Co-culture with granulosa cells improve the in vitro maturation ability of porcine immature oocytes vitrified with cryolock

• Published in: Cryobiology Vol. 69; no. 2; pp. 299 - 304
• Main Authors: Casillas, Fahiel, Teteltitla-Silvestre, Mario, Ducolomb, Yvonne, Lemus, Ana E., Salazar, Zayil, Casas, Eduardo, Betancourt, Miguel
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 01-10-2014
• Subjects: Animals; Cell Survival; Cells, Cultured; Coculture Techniques - methods; Coculture Techniques - veterinary; Cryolock; Cryopreservation - methods; Cryopreservation - veterinary; Cryoprotectants; Cryoprotective Agents - metabolism; Dimethyl Sulfoxide - metabolism; Ethylene Glycol - metabolism; Female; Granulosa Cells - cytology; Granulosa cells co-culture; Immature oocytes; In Vitro Oocyte Maturation Techniques - methods; In Vitro Oocyte Maturation Techniques - veterinary; IVM; Oocytes - cytology; Porcine; SOPS; Swine; Trehalose - metabolism; Vitrification; IVM; Porcine; Vitrification; Cryoprotectants; MTT; Granulosa cells co-culture; OPS; Immature oocytes; NkO-CC; FSH; MI; Egf-L; CPAs; mTBM; EG; COCs; EGF; MII; Cryolock; GV; TCM-199; BES; GVB; FCS; SSV; SOPS; PVA; LH; Me2SO
• ISSN: 0011-2240; 1090-2392
• DOI: 10.1016/j.cryobiol.2014.08.004

This study was designed to evaluate the efficiency of two oocyte vitrification–warming procedures using two different devices: Superfine Open Pulled Straws (SOPS) and Cryolock, as well as the effect of the co-culture of vitrified immature oocytes with fresh granulosa cells to improve in vitro maturation (IVM). Immature oocytes were vitrified with two procedures: A) Oocytes were exposed to an increasing concentration of ethylene glycol (EG) from 4% to 35% with 0.5M trehalose. They then, were loaded in SOPS or Cryolock. For warming, oocytes were exposed to decreasing concentrations of trehalose 0.3, 0.2 and 0.1M for IVM. B) Oocytes were exposed to two mixtures of EG and dimethylsulfoxide (Me2SO), at 7.5% and 16%, both with 0.4M of sucrose and then loaded in SOPS or Cryolock and stored in liquid nitrogen. For warming, oocytes were exposed to a single concentration of sucrose 0.5M. After warming, viability was determined; and after 44h of IVM both viability and meiotic stages were evaluated. The results indicate no significant differences between procedures A and B with SOPS in all maturation stages, reaching a maximum maturation rate of 21%. As to Cryolock, significant differences were observed between both procedures, being procedure B, more efficient with a yield of 38% in MII stage and increased to 49% due to the co-culture with fresh granulosa cells. In conclusion, viability and maturation rates were improved with Cryolock and procedure B with the co-culture system in vitrified immature oocytes.