Bassols J, Kádár E, Briz M, Pinart E, Sancho S, Garcia-Gil N, Badia E, Pruneda A, Bussalleu E, Yeste M, Casas I, Bonet S
Biotechnology of Porcine Reproduction, Department of Biology, INTEA, Faculty of Sciences, University of Girona, Campus Montilivi s/n, 17071 Girona, Spain.
Anim Reprod Sci. 2006 Oct;95(3-4):262-72. doi: 10.1016/j.anireprosci.2005.10.005. Epub 2005 Nov 14.
The goal of this study was to investigate the effect of the collagenase digestion time, the initial density of fragments and the culture temperature on the obtention of a boar epididymal epithelial cell culture, which is a useful methodology for the study of epididymal functions. A confluent monolayer of caput, corpus and cauda epididymal epithelial cells was only obtained when an adequate enzymatic digestion of the connective tissue surrounding the epididymal tubule was performed. For the correct digestion of caput and corpus fragments two collagenase digestions of 2 and 1h, respectively, were enough. Cauda fragments, however, needed two collagenase digestions of 3h each. A confluent monolayer of caput, corpus and cauda epididymal epithelial cells was obtained regardless of the initial density tested (15, 30, 60 and 90fragments/well). However, cultures originated from 15 and 30fragments/well showed higher cell concentration during the first 2 weeks of culture than cultures originated from 60 and 90fragments/well. A confluent monolayer of caput, corpus and cauda epididymal epithelial cells was obtained at both 32 and 37 degrees Celsius, but at 32 degrees Celsius cells grew very slowly and confluence was not reached until a week later than it was with cells growing at 37 degrees Celsius. In conclusion, we have observed that the time of digestion with collagenase is an important factor for the successful establishment of boar epididymal cell monolayers, and that the initial density of fragments and the culture temperature should be taken into account.
本研究的目的是调查胶原酶消化时间、片段初始密度和培养温度对猪附睾上皮细胞培养物获取的影响,这是一种用于研究附睾功能的有用方法。只有在对附睾管周围的结缔组织进行充分的酶消化后,才能获得附睾头、体和尾上皮细胞的汇合单层。对于附睾头和体片段的正确消化,分别进行2小时和1小时的两次胶原酶消化就足够了。然而,附睾尾片段需要两次每次3小时的胶原酶消化。无论测试的初始密度如何(15、30、60和90个片段/孔),都能获得附睾头、体和尾上皮细胞的汇合单层。然而,起源于15和30个片段/孔的培养物在培养的前两周显示出比起源于60和90个片段/孔的培养物更高的细胞浓度。在32摄氏度和37摄氏度下均能获得附睾头、体和尾上皮细胞的汇合单层,但在32摄氏度下细胞生长非常缓慢,直到比在37摄氏度下生长的细胞晚一周才达到汇合。总之,我们观察到胶原酶消化时间是成功建立猪附睾细胞单层的重要因素,并且应考虑片段的初始密度和培养温度。