AN OSMOTICALLY TOLERANT INNER MEDULLARY COLLECTING DUCT CELL-LINE FROM AN SV40 TRANSGENIC MOUSE

被引:272
作者
RAUCHMAN, MI [1 ]
NIGAM, SK [1 ]
DELPIRE, E [1 ]
GULLANS, SR [1 ]
机构
[1] HARVARD UNIV, SCH MED, HARVARD CTR STUDY KIDNEY DIS, BOSTON, MA 02115 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1993年 / 265卷 / 03期
关键词
HYPEROSMOTIC STRESS; ORGANIC OSMOLYTES; SODIUM CHANNEL; ATRIAL NATRIURETIC PEPTIDE; RENAL MEDULLA; DEXAMETHASONE; ZO-1; DESMOPLAKIN;
D O I
10.1152/ajprenal.1993.265.3.F416
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The terminal inner medullary collecting duct (IMCD) plays an important role in determining the final urinary composition. Currently, there is no continuous cell line derived from this nephron segment. We have developed a cell line derived from the terminal IMCD of mice transgenic for the early region of simian virus SV40 (large T antigen). This cell line, mIMCD-3, retains many differentiated characteristics of this nephron segment including high transepithelial resistance (1,368 +/- 172 OMEGA.cm2), inhibition of apical-to-basal sodium flux by amiloride (41 +/- 7%) and by atrial natriuretic peptide (ANP) (40 +/- 9%), the presence of the amiloride-sensitive sodium channel as determined by Western blot analysis, and accumulation of the major organic osmolytes in response to hypertonic stress. Significantly, mIMCD-3 cells adapted readily and were able to grow in hypertonic medium supplemented with NaCl and urea up to 910 mosmol/kgH2O. These extreme osmotic conditions exist in the renal medulla in vivo but are known to be lethal to most other cells. This cell line should be highly useful for the study of the cellular adaptation to osmotic stress and the cell biology and transport physiology of this nephron segment.
引用
收藏
页码:F416 / F424
页数:9
相关论文
共 38 条
[1]   ADENOSINE-SENSITIVE PHOSPHOINOSITIDE TURNOVER IN A NEWLY ESTABLISHED RENAL-CELL LINE [J].
AREND, LJ ;
HANDLER, JS ;
RHIM, JS ;
GUSOVSKY, F ;
SPIELMAN, WS .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (06) :F1067-F1074
[2]  
BEUTLER HO, 1974, METHOD ENZYMAT AN, P1708
[3]  
FAUTH C, 1991, RENAL PHYSIOL BIOCH, V14, P128
[4]   TUBULAR SITE(S) OF ACTION OF ATRIAL NATRIURETIC PEPTIDE IN THE RAT [J].
FRIED, TA ;
OSGOOD, RW ;
STEIN, JH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (02) :F313-F316
[5]  
GSTRAUNTHALER GJA, 1988, RENAL PHYSIOL BIOCH, V11, P1
[6]   ACCUMULATION OF MAJOR ORGANIC OSMOLYTES IN RAT RENAL INNER MEDULLA IN DEHYDRATION [J].
GULLANS, SR ;
BLUMENFELD, JD ;
BALSCHI, JA ;
KALETA, M ;
BRENNER, RM ;
HEILIG, CW ;
HEBERT, SC .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (04) :F626-F634
[7]   THE MDCK EPITHELIAL-CELL LINE EXPRESSES A CELL-SURFACE ANTIGEN OF THE KIDNEY DISTAL TUBULE [J].
HERZLINGER, DA ;
EASTON, TG ;
OJAKIAN, GK .
JOURNAL OF CELL BIOLOGY, 1982, 93 (02) :269-277
[8]   ENHANCEMENT OF ELECTROGENIC NA+ TRANSPORT ACROSS RAT INNER MEDULLARY COLLECTING DUCT BY GLUCOCORTICOID AND BY MINERALOCORTICOID HORMONES [J].
HUSTED, RF ;
LAPLACE, JR ;
STOKES, JB .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (02) :498-506
[9]   A SPECTROSCOPIC METHOD FOR ASSESSING CONFLUENCE OF EPITHELIAL-CELL CULTURES [J].
JOVOV, B ;
WILLS, NK ;
LEWIS, SA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (06) :C1196-C1203
[10]  
KELLEY KA, 1991, J AM SOC NEPHROL, V2, P84