Shen H, Smith D E, Yang T, Huang Y G, Schnermann J B, Brosius F C
College of Pharmacy and Upjohn Center for Clinical Pharmacology, Department of Internal Medicine, University of Michigan, Ann Arbor Michigan 48109, USA.
Am J Physiol. 1999 May;276(5):F658-65. doi: 10.1152/ajprenal.1999.276.5.F658.
To determine the renal localization of oligopeptide transporters, Northern blot analyses were performed and polyclonal antisera were generated against PEPT1 and PEPT2, the two cloned rat H+/peptide transporters. Under high-stringency conditions, a 3.0-kb mRNA transcript of rat PEPT1 was expressed primarily in superficial cortex, whereas a 3.5-kb mRNA transcript of PEPT2 was expressed primarily in deep cortex/outer stripe of outer medulla. PEPT1 antisera detected a specific band on immunoblots of renal and intestinal brush-border membrane vesicles (BBMV) with an apparent mobility of approximately 90 kDa. PEPT2 antisera detected a specific broad band of approximately 85 kDa in renal but not in intestinal BBMV. PEPT1 immunolocalization experiments showed detection of a brush border antigen in S1 segments of the proximal tubule and in the brush border of villi from all segments of the small intestine. In contrast, PEPT2 immunolocalization was primarily confined to the brush border of S3 segments of the proximal tubule. All other nephron segments in rat were negative for PEPT1 and PEPT2 staining. Overall, our results conclusively demonstrate that although PEPT1 is expressed in early regions of the proximal tubule (pars convoluta), PEPT2 is specific for the latter regions of proximal tubule (pars recta).
为了确定寡肽转运体的肾脏定位,进行了Northern印迹分析,并制备了针对两种克隆的大鼠H⁺/肽转运体PEPT1和PEPT2的多克隆抗血清。在高严格条件下,大鼠PEPT1的3.0 kb mRNA转录本主要在浅表皮质表达,而PEPT2的3.5 kb mRNA转录本主要在深皮质/外髓质外带表达。PEPT1抗血清在肾脏和肠道刷状缘膜囊泡(BBMV)的免疫印迹上检测到一条特异性条带,其表观迁移率约为90 kDa。PEPT2抗血清在肾脏BBMV中检测到一条约85 kDa的特异性宽带,但在肠道BBMV中未检测到。PEPT1免疫定位实验显示,在近端小管的S1段和小肠各段绒毛的刷状缘检测到一种刷状缘抗原。相比之下,PEPT2免疫定位主要局限于近端小管S3段的刷状缘。大鼠的所有其他肾单位段对PEPT1和PEPT2染色均为阴性。总体而言,我们的结果确凿地表明,虽然PEPT1在近端小管的早期区域(曲部)表达,但PEPT2对近端小管的后期区域(直部)具有特异性。