Keely P J, Wu J E, Santoro S A
Department of Pathology, Washington University School of Medicine, St. Louis, MO 63110-1093, USA.
Differentiation. 1995 Jul;59(1):1-13. doi: 10.1046/j.1432-0436.1995.5910001.x.
To begin to determine the role of the alpha 2 beta 1 integrin and its ligands, collagen I, collagen IV, and laminin, in mammary epithelial differentiation in vivo, we determined the expression of these molecules by in situ hybridization and immunofluorescence in the developing mouse mammary gland. Expression of collagen I, collagen IV, and laminin mRNAs in the mammary gland during puberty corresponded to the period of greatest growth of the gland, 4-7 weeks postnatally. Collagen I expression preceded collagen IV expression, both of which preceded laminin expression, suggesting an important temporal sequence of extracellular matrix (ECM) production. When growth of the epithelium ceased in the adult virgin gland, expression of all three mRNAs became undetectable. Following the onset of pregnancy these molecules were re-expressed with the same chronology observed during puberty. Collagen I, collagen IV, and laminin were expressed by stromal cells immediately surrounding the developing ductal epithelium. Surprisingly, we found no expression of ECM components in the epithelial cells, suggesting the mammary epithelium does not synthesize its own basement membrane. The distribution of collagen I was consistent with a role in duct formation, since collagen I was strikingly abundant around larger mammary ducts, but was sparse around growing endbuds or alveoli. Conversely, there was abundant laminin near growing endbuds and around alveoli, and less around large ducts, suggesting its role is different than collagen I. The alpha 2 beta 1 integrin was present on the basal, lateral, and apical surfaces of the mammary epithelium throughout postnatal development and pregnancy. The alpha 2 beta 1 integrin expression was strongest at midpregnancy, suggesting a role for alpha 2 beta 1 integrin in the alveolar formation that occurs at this time. The alpha 2 beta 1 integrin expression decreased dramatically in the lactating gland. Our results suggest that alpha 2 beta 1 integrin interactions with its temporally and spatially regulated ligands, collagen I, collagen IV, and laminin, could play an important role in mammary morphogenesis in vivo.
为了开始确定α2β1整合素及其配体(I型胶原、IV型胶原和层粘连蛋白)在体内乳腺上皮分化中的作用,我们通过原位杂交和免疫荧光法测定了这些分子在发育中的小鼠乳腺中的表达。青春期乳腺中I型胶原、IV型胶原和层粘连蛋白mRNA的表达与腺体生长最旺盛的时期相对应,即出生后4 - 7周。I型胶原的表达先于IV型胶原,两者又都先于层粘连蛋白的表达,这表明细胞外基质(ECM)产生存在重要的时间顺序。当成年未孕腺体中上皮生长停止时,所有这三种mRNA的表达都无法检测到。怀孕开始后,这些分子以与青春期观察到的相同时间顺序重新表达。I型胶原、IV型胶原和层粘连蛋白由紧邻发育中的导管上皮的基质细胞表达。令人惊讶的是,我们发现上皮细胞中没有ECM成分的表达,这表明乳腺上皮不合成其自身的基底膜。I型胶原的分布与导管形成中的作用一致,因为I型胶原在较大的乳腺导管周围显著丰富,但在生长中的终末芽或肺泡周围稀疏。相反,生长中的终末芽附近和肺泡周围有丰富的层粘连蛋白,而在大导管周围较少,这表明其作用与I型胶原不同。在出生后发育和怀孕过程中,α2β1整合素存在于乳腺上皮的基底、侧面和顶端表面。α2β1整合素的表达在妊娠中期最强,这表明α2β1整合素在此时发生的肺泡形成中起作用。α2β1整合素的表达在泌乳腺中急剧下降。我们的结果表明,α2β1整合素与其在时间和空间上受调控的配体(I型胶原、IV型胶原和层粘连蛋白)之间的相互作用可能在体内乳腺形态发生中起重要作用。