Sears S, Erickson A, Hendrickson A
Department of Biological Structure, University of Washington, Seattle 98195, USA.
Invest Ophthalmol Vis Sci. 2000 Apr;41(5):971-9.
To characterize the spatial and temporal expression of key structural and phototransduction cascade proteins in the monkey cone outer segment (OS).
Retinas from Macaca monkeys from ages fetal day (Fd) 89 through adulthood were double labeled using immunofluorescence for short (S) or long/medium (L/M) wavelength-sensitive cone opsin and either a structural protein (peripherin) or a phototransduction cascade protein (alpha-transducin [alpha-T], phosphodiesterase [PDE], or rhodopsin kinase [RK]). The spatial and temporal patterns of expression for each protein at each age were determined and graphed as a percentage of retinal coverage.
In both cone types, opsins and phototransduction proteins appear first in the fovea and last at the retinal edge. Peripherin appears concomitantly with opsin in both S and L/M cones, but S cones express peripherin and opsin 1 to 3 weeks before neighboring L/M cones. Alpha-T, PDE, and RK are expressed together in the L/M cone OS shortly after L/M opsin appears. Phototransduction proteins are not expressed in S cones until 1 to 3 weeks after the appearance of S opsin and at the same time that neighboring cones are expressing both L/M opsin and phototransduction proteins.
The concomitant appearance of opsin and peripherin strongly suggests roles in promoting the structural integrity of the developing OS. Phototransduction cascade proteins appear in the developing OS at the same time as one another, but after opsin. The significant lag between their expression and that of S cone opsin indicates that phototransduction proteins are not essential for OS formation, nor does opsin expression trigger their expression. The different temporal but similar spatial expression patterns of phototransduction proteins within S and L/M cones suggests that some local signal(s) coordinates their appearance.
表征猴视锥细胞外段(OS)中关键结构蛋白和光转导级联蛋白的时空表达情况。
使用免疫荧光法对胎龄89天至成年的猕猴视网膜进行双重标记,分别针对短(S)或长/中(L/M)波长敏感视锥视蛋白以及一种结构蛋白(外周蛋白)或一种光转导级联蛋白(α-转导蛋白[α-T]、磷酸二酯酶[PDE]或视紫红质激酶[RK])。确定每个年龄段每种蛋白的时空表达模式,并将其绘制成视网膜覆盖百分比的图表。
在两种视锥细胞类型中,视蛋白和光转导蛋白均首先出现在中央凹,最后出现在视网膜边缘。外周蛋白在S和L/M视锥细胞中均与视蛋白同时出现,但S视锥细胞比相邻的L/M视锥细胞早1至3周表达外周蛋白和视蛋白。L/M视蛋白出现后不久,α-T、PDE和RK在L/M视锥细胞OS中共同表达。直到S视蛋白出现1至3周后,且相邻视锥细胞同时表达L/M视蛋白和光转导蛋白时,光转导蛋白才在S视锥细胞中表达。
视蛋白和外周蛋白的同时出现强烈表明它们在促进发育中的OS的结构完整性方面发挥作用。光转导级联蛋白在发育中的OS中彼此同时出现,但在视蛋白之后。它们的表达与S视锥细胞视蛋白的表达之间存在显著滞后表明,光转导蛋白对于OS形成并非必不可少,视蛋白表达也不会触发它们的表达。S和L/M视锥细胞内光转导蛋白不同的时间但相似的空间表达模式表明,某些局部信号协调了它们的出现。