Hayashi Toru, Koyama Noriko, Gresik Edward W, Kashimata Masanori
Department of Pharmacology, Asahi University School of Dentistry, Mizuho, Japan.
J Med Invest. 2009;56 Suppl:250-2. doi: 10.2152/jmi.56.250.
Fetal murine submandibular salivary gland (SMG) is known as a model to study organogenesis including branching morphogenesis, which is a basic developmental process for formation of a wide variety of arborized organs. Branching morphogenesis is under the control of a complex network of regulatory proteins, such as the ErbB family of tyrosine kinase receptors, activated by members of the epidermal growth factor (EGF) family of ligands. Recent reports identify critical roles for micro RNAs (miRNAs) on many developmental processes through regulation of gene expression. We hypothesize that miRNAs regulating branching morphogenesis are expressed in fetal murine SMG and that expression of the miRNAs associated with branching morphogenesis is modulated in part by EGF. Using cloning methods, we obtained the expression profiles on miRNAs derived from fetal murine SMG under three different conditions: (1) native E13 SMGs (freshly isolated), (2) E13 SMGs cultured for 24 hours with no added EGF (controls), or (3) cultured with EGF. There were 44 known miRNAs and four novel miRNAs candidates in native SMG at E13. Comparing the three profiles revealed that several miRNAs were expressed specifically at each condition. These results suggested that these miRNAs were associated with regulating organogenesis, possibly including branching morphogenesis.
胎鼠下颌下唾液腺(SMG)是研究器官发生包括分支形态发生的一种模型,分支形态发生是形成多种树状器官的基本发育过程。分支形态发生受复杂的调节蛋白网络控制,如酪氨酸激酶受体的ErbB家族,由表皮生长因子(EGF)配体家族成员激活。最近的报道表明,微小RNA(miRNA)通过调节基因表达在许多发育过程中发挥关键作用。我们假设调节分支形态发生的miRNA在胎鼠SMG中表达,并且与分支形态发生相关的miRNA的表达部分受EGF调节。使用克隆方法,我们获得了在三种不同条件下源自胎鼠SMG的miRNA的表达谱:(1)天然E13 SMG(新鲜分离),(2)未添加EGF培养24小时的E13 SMG(对照),或(3)用EGF培养。在E13的天然SMG中有44种已知的miRNA和4种新的miRNA候选物。比较这三种表达谱发现,几种miRNA在每种条件下特异性表达。这些结果表明,这些miRNA与调节器官发生有关,可能包括分支形态发生。