INSITU LOCALIZATION OF TRANSFORMING GROWTH FACTOR-BETA-1 IN PORCINE HEART - ENHANCED EXPRESSION AFTER CHRONIC CORONARY-ARTERY CONSTRICTION

被引:60
作者
WUNSCH, M [1 ]
SHARMA, HS [1 ]
MARKERT, T [1 ]
BERNOTATDANIELOWSKI, S [1 ]
SCHOTT, RJ [1 ]
KREMER, P [1 ]
BLEESE, N [1 ]
SCHAPER, W [1 ]
机构
[1] MAX PLANCK INST, W-6350 BAD NAUHEIM, GERMANY
关键词
TGF-BETA-1; ANGIOGENESIS; CORONARY CONSTRICTION; SWINE HEART; INSITU TECHNIQUES;
D O I
10.1016/0022-2828(91)91640-D
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We investigated the expression of transforming growth factor beta 1 (TGF-β1), a polypeptide differentiation factor probably associated with angiogenic properties in chronically hypoperfused heart tissue. A slowly swelling ameroid constrictor was implanted around the coronary circumflex artery (CX) of young domestic pigs. Two to three weeks after, significant CX stenosis of more than 90% and coronary collateralization could be demonstrated angiographically. The CX dependent experimental myocardial tissue (E) was investigated, with the LAD dependent area of the same pig serving as a control (C). We found significantly enhanced TGF-β1 mRNA expression by northern blot hybridization in the experimental myocardium (E) of those pigs with demonstrable coronary collaterals in the absence of a major myocardial infarction. The presence of TGF-β1 protein could be demonstrated quantitatively in extracts of the experimental and the control area by immunoblot analysis. By in situ techniques, TGF-β1 mRNA and protein could be localized predominantly in cardiac myocytes. We conclude that one adaptive mechanism of the pig heart in chronic coronary artery constriction is the enhanced expression of TGF-β1. Cardiac myocytes are a major source of TGF-β1. The observed coronary collateralization could be mediated - at least in part - by the angiogenic properties of TGF-β1. © 1991.
引用
收藏
页码:1051 / 1062
页数:12
相关论文
共 56 条
  • [1] ANZANO MA, 1982, CANCER RES, V42, P4776
  • [2] ASSOIAN RK, 1983, J BIOL CHEM, V258, P7155
  • [3] EXPRESSION AND SECRETION OF TYPE-BETA TRANSFORMING GROWTH-FACTOR BY ACTIVATED HUMAN MACROPHAGES
    ASSOIAN, RK
    FLEURDELYS, BE
    STEVENSON, HC
    MILLER, PJ
    MADTES, DK
    RAINES, EW
    ROSS, R
    SPORN, MB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (17) : 6020 - 6024
  • [4] BRAHIC M, 1978, P NATL ACAD SCI USA, V75, P5125
  • [5] CHEIFETZ S, 1989, J BIOL CHEM, V264, P12025
  • [6] ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE
    CHIRGWIN, JM
    PRZYBYLA, AE
    MACDONALD, RJ
    RUTTER, WJ
    [J]. BIOCHEMISTRY, 1979, 18 (24) : 5294 - 5299
  • [7] DETECTION OF MESSENGER-RNAS IN SEA-URCHIN EMBRYOS BY INSITU HYBRIDIZATION USING ASYMMETRIC RNA PROBES
    COX, KH
    DELEON, DV
    ANGERER, LM
    ANGERER, RC
    [J]. DEVELOPMENTAL BIOLOGY, 1984, 101 (02) : 485 - 502
  • [8] DANIEL TO, 1987, J BIOL CHEM, V262, P11893
  • [9] SEQUENCE OF THE PORCINE TRANSFORMING GROWTH-FACTOR-BETA PRECURSOR
    DERYNCK, R
    RHEE, L
    [J]. NUCLEIC ACIDS RESEARCH, 1987, 15 (07) : 3187 - 3187
  • [10] HUMAN TRANSFORMING GROWTH FACTOR-BETA COMPLEMENTARY-DNA SEQUENCE AND EXPRESSION IN NORMAL AND TRANSFORMED-CELLS
    DERYNCK, R
    JARRETT, JA
    CHEN, EY
    EATON, DH
    BELL, JR
    ASSOIAN, RK
    ROBERTS, AB
    SPORN, MB
    GOEDDEL, DV
    [J]. NATURE, 1985, 316 (6030) : 701 - 705