Department of Ophthalmology and Visual Sciences, Washington University Medical School, St. Louis, Missouri, USA.
Invest Ophthalmol Vis Sci. 2012 Jan 25;53(1):454-60. doi: 10.1167/iovs.11-8717.
Mice lacking rods and cones retain pupillary light reflexes that are mediated by intrinsically photosensitive retinal ganglion cells (ipRGCs). Melanopsin is necessary and sufficient for this nonvisual photoreception. The mammalian inner retina also expresses the potential blue light photopigments cryptochromes 1 and 2. Previous studies have shown that outer retinal degenerate mice lacking cryptochromes have lower nonvisual photic sensitivity than retinal degenerate mice, suggesting a role for cryptochrome in inner retinal photoreception.
Nonvisual photoreception (pupillary light responses, circadian entrainment, and in vitro sensitivity of intrinsically photosensitive retinal ganglion cells) were studied in wild-type, rd/rd, and circadian clock-mutant mice with and without rd/rd mutation.
Loss of cryptochrome in retinal degenerate mice reduces the sensitivity of the pupillary light response at all wavelengths but does not alter the form of the action spectrum, suggesting that cryptochrome does not function as a photopigment in the inner retina. The authors compounded the rd/rd retinal degeneration mutation with mutations in other essential circadian clock genes, mPeriod and Bmal1. Both mPeriod1⁻/⁻; mPeriod2⁻/⁻;rd/rd and Bmal1⁻/⁻;rd/rd mice showed significantly lower pupillary light sensitivity than rd/rd mice alone. A moderate amplitude (0.5 log) circadian rhythm of pupillary light responsiveness was observed in rd/rd mice. Multielectrode array recordings of ipRGC responses of mCryptochrome1⁻/⁻;mCryptochrome2⁻/⁻ and mPeriod1⁻/⁻;mPeriod2⁻/⁻ mice showed minimal sensitivity decrement compared with wild-type animals. mCryptochrome1⁻/⁻;mCryptochrome2⁻/⁻;rd/rd, mPeriod1⁻/⁻;mPeriod2⁻/⁻;rd/rd and Bmal1⁻/⁻;rd/rd mice all showed comparable weak behavioral synchronization to a 12-hour light/12-hour dark cycle.
The effect of cryptochrome loss on nonvisual photoreception is due to loss of the circadian clock nonspecifically. The circadian clock modulates the sensitivity of nonvisual photoreception.
缺乏视杆和视锥细胞的小鼠保留瞳孔对光反射,该反射由内在光敏视网膜神经节细胞(ipRGC)介导。黑视素对于这种非视觉光感受是必需和充分的。哺乳动物的内视网膜也表达潜在的蓝光视色素隐花色素 1 和 2。先前的研究表明,外视网膜退化的缺乏隐花色素的小鼠比视网膜退化的小鼠具有更低的非视觉光敏感性,这表明隐花色素在视网膜内光感受中起作用。
在野生型、rd/rd 和生物钟突变小鼠中,研究了非视觉光感受(瞳孔光反应、昼夜节律同步和内在光敏视网膜神经节细胞的体外敏感性),并在有和没有 rd/rd 突变的情况下进行了研究。
在视网膜退化的小鼠中,隐花色素的缺失降低了瞳孔光反应在所有波长的敏感性,但不改变作用光谱的形式,这表明隐花色素在视网膜内不起光色素的作用。作者将 rd/rd 视网膜退化突变与其他必需的生物钟基因 mPeriod 和 Bmal1 的突变复合。mPeriod1⁻/⁻; mPeriod2⁻/⁻; rd/rd 和 Bmal1⁻/⁻; rd/rd 小鼠均显示出比单独 rd/rd 小鼠更低的瞳孔光敏感性。在 rd/rd 小鼠中观察到中等幅度(0.5 log)的瞳孔光反应昼夜节律。mCryptochrome1⁻/⁻; mCryptochrome2⁻/⁻ 和 mPeriod1⁻/⁻; mPeriod2⁻/⁻ 小鼠的 ipRGC 反应的多电极阵列记录显示,与野生型动物相比,敏感性降低幅度较小。mCryptochrome1⁻/⁻; mCryptochrome2⁻/⁻; rd/rd、mPeriod1⁻/⁻; mPeriod2⁻/⁻; rd/rd 和 Bmal1⁻/⁻; rd/rd 小鼠对 12 小时光照/12 小时黑暗周期的行为同步性均相当弱。
隐花色素缺失对非视觉光感受的影响归因于昼夜节律钟的非特异性缺失。昼夜节律调节非视觉光感受的敏感性。