中国农业科学 ›› 2026, Vol. 59 ›› Issue (19): 4400-4416.doi: 10.3864/j.issn.0578-1752.2026.19.017

• 畜牧·兽医 • 上一篇    下一篇

低氧相关因子在牦牛和黄牛小肠组织中的表达差异分析

张叶琼1(), 王军1, 徐铭蔚1, 胡嘉琦1, 刘莎莎1, 蓝雯琳1, 谈笑1, 杨琨1,2,3()   

  1. 1 西北民族大学生命科学与工程学院, 兰州 730000
    2 西北民族大学生物医学研究中心甘肃省动物细胞技术创新中心, 兰州 730030
    3 西北民族大学生物医学研究中心生物工程与技术国家民委重点实验室, 兰州 730030
  • 收稿日期:2025-12-29 接受日期:2026-04-10 出版日期:2026-10-01 发布日期:2026-10-10
  • 通信作者:
    杨琨,E-mail:
  • 联系方式: 张叶琼,E-mail:2074647593@qq.com。
  • 基金资助:
    甘肃省青年人才项目(2025QNGR63); 中央高校基本科研业务费专项(31920250051); 中央高校基本科研业务费专项(31920260071); 兰州青年科技人才创新项目(2023-QN-70)

Differential Analysis of Hypoxia-Related Factors in the Small Intestines of Yaks and Yellow Cattle

ZHANG YeQiong1(), WANG Jun1, XU MingWei1, HU JiaQi1, LIU ShaSha1, LAN WenLin1, TAN Xiao1, YANG Kun1,2,3()   

  1. 1 College of Life Science and Engineering, Northwest Minzu University, Lanzhou 730000
    2 Gansu Provincial Technology Innovation Center for Animal Cells, Biomedical Research Center, Northwest Minzu University, Lanzhou 730030
    3 Key Laboratory of Bioengineering and Technology, State Ethnic Affairs Commission, Biomedical Research Center, Northwest Minzu University, Lanzhou 730030
  • Received:2025-12-29 Accepted:2026-04-10 Published:2026-10-01 Online:2026-10-10

摘要:

【目的】探究丙酮酸脱氢酶激酶1 (pyruvate dehydrogenase kinase1, PDK1)、缺氧诱导因子1α (hypoxia inducible factor-1α, HIF-1α)、转化生长因子-β(transforming growth factor-β, TGF-β)、血管内皮生长因子 (vascular endothelial growth factor,VEGF)、母系抗皮节蛋白同源物2 (mothers against decapentaplegic homolog 2, Smad2)和母系抗皮节蛋白同源物3 (mothers against decapentaplegic homolog 3, Smad3)等低氧相关因子在小肠组织中的表达差异,揭示牦牛对低氧环境的肠道适应机制。【方法】选取高原牦牛和平原黄牛的小肠组织(十二指肠、空肠、回肠)作为研究对象,采用苏木精-伊红染色(hematoxylin-eosin staining, H.E)、过碘酸雪夫染色(periodic acid-Schiff staining, PAS)、Masson三色染色(Masson’s trichrome staining)以及免疫组织化学染色。在光学显微镜下对以上染色后的组织切片拍照,利用图像分析软件对H.E染色下的肠绒毛高度(villus height, V)、隐窝深度(crypt depth, C)以及PAS、Masson、免疫组织化学染色的平均光密度(average optical density analysis, AOD)进行分析,并用平均光密度值表示阳性表达结果,从而探究低氧相关因子在不同物种、不同肠段组织中的分布特征与表达差异。【结果】H.E染色结果显示,牦牛与黄牛十二指肠肠道消化指标V/C值(肠绒毛高度/隐窝深度,villus height/crypt depth)均显著高于空肠和回肠(P<0.05),且牦牛十二指肠V/C值显著高于黄牛同肠段(P<0.05)。PAS染色结果进一步显示,PAS阳性物质在十二指肠的表达强度显著高于空肠和回肠(P<0.05),且在纹状缘、杯状细胞和潘氏细胞中呈强阳性表达,牦牛各肠段中的表达显著高于黄牛(P<0.05)。Masson三色染色结果显示,牦牛与黄牛小肠组织的胶原纤维含量均存在显著种间与肠段差异(P<0.05),其中黄牛十二指肠和空肠纤维含量占比显著高于牦牛对应肠段(P<0.05)。免疫组织化学检测到,PDK1、HIF-1α、TGF-β、VEGF在牦牛和黄牛小肠组织的阳性表达区域呈现清晰的棕黄色,主要定位于纹状缘、潘氏细胞及杯状细胞,且在小肠腺部位的表达特征存在明显的种间差异,黄牛十二指肠和空肠肠腺呈弱阳性表达,牦牛对应部位呈强阳性表达。组织差异分析显示,上述因子在十二指肠的表达量显著高于空肠和回肠(P<0.05)。物种差异上,牦牛小肠组织的整体表达水平显著高于黄牛(P<0.05);但Smad2和Smad3的表达与上述因子有差异,Smad2和Smad3在十二指肠中的表达显著低于回肠和空肠(P<0.05),并且在牦牛十二指肠和回肠中的表达显著低于黄牛(P<0.05),在牦牛空肠中的表达显著高于黄牛(P<0.05)。【结论】H.E染色、特殊染色及免疫组织化学染色结果显示,牦牛与黄牛小肠在形态结构、糖类物质分布及低氧相关因子表达方面存在显著差异,提示牦牛肠道在结构与分子层面具有独特的低氧适应特征,PDK1、HIF-1α及VEGF等因子可能在牦牛肠道低氧适应机制中发挥了重要作用。研究为高原动物肠道适应研究提供了基础数据,也为低氧相关肠道疾病的机制探讨与防治提供了参考。

关键词: 牦牛, 小肠, 低氧, 丙酮酸脱氢酶激酶1(PDK1), 缺氧诱导因子1α(HIF-1α), 血管内皮生长因子(VEGF)

Abstract:

【Objective】This study aimed to investigate the differential expression of hypoxia-related factors—Pyruvate dehydrogenase kinase 1 (PDK1), Hypoxia-inducible factor-1α (HIF-1α), Transforming growth factor-β (TGF-β), Vascular endothelial growth factor (VEGF), Mothers against decapentaplegic homolog 2 (Smad2), and Mothers against decapentaplegic homolog 3 (Smad3)—in the small intestinal tissues of yaks, to elucidate the intestinal adaptation mechanisms of yaks to hypoxic environments.【Method】Small intestinal tissues (duodenum, jejunum, and ileum) from plateau yaks and plain yellow cattle were selected as research subjects. Hematoxylin-eosin staining (H.E), periodic acid-Schiff staining (PAS), Masson’s trichrome staining, and immunohistochemical staining were performed. Tissue sections after staining were photographed under a light microscope. Image analysis software was used to measure villus height (V) and crypt depth (C) in H.E-stained sections, as well as the average optical density (AOD) of PAS, Masson, and immunohistochemical staining. The average optical density value was employed to represent positive expression results, thereby investigating the distribution characteristics and expression differences of hypoxia-related factors in different species and intestinal segments.【Result】H.E staining results indicated that the V/C ratio (villus height/crypt depth), an indicator of intestinal digestion, in both yaks and yellow cattle was significantly higher in the duodenum compared to the jejunum and ileum (P<0.05). Furthermore, the duodenal V/C ratio of yaks was significantly higher than that of yellow cattle (P<0.05). PAS staining showed that PAS-positive substances were expressed with significantly higher intensity in the duodenum than in the jejunum and ileum (P<0.05), with strong positive expression observed in the striated border, goblet cells, and Paneth cells. The expression in all intestinal segments of yaks was significantly higher than in yellow cattle (P<0.05). Masson's trichrome staining results revealed significant interspecies and segmental differences in collagen fiber content within the small intestinal tissues of both yaks and yellow cattle (P<0.05). Specifically, the proportion of collagen fibers in the duodenum and jejunum of yellow cattle was significantly higher than in the corresponding segments of yaks (P<0.05). Immunohistochemical analysis detected distinct positive brown-yellow expression of PDK1, HIF-1α, TGF-β, and VEGF in the small intestinal tissues, primarily localized to the striated border, Paneth cells, and goblet cells. Differences in intestinal gland expression were observed between species: weak positive expression was seen in the duodenal and jejunal glands of yellow cattle, while strong positive expression was observed in the corresponding locations in yaks. Tissue segment analysis showed that the expression levels of these factors were significantly higher in the duodenum than in the jejunum (P<0.05). Regarding species differences, the overall expression levels in yak small intestinal tissues were significantly higher than in yellow cattle (P<0.05). However, the expression patterns of Smad2 and Smad3 differed from those of the aforementioned factors. The expressions of Smad2 and Smad3 in the duodenum were significantly lower than those in the ileum and jejunum, respectively (P<0.05). Furthermore, the expression of Smad2/3 in the duodenum and ileum of yaks was significantly lower than in yellow cattle (P<0.05), while in the jejunum of yaks, it was significantly higher than in yellow cattle (P<0.05).【Conclusion】Results from H&E staining, special staining, and immunohistochemical staining revealed significant differences between yaks and yellow cattle in the morphological structure, carbohydrate distribution, and expression of hypoxia-related factors in the small intestine. These findings suggest that yak intestines possess unique structural and molecular adaptive features to hypoxia, and that factors such as PDK1, HIF-1α, and VEGF may play important roles in the intestinal hypoxic adaptation mechanisms of yaks. This study provides fundamental data for research on intestinal adaptation in high-altitude animals and offers a reference for exploring the mechanisms and prevention of hypoxia-related intestinal diseases.

Key words: yak, small intestine, hypoxia, pyruvate dehydrogenase kinase 1 (PDK1), hypoxia inducible factor 1α (HIF-1α), vascular endothelial growth factor (VEGF)