pH, which may damage the process of keratinization of the ruminal stratified squamous epithelium, leading to areas of abnormal keratinization (AK). However, the comprehension of molecular biological processes leading to the development of an AK area in the rumen is limited. A total of 48 wethers (2-month-old) were fed a diet containing 48% barley and 24% starch (DM basis) to induce AK development. Rumen fluid samples were collected via an oral stomach tube at 0, 2.5, and 6 h post-morning feeding on three consecutive days (d 58, 59, and 60) to measure pH. Following a 63-day feeding period, all lambs were slaughtered, and based on macroscopic pathological observation of the rumen, they were retrospectively classified into two categories of individuals: individuals with normal rumen (INR; n = 38) and individuals with abnormal keratinization rumen (IAKR; n = 10). Tissue samples from the AK and adjacent morphologically normal (MN) areas of IAKR were analyzed histologically and via RNA sequencing and quantitative real-time PCR (qRT-PCR). Statistical analysis used Shapiro-Wilk tests for histological and qRT-PCR data and linear mixed models for pH comparisons. Key genes and pathways were identified through Differential Expression Analysis (DEA), Weighted Gene Co-expression Network Analysis (WGCNA), and Gene Set Enrichment Analysis (GSEA). Compared to the INR, the IAKR had a lower rumen pH at 2.5 h post-morning feeding (5.352 vs 6.035, P < 0.01). Histological examination showed significant reductions in papillae length, width, and stratum corneum thickness in the AK area compared to the MN area (P < 0.01). Transcriptomic analysis revealed the gene expression downregulation of ACTR2, which play a role in tight junctions; Downregulation of SLC38A2, a gene involved in the protein digestion and absorption pathway, was also observed; The upregulation of MMP9 was observed in the IL-17 signaling pathway, contributing to tissue damage; The expression of ITGB7 was also upregulated, which intensified the local immune response. The expression patterns of these genes were further confirmed by qRT-PCR analysis. In conclusion, the current study revealed molecular processes involved in the disruption of intercellular connections and structural support in tissue cells and impaired ability of cells to absorb nutrients and capture signaling molecules within these AK areas caused by high grain feeding.
高粒饲粮可降低瘤胃pH值,从而破坏瘤胃分层鳞状上皮的角化过程,导致角化异常区(AK)。然而,对导致瘤胃AK区发育的分子生物学过程的理解是有限的。本试验共48头2月龄仔猪,饲喂含48%大麦和24%淀粉(DM基础)的饲粮诱导AK发育。在连续3天(第58、59和60天)晨饲后0、2.5和6 h,通过口胃管采集瘤胃液,测量ph值。饲喂63 d后,屠宰羔羊,根据瘤胃宏观病理观察,将羔羊回顾性分为正常瘤胃组(INR, n = 38)和异常角化瘤胃组(IAKR, n = 10)。通过RNA测序和实时荧光定量PCR (qRT-PCR)对IAKR AK区和相邻形态学正常(MN)区的组织样本进行组织学分析。统计分析采用Shapiro-Wilk检验组织学和qRT-PCR数据,并采用线性混合模型进行pH比较。通过差异表达分析(DEA)、加权基因共表达网络分析(WGCNA)和基因集富集分析(GSEA)确定关键基因和通路。与INR相比,IAKR在晨饲后2.5 h的瘤胃pH较低(5.352 vs 6.035, P < 0.01)。组织学检查显示,与MN区相比,AK区乳头长度、宽度和角质层厚度均显著减少(P < 0.01)。转录组学分析显示,参与紧密连接的ACTR2基因表达下调;SLC38A2(参与蛋白质消化吸收途径的基因)的下调也被观察到;在IL-17信号通路中观察到MMP9的上调,导致组织损伤;ITGB7表达上调,增强了局部免疫应答。qRT-PCR分析进一步证实了这些基因的表达模式。总之,目前的研究揭示了高谷物喂养引起的细胞间连接和组织细胞结构支持的破坏以及细胞吸收营养和捕获这些AK区域信号分子的能力受损的分子过程。
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.