SIMULTANEOUS IMAGING OF INTRACELLULAR [CA2+] AND PH IN SINGLE MDCK AND GLOMERULAR EPITHELIAL-CELLS

被引:52
作者
WIEGMANN, TB
WELLING, LW
BEATTY, DM
HOWARD, DE
VAMOS, S
MORRIS, SJ
机构
[1] UNIV MISSOURI, SCH BIOL SCI, DIV MOLEC BIOL & BIOCHEM, KANSAS CITY, MO 64110 USA
[2] VET AFFAIRS MED CTR, RENAL SECT, KANSAS CITY, MO 64128 USA
[3] VET AFFAIRS MED CTR, LAB SERV, KANSAS CITY, MO 64128 USA
[4] UNIV KANSAS, MED CTR, DEPT MED, KANSAS CITY, KS 66103 USA
[5] UNIV KANSAS, MED CTR, DEPT PATHOL, KANSAS CITY, KS 66103 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1993年 / 265卷 / 04期
关键词
VIDEO MICROSCOPY; FLUORESCENCE MICROSCOPY; FLUORESCENCE DYES; CELL CULTURE; CALCIUM; MADIN-DARBY CANINE KIDNEY CELLS;
D O I
10.1152/ajpcell.1993.265.4.C1184
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The interrelationships between changes in intracellular calcium concentration ([Ca2+]i) and intracellular pH in Madin-Darby canine kidney cells and kidney glomerular epithelial cells exposed to various stimuli were analyzed simultaneously using a new design of a fluorescence video microscope. Cells were double labeled with indo 1 and SNARF 1 dyes and were excited simultaneously at 350 and 540 nm. Images at four emission wavelengths were captured simultaneously at 405, 475, 575, and 640 nm at 30 frames/s for the two ratio dyes. SNARF sensitivity to pH between 6.5 and 8.0 was unchanged by [Ca2+]i. The SNARF ratio maps were used to correct the pH-dependent changes in the calculation of local cell calcium. NH4Cl loading produced the expected alkalinization and a concurrent rise in [Ca2+]i. When the NH4Cl was removed and the cells became acidic, a second rise in [Ca2+]i was recorded. Both changes in [Ca2+], were from intracellular stores since they persisted in the absence of extracellular calcium. The findings demonstrate the need for pH correction of indo 1 recordings.
引用
收藏
页码:C1184 / C1190
页数:7
相关论文
共 25 条
[1]   DIFFERENTIAL-EFFECTS OF PHORBOL ESTERS ON PGE2 AND BRADYKININ-INDUCED ELEVATION OF [CAI2+] IN MDCK-CELLS [J].
ABOOLIAN, A ;
VANDERMOLEN, M ;
NORD, EP .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (06) :F1135-F1143
[2]  
BUSA WB, 1986, ANNU REV PHYSIOL, V48, P389
[3]   METABOLIC-REGULATION VIA INTRACELLULAR PH [J].
BUSA, WB ;
NUCCITELLI, R .
AMERICAN JOURNAL OF PHYSIOLOGY, 1984, 246 (04) :R409-R438
[4]   ISOPROTERENOL AND CYCLIC-AMP INCREASE INTRACELLULAR FREE [CA] IN MDCK CELLS [J].
CHASE, HS ;
WONG, SME .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 254 (03) :F374-F384
[5]   INTERACTIONS BETWEEN INTRACELLULAR PH AND CALCIUM IN SINGLE-MOUSE NEURO-BLASTOMA (N2A) AND RAT PHEOCHROMOCYTOMA CELLS (PC12) [J].
DICKENS, CJ ;
GILLESPIE, JI ;
GREENWELL, JR .
QUARTERLY JOURNAL OF EXPERIMENTAL PHYSIOLOGY AND COGNATE MEDICAL SCIENCES, 1989, 74 (05) :671-679
[6]  
GEIBEL J, 1992, FASEB J, V6, pA1548
[7]  
HAUGLAND RP, 1992, MOL PROBES HDB FLUOR
[8]   CA-2+ BINDING-KINETICS OF FURA-2 AND AZO-1 FROM TEMPERATURE-JUMP RELAXATION MEASUREMENTS [J].
KAO, JPY ;
TSIEN, RY .
BIOPHYSICAL JOURNAL, 1988, 53 (04) :635-639
[9]   THE EFFECT OF PH ON RATE CONSTANTS, ION SELECTIVITY AND THERMODYNAMIC PROPERTIES OF FLUORESCENT CALCIUM AND MAGNESIUM INDICATORS [J].
LATTANZIO, FA ;
BARTSCHAT, DK .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 177 (01) :184-191
[10]   THE EFFECTS OF PH AND TEMPERATURE ON FLUORESCENT CALCIUM INDICATORS AS DETERMINED WITH CHELEX-100 AND EDTA BUFFER SYSTEMS [J].
LATTANZIO, FA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 171 (01) :102-108