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1 May 2003 Expression of Vascular Endothelial Growth Factor Isoforms and Receptors Flt-1 and KDR During the Peri-Implantation Period in the Mink, Mustela vison
Flavia L. Lopes, Joëlle Desmarais, Nicolas Y. Gévry, Sandra Ledoux, Bruce D. Murphy
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Abstract

Expression of vascular endothelial growth factor (VEGF) isoforms and its receptors, Flt-1 and KDR, was investigated during the period of peri-implantation in mink, a species that displays obligate embryonic diapause. Uterine samples were collected during diapause, embryo activation, and implantation from pseudopregnant and anestrous animals and analyzed by semiquantitative reverse transcription polymerase chain reaction and immunohistochemistry. The abundance of mRNA of VEGF isoforms 120, 164, and 188 was highest during late embryo activation and at implantation. VEGF protein was localized to the glandular epithelium at all stages of peri-implantation, whereas the luminal epithelium lacked VEGF reactivity during diapause. Endometrial stroma and luminal and glandular epithelia were positive for VEGF in implanted uteri. The invasive trophoblast cells of the implanting embryo were intensively stained. High levels of VEGF mRNA in pseudopregnant uteri indicates that VEGF upregulation leading to implantation is dependent upon maternal rather than embryonic factors. The abundance of the two receptors, KDR and Flt-1, increased in the uterus during implantation. Low levels of the receptors in pseudopregnant uteri compared with those containing activated or implanted embryos indicates that the embryo regulates receptor expression. These results demonstrate VEGF and VEGF receptor expression during early gestation in mink and suggest that maternal and embryonic input regulates different aspects of the angiogenic process.

Flavia L. Lopes, Joëlle Desmarais, Nicolas Y. Gévry, Sandra Ledoux, and Bruce D. Murphy "Expression of Vascular Endothelial Growth Factor Isoforms and Receptors Flt-1 and KDR During the Peri-Implantation Period in the Mink, Mustela vison," Biology of Reproduction 68(5), 1926-1933, (1 May 2003). https://doi.org/10.1095/biolreprod.102.013441
Received: 15 November 2002; Accepted: 1 December 2002; Published: 1 May 2003
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