Department of Surgery, Medical College of Georgia, Augusta, GA 30912, USA.
J Gastrointest Surg. 2010 Mar;14(3):449-61. doi: 10.1007/s11605-009-1045-x. Epub 2009 Dec 22.
Butyrate is a bacterial fermentation product that produces its beneficial effects on colon through GPR109A, a butyrate receptor, and SLC5A8, a butyrate transporter. In this study, we compared the expression of GPR109A and SLC5A8 between conventional mice and germ-free mice to test the hypothesis that the expression of these two proteins will be decreased in germ-free mice compared to conventional mice because of the absence of bacterial fermentation products and that colonization of germ-free mouse colon with conventional bacteria will reverse these changes.
RNA was prepared from the ileum and colon of conventional mice and germ-free mice and used for RT-PCR to determine mRNA levels. Tissue sections were used for immunohistochemical analysis to monitor the expression of GPR109A and SLC5A8 at the protein level. cDNA microarray was used to determine the differential expression of the genes in the colon between conventional mice and germ-free mice.
In conventional mice with normal bacterial colonization of the intestinal tract, GPR109A and SLC5A8 are expressed on the apical membrane of epithelial cells lining the ileum and colon. In germ-free mice, the expression of GPR109A and SLC5A8 is reduced markedly in the ileum and colon. The expression returns to normal levels when the intestinal tract of germ-free mice is colonized with bacteria. The expression of the Na(+)-coupled glucose transporter, SGLT1, follows a similar pattern. Microarray analysis identifies approximately 700 genes whose expression is altered more than twofold in germ-free mice compared to conventional mice. Among these genes are the chloride/bicarbonate exchanger SLC26A3 and the water channel aquaporin 4. The expression of SLC26A3 and AQP4 in ileum and colon is reduced in germ-free mice, but the levels return to normal upon bacterial colonization.
Gut bacteria play an active role in the control of gene expression in the host intestinal tract, promoting the expression of the genes that are obligatory for the biological actions of the bacterial fermentation product butyrate and also the genes that are related to electrolyte and water absorption.
丁酸是一种细菌发酵产物,通过 GPR109A(丁酸受体)和 SLC5A8(丁酸转运体)在结肠中发挥有益作用。在这项研究中,我们比较了常规小鼠和无菌小鼠中 GPR109A 和 SLC5A8 的表达,以检验以下假设:由于缺乏细菌发酵产物,无菌小鼠中这两种蛋白的表达将低于常规小鼠,而用常规细菌定植无菌小鼠结肠可逆转这些变化。
从常规小鼠和无菌小鼠的回肠和结肠中提取 RNA,用于 RT-PCR 以确定 mRNA 水平。使用组织切片进行免疫组织化学分析以监测 GPR109A 和 SLC5A8 在蛋白质水平上的表达。使用 cDNA 微阵列确定常规小鼠和无菌小鼠结肠中基因的差异表达。
在肠道有正常细菌定植的常规小鼠中,GPR109A 和 SLC5A8 表达于回肠和结肠的上皮细胞顶膜。在无菌小鼠中,GPR109A 和 SLC5A8 在回肠和结肠中的表达明显降低。当无菌小鼠的肠道定植细菌时,其表达恢复正常水平。钠依赖性葡萄糖转运体 SGLT1 的表达也呈现相似的模式。微阵列分析确定了约 700 个基因,其在无菌小鼠中的表达与常规小鼠相比改变超过两倍。这些基因包括氯离子/碳酸氢根交换体 SLC26A3 和水通道 Aquaporin 4。SLC26A3 和 AQP4 在回肠和结肠中的表达在无菌小鼠中降低,但在细菌定植后恢复正常。
肠道细菌在宿主肠道基因表达的控制中发挥积极作用,促进了丁酸的生物学作用所必需基因的表达,也促进了与电解质和水吸收相关的基因的表达。