McBryan Jean, Howlin Jillian
Department of Molecular Medicine Royal College of Surgeons in Ireland Education and Research Centre, Beaumont Hospital, Dublin, 9, Ireland.
Division of Oncology-Pathology, Lund University Cancer Center/Medicon Village, Building 404:B2, Scheelevägen 2, 223 81, Lund, Sweden.
Methods Mol Biol. 2017;1501:77-114. doi: 10.1007/978-1-4939-6475-8_3.
During the past 25 years, the combination of increasingly sophisticated gene targeting technology with transplantation techniques has allowed researchers to address a wide array of questions about postnatal mammary gland development. These in turn have significantly contributed to our knowledge of other branched epithelial structures. This review chapter highlights a selection of the mouse models exhibiting a pubertal mammary gland phenotype with a focus on how they have contributed to our overall understanding of in vivo mammary morphogenesis. We discuss mouse models that have enabled us to assign functions to particular genes and proteins and, more importantly, have determined when and where these factors are required for completion of ductal outgrowth and branch patterning. The reason for the success of the mouse mammary gland model is undoubtedly the suitability of the postnatal mammary gland to experimental manipulation. The gland itself is very amenable to investigation and the combination of genetic modification with accessibility to the tissue has allowed an impressive number of studies to inform biology. Excision of the rudimentary epithelial structure postnatally allows genetically modified tissue to be readily transplanted into wild type stroma or vice versa, and has thus defined the contribution of each compartment to particular phenotypes. Similarly, whole gland transplantation has been used to definitively discern local effects from indirect systemic effects of various growth factors and hormones. While appreciative of the power of these tools and techniques, we are also cognizant of some of their limitations, and we discuss some shortcomings and future strategies that can overcome them.
在过去25年里,日益成熟的基因靶向技术与移植技术相结合,使研究人员能够解决一系列关于产后乳腺发育的问题。这些问题反过来又极大地增进了我们对其他分支上皮结构的了解。本章综述重点介绍了一些表现出青春期乳腺表型的小鼠模型,着重阐述它们如何有助于我们全面理解体内乳腺形态发生。我们讨论了一些小鼠模型,这些模型使我们能够确定特定基因和蛋白质的功能,更重要的是,确定了导管生长和分支模式完成时这些因子在何时何地发挥作用。小鼠乳腺模型取得成功的原因无疑是产后乳腺适合进行实验操作。乳腺本身非常便于研究,基因改造与组织可及性的结合使得大量研究能够为生物学提供信息。产后切除原始上皮结构可使转基因组织轻松移植到野生型基质中,反之亦然,从而明确了每个隔室对特定表型的贡献。同样,全腺移植已被用于明确区分各种生长因子和激素的局部效应与间接全身效应。尽管我们认识到这些工具和技术的强大之处,但也意识到它们存在一些局限性,并讨论了一些缺点以及能够克服这些缺点的未来策略。