Quarrie L H, Addey C V, Wilde C J
Hannah Research Institute, United Kingdom.
J Cell Physiol. 1996 Sep;168(3):559-69. doi: 10.1002/(SICI)1097-4652(199609)168:3<559::AID-JCP8>3.0.CO;2-O.
Programmed cell death in mammary tissue was studied during natural weaning in lactating mice and after litter removal or milk stasis. All treatments stimulated mammary apoptosis, indicating that this process is an integral part of the tissue's involution after lactation. Induction of apoptosis was slower in natural weaning than after litter removal but occurred earlier when mice were concurrently pregnant during natural weaning. Ipsilateral induction of apoptosis by milk stasis in teat-sealed glands indicates that cell death is under local (i.e., intramammary) as well as endocrine regulation. Apoptosis detected by DNA laddering was associated with changes in expression of p53 and bax, two genes implicated in the regulation of cell death, and was accompanied by structural degeneration characteristic of mammary involution. Reciprocal changes in stromelysin mRNA, and that of its inhibitor TIMP-2, suggested that this structural reorganisation was the result of coordinated changes in gene expression favouring proteolysis of the extracellular matrix.
在哺乳期小鼠自然断奶期间以及去除幼崽或乳汁淤积后,对乳腺组织中的程序性细胞死亡进行了研究。所有处理均刺激了乳腺细胞凋亡,表明该过程是泌乳后组织退化的一个组成部分。自然断奶时细胞凋亡的诱导比去除幼崽后要慢,但在自然断奶期间小鼠同时怀孕时则发生得更早。乳头封闭腺体中乳汁淤积对同侧细胞凋亡的诱导表明,细胞死亡受局部(即乳腺内)以及内分泌调节。通过DNA梯带检测到的细胞凋亡与p53和bax表达的变化有关,这两个基因参与细胞死亡的调节,并伴有乳腺退化的结构变性特征。基质溶素mRNA及其抑制剂TIMP-2的相互变化表明,这种结构重组是有利于细胞外基质蛋白水解的基因表达协调变化的结果。