Alginate scaffold for organ culture of cryopreserved-thawed human ovarian cortical follicles.

Alon Kedem*, Ariel Hourvitz, Benjamin Fisch, Michal Shachar, Smadar Cohen, Avi Ben-Haroush, Joshua Dor, Enrique Freud, Carmela Felz, Ronit Abir

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

32 Scopus citations

Abstract

To compare macroporous alginate scaffolds with Matrigel for culturing frozen-thawed human primordial follicles in organ culture. Twelve girls/women donated ovarian tissue. One tissue sample was fixed immediately after thawing (uncultured samples). Slices were cultured for 2 weeks on either Matrigel or on alginate scaffolds with a serum-free culture medium. Growth evaluation consisted of follicular counts and classification, immunohistochemistry and measurement of 17β-Estradiol (E(2)) production. The number of developing follicles was significantly higher in alginate scaffold-cultured samples than on Matrigel with a concomitant decrease in the number of primordial follicles in alginate scaffold-cultured samples than uncultured samples. The number of atretic follicles after 1 week was significantly higher in the Matrigel-cultured samples than in the alginate scaffold cultured samples. E(2) production was similar in both groups. Three dimensional alginate scaffolds are a promising putative in vitro technology for developing human primordial follicles.

Original languageEnglish
Pages (from-to)761-769
Number of pages9
JournalJournal of Assisted Reproduction and Genetics
Volume28
Issue number9
DOIs
StatePublished - 2011

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