In vitro maturation of human preovulatory oocytes reconstructed by germinal vesicle transfer

Objective: To describe a micromanipulation-electrofusion procedure for tran sferring germinal vesicles (GVs) between immature human oocytes. Design: Pilot study to assess oocyte maturation after an invasive micromani pulation procedure. Setting: Research laboratory at a university medical center. Patient(s): Immature oocytes were discarded from intracytoplasmic sperm inj ection (ICSI)-IVF cycles of patients 23-48 years of age. Intervention(s): Initially, GV removal and transfer were performed on the s ame oocyte; these "self-reconstructed" oocytes were then cultured in vitro for up to 50 hours and examined periodically for maturation as judged by th e extrusion of the first polar body. In a second study, GVs from oocytes of "old" patients (>38 years old) were successfully transferred into enucleat ed immature oocytes of "young" patients ((31 years old). Main Outcome Measure(s): Extrusion of the first polar body was monitored in "reconstructed" and control oocytes; karyotypes also were analyzed at meio sis IJ. Result(s): From 48 oocytes from old patients, 12 GVs were successfully remo ved, transferred, and fused into previously enucleated oocytes from young p atients. After in vitro culture, 7 of these "reconstructed" oocytes matured to meiosis II, a maturation rate not significantly different from that obs erved in nonmanipulated controls. A normal, second meiotic metaphase chromo some complement was observed in 4 of 5 reconstructed oocytes. Conclusion(s): Normal meiosis can occur after the transfer of a GV into an enucleated host oocyte. Germinal vesicle transfer may be a valuable researc h procedure that generates cell models to characterize the cytoplasmic-nucl ear interplay for cell cycle regulation, maturation, and fertilization in t he human oocyte; it also may be a potentially attractive alternative to ooc yte donation.