摘要

BACKGROUND: A solution-based vitrification protocol is a process of sequentially changing-solutions from. which both influx of cryoprotectants (loading) and efflux of water (dehydration) were accomplished before cryo-exposure. Hence, we need to properly control the concentration /composition of the cryoprotectant solutions. OBJECTIVE: The study was, using a systematic approach, to develop a protocol for Rubio akane hairy roots, a, very sensitive material to cytotoxicity of vitrification solutions, METHODS: Due to the poor response of 10-year in vitro maintained R. akane hairy roots to already established cryopreservation protocols, the following sets of experiments were,designed: 1) combinational, effect of preculture, osmoprotection and cryoprotection with PVS3-based (A3-70%) %26apos;and PVS3-based (B5-80%) vitrification solutions; 2) different cooling/warming rates and, warming temperature; 3) varying unloading solutions (25%, 35% and 45% sucroSe) and durations (7 min and 30 min) with or without changing the unloading solutions RESULTS Preculture and osmoprotection treatments were necessary to acquire cytotoxicity tolerance in both vitrification solutions tested and osnioprotection treatment was More critical, especially in B5-80%. A sequential osmoprotection treatment (C10-50%) following conventional osmoprotection (C4-35%) was needed to increase the post-cryopreservation regrowth. Al.uinitituri foil strips were superior to Cryovials, but the warming temperature tested (20 degrees C and 40 degrees c) did not affect post-cryopreservation recovery. In the unloading procedure, a longer duration (30 min) with a higher sucrose solution (S-45%) was harmful, possibly due, to osmotic stress. CONCLUSION: R. akane hairy roots are very sensitive, to cytotoxicity (both osmotic stress and chemical toxicity) and thus a proper process (preculture, osmoprotection, cryoprotection and Unloading) is necessary for higher post-Cryopreservation recovery.

  • 出版日期2014-4