Søndergaard Helle Bach, Brodin Birger, Nielsen Carsten Uhd
Department of Pharmaceutics and Analytical Chemistry, The Faculty of Pharmaceutical Sciences, University of Copenhagen, Universitetsparken 2, Copenhagen, Denmark.
Pflugers Arch. 2008 Jun;456(3):611-22. doi: 10.1007/s00424-007-0421-1. Epub 2007 Dec 20.
The purpose of this work was to investigate the apical uptake and transepithelial transport of Gly-Sar along with the expression of the di-/tripeptide transporters hPEPT1 and hPEPT2 in human Calu-3 bronchial epithelial cells. The apical Gly-Sar uptake rate in Calu-3 cells followed Michaelis-Menten kinetics with a Km value of 1.3 +/- 0.3 mM and a Vmax value of 0.60 +/- 0.06 nmol cm(-2) min(-1). Transepithelial apical to basolateral transport of 50 microM [3H]-labelled Gly-Sar across the Calu-3 cell monolayer was pH-dependent. The Gly-Sar flux was significantly reduced in the presence of delta-aminolevulinic acid (2.5 mM), cephalexin (25 mM), and captopril (25 mM; p < 0.05, n = 3). Reverse transcriptase polymerase chain reaction (RT-PCR) revealed the presence of both hPEPT1 and hPEPT2 mRNA in the Calu-3 cells. These findings were confirmed in healthy human bronchial cDNA. Restriction-endonuclease analysis identified hPEPT2 in Calu-3 cells to be the hPEPT21 haplotype. Western blotting demonstrated expression of the hPEPT1 protein (approximately 80 kDa), and the immunolabel was mainly localized in the apical membrane as judged by immunolocalization studies using confocal laser scanning microscopy (CLSM). This work presents for the first time hPEPT1 and hPEPT21 expression in human Calu-3 cells. Surprisingly, the results indicate that Gly-Sar uptake and transport in Calu-3 cells are hPEPT1-mediated rather than hPEPT2-mediated.
本研究旨在探讨甘氨酰 - 肌氨酸(Gly - Sar)在人Calu - 3支气管上皮细胞中的顶端摄取和跨上皮转运,以及二肽/三肽转运体hPEPT1和hPEPT2的表达情况。Calu - 3细胞中Gly - Sar的顶端摄取速率符合米氏动力学,Km值为1.3±0.3 mM,Vmax值为0.60±0.06 nmol cm(-2) min(-1)。50 μM [3H]标记的Gly - Sar跨Calu - 3细胞单层的顶端到基底外侧的跨上皮转运是pH依赖性的。在存在δ-氨基乙酰丙酸(2.5 mM)、头孢氨苄(25 mM)和卡托普利(25 mM;p < 0.05,n = 3)的情况下,Gly - Sar通量显著降低。逆转录聚合酶链反应(RT - PCR)显示Calu - 3细胞中同时存在hPEPT1和hPEPT2 mRNA。这些发现在健康人支气管cDNA中得到证实。限制性内切酶分析确定Calu - 3细胞中的hPEPT2为hPEPT21单倍型。蛋白质免疫印迹法证实了hPEPT1蛋白(约80 kDa)的表达,通过共聚焦激光扫描显微镜(CLSM)进行的免疫定位研究判断,免疫标记主要定位于顶端膜。本研究首次展示了hPEPT1和hPEPT21在人Calu - 3细胞中的表达。令人惊讶的是,结果表明Calu - 3细胞中Gly - Sar的摄取和转运是由hPEPT1介导的,而非hPEPT2介导。