Schmidt Thomas, Fischer Dietmar, Andreadaki Anastasia, Bartelt-Kirbach Britta, Golenhofen Nikola
Institute of Anatomy and Cell Biology, University of Ulm, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
Department of Experimental Neurology, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
Cell Stress Chaperones. 2016 Jan;21(1):167-178. doi: 10.1007/s12192-015-0650-8.
Several eye diseases are associated with axonal injury in the optic nerve, which normally leads to degeneration of retinal ganglion cells (RGCs) and subsequently to loss of vision. There is experimental evidence that some members of the small heat shock protein family (HspBs) are upregulated upon optic nerve injury (ONI) in the retina and sufficient to promote RGC survival. These data raise the question as to whether other family members may play a similar role in this context. Here, we performed a comprehensive comparative study comprising all HspBs in an experimental model of ONI. We found that five HspBs were expressed in the adult rat retina at control conditions but only HspB1 and HspB5 were upregulated in response to ONI. Furthermore, HspB1 and HspB5 were constitutively phosphorylated in Müller cells at serine 15 and serine 59, respectively. In RGCs, phosphorylation was stimulated by ONI and occurred at serine 86 of HspB1 and at serine 19 and 45 of HspB5. These data suggest that of all small heat shock proteins, only HspB1 and HspB5 might be of protective value for RGCs after ONI and that this process might be regulated by phosphorylation at serine 86 of HspB1 and serine 19 and serine 45 of HspB5. The molecular targets of phosphoHspB1 and phosphoHspB5 remain to be identified.
几种眼部疾病与视神经轴突损伤相关,这通常会导致视网膜神经节细胞(RGCs)变性,进而导致视力丧失。有实验证据表明,小热休克蛋白家族(HspBs)的一些成员在视网膜视神经损伤(ONI)后会上调,并且足以促进RGCs存活。这些数据提出了一个问题,即在这种情况下其他家族成员是否可能发挥类似作用。在这里,我们在ONI实验模型中对所有HspBs进行了全面的比较研究。我们发现,在对照条件下,五种HspBs在成年大鼠视网膜中表达,但只有HspB1和HspB5在ONI反应中上调。此外,HspB1和HspB5分别在Müller细胞中丝氨酸15和丝氨酸59处组成性磷酸化。在RGCs中,磷酸化由ONI刺激,发生在HspB1的丝氨酸86以及HspB5的丝氨酸19和45处。这些数据表明,在所有小热休克蛋白中,只有HspB1和HspB5可能在ONI后对RGCs具有保护价值,并且这个过程可能由HspB1的丝氨酸86以及HspB5的丝氨酸19和丝氨酸45处的磷酸化调节。磷酸化HspB1和磷酸化HspB5的分子靶点仍有待确定。