Absence of aquaporin-4 water channels from kidneys of the desert rodent Dipodomys merriami merriami

被引:34
作者
Huang, Y
Tracy, R
Walsberg, GE
Makkinje, A
Fang, P
Brown, D
Van Hoek, AN
机构
[1] Massachusetts Gen Hosp, Renal Unit, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Program Membrane Biol, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Boston, MA 02114 USA
[4] Arizona State Univ, Dept Biol, Tempe, AZ 85287 USA
[5] Massachusetts Gen Hosp, Diabet Unit, Charlestown, MA 02129 USA
[6] Harvard Univ, Sch Med, Charlestown, MA 02129 USA
关键词
freeze fracture electron microscopy; immunocytochemistry; Merriam's kangaroo rat; in situ hybridization;
D O I
10.1152/ajprenal.2001.280.5.F794
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Recently, we found that aquaporin-4 (AQP4) is expressed in the S3 segment of renal proximal tubules of mice but not in rat proximal tubules. Because mice have relatively larger papillae than rats, it was proposed that the renal distribution of AQP4 in various species could be related to their maximum urinary concentrating ability. Therefore, kidneys and other tissues of Merriam's desert kangaroo rat, Dipodomys merriami merriami, which produce extremely concentrated urine (up to 5,000 mosmol/kgH(2)O), were examined for AQP4 expression and localization. Contrary to our expectation, AQP4 immunostaining was undetectable in any region of the kidney, and the absence of AQP4 protein was confirmed by Western blotting. By freeze fracture electron microscopy, orthogonal arrays of intramembraneous particles (OAPs) were not detectable in plasma membranes of principal cells and proximal tubules. However, AQP4 protein was readily detectable in gastric parietal and brain astroglial cells. Northern blotting failed to detect AQP4 mRNA in kangaroo rat kidneys, whereas both in situ hybridization and RT-PCR experiments did reveal AQP4 mRNA in collecting ducts and proximal tubules of the S3 segment. These results suggest that renal expression of AQP4 in the kangaroo rat kidney is regulated at the transcriptional or translational level, and the absence of AQP4 may be critical for the extreme urinary concentration that occurs in this species.
引用
收藏
页码:F794 / F802
页数:9
相关论文
共 33 条
[21]  
Nielsen S, 1999, J AM SOC NEPHROL, V10, P647
[22]   LOCALIZATION OF THE CHIP28 WATER CHANNEL IN RAT-KIDNEY [J].
SABOLIC, I ;
VALENTI, G ;
VERBAVATZ, JM ;
VANHOEK, AN ;
VERKMAN, AS ;
AUSIELLO, DA ;
BROWN, D .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (06) :C1225-C1233
[23]  
Sambrook J., 1989, MOL CLONING
[24]   Molecular characterization of a broad selectivity neutral solute channel [J].
Tsukaguchi, H ;
Shayakul, C ;
Berger, UV ;
Mackenzie, B ;
Devidas, S ;
Guggino, WB ;
van Hoek, AN ;
Hediger, MA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (38) :24737-24743
[25]   The role of the 5′ untranslated region of an mRNA in translation regulation during development [J].
van der Velden, AW ;
Thomas, AAM .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 1999, 31 (01) :87-106
[26]   Aquaporin-4 is expressed in basolateral membranes of proximal tubule S3 segments in mouse kidney [J].
Van Hoek, AN ;
Ma, TH ;
Yang, BX ;
Verkman, AS ;
Brown, D .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2000, 278 (02) :F310-F316
[27]  
Verbavatz JM, 1997, J CELL SCI, V110, P2855
[28]  
Verkman AS, 1999, J AM SOC NEPHROL, V10, P1126
[29]   Aquaporins in the kidney: Emerging new aspects [J].
Yamamoto, T ;
Sasaki, S .
KIDNEY INTERNATIONAL, 1998, 54 (04) :1041-1051
[30]  
Yang BX, 1996, J BIOL CHEM, V271, P4577