TY - JOUR
T1 - Isoform 165 of vascular endothelial growth factor in collagen matrix improves ovine cryopreserved ovarian tissue revascularisation after xenotransplantation in mice
AU - Henry, Laurie
AU - Labied, Soraya
AU - Fransolet, Maïté
AU - Kirschvink, Nathalie
AU - Blacher, Silvia
AU - Noel, Agnès
AU - Foidart, Jean Michel
AU - Nisolle, Michelle
AU - Munaut, Carine
PY - 2015/3/7
Y1 - 2015/3/7
N2 - Background: Aggressive anti-cancer treatments can result in ovarian failure. Ovarian cryopreservation has been developed to preserve the fertility of young women, but early graft revascularisation still requires improvement. Methods: Frozen/thawed sheep ovarian cortical biopsies were embedded in collagen matrix with or without isoform 165 of vascular endothelial growth factor (VEGF165) and transplanted into ovaries of immunodeficient mice. Ovaries were chosen as transplantation sites to more closely resemble clinical conditions in which orthotopic transplantation has previously allowed several spontaneous pregnancies. Results: We found that VEGF165 significantly increased the number of Dextran-FITC positive functional vessels 3days after grafting. Dextran- fluorescein isothiocyanate (FITC) positive vessels were detectable in 53% and 29% of the mice in the VEGF-treated and control groups, respectively. Among these positive fragments, 50% in the treated group displayed mature smooth-muscle-actin-alpha (alpha-SMA) positive functional vessels compared with 0% in the control group. CD31 positive murine blood vessels were observed in 40% of the VEGF165 transplants compared with 21% of the controls. After 3weeks, the density of murine vessels was significantly higher in the VEGF165 group. Conclusion: The encapsulation of ovarian tissue in collagen matrix in the presence of VEGF165 before grafting has a positive effect on functional blood vessel recruitment. It can be considered as a useful technique to be improved and further developed before human clinical applications in female cancer patients in the context of fertility preservation.
AB - Background: Aggressive anti-cancer treatments can result in ovarian failure. Ovarian cryopreservation has been developed to preserve the fertility of young women, but early graft revascularisation still requires improvement. Methods: Frozen/thawed sheep ovarian cortical biopsies were embedded in collagen matrix with or without isoform 165 of vascular endothelial growth factor (VEGF165) and transplanted into ovaries of immunodeficient mice. Ovaries were chosen as transplantation sites to more closely resemble clinical conditions in which orthotopic transplantation has previously allowed several spontaneous pregnancies. Results: We found that VEGF165 significantly increased the number of Dextran-FITC positive functional vessels 3days after grafting. Dextran- fluorescein isothiocyanate (FITC) positive vessels were detectable in 53% and 29% of the mice in the VEGF-treated and control groups, respectively. Among these positive fragments, 50% in the treated group displayed mature smooth-muscle-actin-alpha (alpha-SMA) positive functional vessels compared with 0% in the control group. CD31 positive murine blood vessels were observed in 40% of the VEGF165 transplants compared with 21% of the controls. After 3weeks, the density of murine vessels was significantly higher in the VEGF165 group. Conclusion: The encapsulation of ovarian tissue in collagen matrix in the presence of VEGF165 before grafting has a positive effect on functional blood vessel recruitment. It can be considered as a useful technique to be improved and further developed before human clinical applications in female cancer patients in the context of fertility preservation.
KW - Collagen matrix
KW - Fertility preservation
KW - VEGF165
KW - Xenotransplantation and angiogenesis
UR - http://www.scopus.com/inward/record.url?scp=84925244178&partnerID=8YFLogxK
U2 - 10.1186/s12958-015-0015-2
DO - 10.1186/s12958-015-0015-2
M3 - Article
AN - SCOPUS:84925244178
VL - 13
JO - In Reproductive Biology and endocrinology
JF - In Reproductive Biology and endocrinology
IS - 1
M1 - 12
ER -