Inhibition of human trophoblast invasiveness by high glucose concentrations

被引:41
作者
Belkacemi, L [1 ]
Lash, GE [1 ]
Macdonald-Goodfellow, SK [1 ]
Caldwell, JD [1 ]
Graham, CH [1 ]
机构
[1] Queens Univ, Dept Anat & Cell Biol, Kingston, ON K7L 3N6, Canada
关键词
D O I
10.1210/jc.2004-2242
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Trophoblast invasion of the uterus is regulated by local microenvironmental factors. Objective: Because certain conditions may affect uterine glucose levels during placentation, the aim of this study was to determine the effect of glucose concentration on trophoblast invasion. Results: Compared with incubation in 0.2 and 2.5mM glucose, a 24-h incubation in increasing glucose concentrations (5 and 10 mM) resulted in up to a 62% inhibition (P < 0.01) of the in vitro invasiveness of immortalized HTR-8/SVneo trophoblasts. This decreased invasiveness in 5 and 10 mM glucose was paralleled by inhibition of a plasminogen activator (PA) activity corresponding to active urokinase-type PA ( uPA). Inhibition of pro-uPA binding to the uPA receptor decreased the invasiveness of cells incubated in 0.2 and 2.5 mM glucose to levels observed in cells incubated in higher glucose concentrations (P < 0.05). Gelatin zymography and Western blot analysis revealed that the levels of matrix metalloproteinase-2 and -9, PA inhibitor-1, and uPA receptor were unaffected by glucose. Glucose transporter-1 levels were 26 and 34% higher in cells cultured in 2.5 and 0.2 mM glucose, respectively, vs. 5 or 10 mM glucose (P < 0.05). In contrast, glucose transporter-3 levels were not affected by incubation in various glucose concentrations. Conclusions: These findings indicate that high glucose concentrations inhibit the invasiveness of HTR-8/SVneo cells by preventing uPA activation. Therefore, through its effects on uPA activity, glucose may be an important regulator of trophoblast invasiveness during implantation and placentation.
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收藏
页码:4846 / 4851
页数:6
相关论文
共 41 条
[1]   Diabetes and the maternal resistance vasculature [J].
Ang, C ;
Lumsden, MA .
CLINICAL SCIENCE, 2001, 101 (06) :719-729
[2]   Tumor necrosis factor-α inhibits trophoblast migration through elevation of plasminogen activator inhibitor-1 in first-trimester villous explant cultures [J].
Bauer, S ;
Pollheimer, J ;
Hartmann, J ;
Husslein, P ;
Aplin, JD ;
Knöfler, M .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (02) :812-822
[3]  
BEHRENDT N, 1995, BIOL CHEM H-S, V376, P269
[4]   Influence of maternal diabetes on placental fibroblast growth factor-2 expression, proliferation, and apoptosis [J].
Burleigh, DW ;
Stewart, K ;
Grindle, KM ;
Kay, HH ;
Golos, TG .
JOURNAL OF THE SOCIETY FOR GYNECOLOGIC INVESTIGATION, 2004, 11 (01) :36-41
[5]   Hepatocyte growth factor regulates human trophoblast motility and invasion: a role for nitric oxide [J].
Cartwright, JE ;
Holden, DP ;
Whitley, GS .
BRITISH JOURNAL OF PHARMACOLOGY, 1999, 128 (01) :181-189
[6]   Plasminogen activator activity is decreased in rat gingiva during diabetes [J].
Chang, KM ;
Rani, AS ;
Chang, KC ;
Kumar, S .
JOURNAL OF PERIODONTOLOGY, 1996, 67 (08) :743-747
[7]  
Cuvier C, 1997, CLIN EXP METASTAS, V15, P19
[8]   THE UROKINASE RECEPTOR - PROTEIN-STRUCTURE AND ROLE IN PLASMINOGEN ACTIVATION AND CANCER INVASION [J].
DANO, K ;
BEHRENDT, N ;
BRUNNER, N ;
ELLIS, V ;
PLOUG, M ;
PYKE, C .
FIBRINOLYSIS, 1994, 8 :189-203
[9]  
ELLIS V, 1991, J BIOL CHEM, V266, P12752
[10]   High glucose reduces generation of plasmin activity by mesangial cells [J].
Fisher, EJ ;
McLennan, SV ;
Yue, DK ;
Turtle, JR .
MICROVASCULAR RESEARCH, 1997, 53 (02) :173-178