Skowronski Mariusz T, Lebeck Janne, Rojek Aleksandra, Praetorius Jeppe, Füchtbauer Ernst-Martin, Frøkiaer Jørgen, Nielsen Søren
The Water and Salt Research Center, Institute of Anatomy, University of Aarhus, DK-8000 Aarhus C, Denmark.
Am J Physiol Renal Physiol. 2007 Mar;292(3):F956-65. doi: 10.1152/ajprenal.00314.2006. Epub 2006 Oct 31.
Aquaporin (AQP7) is expressed in proximal tubules and is involved in glycerol uptake. The cellular expression and physiological function in other organs remain largely undefined. AQP7 knockout (KO) mice were generated and used for immunohistochemical analyses to define the organ and cellular expression of AQP7. AQP7 labeling was found in kidney proximal tubule, heart, skeletal muscle, testis, epididymis, as well as in white and brown adipose tissue (WAT and BAT) of wild-type mice. Importantly, immunoreactivity was completely absent from these tissues in AQP7 KO mice. At the cellular level, the capillary endothelium WAT and BAT displayed prominent staining, whereas AQP7 labeling in adipocyte membranes was undetectable. Double-labeling confocal microscopy revealed coexpression of AQP7 with capillary AQP1 but not with adipocyte GLUT4. Moreover, immunoelectron microscopy and RT-PCR of isolated microvessels confirmed the vascular AQP7 expression. Distinct immunolabeling of the capillary endothelium was also observed in both skeletal and heart muscle with no apparent staining of skeletal or cardiac myocytes. As previously reported, specific immunolabeling was confined to brush border in segment 3 renal proximal tubules and to spermatids and spermatozoa in male reproductive tract. The expression of AQP7 was induced up to 2.2-fold in WAT of mice with streptozotocin-induced diabetes mellitus (S-DM) compared with controls and fasting for 72 h (but not 24 h) induced significant increase in AQP7 expression. In conclusion, AQP7 is expressed in capillary endothelia of adipose tissue (and cardiac and striated muscle) and is upregulated in WAT in response to S-DM supporting its role in glycerol metabolism.
水通道蛋白(AQP7)在近端小管中表达,参与甘油摄取。其在其他器官中的细胞表达和生理功能仍 largely 未明确。构建了 AQP7 基因敲除(KO)小鼠,并用于免疫组织化学分析以确定 AQP7 的器官和细胞表达。在野生型小鼠的肾近端小管、心脏、骨骼肌、睾丸、附睾以及白色和棕色脂肪组织(WAT 和 BAT)中发现了 AQP7 标记。重要的是,在 AQP7 KO 小鼠的这些组织中完全没有免疫反应性。在细胞水平上,毛细血管内皮 WAT 和 BAT 显示出明显的染色,而在脂肪细胞膜中未检测到 AQP7 标记。双标记共聚焦显微镜显示 AQP7 与毛细血管 AQP1 共表达,但与脂肪细胞 GLUT4 不共表达。此外,分离微血管的免疫电子显微镜和 RT-PCR 证实了血管 AQP7 的表达。在骨骼肌和心肌中也观察到毛细血管内皮的明显免疫标记,而骨骼肌或心肌细胞没有明显染色。如先前报道,特异性免疫标记局限于肾近端小管 3 段的刷状缘以及雄性生殖道中的精子细胞和精子。与对照组相比,链脲佐菌素诱导的糖尿病(S-DM)小鼠的 WAT 中 AQP7 的表达诱导增加至 2.2 倍,禁食 72 小时(而非 24 小时)诱导 AQP7 表达显著增加。总之,AQP7 在脂肪组织(以及心脏和横纹肌)的毛细血管内皮中表达,并在 WAT 中因 S-DM 而上调,支持其在甘油代谢中的作用。