FATTY-ACID OXIDATION CAPACITY AND FATTY ACID-BINDING PROTEIN-CONTENT OF DIFFERENT CELL-TYPES ISOLATED FROM RAT-HEART

被引:49
作者
LINSSEN, MCJG [1 ]
VORK, MM [1 ]
DEJONG, YF [1 ]
GLATZ, JFC [1 ]
VANDERVUSSE, GJ [1 ]
机构
[1] STATE UNIV LIMBURG,DEPT MOT SCI,6200 MD MAASTRICHT,NETHERLANDS
关键词
cardiomyocytes; ELISA; endothelial cells; fatty acid oxidation; fatty acid-binding protein; fibroblast-like cells; rat heart;
D O I
10.1007/BF00231363
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Heart tissue contains appreciable amounts of fatty acid-binding protein (FABP). FABP is thought to play a crucial role in the transport of fatty acids from the cellular membrane to the intracellular site of oxidation and also, in case of endothelial cells, in the transfer of fatty acids from the vascular to the interstitial compartment through the endothelial cytoplasm. The present study was designed to delineate a possible quantitative relationship between the capacity of different cell types in the heart to oxidize fatty acids and the presence of FABP. Palmitate oxidation capacity, measured in homogenates of cells isolated from adult rat hearts, was 2 nmol/min per mg tissue protein in freshly isolated cardiomyocytes (CMC), but only 0.09 and 0.31 nmol/min per mg tissue protein in cultivated endothelial (CEC) and fibroblast-like cells (CFLC), respectively. Palmitate oxidation rates were closely related to the cytochrome C oxidase activity and, hence, to the mitochondrial density in the cells under investigation. In CMC the content of cytosolic H-FABP (H-FABPc) was about 4.51 μg/mg tissue protein. However, in CEC and CFLC the FABP content was less than 0.01 and 0.004 μg/mg tissue protein, respectively, corresponding to at maximum 0.2% of the FABP content of CMC. These findings indicate a marked difference between CMC and non-myocytal cells in the heart regarding their capacity to oxidize fatty acids, and a marked disproportion between the fatty acid oxidation capacity and immunochemically determined FABP content in both CEC and CFLC. The functional implication of these observations remains to be elucidated. © 1990 Kluwer Academic Publishers.
引用
收藏
页码:19 / 25
页数:7
相关论文
共 20 条
[1]   THE CELLULAR FATTY-ACID BINDING-PROTEINS - ASPECTS OF STRUCTURE, REGULATION, AND FUNCTION [J].
BASS, NM .
INTERNATIONAL REVIEW OF CYTOLOGY-A SURVEY OF CELL BIOLOGY, 1988, 111 :143-184
[2]  
BASSINGTHWAIGHT.JB, 1989, MOL CELL BIOCHEM, V88, P45
[3]   FATTY ACID-BINDING PROTEINS .10. SUBCELLULAR-DISTRIBUTION OF CARDIAC FATTY ACID-BINDING PROTEIN IN BOVINE HEART-MUSCLE AND QUANTITATION WITH AN ENZYME-LINKED IMMUNOSORBENT-ASSAY [J].
BORCHERS, T ;
UNTERBERG, C ;
RUDEL, H ;
ROBENEK, H ;
SPENER, F .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 1002 (01) :54-61
[4]   MEASUREMENT OF RAT-HEART FATTY-ACID BINDING-PROTEIN BY ELISA - TISSUE DISTRIBUTION, DEVELOPMENTAL-CHANGES AND SUBCELLULAR-DISTRIBUTION [J].
CRISMAN, TS ;
CLAFFEY, KP ;
SAOUAF, R ;
HANSPAL, J ;
BRECHER, P .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1987, 19 (05) :423-431
[5]   RAT HEART-DERIVED ENDOTHELIAL AND SMOOTH-MUSCLE CELL-CULTURES - ISOLATION, CLONING AND CHARACTERIZATION [J].
DIGLIO, CA ;
GRAMMAS, P ;
GIACOMELLI, F ;
WIENER, J .
TISSUE & CELL, 1988, 20 (04) :477-492
[6]   CONTROL OF ENERGY-PRODUCTION IN THE HEART - A NEW FUNCTION FOR FATTY-ACID BINDING-PROTEIN [J].
FOURNIER, NC ;
RAHIM, M .
BIOCHEMISTRY, 1985, 24 (09) :2387-2396
[7]  
GLATZ JFC, 1984, J BIOL CHEM, V259, P4295
[8]   INTRACELLULAR-TRANSPORT OF LIPIDS [J].
GLATZ, JFC ;
VANDERVUSSE, GJ .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1989, 88 (1-2) :37-44
[9]   POSTNATAL-DEVELOPMENT OF PALMITATE OXIDATION AND MITOCHONDRIAL ENZYME-ACTIVITIES IN RAT CARDIAC AND SKELETAL-MUSCLE [J].
GLATZ, JFC ;
VEERKAMP, JH .
BIOCHIMICA ET BIOPHYSICA ACTA, 1982, 711 (02) :327-335
[10]   ANALYSIS OF MUSCLE MITOCHONDRIAL-FUNCTION WITH TECHNIQUES APPLICABLE TO NEEDLE-BIOPSY SAMPLES [J].
GOHIL, K ;
JONES, DA ;
EDWARDS, RHT .
CLINICAL PHYSIOLOGY, 1981, 1 (02) :195-207