Autocrine and paracrine regulation of myocardial cell growth in vitro - The TGF beta paradigm

被引:27
作者
Long, CS
机构
[1] VET ADM MED CTR, RES SERV, SAN FRANCISCO, CA 94121 USA
[2] UNIV CALIF SAN FRANCISCO, DEPT MED, SAN FRANCISCO, CA USA
关键词
D O I
10.1016/S1050-1738(96)00090-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Over the past few years, there has been an increasing appreciation of the role that growth factors/cytokines play in cardiac growth/development and the myocardial response to injury. This has derived, at least in part, from two observations: (a) that a number of these factors are expressed in response to myocardial stress, and (b) that some of these factors can stimulate myocardial growth in culture along with the characteristic set of gene products that are associated with hypertrophy in vivo. Virtually all of the cells that make up the adult myocardium have at one time or another been reported to either be the source, the site of action, or both, of many of these cytokines. Although the cell specificity of cytokine production is not critical to the understanding of the complex nature of intracardiac cell-cell interactions as a mechanism of cardiac growth/development, this distinction does have some importance as myocardial cell culture gains increased popularity in the research community Because there ave MO true cardiac muscle cell lines, all of the myocyte cultures used in these studies are, in essence, ''cocultures'' of cardiac myocytes and nonmyocytes (predominantly fibroblasts), with absolute numbers of these ''contaminating'' cells a function of plated cell density. As such, the cell specificity of some substances on myocardial cell growth and transcriptional program (of both myocytes and fibroblasts) is not always clear. This makes the critical examination of the expression (and effects) of these growth-promoting substances in culture of particular importance with attention to the specific culture conditions employed. The complexity of the situation in the heart is compounded by the observation that many of these substances have differential effects on the individual myocardial cell types and can induce the expression of other cytokines/cytokine receptors by these cells. In this report, the investigations published to date on the autocrine/paracrine effects of these factors on myocardial cell growth in culture are reviewed. The complexity of the subject is illustrated with the findings from our laboratory investigating one of the cytokines with growth-promoting effects on myocardial cells in culture, transforming growth factor beta (TGF beta). (C) 1996, Elsevier Science Inc.
引用
收藏
页码:217 / 226
页数:10
相关论文
共 91 条
[1]  
AKHURST RJ, 1990, DEVELOPMENT, V108, P645
[2]   THE ROLE OF TGF-BETA-S IN MAMMALIAN DEVELOPMENT AND NEOPLASIA [J].
AKHURST, RJ ;
FITZPATRICK, DR ;
FOWLIS, DJ ;
GATHERER, D ;
MILLAN, FA ;
SLAGER, H .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1992, 32 (02) :127-135
[3]   AN ACTIVATED FORM OF TRANSFORMING GROWTH FACTOR-BETA IS PRODUCED BY COCULTURES OF ENDOTHELIAL-CELLS AND PERICYTES [J].
ANTONELLIORLIDGE, A ;
SAUNDERS, KB ;
SMITH, SR ;
DAMORE, PA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (12) :4544-4548
[4]   CONTROL OF CARDIAC-MUSCLE CELL-FUNCTION BY AN ENDOGENOUS NITRIC-OXIDE SIGNALING SYSTEM [J].
BALLIGAND, JL ;
KELLY, RA ;
MARSDEN, PA ;
SMITH, TW ;
MICHEL, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (01) :347-351
[5]   TGF-BETA INDUCES BIMODAL PROLIFERATION OF CONNECTIVE-TISSUE CELLS VIA COMPLEX CONTROL OF AN AUTOCRINE PDGF LOOP [J].
BATTEGAY, EJ ;
RAINES, EW ;
SEIFERT, RA ;
BOWENPOPE, DF ;
ROSS, R .
CELL, 1990, 63 (03) :515-524
[6]  
BHAMBI B, 1991, AM J PATHOL, V139, P1131
[7]   ADRENERGIC REGULATION OF THE SKELETAL ALPHA-ACTIN GENE PROMOTER DURING MYOCARDIAL-CELL HYPERTROPHY [J].
BISHOPRIC, NH ;
KEDES, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (06) :2132-2136
[8]  
BRAND T, 1993, J BIOL CHEM, V268, P11500
[9]   Physicochemical Activation of Recombinant Latent Transforming Growth Factor-beta's 1, 2, and 3 [J].
Brownh, Peter D. ;
Wakefiel, Lalage M. ;
Levinson, Arthur D. ;
Sporn, Michael B. .
GROWTH FACTORS, 1990, 3 (01) :35-43
[10]   PRESSURE-INDUCED AND VOLUME-INDUCED LEFT-VENTRICULAR HYPERTROPHIES ARE ASSOCIATED WITH DISTINCT MYOCYTE PHENOTYPES AND DIFFERENTIAL INDUCTION OF PEPTIDE GROWTH-FACTOR MESSENGER-RNAS [J].
CALDERONE, A ;
TAKAHASHI, N ;
IZZO, NJ ;
THAIK, CM ;
COLUCCI, WS .
CIRCULATION, 1995, 92 (09) :2385-2390