Neuenschwander S, Schwartz A, Wood T L, Roberts C T, Hennighausen L, LeRoith D
Diabetes Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
J Clin Invest. 1996 May 15;97(10):2225-32. doi: 10.1172/JCI118663.
Development of the mammary gland during puberty, pregnancy, and lactation is controlled by steroid and peptide hormones and growth factors. To determine the role of the insulin-like growth factors (IGFs) in this process we developed a transgenic model using the whey acidic protein (WAP) gene to direct expression of rat IGF-I and human IGF binding protein-3 (IGFBP-3) to mammary tissue during late pregnancy and throughout lactation. High levels of expression of transgenic IGF-I and IGFBP-3 were seen in lobular-alveolar cells by in situ hybridization. There was no obvious effect on mammary development during pregnancy and lactation; indeed, mothers were capable of nursing their pups normally and the only structural difference seen in the mammary glands at peak lactation was an overall smaller size of the alveoli. We also evaluated the role of IGF-I and IGFBP-3 in the remodeling of mammary tissue during involution. Compared with control animals, the process of involution was modified in both transgenic lines. The degree of apoptotic cells was lower in the WAP-IGF-I and WAP-BP-3 expressing mice. In addition, there was a more quiescent pattern of involution with residual lobular secretary ability and a muted host inflammatory reaction with fewer lumenal microcalcifications. These results demonstrate that IGF-I and IGFBP-3 may modulate the involutionary process of the lactating mammary gland.
青春期、孕期及哺乳期乳腺的发育受类固醇激素、肽类激素及生长因子的调控。为确定胰岛素样生长因子(IGF)在此过程中的作用,我们构建了一种转基因模型,利用乳清酸性蛋白(WAP)基因在妊娠后期及整个哺乳期将大鼠IGF-I和人IGF结合蛋白-3(IGFBP-3)定向表达于乳腺组织。通过原位杂交在小叶-腺泡细胞中观察到转基因IGF-I和IGFBP-3的高表达。在妊娠和哺乳期对乳腺发育没有明显影响;实际上,母鼠能够正常哺育幼崽,在泌乳高峰期乳腺中唯一可见的结构差异是腺泡总体尺寸较小。我们还评估了IGF-I和IGFBP-3在乳腺退化过程中乳腺组织重塑的作用。与对照动物相比,两个转基因品系的退化过程均发生了改变。在表达WAP-IGF-I和WAP-BP-3的小鼠中,凋亡细胞的程度较低。此外,退化过程更为静止,保留了小叶分泌能力,且宿主炎症反应减弱,管腔内微钙化减少。这些结果表明,IGF-I和IGFBP-3可能调节泌乳期乳腺的退化过程。