INDUCTION OF RESISTANCE TO MINERALOCORTICOID HORMONE IN CULTURED INNER MEDULLARY COLLECTING DUCT CELLS BY TGF-BETA-1

被引:30
作者
HUSTED, RF
MATSUSHITA, K
STOKES, JB
机构
[1] UNIV IOWA, COLL MED, DEPT INTERNAL MED, EPITHELIAL TRANSPORT LAB, IOWA CITY, IA 52242 USA
[2] DEPT VET AFFAIRS MED CTR, IOWA CITY, IA 52242 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL FLUID AND ELECTROLYTE PHYSIOLOGY | 1994年 / 267卷 / 05期
关键词
KIDNEY; SODIUM ION TRANSPORT; ALDOSTERONE; TRANSFORMING GROWTH FACTOR-BETA; COLLECTING DUCT;
D O I
10.1152/ajprenal.1994.267.5.F767
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The renal collecting duct is a major target for the mineralocorticoid hormone aldosterone which acts to enhance electrogenic Na+ absorption. The cortical portion of the collecting duct displays a vigorous response to mineralocorticoids administered in vivo. The terminal, or inner medullary portion, does not usually display such a vigorous response; the reason for this difference is unknown. To explore one possible mechanism for this lack of response, we varied the conditions of culturing these cells and determined that serum inhibited the ability of aldosterone to enhance Naf transport. By screening 11 peptides, we found that transforming growth factor (TGF)-beta 1 produced a concentration-dependent inhibition of the action of aldosterone. The action of TGF-beta 1 required at least several hours of incubation. Resistance to the action of aldosterone could be produced by preincubating the monolayers with TGF-beta 1 for a few hours; subsequent exposure to aldosterone for up to 48 h failed to stimulate Na+ transport. TGF-beta 1 did not produce a change in cell morphology or the content of DNA, ATP, or ADP; there was a small reduction in protein content. Pretreatment with cycloheximide failed to reproduce the TGF-beta 1 effect. The induction of resistance to mineralocorticoid hormone may play an important role in modulating the effects of aldosterone on Na+ homeostasis.
引用
收藏
页码:F767 / F775
页数:9
相关论文
共 49 条
[1]   PREPARATION AND PROPERTIES OF PLASMA MEMBRANE AND ENDOPLASMIC RETICULUM FRAGMENTS FROM ISOLATED RAT FAT CELLS [J].
AVRUCH, J ;
WALLACH, DFH .
BIOCHIMICA ET BIOPHYSICA ACTA, 1971, 233 (02) :334-&
[2]   IMMUNOCYTOCHEMICAL LOCALIZATION OF NA+ CHANNELS IN RAT-KIDNEY MEDULLA [J].
BROWN, D ;
SORSCHER, EJ ;
AUSIELLO, DA ;
BENOS, DJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (02) :F366-F369
[3]   TGF-BETA INHIBITS GROWTH FACTOR-INDUCED DNA-SYNTHESIS IN HAMSTER FIBROBLASTS WITHOUT AFFECTING THE EARLY MITOGENIC EVENTS [J].
CHAMBARD, JC ;
POUYSSEGUR, J .
JOURNAL OF CELLULAR PHYSIOLOGY, 1988, 135 (01) :101-107
[4]   DIFFERENCES IN SYNERGISTIC ACTIONS OF VASOPRESSIN AND DEOXYCORTICOSTERONE IN RAT AND RABBIT CCD [J].
CHEN, L ;
WILLIAMS, SK ;
SCHAFER, JA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 259 (01) :F147-F156
[5]   KININ EFFECTS ON ELECTROGENIC ION-TRANSPORT IN PRIMARY CULTURES OF PIG RENAL PAPILLARY COLLECTING TUBULE CELLS [J].
CUTHBERT, AW ;
GEORGE, AM ;
MACVINISH, L .
AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 249 (03) :F439-F447
[6]   MICROPUNCTURE STUDY OF ELECTROLYTE TRANSPORT ACROSS PAPILLARY COLLECTING DUCT OF RAT [J].
DIEZI, J ;
MICHOUD, P ;
ACEVES, J ;
GIEBISCH, G .
AMERICAN JOURNAL OF PHYSIOLOGY, 1973, 224 (03) :623-634
[7]   FORMATION OF 6-KETO-PGF1-ALPHA BY COLLECTING TUBULE CELLS ISOLATED FROM RABBIT RENAL PAPILLAE [J].
GRENIER, FC ;
SMITH, WL .
PROSTAGLANDINS & OTHER LIPID MEDIATORS, 1978, 16 (05) :759-772
[8]   TRANSFORMING GROWTH-FACTOR-BETA-1 REDUCES INFARCT SIZE AFTER EXPERIMENTAL CEREBRAL-ISCHEMIA IN A RABBIT MODEL [J].
GROSS, CE ;
BEDNAR, MM ;
HOWARD, DB ;
SPORN, MB .
STROKE, 1993, 24 (04) :558-562
[9]   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
[10]   CHARACTERISTICS OF PAPILLARY COLLECTING DUCT CELLS IN PRIMARY CULTURE [J].
HUSTED, RF ;
HAYASHI, M ;
STOKES, JB .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (06) :F1160-F1169