Ogorevc J, Dovč P
Department of Animal Science, Biotechnical Faculty, University of Ljubljana, Domzale, Slovenia.
Department of Animal Science, Biotechnical Faculty, University of Ljubljana, Domzale, Slovenia
Genet Mol Res. 2015 Apr 15;14(2):3481-90. doi: 10.4238/2015.April.15.12.
Primary mammary epithelial cell cultures were established from mammary tissue of lactating and non-lactating goats to assess the expression of beta-casein (CSN2) in vitro. Primary cell cultures were established by enzymatic digestion of mammary tissue and characterized using antibodies against cytokeratin 14, cytokeratin 18, and vimentin. The established primary cell lines in the second passage were grown in basal medium on plastic and in hormone-supplemented (lactogenic) medium on plastic and on an extracellular matrix-covered surface, respectively. CSN2 gene expression was evaluated using quantitative reverse transcription PCR. The presence of CSN2 transcripts was detected in all samples, including cells originating from non-lactating goat, grown in basal medium. The presence of CSN2 protein was confirmed using immunofluorescence. Response to the hormonal treatment and cell morphology differed between the cell lines and treatments. In 2 cell lines supplemented with lactogenic hormones in the medium, CSN2 expression was increased, while CSN2 levels in one of the cell lines remained constant, regardless of the treatment. Addition of extracellular matrix showed positive effects on CSN2 transcription activity in 1 of the cell lines, while in the other 2 showed no statistically significant effects. CSN2 expression appeared to depend on subtle differences in physiological state of the starting tissue material, growth conditions, cell types present in the culture, and methods used for cell culture establishment. Further studies are necessary to identify factors that determine hormone-responsiveness and transcriptional activity of milk protein genes in goat primary mammary cell cultures.
从泌乳期和非泌乳期山羊的乳腺组织中建立原代乳腺上皮细胞培养物,以评估β-酪蛋白(CSN2)在体外的表达。通过酶消化乳腺组织建立原代细胞培养物,并使用抗细胞角蛋白14、细胞角蛋白18和波形蛋白的抗体进行鉴定。第二代建立的原代细胞系分别在塑料培养皿上的基础培养基中、在塑料培养皿上的激素补充(产乳)培养基中以及在细胞外基质覆盖的表面上生长。使用定量逆转录PCR评估CSN2基因表达。在所有样品中都检测到了CSN2转录本的存在,包括在基础培养基中生长的来自非泌乳期山羊的细胞。使用免疫荧光法确认了CSN2蛋白的存在。细胞系和处理之间对激素处理的反应和细胞形态有所不同。在培养基中添加产乳激素的2个细胞系中,CSN2表达增加,而其中一个细胞系中的CSN2水平保持不变,无论处理如何。添加细胞外基质对其中1个细胞系的CSN2转录活性有积极影响,而在另外2个细胞系中则没有统计学上的显著影响。CSN2的表达似乎取决于起始组织材料的生理状态、生长条件、培养物中存在的细胞类型以及用于建立细胞培养的方法的细微差异。有必要进行进一步的研究,以确定决定山羊原代乳腺细胞培养物中乳蛋白基因激素反应性和转录活性的因素。