Stiening C M, Hoying J B, Abdallah M B, Hoying A M, Pandey R, Greer K, Collier R J
Department of Animal Science, University of Arizona, Tucson 85721, USA.
J Dairy Sci. 2008 Mar;91(3):1053-66. doi: 10.3168/jds.2007-0161.
The study objective was to evaluate the effect of endocrine and mechanical (gel release) signaling on bovine mammary epithelial cell ultrastructure and gene expression. Cultures receiving only one stimulus demonstrated partially differentiated ultrastructure, which included abundant polysomes, limited rough endoplasmic reticulum, and absence of secretory products, whereas the 2 stimuli together induced a more complete lactogenic phenotype that included increased rough endoplasmic reticulum, abundant lipid droplets, and secretory vesicles containing casein micelles. The structural data indicated that although synthesis of milk components was initiated, the copious synthesis and secretion associated with stage II lactogenesis was not evident. Microarray analysis revealed that both prolactin and gel release independently regulated several genes linked to a wide array of cellular activities. In combination, they regulated fewer genes targeted to lactogenesis. Genes regulated by the combination treatment included claudin 7, multiple caseins, xanthine oxidoreductase, and several protein synthesis, packaging, and transport genes. Genes related to structural activity including keratin 15 (morphogenesis), alpha-spectrin (cell shape via actin cytoskeleton), and chitinase-like protein 1 (tissue remodeling) were up-regulated by the combination treatment as was the transcription factor Kruppel-like factor 2 (KLF-2). However, Snail 2, which down-regulates and inhibits tight junction components, was repressed in response to the combination treatment. These results suggest coordination between endocrine and physical signals at the genomic level that produces a more specific and targeted transcriptional response associated with stage I lactogenesis. A molecular pathway analysis of the differentially expressed genes revealed that genes regulating cell signaling were linked to those regulating cell structure and adhesion.
本研究的目的是评估内分泌信号和机械信号(凝胶释放)对牛乳腺上皮细胞超微结构和基因表达的影响。仅接受一种刺激的培养物表现出部分分化的超微结构,包括丰富的多核糖体、有限的粗面内质网且无分泌产物,而两种刺激共同作用则诱导出更完整的泌乳表型,包括粗面内质网增加、丰富的脂滴以及含有酪蛋白胶粒的分泌小泡。结构数据表明,尽管已启动了乳成分的合成,但与泌乳第二期相关的大量合成和分泌并不明显。微阵列分析显示,催乳素和凝胶释放均独立调节了与多种细胞活动相关的多个基因。两者共同作用时,它们调节的与泌乳相关的基因较少。联合处理所调节的基因包括闭合蛋白7、多种酪蛋白、黄嘌呤氧化还原酶以及一些蛋白质合成、包装和运输基因。联合处理上调了与结构活性相关的基因,包括角蛋白15(形态发生)、α-血影蛋白(通过肌动蛋白细胞骨架决定细胞形状)和几丁质酶样蛋白1(组织重塑),转录因子Kruppel样因子2(KLF-2)也被上调。然而,下调并抑制紧密连接成分的Snail 2在联合处理后受到抑制。这些结果表明,内分泌信号和物理信号在基因组水平上存在协同作用,从而产生了与泌乳第一期相关的更特异且有针对性的转录反应。对差异表达基因的分子通路分析表明,调节细胞信号传导的基因与调节细胞结构和黏附的基因相关联。