Elevated DNase I levels in human idiopathic dilated cardiomyopathy: An indicator of apoptosis?

被引:52
作者
Yao, M
Keogh, A
Spratt, P
dosRemedios, G
Kiessling, PC
机构
[1] UNIV SYDNEY, DEPT ANAT & HISTOL, MUSCLE RES UNIT, SYDNEY, NSW 2006, AUSTRALIA
[2] ST VINCENTS HOSP, HEART & LUNG TRANSPLANT UNIT, DARLINGHURST, NSW 2010, AUSTRALIA
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
dilated cardiomyopathy; deoxyribonuclease I; deoxyribonucleic acid; apoptosis; zymogram;
D O I
10.1006/jmcc.1996.0009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This is the first report to determine deoxyribonuclease I (DNase I) levels in the human myocardium and the first to demonstrate an increased DNase I level associated with end-stage heart failure due to idiopathic dilated cardiomyopathy (IDCM) compared to non-diseased heart samples. Left ventricular samples were obtained following transplantation from failing hearts of 13 patients diagnosed with IDCM and from four unused donor hearts. Using a zymogram technique, we show that the DNase I levels of the 1DCM heart samples were significantly elevated (range 0.65-2.75 pg DNase I/mu g protein, mean+/-S.E. of 1.69+/-0.22 pg/mu g) compared to four nondiseased, donor heart samples (range 0.12-0.35 pg/mu g protein, mean+/-S.E. of 0.22+/-0.05 pg/mu g). The DNase I extracted from heart tissue was characterized by: (1) a co-migration with bovine pancreatic DNase I; (2) a pH dependence consistent with DNase I; (3) a dependence of its activity on both Ca2+ and Mg2+ and an inhibition by Zn2+; and (4) an inhibition of its activity in the presence of monomeric rabbit skeletal muscle actin. The elevated DNase I levels associated with heart failure due to IDCM suggests that apoptosis may be implicated in pathophysiology of this disorder. (C) 1996 Academic Press Limited
引用
收藏
页码:95 / 101
页数:7
相关论文
共 16 条
[1]   STUDIES ON ACID DEOXYRIBONUCLEASE .2. ISOLATION + CHARACTERIZATION OF SPLEEN-ACID DEOXYRIBONUCLEASE [J].
BERNARDI, G ;
GRIFFE, M .
BIOCHEMISTRY, 1964, 3 (10) :1419-&
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]   APOPTOSIS AND DISEASE [J].
CARSON, DA ;
RIBEIRO, JM .
LANCET, 1993, 341 (8855) :1251-1254
[4]   IDIOPATHIC DILATED CARDIOMYOPATHY [J].
DEC, GW ;
FUSTER, V .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (23) :1564-1575
[5]   CA2+/MG2+-DEPENDENT NUCLEASE - TISSUE DISTRIBUTION, RELATIONSHIP TO INTER-NUCLEOSOMAL DNA FRAGMENTATION AND INHIBITION BY ZN2+ [J].
GIANNAKIS, C ;
FORBES, IJ ;
ZALEWSKI, PD .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 181 (02) :915-920
[6]   REPERFUSION INJURY INDUCES APOPTOSIS IN RABBIT CARDIOMYOCYTES [J].
GOTTLIEB, RA ;
BURLESON, KO ;
KLONER, RA ;
BABIOR, BM ;
ENGLER, RL .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (04) :1621-1628
[7]  
JAMES TN, 1993, J LAB CLIN MED, V122, P309
[8]   NORMAL AND ABNORMAL CONSEQUENCES OF APOPTOSIS IN THE HUMAN HEART - FROM POSTNATAL MORPHOGENESIS TO PAROXYSMAL ARRHYTHMIAS [J].
JAMES, TN .
CIRCULATION, 1994, 90 (01) :556-573
[9]   ISOLATION, CHARACTERIZATION AND CRYSTALLIZATION OF DEOXYRIBONUCLEASE-I FROM BOVINE AND RAT PAROTID-GLAND AND ITS INTERACTION WITH RABBIT SKELETAL-MUSCLE ACTIN [J].
KREUDER, V ;
DIECKHOFF, J ;
SITTIG, M ;
MANNHERZ, HG .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1984, 139 (02) :389-400
[10]  
LACKS SA, 1981, J BIOL CHEM, V256, P2644