• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

牛血管生成素样蛋白 4 的组织表达。

Tissue expression of angiopoietin-like protein 4 in cattle.

机构信息

Department of Animal Sciences and Industry, Kansas State University, Manhattan 66506, USA.

出版信息

J Anim Sci. 2010 Jan;88(1):124-30. doi: 10.2527/jas.2009-2258. Epub 2009 Sep 25.

DOI:10.2527/jas.2009-2258
PMID:19783696
Abstract

Angiopoietin-like protein 4 (ANGPTL4; also known as fasting-induced adipose factor) is a plasma protein that stimulates oxidation of fatty acids and inhibits fat accumulation. The gastrointestinal tract appears to play an important role in regulating plasma ANGPTL4 concentration in some situations and may be influenced by microbes within the gastrointestinal tract. Our aim was to determine which tissues express ANGPTL4 in the bovine. Rumen, omasum, abomasum, duodenum, jejunum, ileum, colon, pancreas, liver, and subcutaneous adipose tissue samples were collected postmortem from 2 steers. Abundance of ANGPTL4 messenger RNA was quantified by quantitative real-time PCR, and was most abundant in liver and adipose tissue (P < 0.05). We also detected ANGPTL4 messenger RNA throughout the gastrointestinal tract, although its abundance was approximately 10% of that found in liver and adipose tissue. Western blot analysis revealed that ANGPTL4 protein was most abundant in liver and adipose tissue (P < 0.05), but omasal, abomasal, and ileal samples contained at least 60% as much ANGPTL4 protein as the liver and adipose tissue samples, and the protein was detected in all tissues. Finally, cross-sections of the liver, pancreas, and rumen wall were used for indirect immunofluorescent detection of ANGPTL4. Despite the low abundance of ANGPTL4 measured by quantitative real-time PCR and Western blot in ruminal tissue, immunofluorescence demonstrated that expression of ANGPTL4 in ruminal epithelial cells was equivalent to or greater than that in liver hepatocytes. These findings indicate that, as in other species studied, liver and adipose tissue are key sources of ANGPTL4 in cattle. However, the protein was also highly abundant in ruminal epithelium, making it possible that commensal microbes may influence ANGPTL4 synthesis and secretion in the ruminant gastrointestinal tract.

摘要

血管生成素样蛋白 4(ANGPTL4;也称为禁食诱导脂肪因子)是一种血浆蛋白,可刺激脂肪酸的氧化并抑制脂肪堆积。在某些情况下,胃肠道似乎在调节血浆 ANGPTL4 浓度方面发挥着重要作用,并且可能受到胃肠道内微生物的影响。我们的目的是确定牛中哪些组织表达 ANGPTL4。从 2 头公牛死后采集瘤胃、网胃、瓣胃、十二指肠、空肠、回肠、结肠、胰腺、肝脏和皮下脂肪组织样本。通过定量实时 PCR 定量 ANGPTL4 信使 RNA 的丰度,其在肝脏和脂肪组织中最丰富(P <0.05)。我们还在整个胃肠道中检测到 ANGPTL4 信使 RNA,尽管其丰度约为肝脏和脂肪组织的 10%。Western blot 分析显示 ANGPTL4 蛋白在肝脏和脂肪组织中最丰富(P <0.05),但网胃、瓣胃和回肠样本中的 ANGPTL4 蛋白含量至少为肝脏和脂肪组织样本的 60%,并且在所有组织中都检测到该蛋白。最后,使用肝、胰腺和瘤胃壁的横截面进行 ANGPTL4 的间接免疫荧光检测。尽管瘤胃组织中通过定量实时 PCR 和 Western blot 测量的 ANGPTL4 丰度较低,但免疫荧光显示 ANGPTL4 在瘤胃上皮细胞中的表达与肝脏肝细胞中的表达相当或更高。这些发现表明,与在其他研究物种中一样,肝脏和脂肪组织是牛中 ANGPTL4 的主要来源。然而,该蛋白在瘤胃上皮细胞中也高度丰富,这使得共生微生物可能影响反刍动物胃肠道中 ANGPTL4 的合成和分泌。

相似文献

1
Tissue expression of angiopoietin-like protein 4 in cattle.牛血管生成素样蛋白 4 的组织表达。
J Anim Sci. 2010 Jan;88(1):124-30. doi: 10.2527/jas.2009-2258. Epub 2009 Sep 25.
2
Regulation of angiopoietin-like protein 4/fasting-induced adipose factor (Angptl4/FIAF) expression in mouse white adipose tissue and 3T3-L1 adipocytes.血管生成素样蛋白4/禁食诱导脂肪因子(Angptl4/FIAF)在小鼠白色脂肪组织和3T3-L1脂肪细胞中的表达调控
Br J Nutr. 2008 Jul;100(1):18-26. doi: 10.1017/S0007114507882961. Epub 2007 Dec 17.
3
Influence of ruminal and postruminal carbohydrate infusion on visceral organ mass and adipose tissue accretion in growing beef steers.瘤胃和瘤胃后碳水化合物灌注对生长肉牛内脏器官质量和脂肪组织蓄积的影响。
J Anim Sci. 2007 Sep;85(9):2256-70. doi: 10.2527/jas.2006-359. Epub 2007 Apr 12.
4
Fatty acids and hypoxia stimulate the expression and secretion of the adipokine ANGPTL4 (angiopoietin-like protein 4/ fasting-induced adipose factor) by human adipocytes.脂肪酸和缺氧刺激人类脂肪细胞中脂肪因子ANGPTL4(血管生成素样蛋白4/禁食诱导脂肪因子)的表达和分泌。
J Nutrigenet Nutrigenomics. 2011;4(3):146-53. doi: 10.1159/000327774. Epub 2011 Jun 28.
5
High-grain diets suppress ruminal tissue abundance of angiopoietin-like protein 4 in cattle.高谷物日粮抑制牛瘤胃组织中血管生成素样蛋白4的丰度。
J Anim Sci. 2014 Sep;92(9):4077-85. doi: 10.2527/jas.2013-7316. Epub 2014 Aug 1.
6
Caloric restriction and exercise increase plasma ANGPTL4 levels in humans via elevated free fatty acids.热量限制和运动通过提高游离脂肪酸水平来增加人体血浆血管生成素样蛋白4(ANGPTL4)的水平。
Arterioscler Thromb Vasc Biol. 2009 Jun;29(6):969-74. doi: 10.1161/ATVBAHA.108.182147. Epub 2009 Apr 2.
7
The acute phase response stimulates the expression of angiopoietin like protein 4.急性期反应刺激血管生成素样蛋白 4 的表达。
Biochem Biophys Res Commun. 2010 Jan 22;391(4):1737-41. doi: 10.1016/j.bbrc.2009.12.145. Epub 2009 Dec 31.
8
Adipogenic gene expression and fatty acid composition in subcutaneous adipose tissue depots of Angus steers between 9 and 16 months of age.9 至 16 月龄安格斯阉牛皮下脂肪组织中脂肪生成基因的表达和脂肪酸组成。
J Anim Sci. 2012 Aug;90(8):2505-14. doi: 10.2527/jas.2011-4602. Epub 2012 Feb 3.
9
Expression of estrogen and androgen receptor in the bovine gastrointestinal tract.雌激素和雄激素受体在牛胃肠道中的表达。
Dtsch Tierarztl Wochenschr. 1995 Apr;102(4):164-8.
10
Angptl4 upregulates cholesterol synthesis in liver via inhibition of LPL- and HL-dependent hepatic cholesterol uptake.血管生成素样蛋白4通过抑制脂蛋白脂肪酶和肝脂酶依赖的肝脏胆固醇摄取来上调肝脏中的胆固醇合成。
Arterioscler Thromb Vasc Biol. 2007 Nov;27(11):2420-7. doi: 10.1161/ATVBAHA.107.151894. Epub 2007 Aug 30.

引用本文的文献

1
Including microbiome information in a multi-trait genomic evaluation: a case study on longitudinal growth performance in beef cattle.在多性状基因组评估中纳入微生物组信息:以肉牛纵向生长性能为例的研究。
Genet Sel Evol. 2024 Mar 15;56(1):19. doi: 10.1186/s12711-024-00887-6.
2
Assessing genomic diversity and signatures of selection in Pinan cattle using whole-genome sequencing data.利用全基因组测序数据评估坪山牛的基因组多样性和选择特征。
BMC Genomics. 2022 Jun 21;23(1):460. doi: 10.1186/s12864-022-08645-y.
3
Transcriptome Adaptation of the Ovine Mammary Gland to Dietary Supplementation of Extruded Linseed.
绵羊乳腺对膨化亚麻籽日粮补充的转录组适应性
Animals (Basel). 2021 Sep 16;11(9):2707. doi: 10.3390/ani11092707.
4
Genome-Wide Association Study Based on Random Regression Model Reveals Candidate Genes Associated with Longitudinal Data in Chinese Simmental Beef Cattle.基于随机回归模型的全基因组关联研究揭示了中国西门塔尔牛纵向数据相关的候选基因。
Animals (Basel). 2021 Aug 27;11(9):2524. doi: 10.3390/ani11092524.
5
Advances in fatty acids nutrition in dairy cows: from gut to cells and effects on performance.奶牛脂肪酸营养研究进展:从肠道到细胞及其对生产性能的影响
J Anim Sci Biotechnol. 2020 Nov 16;11(1):110. doi: 10.1186/s40104-020-00512-8.
6
Expression of messenger RNA encoding two cellular metabolic regulators, AMP-activated protein kinase (AMPK) and O-GlcNAc transferase (OGT), in channel catfish: Their tissue distribution and relationship with changes in food intake.编码两种细胞代谢调节因子——腺苷酸活化蛋白激酶(AMPK)和O-连接N-乙酰葡糖胺转移酶(OGT)的信使核糖核酸在斑点叉尾鮰中的表达:它们的组织分布以及与食物摄入量变化的关系。
Comp Biochem Physiol A Mol Integr Physiol. 2019 Sep;235:12-21. doi: 10.1016/j.cbpa.2019.04.023. Epub 2019 May 12.
7
Serum hepatokines in dairy cows: periparturient variation and changes in energy-related metabolic disorders.奶牛血清肝源性激素:围产期变化及与能量相关的代谢紊乱的变化
BMC Vet Res. 2018 Aug 13;14(1):236. doi: 10.1186/s12917-018-1560-7.
8
Comparative genome-wide methylation analysis of longissimus dorsi muscles between Japanese black (Wagyu) and Chinese Red Steppes cattle.日本黑毛和牛(和牛)与中国草原红牛背最长肌的全基因组甲基化比较分析。
PLoS One. 2017 Aug 3;12(8):e0182492. doi: 10.1371/journal.pone.0182492. eCollection 2017.
9
mRNA Expression of Ovine Angiopoietin-like Protein 4 Gene in Adipose Tissues.绵羊血管生成素样蛋白4基因在脂肪组织中的mRNA表达
Asian-Australas J Anim Sci. 2016 May;29(5):615-23. doi: 10.5713/ajas.15.0090. Epub 2015 Sep 3.
10
Transcriptome adaptation of the bovine mammary gland to diets rich in unsaturated fatty acids shows greater impact of linseed oil over safflower oil on gene expression and metabolic pathways.牛乳腺对富含不饱和脂肪酸日粮的转录组适应性表明,亚麻籽油对基因表达和代谢途径的影响比红花油更大。
BMC Genomics. 2016 Feb 9;17:104. doi: 10.1186/s12864-016-2423-x.