Kellogg Eye Center, 1000 Wall Street, Ann Arbor, MI 48105, USA.
J Physiol. 2014 Apr 1;592(7):1619-36. doi: 10.1113/jphysiol.2013.262782. Epub 2014 Jan 6.
Intrinsically photosensitive retinal ganglion cells (ipRGCs) mediate non-image-forming visual responses, including pupillary constriction, circadian photoentrainment and suppression of pineal melatonin secretion. Five morphological types of ipRGCs, M1-M5, have been identified in mice. In order to understand their functions better, we studied the photoresponses of all five cell types, by whole-cell recording from fluorescently labelled ipRGCs visualized using multiphoton microscopy. All ipRGC types generated melanopsin-based ('intrinsic') as well as synaptically driven ('extrinsic') light responses. The intrinsic photoresponses of M1 cells were lower threshold, higher amplitude and faster than those of M2-M5. The peak amplitudes of extrinsic light responses differed among the ipRGC types; however, the responses of all cell types had comparable thresholds, kinetics and waveforms, and all cells received rod input. While all five types exhibited inhibitory amacrine-cell and excitatory bipolar-cell inputs from the 'on' channel, M1 and M3 received additional 'off'-channel inhibition, possibly through their 'off'-sublamina dendrites. The M2-M5 ipRGCs had centre-surround-organized receptive fields, implicating a capacity to detect spatial contrast. In contrast, the receptive fields of M1 cells lacked surround antagonism, which might be caused by the surround of the inhibitory input nullifying the surround of the excitatory input. All ipRGCs responded robustly to a wide range of motion speeds, and M1-M4 cells appeared tuned to different speeds, suggesting that they might analyse the speed of motion. Retrograde labelling revealed that M1-M4 cells project to the superior colliculus, suggesting that the contrast and motion information signalled by these cells could be used by this sensorimotor area to detect novel objects and motion in the visual field.
内在光敏视网膜神经节细胞(ipRGCs)介导非成像视觉反应,包括瞳孔收缩、昼夜光适应和松果腺褪黑素分泌抑制。在小鼠中已经鉴定出五种形态类型的 ipRGCs,即 M1-M5。为了更好地了解它们的功能,我们通过多光子显微镜可视化荧光标记的 ipRGCs 进行全细胞记录,研究了所有五种细胞类型的光反应。所有 ipRGC 类型都产生基于黑视素的(“内在”)和突触驱动的(“外在”)光反应。M1 细胞的内在光反应的阈值更低、幅度更高、速度更快。外在光反应的峰值幅度在 ipRGC 类型之间存在差异;然而,所有细胞类型的反应都具有可比的阈值、动力学和波形,并且所有细胞都接收视杆细胞输入。虽然所有五种类型都表现出从“on”通道的抑制性无长突细胞和兴奋性双极细胞输入,但 M1 和 M3 还接收额外的“off”通道抑制,可能通过它们的“off”亚层树突。M2-M5 ipRGCs 具有中心-周围组织的感受野,暗示它们具有检测空间对比度的能力。相比之下,M1 细胞的感受野缺乏周围拮抗作用,这可能是由于抑制性输入的周围消除了兴奋性输入的周围。所有 ipRGCs 对广泛的运动速度都有强烈的反应,并且 M1-M4 细胞似乎对不同的速度进行了调谐,表明它们可能分析运动的速度。逆行标记显示 M1-M4 细胞投射到上丘,表明这些细胞发出的对比度和运动信息可以被这个感觉运动区域用来检测视野中的新物体和运动。