Excretion of urinary exosomal AQP2 in rats is regulated by vasopressin and urinary pH

被引:31
作者
Higashijima, Yoshiki [1 ]
Sonoda, Hiroko [1 ]
Takahashi, Saki [1 ]
Kondo, Hiroaki [1 ]
Shigemura, Kanako [1 ]
Ikeda, Masahiro [1 ]
机构
[1] Miyazaki Univ, Dept Vet Pharmacol, Miyazaki 8892192, Japan
基金
日本学术振兴会;
关键词
exosomes; aquaporin-2; vasopressin; urine alkalinization; NEPHROGENIC DIABETES-INSIPIDUS; COLLECTING DUCT CELLS; WATER CHANNEL; AQUAPORIN-2; EXPRESSION; KIDNEY; BIOMARKERS; MARKER; TRAFFICKING; PROTEOMICS; PROSTASIN;
D O I
10.1152/ajprenal.00249.2013
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Excretion of urinary exosomal AQP2 in rats is regulated by vasopressin and urinary pH. Am J Physiol Renal Physiol 305: F1412-F1421, 2013. First published August 28, 2103; doi:10.1152/ajprenal.00249.2013.-Urinary exosomes are small vesicles secreted into urine from all renal epithelial cell types and known to contain proteins that are involved in renal secretion and reabsorption. Among these proteins, urinary exosomal aquaporin-2 (AQP2) has been suggested to be useful for diagnosis of renal disease. However, the mechanisms underlying the excretion of urinary exosomal AQP2 are largely unknown. In this study, we examined the mechanisms of urinary exosomal AQP2 excretion in vivo, using diuretics including furosemide (FS), an inhibitor of the sodium-potassium-chloride symporter; acetazolamide (ACTZ), an inhibitor of carbonic anhydrase; OPC-31260 (OPC), a vasopressin type 2 receptor antagonist; and NaHCO3, a urinary alkalizing agent. Samples of urine from rats were collected for 2 h just after treatment with each diuretic, and urinary exosomes were isolated by ultracentrifugation. Urinary exosomal AQP2 excretion was dramatically increased by treatment with FS accompanied by urine acidification or with ACTZ accompanied by urine alkalization. Immunohistochemistry showed that apical localization of AQP2 was clearly evident and the plasma vasopressin level was increased after each treatment. Although treatment with OPC alone had no significant effect, coadministration of OPC completely inhibited the FS-induced and partially reduced the ACTZ-induced responses, respectively. Treatment with NaHCO3 increased the excretion of urinary exosomal AQP2 accompanied by urine alkalization. This increased response was partially inhibited by coadministration of OPC. These data suggest that an increased plasma level of vasopressin promoted the excretion of urinary exosomal AQP2 and that urine alkalinization also increased it independently of vasopressin.
引用
收藏
页码:F1412 / F1421
页数:10
相关论文
共 46 条
  • [1] Downregulation of renal AQP2 water channel and NKCC2 in mice lacking the apical Na+-H+ exchanger NHE3
    Amlal, H
    Ledoussal, C
    Sheriff, S
    Shull, GE
    Soleimani, M
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 2003, 553 (02): : 511 - 522
  • [2] Amlal H, 2001, AM J PHYSIOL-RENAL, V280, pF531
  • [3] Calcitonin Has a Vasopressin-like Effect on Aquaporin-2 Trafficking and Urinary Concentration
    Bouley, Richard
    Lu, Hua A. J.
    Nunes, Paula
    Da Silva, Nicolas
    McLaughlin, Margaret
    Chen, Ying
    Brown, Dennis
    [J]. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2011, 22 (01): : 59 - 72
  • [4] Exosomes/microvesicles as a mechanism of cell-to-cell communication
    Camussi, Giovanni
    Deregibus, Maria C.
    Bruno, Stefania
    Cantaluppi, Vincenzo
    Biancone, Luigi
    [J]. KIDNEY INTERNATIONAL, 2010, 78 (09) : 838 - 848
  • [5] Renal tubular dysfunction in patients with American cutaneous leishmaniasis
    de Oliveira, Rodrigo A.
    Diniz, Lucyo F. B.
    Teotonio, Leonardo O.
    Lima, Claudio G.
    Mota, Rosa M. S.
    Martins, Alice
    Sanches, Talita R.
    Seguro, Antonio C.
    Andrade, Lucia
    Silva, Geraldo B.
    Liborio, Alexandre B.
    Daher, Elizabeth F.
    [J]. KIDNEY INTERNATIONAL, 2011, 80 (10) : 1099 - 1106
  • [6] Deen PMT, 1996, J AM SOC NEPHROL, V7, P836
  • [7] REGULATION OF COLLECTING DUCT WATER CHANNEL EXPRESSION BY VASOPRESSIN IN BRATTLEBORO RAT
    DIGIOVANNI, SR
    NIELSEN, S
    CHRISTENSEN, EI
    KNEPPER, MA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (19) : 8984 - 8988
  • [8] Elliot S, 1996, J AM SOC NEPHROL, V7, P403
  • [9] Are Sodium Transporters in Urinary Exosomes Reliable Markers of Tubular Sodium Reabsorption in Hypertensive Patients?
    Esteva-Font, Cristina
    Wang, Xiaoyan
    Ars, Elisabet
    Guillen-Gomez, Elena
    Sans, Laia
    Gonzalez Saavedra, Isabel
    Torres, Ferran
    Torra, Roser
    Masilamani, Shyama
    Aurelio Ballarin, Jose
    Fernandez-Llama, Patricia
    [J]. NEPHRON PHYSIOLOGY, 2010, 114 (03): : P25 - P34
  • [10] Large-Scale Proteomics and Phosphoproteomics of Urinary Exosomes
    Gonzales, Patricia A.
    Pisitkun, Trairak
    Hoffert, Jason D.
    Tchapyjnikov, Dmitry
    Star, Robert A.
    Kleta, Robert
    Wang, Nam Sun
    Knepper, Mark A.
    [J]. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2009, 20 (02): : 363 - 379