Crema Virgínia O, Fossati Anna Christina M, Hamassaki Dânia E, Santos Marinilce F
Department of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes 1524, São Paulo, SP, 05508-000, Brazil.
J Mol Histol. 2008 Oct;39(5):519-25. doi: 10.1007/s10735-008-9192-z. Epub 2008 Sep 11.
During the rat submandibular gland (SMG) development, organogenesis and cytodifferentiation depend on the actin cytoskeleton, which is regulated by small Rho GTPases. These proteins link cell surface receptors to pathways that regulate cell motility, polarity, gene expression, vesicular trafficking, proliferation and apoptosis. The aim of this study was to evaluate, by immunohistochemistry, the distribution pattern of RhoA, RhoB, RhoC, Rac1 and Cdc42 during cytodifferentiation of the rat SMG and in male adults. All GTPases were found in epithelial and mesenchymal tissues throughout gland development. Rac1 appeared to be important for parenchyma expansion at the beginning of cytodifferentiation, while RhoC, Cdc42 and the inactive phosphorylated form of Rac1 seemed associated with lumen formation and cell polarization in terminal tubules. RhoA and RhoB labeling was evident throughout development. All GTPases were differentially expressed in the adult gland, suggesting that they play specific roles during differentiation and function of the rat SMG.
在大鼠下颌下腺(SMG)发育过程中,器官发生和细胞分化依赖于肌动蛋白细胞骨架,而肌动蛋白细胞骨架受小Rho GTP酶调节。这些蛋白质将细胞表面受体与调节细胞运动、极性、基因表达、囊泡运输、增殖和凋亡的信号通路联系起来。本研究的目的是通过免疫组织化学方法评估RhoA、RhoB、RhoC、Rac1和Cdc42在大鼠SMG细胞分化过程及成年雄性大鼠中的分布模式。在整个腺体发育过程中,所有GTP酶均在上皮组织和间充质组织中被发现。Rac1似乎在细胞分化开始时对实质扩展很重要,而RhoC、Cdc42和Rac1的无活性磷酸化形式似乎与终末小管中的管腔形成和细胞极化有关。RhoA和RhoB标记在整个发育过程中均很明显。所有GTP酶在成年腺体中均有差异表达,表明它们在大鼠SMG的分化和功能中发挥特定作用。