Department of Anatomy, Cell Death Disease Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Histol Histopathol. 2010 Jan;25(1):33-44. doi: 10.14670/HH-25.33.
Organic anion transporter 1 (OAT1) and OAT3 in the proximal tubules (PT) of the kidney play important roles in the elimination of harmful endogenous compounds and xenobiotics from the body. We investigated the temporal and spatial expression of OAT1 and OAT3 in the differentiating PT in mouse kidney. Ontogenic expression of OAT1 and OAT3 was investigated by immunohistochemical analysis. The S1, S2, and S3 segments of the PT were identified using antibodies to aquaporin 1 (AQP1), Na+-HCO3- cotransporter 1 (kNBC1), and AQP4. OAT1 immunoreactivity was first detected at PT in the inner cortex of 15-day-old fetuses (F15) and in the outer cortex of 7-day old pups. OAT3 was first observed in the distal tubule of F14 and in S2 segment of the PT of F16 and in S1 and S3 segments around the time of birth; expression increased through postpartum day 21. The ontogenic pattern of expression of OAT1 and OAT3 in the differentiating PT suggests that both transporters may function in the S2 segment in the fetus, but not until after birth in S1 and S3 segments.
有机阴离子转运体 1(OAT1)和 OAT3 在肾脏近端小管(PT)中发挥重要作用,可将体内有害的内源性化合物和外源性物质排出体外。我们研究了 OAT1 和 OAT3 在分化中的 PT 中的时空表达。通过免疫组织化学分析研究了 OAT1 和 OAT3 的个体发生表达。使用水通道蛋白 1(AQP1)、Na+-HCO3-共转运蛋白 1(kNBC1)和 AQP4 的抗体鉴定 PT 的 S1、S2 和 S3 节段。OAT1 免疫反应性首先在 15 天龄胎儿(F15)的内皮层和 7 天龄幼崽的外皮层中的 PT 中检测到。OAT3 首先在 F14 的远曲小管和 F16 的 PT 的 S2 节段以及出生时的 S1 和 S3 节段中观察到;表达在产后第 21 天增加。分化中的 PT 中 OAT1 和 OAT3 的个体发生表达模式表明,这两种转运体都可能在胎儿的 S2 节段中发挥作用,但直到出生后 S1 和 S3 节段才起作用。