Sutherland Kate D, Lindeman Geoffrey J, Visvader Jane E
VBCRC Laboratory, The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC 3050, Australia.
J Mammary Gland Biol Neoplasia. 2007 Mar;12(1):15-23. doi: 10.1007/s10911-007-9034-8.
Mammary gland involution, characterized by extensive apoptosis and structural remodelling of the gland, is the process by which the gland is returned to the pre-pregnant state. A key advantage of the mammary gland is the ability to synchronize involution through forced weaning, thus allowing the dissection of biochemical pathways involved in the involution process. Over the past few years, significant advances have been made in understanding the signaling pathways and downstream effectors that regulate epithelial cell apoptosis in the first phase of involution, and the importance of matrix metalloproteinases and their inhibitors in both phases of involution. The precise nature of the triggers for apoptosis, however, and the ultimate perpetrators of cell death are not yet clear. This review focuses on genes whose perturbation, either by targeted deletion or overexpression in transgenic mouse models, leads to precocious involution. The accumulating data point to a complex network of signal transduction pathways that synergize to regulate apoptosis in the involuting mammary gland.
乳腺退化的特征是广泛的细胞凋亡和腺体结构重塑,是乳腺恢复到怀孕前状态的过程。乳腺的一个关键优势是能够通过强制断奶使退化同步,从而便于剖析参与退化过程的生化途径。在过去几年中,在理解调控退化第一阶段上皮细胞凋亡的信号通路和下游效应器,以及基质金属蛋白酶及其抑制剂在退化两个阶段中的重要性方面取得了重大进展。然而,细胞凋亡的触发因素的确切性质以及细胞死亡的最终肇事者尚不清楚。本综述重点关注那些通过转基因小鼠模型中的靶向缺失或过表达而发生扰动从而导致早熟退化的基因。越来越多的数据表明,存在一个协同调节退化乳腺中细胞凋亡的复杂信号转导通路网络。