Department of Ophthalmology and National Clinical Research Center for Geriatrics, West China Hospital of Sichuan University, Chengdu, China.
Research Laboratory of Ophthalmology and Vision Sciences, West China Hospital, Sichuan University, Chengdu, China.
Stem Cells Dev. 2020 Jun 15;29(12):786-794. doi: 10.1089/scd.2019.0268. Epub 2020 Apr 15.
Photoreceptor transplantation can rescue the retinal function of late-stage rd1 mice. Many studies have used synaptic markers to suggest that there are synaptic connections after transplantation, but how donor and host cells are connected remains unknown. Many molecules are needed for triad ribbon synapse formation in wild-type mice. Among them, pikachurin is an important extracellular matrix protein that bridges the pre- and postsynaptic components. To investigate the mechanism of the synaptic connection between donor photoreceptor and host retina, we studied the expression of pikachurin in late-stage rd1 mice before and after transplantation. The results showed that the full-length form of pikachurin could still be detected in the degenerated retina. After photoreceptors were transplanted to the subretinal space of rd1 or wild-type mice, pikachurin was detected in the cytoplasm of most donor photoreceptor cells. Pikachurin puncta may represent the cleaved form of the protein and may indicate synapse generation, but it was barely observed in the donor mass of wild-type mice (3.83 ± 3.17 puncta per 100 donor cells). In contrast, pikachurin puncta could be found in the graft of the rd1 mouse retina, but the number was low (21.35 ± 9.48 puncta per 100 donor cells). In addition, 54.12 ± 8.45% of bassoon puncta were paired with pikachurin puncta and 45.5 ± 6.33% were not, indicating that there were fewer pikachurin puncta than bassoon. These results suggest that pikachurin is involved in only a portion of the synaptic connection between the donor photoreceptor and host retina.
光感受器移植可以挽救晚期 rd1 小鼠的视网膜功能。许多研究都使用突触标记物来表明移植后存在突触连接,但供体和宿主细胞如何连接仍不清楚。野生型小鼠三联体带突触形成需要许多分子。其中,pikachurin 是一种重要的细胞外基质蛋白,可连接突触前和突触后成分。为了研究供体光感受器与宿主视网膜之间的突触连接机制,我们研究了晚期 rd1 小鼠移植前后 pikachurin 的表达。结果表明,在退化的视网膜中仍能检测到 pikachurin 的全长形式。将光感受器移植到 rd1 或野生型小鼠的视网膜下腔后,pikachurin 被检测到在大多数供体光感受器细胞的细胞质中。pikachurin 斑点可能代表蛋白的裂解形式,可能表明突触生成,但在野生型小鼠供体质量中几乎观察不到(每 100 个供体细胞中有 3.83±3.17 个斑点)。相比之下,在 rd1 小鼠视网膜移植物中可以找到 pikachurin 斑点,但数量较低(每 100 个供体细胞中有 21.35±9.48 个斑点)。此外,54.12±8.45%的 bassoon 斑点与 pikachurin 斑点配对,而 45.5±6.33%没有配对,表明 pikachurin 斑点比 bassoon 斑点少。这些结果表明,pikachurin 仅参与供体光感受器与宿主视网膜之间部分突触连接。