Cai Qi, Dmitrieva Natalia I, Ferraris Joan D, Brooks Heddwen L, van Balkom Bas W M, Burg Maurice
Laboratory of Kidney and Electrolyte Metabolism, National Heart, Lung, and Blood Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MD 20892-1603, USA.
Proc Natl Acad Sci U S A. 2005 Jan 11;102(2):503-8. doi: 10.1073/pnas.0408840102. Epub 2004 Dec 27.
Pax2 is a transcription factor that is crucial for kidney development, and it is also expressed in the normal adult kidney, where its physiological function is unknown. In the present study, we find by cDNA microarray analysis that Pax2 expression in second-passage mouse inner-medullary epithelial cells is increased by a high NaCl concentration, which is significant because NaCl levels are normally high in the inner medulla in vivo, and varies with urinary concentration. Furthermore, a high NaCl concentration increases Pax2 mRNA and protein expression in mouse inner medullary collecting duct (mIMCD3) cells, and its transcriptional activity. Pax2 mRNA and protein expression is high in normal adult mouse renal inner medulla but much lower in renal cortex. Pax2 protein is present in collecting duct cells in both renal medulla and cortex and in thin descending limbs of Henle's loop in inner medulla. Treating Brattleboro rats with desamino-Cys-1,d-Arg-8 vasopressin, which increases inner-medullary NaCl concentration, causes a 4-fold increase in inner-medullary Pax2 protein. Treatment with furosemide, which decreases inner-medullary NaCl, reduces inner-medullary Pax2 mRNA and protein. Pax2-specific short interfering RNA increases high NaCl concentration-induced activation of caspase-3 and apoptotic bodies in mIMCD3 cells. We thus conclude that (i) Pax2 is expressed in normal renal medulla, (ii) its expression is regulated there by the normally high and variable NaCl concentration, and (iii) it protects renal medullary cells from high NaCl concentration-induced apoptosis.
Pax2是一种对肾脏发育至关重要的转录因子,它在正常成年肾脏中也有表达,但其生理功能尚不清楚。在本研究中,我们通过cDNA微阵列分析发现,高浓度氯化钠可使传代培养的小鼠髓质内层上皮细胞中Pax2的表达增加,这一点很重要,因为体内髓质内层的氯化钠水平通常较高,且会随尿液浓缩而变化。此外,高浓度氯化钠可增加小鼠髓质内层集合管(mIMCD3)细胞中Pax2的mRNA和蛋白质表达及其转录活性。Pax2的mRNA和蛋白质表达在正常成年小鼠肾髓质中较高,但在肾皮质中则低得多。Pax2蛋白存在于肾髓质和皮质的集合管细胞以及髓质内层亨氏袢细降支中。用去氨基-Cys-1,d-Arg-8血管加压素治疗Brattleboro大鼠可增加髓质内层氯化钠浓度,导致髓质内层Pax2蛋白增加4倍。用呋塞米治疗可降低髓质内层氯化钠水平,减少髓质内层Pax2的mRNA和蛋白质。Pax2特异性短发夹RNA可增加高浓度氯化钠诱导的mIMCD3细胞中caspase-3的激活和凋亡小体的形成。因此,我们得出结论:(i)Pax2在正常肾髓质中表达;(ii)其表达在那里受正常情况下较高且可变的氯化钠浓度调节;(iii)它可保护肾髓质细胞免受高浓度氯化钠诱导的凋亡。