Section of Gene Expression Regulation, Frontier Science Research Center, Kagoshima University, Kagoshima, Japan.
Syst Biol Reprod Med. 2012 Jun;58(3):136-41. doi: 10.3109/19396368.2012.656796. Epub 2012 Feb 10.
Ovarian follicle development is a complex process mediated by interactions between oocytes and surrounding follicular cells. In an ovary, oocytes are ultimately released from Graafian follicles, which develop from antral follicles localized near the surface of an ovary. To examine the molecular interaction between these 2 cell types, direct gene transfer to follicular cells as well as oocytes appears to be a promising approach, but few studies have applied this technique. The aim of the present study was to develop a technique for gene transfer to antral follicle cells based on their accessibility near the surface of an ovary. B6C3F1 (a hybrid between C57BL6/N and C3H/HeN) female mice aged 4 or 8 w were anesthesized and their ovaries were exposed. About 100 nl of a solution containing reporter plasmid DNA (0.5 µg/μl) and 0.1% trypan blue was injected into a follicle using a glass micropipette attached to the mouthpiece. A total of 6 follicles were injected per ovary. After injection, the ovary was immediately subjected to in vivo electroporation (EP) using an electroporator with 8 square electric pulses of 50 ms and 50 V. After 24 h, the treated ovaries were excised to examine the expression of reporter constructs by histochemistry. All the injected follicles expressed reporter genes to different extents. Inspection of cryostat sections of ovaries injected with the lacZ expression plasmid demonstrated that 50-100% of follicular cells within a follicle were successfully transfected. However, there were no oocytes within the antral follicles that were negative for such staining (15 follicles tested). Similar results were obtained when the enhanced green fluorescent protein expression plasmid was introduced. The present method based on in vivo EP was found to be very effective for transfection of follicular cells. This approach might be useful to explore the roles of genes related to oogenesis/folliculogenesis, and for reproductive manipulation targeted to antral follicles.
卵泡发育是一个复杂的过程,由卵母细胞和周围卵泡细胞之间的相互作用介导。在卵巢中,卵母细胞最终从格拉夫氏卵泡中释放出来,这些卵泡是由位于卵巢表面附近的窦卵泡发育而来的。为了研究这两种细胞类型之间的分子相互作用,直接将基因转移到卵泡细胞和卵母细胞似乎是一种很有前途的方法,但很少有研究应用这种技术。本研究旨在建立一种基于卵巢表面附近窦卵泡细胞可及性的基因转移到窦卵泡细胞的技术。4 或 8 周龄 B6C3F1(C57BL6/N 和 C3H/HeN 的杂交种)雌性小鼠麻醉后暴露卵巢。用连接在吹嘴的玻璃微量移液器将含有报告质粒 DNA(0.5μg/μl)和 0.1%台盼蓝的溶液约 100nl 注射到一个卵泡中。每个卵巢共注射 6 个卵泡。注射后,用具有 8 个 50ms 和 50V 的方形电脉冲的电穿孔仪立即对卵巢进行体内电穿孔(EP)。24 小时后,切除处理过的卵巢,通过组织化学法检查报告基因的表达。所有注射的卵泡都不同程度地表达了报告基因。对注射 lacZ 表达质粒的卵巢冷冻切片进行检查表明,一个卵泡内的 50-100%的卵泡细胞被成功转染。然而,在没有这种染色的窦卵泡内没有卵母细胞(测试了 15 个卵泡)。当引入增强型绿色荧光蛋白表达质粒时,得到了类似的结果。基于体内 EP 的这种方法被发现对卵泡细胞的转染非常有效。这种方法可能有助于探索与卵母细胞发生/卵泡发生相关的基因的作用,并用于针对窦卵泡的生殖操作。