Role of placenta growth factor (PIGF) in human extravillous trophoblast proliferation, migration and invasiveness

被引:118
作者
Athanassiades, A [1 ]
Lala, PK [1 ]
机构
[1] Univ Western Ontario, Dept Anat & Cell Biol, London, ON N6A 5C1, Canada
关键词
D O I
10.1016/S0143-4004(98)91039-6
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Placenta growth factor (PlGF) is a homodimeric glycoprotein, 46-50 kDa in size, belonging to the vascular endothelial growth factor (VEGF) sub-family. It exists as two isoforms, PlGF-1 and -2, the latter having a heparin-binding domain. Like VEGF, it is a potent angiogenic factor; however, PlGF homodimers interact with the VEGF receptor Flt-1 (fms-like tyrosine kinase), but not with the kinase domain-containing region (KDR). Since PlGF is made by the human placenta and extravillous trophoblast (EVT) cells of the human placenta express Flt-1 in situ, these cells may be responsive to PlGF. Therefore, this study examined whether first trimester EVT cells propagated in vitro expressed the mRNA or the protein of Flt-1 and PlGF, and whether exogenous PlGF-1 had any effect on EVT cell proliferation, migration or invasiveness. Immunocytochemical and RT-PCR analyses revealed that both normal and SV40 Tag-immortalized EVT cells expressed the protein and mRNA for Flt-1, but not for PlGF-1 or -2. Exogenous PlGF-1 stimulated proliferation (measured by H-3-thymidine uptake) of normal EVT cells in a concentration-dependent manner, but only in the presence of excess heparan sulphate proteoglycans (HSPGs). These results raise two possibilities: that exogenous PlGF-1 (in spite of having a low affinity for heparin) was sequestered away from its receptor because of binding to heparan sulphate proteoglycans on the EVT cell surface or the ECM, or that HSPGs could modify the interaction between Flt-1 and PlGF. PlGF-1, in the presence or absence of HSPGs, however, had no effect on EVT migration or invasiveness, when measured with a transwell invasion (in the presence of Matrigel(R)) or migration (in the absence of Matrigel(R)) assay. These findings place PlGF amongst a large group of growth factors that promote EVT cell proliferation without influencing their migratory or invasive behaviours, and suggest that PlGF-Flt-1 interactions may be regulated by HSPGs in situ. Placenta (1998), 19, 465-473. (C) 1998 W. B. Saunders Company Ltd.
引用
收藏
页码:465 / 473
页数:9
相关论文
共 50 条
  • [1] Ahmed A, 1997, LAB INVEST, V76, P779
  • [2] COLOCALIZATION OF VASCULAR ENDOTHELIAL GROWTH-FACTOR AND ITS FLT-1 RECEPTOR IN HUMAN PLACENTA
    AHMED, A
    LI, XF
    DUNK, C
    WHITTLE, MJ
    RUSHTON, DI
    ROLLASON, T
    [J]. GROWTH FACTORS, 1995, 12 (03) : 235 - 243
  • [3] ATHANASSIADES A, 1998, IN PRESS BIOL REPROD
  • [4] BROWN LF, 1993, AM J PATHOL, V143, P1255
  • [5] Heterodimers of placenta growth factor vascular endothelial growth factor - Endothelial activity, tumor cell expression, and high affinity binding to Flk-1/KDR
    Cao, YH
    Chen, H
    Zhou, L
    Chiang, MK
    AnandApte, B
    Weatherbee, JA
    Wang, YD
    Fang, FY
    Flanagan, JG
    Tsang, MLS
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (06) : 3154 - 3162
  • [6] VASCULAR ENDOTHELIAL GROWTH-FACTOR RECEPTOR LOCALIZATION AND ACTIVATION IN HUMAN TROPHOBLAST AND CHORIOCARCINOMA CELLS
    CHARNOCKJONES, DS
    SHARKEY, AM
    BOOCOCK, CA
    AHMED, A
    PLEVIN, R
    FERRARA, N
    SMITH, SK
    [J]. BIOLOGY OF REPRODUCTION, 1994, 51 (03) : 524 - 530
  • [7] Clark D. E., 1997, Placenta, V18, pA17
  • [8] Clark DE, 1996, HUM REPROD, V11, P1090
  • [9] VEGF(121), A VASCULAR ENDOTHELIAL GROWTH-FACTOR (VEGF) ISOFORM LACKING HEPARIN-BINDING ABILITY, REQUIRES CELL-SURFACE HEPARAN SULFATES FOR EFFICIENT BINDING TO THE VEGF RECEPTORS OF HUMAN-MELANOMA CELLS
    COHEN, T
    GITAYGOREN, H
    SHARON, R
    SHIBUYA, M
    HALABAN, R
    LEVI, BZ
    NEUFELD, G
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (19) : 11322 - 11326
  • [10] PURIFICATION AND CHARACTERIZATION OF A NATURALLY-OCCURRING VASCULAR ENDOTHELIAL GROWTH-FACTOR PLACENTA GROWTH-FACTOR HETERODIMER
    DISALVO, J
    BAYNE, ML
    CONN, G
    KWOK, PW
    TRIVEDI, PG
    SODERMAN, DD
    PALISI, TM
    SULLIVAN, KA
    THOMAS, KA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (13) : 7717 - 7723