Farin C E, Yang L
Department of Animal Science, North Carolina State University, Raleigh 27695-7621.
Mol Reprod Dev. 1994 Mar;37(3):284-92. doi: 10.1002/mrd.1080370307.
5,6-Dichloro-1-beta-D-ribofuranosyl-benzimidazole (DRB) is an analog of the nucleoside adenosine that has been used to inhibit transcription in a variety of cell types. The present studies were designed to evaluate the ability of DRB to block germinal vesicle breakdown (GVBD) in bovine oocytes matured in vitro and to characterize culture conditions required for DRB-mediated arrest of meiosis. Administration of DRB (60-90 microM) at 2-3 h intervals during culture of COC blocked GVBD in approximately 70 percent of oocytes. The inhibitory effect of DRB was reversible and required the presence of cumulus cells. Treatment with DRB was associated with a 57% decrease in 3H-uridine incorporation into total COC RNA and a 90.8% decrease into mRNA but did not affect the incorporation of 3H-leucine into COC proteins. The ability of DRB to arrest meiosis was significantly compromised if supplemental gonadotropin preparations were absent from the maturation media. Gonadotropin-induced GVBD as well as cumulus cell expansion was blocked by treatment with DRB but not with adenosine. GVBD in cultured bovine COC was initially inhibited and then stimulated when supplemental gonadotropin preparations were included in the culture media. DRB treatment in the presence of gonadotropin supplementation blocked the stimulatory effect of gonadotropins on GVBD. In conclusion, DRB can be used to arrest GVBD in bovine COC in a specific and reversible manner. The data support the hypothesis that gene transcription is required for the stimulatory phase of gonadotropin-mediated GVBD in cultured bovine COC.
5,6-二氯-1-β-D-呋喃核糖基苯并咪唑(DRB)是核苷腺苷的类似物,已被用于抑制多种细胞类型中的转录。本研究旨在评估DRB阻断体外成熟的牛卵母细胞生发泡破裂(GVBD)的能力,并确定DRB介导的减数分裂阻滞所需的培养条件。在COC培养期间每隔2 - 3小时给予DRB(60 - 90 microM)可使约70%的卵母细胞阻断GVBD。DRB的抑制作用是可逆的,并且需要卵丘细胞的存在。用DRB处理会使3H-尿苷掺入总COC RNA的量减少57%,掺入mRNA的量减少90.8%,但不影响3H-亮氨酸掺入COC蛋白质。如果成熟培养基中没有补充促性腺激素制剂,DRB阻止减数分裂的能力会显著受损。促性腺激素诱导的GVBD以及卵丘细胞扩张被DRB处理阻断,但腺苷处理则不会。当培养基中包含补充促性腺激素制剂时,培养的牛COC中的GVBD最初受到抑制,然后受到刺激。在补充促性腺激素的情况下进行DRB处理可阻断促性腺激素对GVBD的刺激作用。总之,DRB可用于以特异性和可逆的方式阻断牛COC中的GVBD。数据支持这样的假设,即基因转录是培养的牛COC中促性腺激素介导的GVBD刺激阶段所必需的。