Sorensen M T, Nørgaard J V, Theil P K, Vestergaard M, Sejrsen K
Department of Animal Health, Welfare and Nutrition, Danish Institute of Agricultural Sciences, Research Centre Foulum, PO Box 50, DK-8830, Tjele, Denmark.
J Dairy Sci. 2006 Dec;89(12):4632-9. doi: 10.3168/jds.S0022-0302(06)72513-9.
Milk yield of the dairy cow follows a pattern termed the lactation curve. We have investigated the cellular background for this pattern. Seven mammary biopsies were obtained from each of 10 cows: at the end of lactation (d 347, equal to d 77 before next parturition); during the dry period at d 48 (4 d after dry off); 16 d before parturition; and during lactation at d 14, 42, 88, and 172. The fraction of proliferating (staining positive for Ki-67) alveolar cells was higher during the dry period (8.6%) than during lactation (0.5%). The fraction of apoptotic (staining positive by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling) alveolar cells was higher immediately after dry off (0.37%) and in early lactation (0.76%) than during other periods (0.15%). The enzyme activities of fatty acid synthetase, acetyl CoA-carboxylase, and galactosyl transferase were approximately 12-, 11-, and 4-fold higher, respectively, during lactation than during the dry period. In conclusion, mammary cell proliferation is substantial in a period near parturition but otherwise low, and apoptosis is elevated at dry off and in early lactation. The increase in apoptosis in early lactation may be due to discarding nonfunctional or senescent cells or to removal of a surplus of newly synthesized cells. The activity of selected enzymes central for milk synthesis is probably not limiting for milk production.
奶牛的产奶量遵循一种称为泌乳曲线的模式。我们已经研究了这种模式的细胞背景。从10头奶牛中的每一头获取了7次乳腺活检样本:在泌乳期末(第347天,相当于下次分娩前77天);干奶期第48天(停奶后4天);分娩前16天;以及泌乳期的第14、42、88和172天。增殖的(Ki-67染色阳性)肺泡细胞比例在干奶期(8.6%)高于泌乳期(0.5%)。凋亡的(末端脱氧核苷酸转移酶介导的dUTP缺口末端标记染色阳性)肺泡细胞比例在刚停奶后(0.37%)和泌乳早期(0.76%)高于其他时期(0.15%)。脂肪酸合成酶、乙酰辅酶A羧化酶和半乳糖基转移酶的酶活性在泌乳期分别比干奶期高约12倍、11倍和4倍。总之,乳腺细胞增殖在临近分娩期时大量增加,其他时期则较低,而凋亡在停奶时和泌乳早期升高。泌乳早期凋亡增加可能是由于丢弃无功能或衰老的细胞,或去除多余的新合成细胞。对牛奶合成至关重要的特定酶的活性可能不是牛奶生产的限制因素。