Cavalheiro Gabriel R, Matos-Rodrigues Gabriel E, Gomes Anielle L, Rodrigues Paulo M G, Martins Rodrigo A P
Programa de Biologia Celular e do Desenvolvimento, Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Rio de Janeiro, Brazil.
PLoS One. 2014 Feb 4;9(2):e87182. doi: 10.1371/journal.pone.0087182. eCollection 2014.
Myc protooncogenes play important roles in the regulation of cell proliferation, growth, differentiation and survival during development. In various developing organs, c-myc has been shown to control the expression of cell cycle regulators and its misregulated expression is detected in many human tumors. Here, we show that c-myc gene (Myc) is highly expressed in developing mouse lens. Targeted deletion of c-myc gene from head surface ectoderm dramatically impaired ocular organogenesis, resulting in severe microphtalmia, defective anterior segment development, formation of a lens stalk and/or aphakia. In particular, lenses lacking c-myc presented thinner epithelial cell layer and growth impairment that was detectable soon after its inactivation. Defective development of c-myc-null lens was not caused by increased cell death of lens progenitor cells. Instead, c-myc loss reduced cell proliferation, what was associated with an ectopic expression of Prox1 and p27(Kip1) proteins within epithelial cells. Interestingly, a sharp decrease in the expression of the forkhead box transcription factor Foxe3 was also observed following c-myc inactivation. These data represent the first description of the physiological roles played by a Myc family member in mouse lens development. Our findings support the conclusion that c-myc regulates the proliferation of lens epithelial cells in vivo and may, directly or indirectly, modulate the expression of classical cell cycle regulators in developing mouse lens.
Myc原癌基因在发育过程中对细胞增殖、生长、分化和存活的调控中发挥着重要作用。在各种发育中的器官中,c-myc已被证明可控制细胞周期调节因子的表达,并且在许多人类肿瘤中都检测到其表达失调。在此,我们表明c-myc基因(Myc)在发育中的小鼠晶状体中高度表达。从头部表面外胚层靶向缺失c-myc基因会显著损害眼器官发生,导致严重的小眼症、眼前节发育缺陷、晶状体柄形成和/或无晶状体。特别是,缺乏c-myc的晶状体呈现出较薄的上皮细胞层和生长受损,在其失活后不久即可检测到。c-myc基因缺失的晶状体发育缺陷并非由晶状体祖细胞的细胞死亡增加所致。相反,c-myc的缺失减少了细胞增殖,这与上皮细胞内Prox1和p27(Kip1)蛋白的异位表达有关。有趣的是,在c-myc失活后还观察到叉头框转录因子Foxe3的表达急剧下降。这些数据首次描述了Myc家族成员在小鼠晶状体发育中所起的生理作用。我们的研究结果支持这样的结论,即c-myc在体内调节晶状体上皮细胞的增殖,并且可能直接或间接调节发育中小鼠晶状体中经典细胞周期调节因子的表达。