Successful cryopreservation of mammalian cells requires rapid transport of water and cryoprotective solutes across the plasma membrane. Aquaporin-3 is known as a water/solute channel that can transport water and neutral solutes such as glycerol. In this study we examined whether artificial expression of aquaporin-3 in mouse oocytes can improve water and glycerol permeability and oocyte survival after cryopreservation. Immature mouse oocytes were injected with aquaporin-3 cRNA and were cultured for 12 h. Then the hydraulic conductivity (L(P)) and glycerol permeability (P(GLY)) of matured oocytes were determined from the relative volume changes in 10% glycerol in PB1 medium at 25 degrees C. Mean +/- SD values of L(P) and P(GLY) of cRNA-injected oocytes (3.09 +/- 1.22 micro m min(-1) atm(-1) and 3.69 +/- 1.47 x 10(-3) cm/min, respectively; numbers of oocytes = 25) were significantly higher than those of noninjected oocytes (0.83 +/- 0.02 micro m min(-1) atm(-1) and 0.07 +/- 0.02 x 10(-3) cm/min, respectively; n = 13) and water-injected oocytes (0.87 +/- 0.10 micro m min(-1) atm(-1) and 0.08 +/- 0.02 x 10(-3) cm/min, respectively; n = 20). After cryopreservation in a glycerol-based solution, 74% of cRNA-injected oocytes (n = 27) survived as assessed by their morphological appearance, whereas none of the water-injected oocytes survived (n = 10). When cRNA-injected oocytes that survived cryopreservation were inseminated in vitro, the penetration rate was 40% (n = 48) and the cleavage rate was 31% (n = 70), showing that oocytes retain their ability to be fertilized. This is the first report to show that artificial expression of a water/solute channel in a cell improves its survival after cryopreservation. This approach may enable cryopreservation of cells that have been difficult to cryopreserve.

The cryosensitivity of mammalian embryos depends on the stage of development. Because permeability to water and cryoprotectants plays an important role in cryopreservation, it is plausible that the permeability is involved in the difference in the tolerance to cryopreservation among embryos at different developmental stages. In this study, we examined the permeability to water and glycerol of mouse oocytes and embryos, and tried to deduce the pathway for the movement of water and glycerol. The water permeability (L(P), microm min(-1) atm(-1)) of oocytes and four-cell embryos at 25 degrees C was low (0.63-0.70) and its Arrhenius activation energy (E(a), kcal/mol) was high (11.6-12.3), which implies that the water permeates through the plasma membrane by simple diffusion. On the other hand, the L(p) of morulae and blastocysts was quite high (3.6-4.5) and its E(a) was quite low (5.1-6.3), which implies that the water moves through water channels. Aquaporin inhibitors, phloretin and p-(chloromercuri) benzene-sulfonate, reduced the L(p) of morulae significantly but not that of oocytes. By immunocytochemical analysis, aquaporin 3, which transports not only water but also glycerol, was detected in the morulae but not in the oocytes. Accordingly, the glycerol permeability (P(GLY), x 10(-3) cm/min) of oocytes was also low (0.01) and its E(a) was remarkably high (41.6), whereas P(GLY) of morulae was quite high (4.63) and its E(a) was low (10.0). Aquaporin inhibitors reduced the P(GLY) of morulae significantly. In conclusion, water and glycerol appear to move across the plasma membrane mainly by simple diffusion in oocytes but by facilitated diffusion through water channel(s) including aquaporin 3 in morulae.

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Abstract. Previously, we showed that the exogenous expression of aquaporin 3 (AQP3), an aquaglyceroporin, improved the tolerance of mouse oocytes to vitrification with a glycerol-based solution. In the present study, we examined conditions suitable for the expression of AQP3 and the ability of vitrified oocytes to develop in vitro and in vivo after fertilization. After only partial remove of cumulus cells, immature mouse oocytes (germinal vesicle stage) were injected with 5, 10 or 20 pg of AQP3 cRNA and cultured for 12 h for maturation. When matured oocytes were vitrified with a glycerol-based solution, 57-61% survived regardless of the amount of cRNA injected (5-20 pg). By contrast, no oocytes injected with water (control) survived. When the zona pellucida was removed from the vitrified oocytes and the oocytes were then fertilized in vitro and cultured, the proportions that were fertilized and developed into blastocysts were higher when the amount of cRNA injected was 5 pg than 10-20 pg. When 16 blastocysts were transferred to a pseudopregnant mouse, 5 developed to term, demonstrating that oocytes vitrified after injection of AQP3 cRNA retained the ability to develop to term. The water-permeability of cRNA-injected oocytes was higher than that of control oocytes from the maturing stage to the 1-cell zygote stage, whereas glycerol-permeability was higher only at metaphase II. This indicates that AQP3 was expressed for a relatively short period of time. These results suggest that the transient expression of water/cryoprotectant channels is effective for cryopreserving cells that have low membrane-permeability, such as mammalian oocytes. Key words: Aquaporin, Development, Membrane-permeability, Oocyte, Vitrification (J. Reprod. Dev. 57: [403][404][405][406][407][408] 2011) he permeability of the plasma membrane to water and cryoprotectants is one of the most important factors for successful cryopreservation of oocytes/embryos because it influences the formation of intracellular ice, the toxicity of cryoprotectants and osmotic swelling [1]. For cryopreservation of oocytes/embryos, vitrification has advantages over slow freezing in terms of the simplicity of the method and viability of the cells. As the solution used for vitrification contains a high concentration of cryoprotectants, it is much more toxic than the solution for slow-freezing. Therefore, the permeability of the plasma membrane would affect the survival of cryopreserved cells more in vitrification than in slow freezing. If the permeability is low, insufficient exposure to the cryoprotectants causes formation of intracellular ice. However, excessive exposure results in toxic effects of the cryoprotectants. Therefore, high permeability to water and cryoprotectants would be preferable for vitrification.We showed that a simple one-step method is effective for vitrification of mouse morulae [2] but that a two-step method with a pretreatment with a lower concentration of the cryoprotectant is favorable for vitrifying mouse embryos at early cleavage stages...

Effects of thermal and cycloheximide pre‐treatments on light dependent‐necrosis formation by Pyricularia oryzae toxin(s) on cv. Sekiguchi‐asahi were investigated. Thermal treatments of rice leaves at 55 °C for 10 and 15 sec significantly suppressed leaf necrosis formation. Such heat‐induced insensitivity of rice leaves to toxin(s) was greater at a thermal treatment of 55 °C for 15 sec than that of 55 °C for 10 sec. Cycloheximide pre‐treatment also suppressed leaf necrosis formation under light.

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We examined the effects of D- or L-amino acids on the stimulation of Brassica rapa roots. When 6.7 microM of D-methionine (D-Met) or L-methionine (L-Met) was applied, root hair numbers increased. L-Met (above concentration of 67.0 microM) caused the tip of roots to spiral. When CoCl2 (ethylene synthesis inhibitor) was added into the medium, L-Met lost its activity but COCl2 did not inhibit the bioactivity of D-Met.

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