Department of Ophthalmology and Visual Sciences, University of Michigan School of Medicine, Ann Arbor, Michigan 48105, USA.
Invest Ophthalmol Vis Sci. 2010 Jun;51(6):3244-52. doi: 10.1167/iovs.09-4879. Epub 2010 Jan 13.
The purpose of this study was to identify secreted proteins in the retina of the adult zebrafish that are induced by the selective death of photoreceptors and to test experimentally the function of these proteins during the regeneration of photoreceptors.
Induced selective death of photoreceptors in the retina of the adult zebrafish was combined with in situ hybridization and immunocytochemistry to identify the induced cellular expression of the secreted beta-galactoside binding protein Galectin 1-like 2 (Drgal1-L2). Electroporation of morpholino oligonucleotides was used to knock down protein synthesis, and regenerated photoreceptors were counted in control and experimental retinas after labeling with cell type-specific RNA probes.
Expression analysis and immunocytochemistry showed that Drgal1-L2 is induced de novo by photoreceptor death and is synthesized by microglia and proliferating Müller glia and their mitotic progeny. Knockdown of Drgal1-L2 expression in Müller glia results in reduced regeneration of rod photoreceptors without affecting injury-induced proliferation or the regeneration of cone photoreceptors.
Based on these data, the authors conclude that Drgal1-L2 is induced by photoreceptor cell death and secreted by stem cells and neuronal progenitors and that it regulates the regeneration of rod photoreceptors. Drgal1-L2 is the first secreted factor shown to regulate aspects of regenerative neurogenesis in the teleost retina.
本研究旨在鉴定成年斑马鱼视网膜中受光感受器选择性死亡诱导的分泌蛋白,并在光感受器再生过程中对这些蛋白的功能进行实验测试。
将成年斑马鱼视网膜中光感受器的选择性死亡与原位杂交和免疫细胞化学相结合,以鉴定诱导的分泌β-半乳糖苷结合蛋白半乳糖凝集素 1 样 2(Drgal1-L2)的细胞表达。使用针对特定细胞类型的 RNA 探针对标记的对照和实验性视网膜进行计数,以电穿孔破坏目的基因的翻译来抑制蛋白合成,并计数再生的光感受器。
表达分析和免疫细胞化学显示,Drgal1-L2 是由光感受器死亡新诱导产生的,由小胶质细胞和增殖的 Müller 胶质细胞及其有丝分裂后代合成。Müller 胶质细胞中 Drgal1-L2 表达的敲低会导致杆状光感受器的再生减少,而不影响损伤诱导的增殖或锥状光感受器的再生。
基于这些数据,作者得出结论,Drgal1-L2 是由光感受器细胞死亡诱导产生的,并由干细胞和神经元祖细胞分泌,它调节杆状光感受器的再生。Drgal1-L2 是第一个被证明可调节硬骨鱼视网膜再生神经发生的分泌因子。