NYU School of Medicine, New York, USA.
Cell Cycle. 2010 Nov 1;9(21):4379-86. doi: 10.4161/cc.9.21.13671. Epub 2010 Nov 15.
Fibroblast growth factors (FGFs) negatively regulate long bone development by inhibiting the proliferation of chondrocytes that accumulate in the G₁ phase of the cycle following FGF treatment. Here we report that FGF also causes a striking but transient delay in mitotic entry in RCS chondrocytes by inactivating the cyclin B1-associated CDK1(CDC2) kinase. As a consequence of this inactivation, cells accumulate in the G₂ phase of the cycle for the first 4-6 hours of the treatment. Cyclin B1/CDK1 activity is then restored and cells reach a G₁ arrest. The reduced cyclin B1/CDK1 activity was accompanied by increased CDK1 inhibitory phosphorylation, likely caused by increased activity and expression of the Myt1 kinase. FGF1 also caused dephosphorylation of the CDC25C phosphatase, that however appears due the inactivation of cyclin B1/CDK1 complex in the CDK1 feedback loop, and not the activation of specific phosphatases. the inactivation of the cyclin B1/CDK1 complex is a direct effect of FGF signaling, and not a consequence of the G₂ arrest as it can be observed also in cells blocked at mitosis by Nocodazole. The Chk1 and AtM/ATR kinase are known to play essential roles in the G₂ checkpoint induced by DNA damage/genotoxic stress, but inhibition of Chk1 or ATM/ATR not only did not prevent, but rather potentiated the FGF-induced G₂ arrest. Additionally our results indicate that the transient G₂ arrest is induced by FGF in RCS cell through mechanisms that are independent of the G₁ arrest, and that the G₂ block is not strictly required for the sustained G₁ arrest but may provide a pausing mechanism that allows the FGF response to be fully established.
成纤维细胞生长因子 (FGFs) 通过抑制在 FGF 处理后积累在周期 G₁ 期的软骨细胞增殖来负调控长骨发育。在这里,我们报告 FGF 还通过使 cyclin B1 相关的 CDK1(CDC2)激酶失活,导致 RCS 软骨细胞有丝分裂进入的明显但短暂的延迟。由于这种失活,细胞在处理的前 4-6 小时内积累在周期的 G₂ 期。然后,cyclin B1/CDK1 活性被恢复,细胞达到 G₁ 期阻滞。cyclin B1/CDK1 活性降低伴随着 CDK1 抑制性磷酸化的增加,这可能是由于 Myt1 激酶活性和表达的增加所致。FGF1 还导致 CDC25C 磷酸酶去磷酸化,但这似乎是由于 cyclin B1/CDK1 复合物在 CDK1 反馈环中的失活,而不是特定磷酸酶的激活所致。cyclin B1/CDK1 复合物的失活是 FGF 信号的直接作用,而不是 G₂ 期阻滞的结果,因为即使在细胞被 Nocodazole 阻断有丝分裂时也可以观察到。Chk1 和 AtM/ATR 激酶在由 DNA 损伤/遗传毒性应激诱导的 G₂ 检查点中发挥重要作用,但 Chk1 或 ATM/ATR 的抑制不仅没有阻止,反而增强了 FGF 诱导的 G₂ 期阻滞。此外,我们的结果表明,FGF 通过独立于 G₁ 期阻滞的机制在 RCS 细胞中诱导短暂的 G₂ 期阻滞,并且 G₂ 阻滞不是维持 G₁ 期阻滞所必需的,但可能提供一种暂停机制,允许 FGF 反应得到充分建立。