Embryonic renal collecting duct cell differentiation is influenced in a concentration-dependent manner by the electrolyte environment

被引:5
作者
Schumacher, K
Klotz-Vangerow, S
Tauc, M
Minuth, WW
机构
[1] Univ Regensburg, Dept Anat, D-93053 Regensburg, Germany
[2] Univ Nice, Dept Cellular & Mol Physiol, Nice, France
关键词
renal collecting duct; principal cells; intercalated cells; gradient perfusion culture; electrolyte environment; NaCl load; differentiation;
D O I
10.1159/000046242
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
Background: During kidney development, the embryonic collecting duct (CD) epithelium develops into a heterogeneously composed epithelium consisting of principal and intercalated cells. It is unknown by which molecular mechanism the different cell types arise. We have experimental evidence that the electrolyte environment is involved in the process of terminal cell differentiation. Methods: Embryonic CD epithelia from neonatal rabbit kidneys were microsurgically isolated and maintained in gradient perfusion culture for 13 days under serum-free conditions. Controls were maintained in the same medium (Iscove's modified Dulbecco's medium; IMDM) on basal and luminal sides. Experimental series were performed with IMDM only on the basal side, while on the luminal side IMDM with increasing concentrations of NaCl was used. Finally, the development of principal and intercalated cell features was registered by immunohistochemical labeling with markers specific for adult CD cells. Results: Immunohistochemical markers show that the differentiation pattern is quite different when the embryonic CD epithelia are cultured in IMDM only as compared with specimens kept in IMDM supplemented with 3-24 mmol/l NaCl on the luminal cell side. First signs of changes in development were seen when low doses of 3-6 mmol/l NaCl were added. Conclusions: We conclude that facultative protein expression in embryonic CD epithelium is influenced by the electrolyte environment and starts to be upregulated after administration of unexpectedly low doses of 3-6 mmol/l NaCl added to the luminal perfusion culture medium and increases in a concentration-dependent manner. Copyright (C) 2001 S.KargerAG, Basel.
引用
收藏
页码:165 / 175
页数:11
相关论文
共 48 条
[31]  
Norman JT, 1999, EXP NEPHROL, V7, P463
[32]   Hyperosmolality stimulates Na-K-ATPase gene expression in inner medullary collecting duct cells [J].
Ohtaka, A ;
Muto, S ;
Nemoto, J ;
Kawakami, K ;
Nagano, K ;
Asano, Y .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1996, 270 (05) :F728-F738
[33]   Differential expression of Na+-K+-ATPase, ankyrin, fodrin, and E-cadherin along the kidney nephron [J].
Piepenhagen, PA ;
Peters, LL ;
Lux, SE ;
Nelson, WJ .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1995, 269 (06) :C1417-C1432
[34]  
PLUSKAL MG, 1986, BIOTECHNIQUES, V4, P272
[35]   MORPHOLOGICAL HETEROGENEITY OF THE RABBIT COLLECTING DUCT [J].
RIDDERSTRALE, Y ;
KASHGARIAN, M ;
KOEPPEN, B ;
GIEBISCH, G ;
STETSON, D ;
ARDITO, T ;
STANTON, B .
KIDNEY INTERNATIONAL, 1988, 34 (05) :655-670
[36]  
Sabolic I, 1999, J AM SOC NEPHROL, V10, P913
[37]   POSTNATAL MATURATION OF RABBIT RENAL COLLECTING DUCT .3. PEANUT LECTIN-BINDING INTERCALATED CELLS [J].
SATLIN, LM ;
MATSUMOTO, T ;
SCHWARTZ, GJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (02) :F199-F208
[38]  
SAXEN L, 1992, DEV CELL BIOL SERIES, V19, P13
[39]   Low Na+ diet inhibits Na+ and water transport response to vasopressin in rat cortical collecting duct [J].
Schafer, JA ;
Chen, L ;
Corbitt, BD .
KIDNEY INTERNATIONAL, 1998, 54 (01) :180-187
[40]  
Schumacher K, 1999, IN VITRO CELL DEV-AN, V35, P465