Connor Erin E, Siferd Stephen, Elsasser Theodore H, Evock-Clover Christina M, Van Tassell Curtis P, Sonstegard Tad S, Fernandes Violet M, Capuco Anthony V
Bovine Functional Genomics Laboratory, USDA-ARS, Beltsville Agricultural Research Center, 10300 Baltimore Avenue, Beltsville, MD 20705, USA.
BMC Genomics. 2008 Jul 31;9:362. doi: 10.1186/1471-2164-9-362.
Previous research has demonstrated that increased milking frequency of dairy cattle during the first few weeks of lactation enhances milk yield, and that the effect persists throughout the entire lactation period. The specific mechanisms controlling this increase in milk production are unknown, but suggested pathways include increased mammary epithelial cell number, secretory capacity, and sensitivity to lactogenic hormones. We used serial analysis of gene expression (SAGE) and microarray analysis to identify changes in gene expression in the bovine mammary gland in response to 4x daily milking beginning at d 4 of lactation (IMF4) relative to glands milked 2x daily (Control) to gain insight into physiological changes occurring within the gland during more frequent milking.
Results indicated changes in gene expression related to cell proliferation and differentiation, extracellular matrix (ECM) remodeling, metabolism, nutrient transport, and immune function in IMF4 versus Control cows. In addition, pathways expected to promote neovascularization within the gland appeared to be up regulated in IMF4 cows. To validate this finding, immunolocalization of Von Willebrandt's factor (VWF), an endothelial cell marker, and its co-localization with the nuclear proliferation antigen Ki67 were evaluated in mammary tissue sections at approximately d 7 and d 14 of lactation in cows milked 4x daily versus Controls to estimate endothelial cell abundance and proliferation within the gland. Consistent with expression of genes related to neovascularization, both abundance of VWF and its co-localization with Ki67 appeared to be elevated in cows milked 4x daily, suggesting persistent increased milk yield in response to increased milking frequency may be mediated or complemented by enhanced mammary ECM remodeling and neovascularization within the gland.
Additional study is needed to determine whether changes in ECM remodeling and neovascularization of the mammary gland result in increased milk yield during increased milking frequency, or occur in response to an increased demand for milk production. Gene pathways identified by the current study will provide a basis for future investigations to identify factors mediating the effects of milking frequency on milk yield.
先前的研究表明,在泌乳的最初几周增加奶牛的挤奶频率可提高产奶量,且这种效果在整个泌乳期都持续存在。控制产奶量增加的具体机制尚不清楚,但推测的途径包括乳腺上皮细胞数量增加、分泌能力增强以及对泌乳激素的敏感性提高。我们使用基因表达序列分析(SAGE)和微阵列分析来确定从泌乳第4天开始每天挤奶4次(IMF4)相对于每天挤奶2次(对照)的奶牛乳腺中基因表达的变化,以深入了解在更频繁挤奶期间乳腺内发生的生理变化。
结果表明,与对照奶牛相比,IMF4奶牛在细胞增殖与分化、细胞外基质(ECM)重塑、代谢、营养物质运输和免疫功能方面的基因表达发生了变化。此外,预计可促进乳腺内新血管形成的途径在IMF4奶牛中似乎上调。为了验证这一发现,在泌乳约第7天和第14天的乳腺组织切片中,对每天挤奶4次的奶牛与对照奶牛的血管性血友病因子(VWF,一种内皮细胞标志物)进行免疫定位,并评估其与核增殖抗原Ki67的共定位情况,以估计乳腺内内皮细胞的丰度和增殖情况。与新血管形成相关基因的表达一致,每天挤奶4次的奶牛中VWF的丰度及其与Ki67的共定位似乎都有所升高,这表明对增加挤奶频率的持续产奶量增加可能是由乳腺ECM重塑和乳腺内新血管形成增强介导或补充的。
需要进一步研究以确定乳腺ECM重塑和新血管形成的变化是否会在挤奶频率增加时导致产奶量增加,或者是对产奶需求增加的反应。本研究确定的基因途径将为未来研究确定介导挤奶频率对产奶量影响的因素提供基础。