DISTURBED INTRACELLULAR CALCIUM-RELATED PROCESSES OF HEPATOCYTES AND NEUTROPHILS IN HUMAN ALCOHOLIC LIVER-DISEASE

被引:7
作者
BAFFY, G
VARGA, Z
FORIS, G
LEOVEY, A
机构
[1] First Department of Medicine, University Medical School, Debrecen
关键词
alcoholic liver disease; ATPase; calcium efflux; intracellular free calcium; isolated human hepatocytes;
D O I
10.1016/0009-9120(90)90692-N
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Isolated human hepatocytes and separated neutrophils of 11 patients with alcoholic liver disease (ALD) were used to study some aspects of cellular calcium-related processes compared to nonalcoholic controls. 45Ca2+ efflux from the cells decreased in ALD and the calmodulin-inhibitor trifluoperazine did not influence it further. The intracellular free calcium concentration ([Ca2+]l) of nonstimulated hepatocytes and neutrophils proved to be higher in ALD with the Quin2/AM loading technique. However, the [Ca2+]l rise in hepatocytes and neutrophils, with stimulation by low density lipoprotein (LDL) and N-formyl-methionyl-leucyl phenylalanine (FMLP), respectively, was diminished in ALD compared to appropriate controls. The slower 45Ca2+ extrusion rate, higher basal [Ca2+]l levels, and the diminished [Ca2+]l elevation of activated hepatocytes and neutrophils, suggest disturbed calcium-related intracellular processes in ALD, in particular, impaired regulation of the plasma membrane Ca2+-ATPase. © 1990 The Canadian Society of Clinical Chemists.
引用
收藏
页码:241 / 245
页数:5
相关论文
共 32 条
[1]   CHEMOTACTIC PEPTIDE, CALCIUM AND GUANINE-NUCLEOTIDE REGULATION OF PHOSPHOLIPASE-C ACTIVITY IN MEMBRANES FROM DMSO-DIFFERENTIATED HL60 CELLS [J].
ANTHES, JC ;
BILLAH, MM ;
CALI, A ;
EGAN, RW ;
SIEGEL, MI .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1987, 145 (02) :825-833
[2]   INOSITOL TRISPHOSPHATE AND DIACYLGLYCEROL AS 2ND MESSENGERS [J].
BERRIDGE, MJ .
BIOCHEMICAL JOURNAL, 1984, 220 (02) :345-360
[3]   ARACHIDONIC-ACID METABOLITES AS 2ND MESSENGERS [J].
BEVAN, S ;
WOOD, JN .
NATURE, 1987, 328 (6125) :20-20
[4]   LOW-DENSITY LIPOPROTEIN - AN OLD SUBSTANCE WITH A NEW FUNCTION [J].
BLOCK, LH ;
PLETSCHER, A .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1988, 9 (06) :214-216
[5]   LOW-DENSITY LIPOPROTEIN CAUSES GENERAL CELLULAR ACTIVATION WITH INCREASED PHOSPHATIDYLINOSITOL TURNOVER AND LIPOPROTEIN CATABOLISM [J].
BLOCK, LH ;
KNORR, M ;
VOGT, E ;
LOCHER, R ;
VETTER, W ;
GROSCURTH, P ;
QIAO, BY ;
POMETTA, D ;
JAMES, R ;
REGENASS, M ;
PLETSCHER, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (03) :885-889
[6]  
BOYUM A, 1968, SCAND J CLIN LAB INV, VS 21, P77
[7]   PERTUSSIS TOXIN INHIBITS CHEMOTACTIC PEPTIDE-STIMULATED GENERATION OF INOSITOL PHOSPHATES AND LYSOSOMAL-ENZYME SECRETION IN HUMAN-LEUKEMIC (HL-60) CELLS [J].
BRANDT, SJ ;
DOUGHERTY, RW ;
LAPETINA, EG ;
NIEDEL, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (10) :3277-3280
[8]   BREAKDOWN AND SYNTHESIS OF POLYPHOSPHOINOSITIDES IN FMETLEUPHE-STIMULATED NEUTROPHILS [J].
COCKCROFT, S ;
BARROWMAN, MM ;
GOMPERTS, BD .
FEBS LETTERS, 1985, 181 (02) :259-263
[9]   STUDIES ON CHARACTERIZATION OF HUMAN SERUM LIPOPROTEINS SEPARATED BY ULTRACENTRIFUGATION IN A DENSITY GRADIENT .2. SERUM LIPOPROTEINS IN HYPERLIPEMIC SUBJECTS [J].
CORNWELL, DG ;
HAMWI, GJ ;
BROWN, JB ;
KRUGER, FA .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1961, 9 (01) :41-&
[10]  
DRAZNIN B, 1987, J BIOL CHEM, V262, P14385