4.5 Article

Mouse Cumulus-Denuded Oocytes Restore Developmental Capacity Completely When Matured with Optimal Supplementation of Cysteamine, Cystine, and Cumulus Cells

Journal

BIOLOGY OF REPRODUCTION
Volume 82, Issue 4, Pages 759-768

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1095/biolreprod.109.082206

Keywords

assisted reproductive technology; cumulus cells; cumulus-denuded oocytes; gamete biology; glutathione; in vitro fertilization; in vitro maturation; mouse; ovum

Funding

  1. National Basic Research Project of the China Ministry of Science and Technology [2006CB944003, 2007CB947403]
  2. China National Natural Science Foundation [30771556, 30972096]
  3. National 863'' Project of the China Ministry of Science and Technology [2008AA10Z160, 2008AA101003]

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Our objectives were to study how cysteamine, cystine, and cumulus cells (CCs), as well as oocytes interact to increase oocyte intracellular glutathione (GSH) and thereby to establish an efficient in vitro maturation system for cumulus-denuded oocytes (DOs). Using M16 that contained no thiol as maturation medium, we showed that when supplemented alone, neither cystine nor cysteamine promoted GSH synthesis of mouse DOs, but they did when used together. Although goat CCs required either cysteamine or cystine to promote GSH synthesis, mouse CCs required both. In the presence of cystine, goat CCs produced cysteine but mouse CCs did not. Cysteamine reduced cystine to cysteine in cell-free M16. When TCM-199 that contained 83 mu M cystine was used as maturation medium, supplementation with cysteamine alone had no effect, but supplementation with 100 mu M cysteamine and 200 mu M cystine increased blastulation of DOs matured with CC coculture to a level as high as achieved in cumulus-surrounded oocytes (COCs). Similar numbers of young were produced after two-cell embryos from mouse COCs or CC-cocultured DOs matured with optimal thiol supplementation were transferred to pseudopregnant recipients. It is concluded that 1) mouse CCs can use neither cysteamine nor cystine to promote GSH synthesis, but goat CCs can use either one; 2) goat CCs promote mouse oocyte GSH synthesis by reducing cystine to cysteine, but how they use cysteamine requires further investigation; and 3) mouse DOs can use neither cystine nor cysteamine for GSH synthesis, but they restore developmental capacity completely when matured in the presence of optimum supplementation of cysteamine, cystine, and CCs.

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