Changes of cell volume and nitric oxide concentration in macula densa cells caused by changes in luminal NaCl concentration

被引:56
作者
Liu, RS [1 ]
Pittner, J [1 ]
Persson, AEG [1 ]
机构
[1] Uppsala Univ, Dept Med Cell Biol, S-75123 Uppsala, Sweden
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2002年 / 13卷 / 11期
关键词
D O I
10.1097/01.ASN.0000033275.17169.67
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The luminal NaCl concentration ([NaCl]) at the macula densa (MD) controls both tubuloglomerular feedback (TGF) and renin release. Nitric oxide (NO) inhibits TGF sensitivity to a great extent. The NO concentration in the MD cells is not known. This study measured this concentration in MD cells with confocal microscopy in the isolated perfused thick ascending limb using a NO-sensitive fluorophore 4,5-diaminofluorescein (DAF-2). Calcein was used to measure cell volume changes. The loop perfusion fluid was a modified Ringer solution containing 10, 35, or 135 mM NaCl with a constant total osmolarity (290 mOsm), and the bath was perfused with the 135 mM NaCl solution. The results show that MD cell volume and NO concentration measured with DAF-2 DA increased considerably with increasing luminal [NaCl] and with calcium-free solutions in the lumen and bath. L-arginine (5 mM) increased NO concentration in the MD cells by 30%. 7-nitroindazole could totally inhibit the NO production caused by L-arginine and by increased luminal [NaCl]. In conclusion, the MD cell volume changes caused by the changes of luminal [NaCl] were quantitatively measured, and it was found that increasing the luminal [NaCl] resulted in an increase in cell volume. It was also found that NO formation in MD cells could be measured with DAF-2 and that NO production was increased through neuronal NO synthase activation with an increased luminal [NaCl]. An increased NO production will inhibit the vasoconstriction induced by the TGF and at the same time will reduce TGF sensitivity.
引用
收藏
页码:2688 / 2696
页数:9
相关论文
共 43 条
[21]  
2-G
[22]   Direct evidence of nitric oxide production from bovine aortic endothelial cells using new fluorescence indicators: diaminofluoresceins [J].
Nakatsubo, N ;
Kojima, H ;
Kikuchi, K ;
Nagoshi, H ;
Hirata, Y ;
Maeda, D ;
Imai, Y ;
Irimura, T ;
Nagano, T .
FEBS LETTERS, 1998, 427 (02) :263-266
[23]   Expression of the Na-K-2Cl cotransporter by macula densa and thick ascending limb cells of rat and rabbit nephron [J].
Obermuller, N ;
Kunchaparty, S ;
Ellison, DH ;
Bachmann, S .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (03) :635-640
[24]   Cytosolic [Ca2+] signaling pathway in macula densa cells [J].
Peti-Peterdi, J ;
Bell, PD .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1999, 277 (03) :F472-F476
[25]   Regulation of macula densa Na:H exchange by angiotensin II [J].
Peti-Peterdi, J ;
Bell, PD .
KIDNEY INTERNATIONAL, 1998, 54 (06) :2021-2028
[26]   Role of macula densa nitric oxide and cGMP in the regulation of tubuloglomerular feedback [J].
Ren, YL ;
Garvin, JL ;
Carretero, OA .
KIDNEY INTERNATIONAL, 2000, 58 (05) :2053-2060
[27]   INTRACELLULAR CYTOSOLIC FREE CALCIUM-CONCENTRATION IN THE MACULA DENSA AND IN ASCENDING LIMB CELLS AT DIFFERENT LUMINAL CONCENTRATIONS OF SODIUM-CHLORIDE AND WITH ADDED FUROSEMIDE [J].
SALOMONSSON, M ;
GONZALEZ, E ;
WESTERLUND, P ;
PERSSON, AEG .
ACTA PHYSIOLOGICA SCANDINAVICA, 1991, 142 (02) :283-290
[28]   Dynamic regulation of neuronal NO synthase transcription by calcium influx through a CREB family transcription factor-dependent mechanism [J].
Sasaki, M ;
Gonzalez-Zulueta, M ;
Huang, H ;
Herring, WJ ;
Ahn, SY ;
Ginty, DD ;
Dawson, VL ;
Dawson, TM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (15) :8617-8622
[29]   MACULA DENSA CELLS SENSE LUMINAL NACL CONCENTRATION VIA FUROSEMIDE SENSITIVE NA+2CL-K+ COTRANSPORT [J].
SCHLATTER, E ;
SALOMONSSON, M ;
PERSSON, AEG ;
GREGER, R .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1989, 414 (03) :286-290
[30]   ADAPTATION TO INCREASED DIETARY SALT INTAKE IN THE RAT - ROLE OF ENDOGENOUS NITRIC-OXIDE [J].
SHULTZ, PJ ;
TOLINS, JP .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (02) :642-650