Cell Biology Section, Laboratory of Cell and Developmental Biology, Division of Intramural Research, National Institute of Dental and Craniofacial Research, 30 Convent Drive, MSC 4370, Bethesda, MD 20892, USA.
J Dent Res. 2011 Sep;90(9):1078-84. doi: 10.1177/0022034511413131. Epub 2011 Jun 27.
During organ development, local changes in gene expression govern morphogenesis and cell fate. We have generated a microanatomical atlas of epithelial gene expression of embryonic salivary glands. The mouse submandibular salivary gland first appears as a single mass of epithelial cells surrounded by mesenchyme, and it undergoes rapid branching morphogenesis to form a complex secretory organ with acini connected to an extensive ductal system. Using laser capture microdissection, we collected samples from 14 distinct epithelial locations at embryonic days 12.5, 13.5, 14, and 15, and characterized their gene expression by microarray analysis. These microarray results were evaluated by qPCR of biological replicates and by comparisons of the gene expression dataset with published expression data. Using this gene expression atlas to search for novel regulators of branching morphogenesis, we found a substantial reduction in mRNA levels of GSK3β at the base of forming clefts. This unexpected finding was confirmed by immunostaining, and inhibition of GSK3β activity enhanced salivary gland branching. This first microanatomical expression atlas of a developing gland characterizes changes in local gene expression during salivary gland development and differentiation, which should facilitate the identification of key genes involved in tissue morphogenesis.
在器官发育过程中,基因表达的局部变化控制着形态发生和细胞命运。我们生成了胚胎唾液腺上皮基因表达的微观解剖图谱。小鼠下颌下唾液腺最初作为一团被间质包围的上皮细胞出现,然后经历快速的分支形态发生,形成一个具有与广泛导管系统相连的腺泡的复杂分泌器官。我们使用激光捕获显微解剖术,从胚胎第 12.5、13.5、14 和 15 天的 14 个不同的上皮位置采集样本,并通过微阵列分析来描述它们的基因表达。通过对生物学重复的 qPCR 进行评估,并将基因表达数据集与已发表的表达数据进行比较,对这些微阵列结果进行了验证。我们使用这个基因表达图谱来寻找分支形态发生的新调节因子,发现形成裂隙底部的 GSK3β mRNA 水平显著降低。免疫染色证实了这一意外发现,抑制 GSK3β 活性增强了唾液腺分支。这是发育中腺体的第一个微观解剖表达图谱,描述了唾液腺发育和分化过程中局部基因表达的变化,这应该有助于鉴定参与组织形态发生的关键基因。