Araújo V R, Gastal M O, Wischral A, Figueiredo J R, Gastal E L
Department of Animal Science, Food and Nutrition, Southern Illinois University, 1205 Lincoln Drive, MC 4417, Carbondale, IL, 62901, USA; Laboratory of Manipulation of Oocytes and Preantral Follicles (LAMOFOPA), Veterinary Faculty, State University of Ceará, Av. Paranjana 1700, Campus do Itaperi, Fortaleza, 60740-903 CE, Brazil.
Department of Animal Science, Food and Nutrition, Southern Illinois University, 1205 Lincoln Drive, MC 4417, Carbondale, IL, 62901, USA.
Anim Reprod Sci. 2015 Oct;161:23-31. doi: 10.1016/j.anireprosci.2015.07.006. Epub 2015 Jul 29.
Two culture media and replacement methods were compared during long-term in vitro culture of secondary follicles of cattle using α-MEM(+) or TCM-199(+) as base media. The medium replacement methods were: Conventional - removal and subsequent addition of the same amount (60μl) in a 100μl aliquot (MEM-C and TCM-C), and Small Supplementation - addition of 5μl of fresh medium to an initial small aliquot (50μl), resulting in a final volume of 125μl on the last day of culture (MEM-S and TCM-S). A total of 207 secondary follicles were cultured individually for 32 days at 38.5°C in 5% CO2 and medium replacement was performed every other day. The MEM-S treatment resulted in a larger (P<0.01) follicular diameter, greater (P<0.02) growth rate, greater (P<0.02) antrum formation, as well as greater (P<0.0001) estradiol concentrations when compared with the MEM-C treatment. The medium change methods did not affect (P>0.05) the follicular and estradiol end points for TCM-199(+). The expression of the FSHR gene was greater (P<0.03) with the TCM-C than TCM-S treatment, while the relative amounts of mRNA for IGF1 was greater (P<0.02) with MEM-S than TCM-S treatments and for VEGF was greater (P<0.02) with MEM-C than TCM-C treatment. In conclusion, the type of base medium and the effect of periodic addition of medium differentially affected follicle development, estradiol production, and gene expression. Furthermore, α-MEM(+) can be used to replace TCM-199(+) for culture of preantral follicles of cattle if progressive addition of medium is used for medium change.
在牛次级卵泡的长期体外培养过程中,比较了两种培养基及其更换方法,以α-MEM(+)或TCM-199(+)作为基础培养基。培养基更换方法为:传统方法——在100μl分装液中去除并随后添加相同量(60μl)的培养基(MEM-C和TCM-C),以及少量补充法——向初始少量分装液(50μl)中添加5μl新鲜培养基,在培养的最后一天最终体积达到125μl(MEM-S和TCM-S)。总共207个次级卵泡在38.5°C、5%二氧化碳条件下单独培养32天,每隔一天更换培养基。与MEM-C处理相比,MEM-S处理导致卵泡直径更大(P<0.01)、生长速率更高(P<0.02)、腔形成更多(P<0.02)以及雌二醇浓度更高(P<0.0001)。培养基更换方法对TCM-199(+)的卵泡和雌二醇终点指标没有影响(P>0.05)。与TCM-S处理相比,TCM-C处理的FSHR基因表达更高(P<0.03),而与TCM-S处理相比,MEM-S处理的IGF1 mRNA相对量更高(P<0.02),与TCM-C处理相比,MEM-C处理的VEGF mRNA相对量更高(P<0.02)。总之,基础培养基类型和定期添加培养基的效果对卵泡发育、雌二醇产生和基因表达有不同影响。此外,如果采用逐步添加培养基的方法更换培养基,α-MEM(+)可用于替代TCM-199(+)培养牛的窦前卵泡。