OXYGEN-TENSION REGULATES THE EXPRESSION OF THE PLATELET-DERIVED GROWTH FACTOR-B CHAIN GENE IN HUMAN ENDOTHELIAL-CELLS

被引:362
作者
KOUREMBANAS, S
HANNAN, RL
FALLER, DV
机构
[1] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,44 BINNEY ST,BOSTON,MA 02115
[2] BRIGHAM & WOMENS HOSP,CHILDRENS HOSP,JOINT PROGRAM NEONATOL,BOSTON,MA 02115
[3] HARVARD UNIV,SCH MED,DEPT PEDIAT,BOSTON,MA 02115
[4] HARVARD UNIV,SCH MED,DEPT SURG,BOSTON,MA 02115
关键词
Gene expression; Hypoxia; Transcriptional regulation; Vascular tone; Vasoconstrictor;
D O I
10.1172/JCI114759
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Hypoxic states are associated with abnormal proliferation and constriction of the smooth muscle cells surrounding the distal vessels of the lung. In hypoxic as well as in normal states, the endothelial cell layer may play a key role in controlling smooth muscle tone by secreting a number of vasoactive agents. Platelet-derived growth factor (PDGF), produced by endothelial cells, is a major growth factor for vascular smooth muscle cells and a powerful vasoconstrictor. It consists of a disulfide-linked dimer of two related peptides, A and B, that are products of two different genes. We found that hypoxic conditions (0-3% oxygen environments) significantly increased PDGF-B mRNA in cultured human umbilical vein endothelial cells by enhancing the transcriptional rate of this gene. This increase was inversely proportional to oxygen tension and was reversible upon reexposure of cells to a 21% oxygen atmosphere. mRNA levels of PDGF-A were not affected nor was the overall rate of cellular gene transcription increased in response to hypoxia. These studies indicate that endothelial cells are not only capable of sensing oxygen tension, but are also able to discriminate and respond to even small differences in oxygen tension resulting in dramatic upregulation of the PDGF-B chain gene.
引用
收藏
页码:670 / 674
页数:5
相关论文
共 27 条
[1]   VASOCONSTRICTION - A NEW ACTIVITY FOR PLATELET-DERIVED GROWTH-FACTOR [J].
BERK, BC ;
ALEXANDER, RW ;
BROCK, TA ;
GIMBRONE, MA ;
WEBB, RC .
SCIENCE, 1986, 232 (4746) :87-90
[2]   CDNA SEQUENCE AND CHROMOSOMAL LOCALIZATION OF HUMAN PLATELET-DERIVED GROWTH-FACTOR A-CHAIN AND ITS EXPRESSION IN TUMOR-CELL LINES [J].
BETSHOLTZ, C ;
JOHNSSON, A ;
HELDIN, CH ;
WESTERMARK, B ;
LIND, P ;
URDEA, MS ;
EDDY, R ;
SHOWS, TB ;
PHILPOTT, K ;
MELLOR, AL ;
KNOTT, TJ ;
SCOTT, J .
NATURE, 1986, 320 (6064) :695-699
[3]  
BOWENPOPE DF, 1989, J BIOL CHEM, V264, P2502
[4]  
CHIRGWIN JM, 1979, BIOCHEMISTRY-US, V18, P5924
[5]  
DANIEL TO, 1986, J BIOL CHEM, V261, P9579
[6]  
DANIEL TO, 1987, J BIOL CHEM, V262, P11893
[7]   HUMAN TRANSFORMING GROWTH FACTOR-BETA COMPLEMENTARY-DNA SEQUENCE AND EXPRESSION IN NORMAL AND TRANSFORMED-CELLS [J].
DERYNCK, R ;
JARRETT, JA ;
CHEN, EY ;
EATON, DH ;
BELL, JR ;
ASSOIAN, RK ;
ROBERTS, AB ;
SPORN, MB ;
GOEDDEL, DV .
NATURE, 1985, 316 (6030) :701-705
[8]  
DEUEL TF, 1984, BLOOD, V64, P951
[9]   THE OBLIGATORY ROLE OF ENDOTHELIAL-CELLS IN THE RELAXATION OF ARTERIAL SMOOTH-MUSCLE BY ACETYLCHOLINE [J].
FURCHGOTT, RF ;
ZAWADZKI, JV .
NATURE, 1980, 288 (5789) :373-376
[10]   DELETIONS OF SPECIFIC REGIONS OF THE SIMIAN SARCOMA-ASSOCIATED VIRUS GENOME ARE FOUND IN DEFECTIVE VIRUSES AND IN THE SIMIAN SARCOMA-VIRUS [J].
GELMANN, EP ;
PETRI, E ;
CETTA, A ;
WONGSTAAL, F .
JOURNAL OF VIROLOGY, 1982, 41 (02) :593-604