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首页> 外文期刊>The Journal of Comparative Neurology >Spatial and temporal expression of short, long/medium, or both opsins in human fetal cones.
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Spatial and temporal expression of short, long/medium, or both opsins in human fetal cones.

机译:人视锥细胞中短视蛋白,长视蛋白或中视蛋白或二者的时空表达。

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摘要

Human cone photoreceptors are characterized by long (L), medium (M), or short (S) wavelength-specific opsin. No reports have described the developmental pattern of human cone opsin expression, nor has the existence of human cones containing more than one opsin been tested. Single-and double-label immunocytochemistry and in situ hybridization have been used to determine the developmental pattern of opsin appearance and to investigate the presence of double-labeled cones in sections and wholemounts of human fetal, neonatal, infant, and adult retina. S opsin protein appears in and around the fovea at fetal week (Fwk) 10.9, whereas L/M opsin first appears in the fovea at Fwk 14-15. S opsin mRNA and protein are consistently detected much farther into peripheral retina than L/M opsin, indicating that S appears before L/M opsin. S cones cover 90% of the retina by Fwk 19. L/M cones appear outside the central retina by Fwk 21.5 and reach the retinal edge by Fwk 34-37. The spatial pattern of mRNA expression closely matches that for protein, but mRNA appears slightly earlier than protein at a given retinal point, indicating that only short delays occur between mRNA expression and translation into protein. Cones containing both S and L/M opsin (S+L/M) appear around the fovea shortly after L/M opsin is expressed, are found in more peripheral retina at older ages, and decrease in number after birth. Some S+L/M cones are still detected in adult retina. Both S opsin protein and mRNA appear significantly earlier than L/M mRNA or protein across the human retina, suggesting that the two cone types differentiate under independent controlling factors. However, the presence of single cones containing both S and L/M opsin during development suggests that human cones can respond to the factors controlling expression of each opsin. Copyright 2000 Wiley-Liss, Inc.
机译:人视锥细胞感光细胞的特征是长波长(L),中波长(M)或短波长(S)的视蛋白。没有报道描述人视锥蛋白表达的发展模式,也没有测试包含多个视蛋白的人视锥蛋白的存在。单和双标签免疫细胞化学和原位杂交已被用来确定视蛋白外观的发育模式,并调查在人类胎儿,新生儿,婴儿和成人视网膜的切片和整个切片中双标签视锥细胞的存在。 S视蛋白在胎儿周(Fwk)10.9时出现在中央凹及其周围,而L / M视蛋白则首先在Fwk 14-15的中央凹出现。一致地检测到S视蛋白mRNA和蛋白比L / M视蛋白更深入外周视网膜,这表明S出现在L / M视蛋白之前。 S视锥在Fwk 19处覆盖了90%的视网膜。L/ M视锥在Fwk 21.5处出现在视网膜中央,并在Fwk 34-37处到达视网膜边缘。 mRNA表达的空间模式与蛋白质的紧密匹配,但是在给定的视网膜点,mRNA的出现要早于蛋白质,这表明在mRNA表达和翻译成蛋白质之间只有很短的延迟。含有S和L / M视蛋白(S + L / M)的锥体在表达L / M视蛋白后不久出现在中央凹周围,在老年人中更多见于周边视网膜,出生后数量减少。在成年视网膜中仍检测到一些S + L / M视锥细胞。 S视蛋白的蛋白和mRNA的出现明显早于整个人视网膜中的L / M mRNA或蛋白,这表明这两种视锥细胞类型在独立的控制因素下分化。但是,在发育过程中同时含有S和L / M视蛋白的视锥细胞的存在表明,人类视锥细胞可以对控制每种视蛋白表达的因子作出反应。版权所有2000 Wiley-Liss,Inc.

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