Molecular Human Reproduction, Vol. 7, No. 1, 57-63,
January 2001
© 2001 European Society of Human Reproduction and Embryology
Embryology |
Vascular endothelial growth factor (VEGF) mRNA splice variants are differentially expressed in human blastocysts*
1 Department of Obstetrics and Gynecology, Heinrich-Heine-University Medical Center, Moorenstraße 5, D-40225, Düsseldorf, Germany, and 2 Department of GYN/OB, Reproductive Immunology Laboratory, Stanford University Medical Center, Stanford, CA, USA
Abstract
The aim of our study was to detect and characterize mRNA expression of VEGF isoforms VEGF121, VEGF145, VEGF165, VEGF189, and VEGF206 in human blastocysts. We recently demonstrated VEGF mRNA expression during human preimplantation embryo development, and further information regarding the alternatively spliced mRNAs resulting in freely secreted proteins or proteins bound to cell surface heparansulphate proteoglycans is needed to better understand the process of angiogenesis during implantation. Human blastocysts unsuitable for transfer obtained from the IVF programme at Stanford University were examined by reverse transcription/hemi-nested polymerase chain reaction for their expression of VEGF mRNA splice variants. VEGF mRNA was expressed in 17 out of 19 (89%) blastocysts. Of the 17 blastocysts, VEGF121 mRNA was detected in 88%, VEGF145 mRNA in 100%, VEGF165 mRNA in 71%, and VEGF189 mRNA in 24% of blastocysts. There was co-expression of mRNA for VEGF121 and VEGF145 only in 29% blastocysts, of mRNA for VEGF165 and VEGF145 only in 12%, and of mRNA for VEGF121, VEGF145 and VEGF165 in 59% blastocysts. VEGF206 mRNA could not be detected. In conclusion, we demonstrated that blastocysts express the mRNAs encoding for the free VEGF proteins, enabling the implanting embryo to immediately induce angiogenesis at the implantation site.
angiogenesis/cytokines/gene expression/growth factors/implantation
Notes
3 To whom correspondence should be addressed. E-mail: kruessel{at}uni-duesseldorf.de
* Presented in part at the 16th annual meeting of ESHRE, Bologna, Italy, June 2528, 2000.
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