Animal Genomics and Improvement Laboratory, USDA-Agricultural Research Service, Beltsville, MD 20705.
College of Animal Biotechnology, Guru Angad Dev Veterinary and Animal Sciences University, Ludhiana, Punjab 141004, India.
J Dairy Sci. 2020 Mar;103(3):2928-2940. doi: 10.3168/jds.2019-17241. Epub 2019 Nov 6.
The mammary gland undergoes distinct periods of growth, development, and secretory activity. During bovine lactation, a gradual decrease in the number of mammary epithelial cells largely accounts for the decline in milk production with advancing lactation. The net decline in cell number (approx. 50%) is due to cell death but is simultaneously accompanied by cell renewal. Although the rate of cell proliferation is slow, by the end of lactation most cells in the gland were formed after calving. Typically milking is terminated when cows are in the final 2 mo of pregnancy. This causes regenerative involution, wherein extensive cell replacement and mammary growth occurs. We hypothesized that replacement of senescent secretory cells and progenitor cells during the dry period increases milk yield in the next lactation. Analysis of global gene expression revealed networks and canonical pathways during regenerative involution that support cell turnover and mammary growth, and reflect oxidative stress, mitochondrial dysfunction, and endoplasmic reticulum (ER) stress. Immune responses consistent with influx of neutrophils, macrophages, and lymphocytes, and processes that support mammary differentiation and lactogenesis were also evident. Data also suggest that replication of stem and progenitor cells occurs during the dry period. Relying on long-term retention of bromodeoxyuridine-labeled DNA, we identified putative bovine mammary stem cells. These label-retaining epithelial cells (LREC) are in low abundance within mammary epithelium (<1%), predominantly estrogen receptor-negative, and localized in a basal or suprabasal layer of the epithelium. Analyses of gene expression in laser-microdissected LREC are consistent with the concept that LREC represent stem cells and progenitor cells, which differ in properties and location within the epithelial layer. We identified potential markers for these cells and have increased their number by infusing xanthosine through the teat canal of prepubertal heifers. Altering population dynamics of mammary stem and progenitor cells during the mammary cycle may be a means to increase efficiency of milk production.
乳腺经历了明显的生长、发育和分泌活动期。在奶牛泌乳期间,乳腺上皮细胞数量逐渐减少,在泌乳后期乳汁产量下降在很大程度上是由于细胞死亡,但同时伴随着细胞更新。细胞数量的净减少(约 50%)是由于细胞死亡,但同时伴随着细胞更新。尽管细胞增殖速度缓慢,但到泌乳期末,乳腺中大多数细胞都是在产犊后形成的。通常在奶牛怀孕的最后 2 个月停止挤奶。这会导致再生性萎缩,其中会发生广泛的细胞替代和乳腺生长。我们假设在干奶期替换衰老的分泌细胞和祖细胞会增加下一泌乳期的产奶量。对再生性萎缩过程中的全基因表达分析揭示了支持细胞更替和乳腺生长的网络和典型途径,反映了氧化应激、线粒体功能障碍和内质网(ER)应激。也有迹象表明,在干奶期有大量中性粒细胞、巨噬细胞和淋巴细胞流入,并且支持乳腺分化和泌乳的过程也在进行。数据还表明,干细胞和祖细胞的复制发生在干奶期。通过长期保留溴脱氧尿苷标记的 DNA,我们鉴定了牛乳腺干细胞的假设。这些持续标记的上皮细胞(LREC)在乳腺上皮细胞中含量较低(<1%),主要为雌激素受体阴性,位于上皮细胞的基底层或基底上层。对激光微切割的 LREC 进行基因表达分析的结果与 LREC 代表干细胞和祖细胞的概念一致,这些细胞在性质和位置上存在差异上皮层。我们鉴定了这些细胞的潜在标记物,并通过向青春期前小母牛的乳头管中注入黄嘌呤核苷增加了它们的数量。改变乳腺干细胞和祖细胞在乳腺周期中的群体动态可能是提高产奶效率的一种方法。