Cui L, Blanchard R K, Cousins R J
Food Science and Human Nutrition Department and Center for Nutritional Sciences, University of Florida, Gainesville, Florida 32611-0370, USA.
Kidney Int. 2001 Apr;59(4):1424-31. doi: 10.1046/j.1523-1755.2001.0590041424.x.
Zinc deficiency in humans produces a secretory diarrhea that is corrected by zinc supplementation. In rats, differential mRNA display analysis has shown that intestinal uroguanylin gene expression is increased in zinc deficiency. An endocrine axis involving intestinal uroguanylin and the kidney may exist. Therefore, we conducted this study to examine whether zinc deficiency would affect uroguanylin expression in the kidney of rats.
A purified diet, deficient or adequate in zinc content, was fed to rats. Preprouroguanylin mRNA was localized in kidney by in situ hybridization, and prouroguanylin/uroguanylin peptides were localized in the kidney by immunohistochemistry. Abundance was measured by Western blotting and slot blotting analyses.
In situ hybridization demonstrated that preprouroguanylin mRNA-expressing cells were localized in the proximal tubules, being primarily limited to the cortical-medullary junction. Zinc deficiency did not alter the abundance or distribution of the mRNA. Immunohistochemistry, using a uroguanylin peptide-specific, affinity-purified antibody, demonstrated that immunoreactive uroguanylin peptide was localized to the same cells but that the staining was stronger in zinc-deficient rats. Western blotting analysis of kidney extracts showed that there was no difference in abundance of prouroguanylin between zinc adequate and deficient rats. However, slot blotting analysis demonstrated that the abundance of a low molecular weight immunoreactive peptide, presumably uroguanylin, was higher in extracts of zinc-deficient rats.
The results suggest that production of prouroguanylin by the kidney, in contrast to the intestine, is not influenced by dietary zinc intake, but that higher amounts of uroguanylin in kidney extracts may reflect renal processing of the hormone obtained from the systemic circulation.
人体缺锌会导致分泌性腹泻,补锌后可得到纠正。在大鼠中,差异mRNA显示分析表明,缺锌时肠道尿鸟苷素基因表达增加。可能存在一个涉及肠道尿鸟苷素和肾脏的内分泌轴。因此,我们进行了这项研究,以检查缺锌是否会影响大鼠肾脏中尿鸟苷素的表达。
给大鼠喂食锌含量不足或充足的纯化饮食。通过原位杂交将前尿鸟苷素原mRNA定位在肾脏中,通过免疫组织化学将尿鸟苷素原/尿鸟苷素肽定位在肾脏中。通过蛋白质印迹和狭缝印迹分析测量丰度。
原位杂交表明,表达前尿鸟苷素原mRNA的细胞位于近端小管,主要局限于皮质-髓质交界处。缺锌并未改变mRNA的丰度或分布。使用尿鸟苷素肽特异性亲和纯化抗体进行的免疫组织化学表明,免疫反应性尿鸟苷素肽定位于相同的细胞,但在缺锌大鼠中染色更强。对肾脏提取物的蛋白质印迹分析表明,锌充足和缺锌大鼠之间尿鸟苷素原的丰度没有差异。然而,狭缝印迹分析表明,缺锌大鼠提取物中一种低分子量免疫反应性肽(可能是尿鸟苷素)的丰度更高。
结果表明,与肠道不同,肾脏中尿鸟苷素原的产生不受饮食锌摄入量的影响,但肾脏提取物中较高量的尿鸟苷素可能反映了从体循环获得的激素的肾脏加工过程。