Meissner Svenja, Hagen Franziska, Deiner Carolin, Günzel Dorothee, Greco Gabriele, Shen Zanming, Aschenbach Jörg R
Institute of Veterinary Physiology, Freie Universität Berlin, D-14163 Berlwin, Germany.
Institute of Clinical Physiology, Charité-Universitätsmedizin Berlin, D-12203 Berlin, Germany.
J Dairy Sci. 2017 Aug;100(8):6662-6675. doi: 10.3168/jds.2016-12262. Epub 2017 May 24.
Subacute ruminal acidosis is induced by high concentrations of short-chain fatty acids (SCFA, mainly acetate, propionate, and butyrate) that release protons to decrease the pH of the ruminal digesta. This low pH, in turn, is thought to damage epithelial barrier function. The present study applied a model of simulated ruminal acidosis ex vivo to investigate if SCFA directly contribute to epithelial barrier failure beyond their role as proton donors. Epithelial tissues from the rumen of slaughtered sheep were mounted in Ussing chambers and incubated under 3 different conditions. Two groups were incubated in the absence of SCFA at mucosal pH 6.1 (control) and pH 5.1, respectively, for 7 h. A third group was first incubated in a mucosal solution containing 100 mM SCFA at pH 5.1 for 2 h and, thereafter, in a mucosal solution without SCFA at pH 6.1 for the remaining 5 h. Transepithelial conductance (G), short-circuit current (I), and fluorescein fluxes were determined. After 7 h of incubation, the expression levels of claudin-1, claudin-4, claudin-7, and occludin were measured by quantitative reverse-transcription PCR and Western blot. Furthermore, the local distribution of these tight junction (TJ) proteins was examined by confocal laser scanning microscopy. A 7-h incubation at pH 5.1 in the absence of SCFA did not influence either G or fluorescein flux rates of ruminal tissues ex vivo compared with the control. In contrast, incubation at pH 5.1 with SCFA for only 2 h induced increases in G and fluorescein flux rates that continued even after tissues were returned back to pH 6.1. Expression analysis showed that pH 5.1 without SCFA for 7 h induced no changes in mRNA expression of claudin-1, claudin-4, claudin-7, and occludin and a selective decrease in protein expression of only claudin-4 compared with the control. However, a 2-h incubation at pH 5.1 in the presence of SCFA decreased the mRNA-expression of claudin-7, as well as the protein expression of claudin-4, claudin-7, and occludin. The decreased expression of these TJ proteins in the group incubated with SCFA was also evident in immunohistochemistry. Immunohistochemistry additionally evidenced a considerable retraction of all tested TJ proteins out of the TJ in that group. We conclude that a low mucosal pH of 5.1 is tolerated well by ruminal epithelia for several hours. However, a low pH in combination with SCFA induces damage to the TJ and disturbs barrier function, which is not immediately reversible upon the removal of the acidotic insult.
亚急性瘤胃酸中毒是由高浓度的短链脂肪酸(SCFA,主要是乙酸、丙酸和丁酸)引起的,这些短链脂肪酸释放质子以降低瘤胃消化物的pH值。反过来,这种低pH值被认为会损害上皮屏障功能。本研究应用体外模拟瘤胃酸中毒模型,以研究SCFA是否除了作为质子供体的作用外,还直接导致上皮屏障功能障碍。将屠宰羊瘤胃的上皮组织安装在尤斯灌流小室中,并在3种不同条件下孵育。两组分别在不存在SCFA的情况下,于黏膜pH值6.1(对照组)和pH值5.1下孵育7小时。第三组首先在含有100 mM SCFA、pH值5.1的黏膜溶液中孵育2小时,然后在不含SCFA、pH值6.1的黏膜溶液中孵育剩余的5小时。测定跨上皮电导(G)、短路电流(I)和荧光素通量。孵育7小时后,通过定量逆转录PCR和蛋白质免疫印迹法测量紧密连接蛋白1(claudin-1)、紧密连接蛋白4(claudin-4)、紧密连接蛋白7(claudin-7)和闭合蛋白(occludin)的表达水平。此外,通过共聚焦激光扫描显微镜检查这些紧密连接(TJ)蛋白的局部分布。与对照组相比,在不存在SCFA的情况下于pH值5.1孵育7小时对体外瘤胃组织的G或荧光素通量率没有影响。相反,在pH值5.1下与SCFA一起孵育仅2小时会导致G和荧光素通量率增加,即使组织恢复到pH值6.1后这种增加仍会持续。表达分析表明,在不存在SCFA的情况下于pH值5.1孵育7小时,与对照组相比,紧密连接蛋白1、紧密连接蛋白4、紧密连接蛋白7和闭合蛋白的mRNA表达没有变化,仅紧密连接蛋白4的蛋白质表达有选择性降低。然而,在存在SCFA的情况下于pH值5.1孵育2小时会降低紧密连接蛋白7的mRNA表达,以及紧密连接蛋白4、紧密连接蛋白7和闭合蛋白的蛋白质表达。在免疫组织化学中,与SCFA一起孵育的组中这些TJ蛋白的表达降低也很明显。免疫组织化学还证明该组中所有测试的TJ蛋白从紧密连接中大量回缩。我们得出结论,瘤胃上皮对5.1的低黏膜pH值能耐受数小时。然而,低pH值与SCFA相结合会导致紧密连接受损并扰乱屏障功能,在消除酸中毒刺激后这种损害不会立即逆转。