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PACAP 缺乏小鼠在非视觉光感受器和早期活动开始方面表现出光参数依赖性异常。

PACAP-deficient mice exhibit light parameter-dependent abnormalities on nonvisual photoreception and early activity onset.

机构信息

Graduate School of Pharmaceutical Sciences, Osaka University, Osaka, Japan.

出版信息

PLoS One. 2010 Feb 18;5(2):e9286. doi: 10.1371/journal.pone.0009286.

Abstract

BACKGROUND

The photopigment melanopsin has been suggested to act as a dominant photoreceptor in nonvisual photoreception including resetting of the circadian clock (entrainment), direct tuning or masking of vital status (activity, sleep/wake cycles, etc.), and the pupillary light reflex (PLR). Pituitary adenylate cyclase-activating polypeptide (PACAP) is exclusively coexpressed with melanopsin in a small subset of retinal ganglion cells and is predicted to be involved extensively in these responses; however, there were inconsistencies in the previous reports, and its functional role has not been well understood.

METHODOLOGY/PRINCIPAL FINDINGS: Here we show that PACAP-deficient mice exhibited severe dysfunctions of entrainment in a time-dependent manner. The abnormalities in the mutant mice were intensity-dependent in phase delay and duration-dependent in phase advance. The knockout mice also displayed blunted masking, which was dependent on lighting conditions, but not completely lost. The dysfunctions of masking in the mutant mice were recovered by infusion of PACAP-38. By contrast, these mutant mice show a normal PLR. We examined the retinal morphology and innervations in the mutant mice, and no apparent changes were observed in melanopsin-immunoreactive cells. These data suggest that the dysfunctions of entrainment and masking were caused by the loss of PACAP, not by the loss of light input itself. Moreover, PACAP-deficient mice express an unusually early onset of activities, from approximately four hours before the dark period, without influencing the phase of the endogenous circadian clock.

CONCLUSIONS/SIGNIFICANCE: Although some groups including us reported the abnormalities in photic entrainments in PACAP- and PAC(1)-knockout mice, there were inconsistencies in their results. The time-dependent dysfunctions of photic entrainment in the PACAP-knockout mice described in this paper can integrate the incompatible data in previous reports. The recovery of impaired masking by infusion of PACAP-38 in the mutant mice is the first direct evidence of the relationship between PACAP and masking. These results indicate that PACAP regulates particular nonvisual light responses by conveying parametric light information--that is, intensity and duration. The "early-bird" phenotype in the mutant mice originally reported in this paper supposed that PACAP also has a critical role in daily behavioral patterns, especially during the light-to-dark transition period.

摘要

背景

视蛋白黑视素被认为是光感受器在非视觉光感受中的主要受体,包括重置生物钟(同步)、直接调节或掩盖生命状态(活动、睡眠/觉醒周期等)以及瞳孔对光反射(PLR)。垂体腺苷酸环化酶激活肽(PACAP)仅与一小部分视网膜神经节细胞中的黑视素共表达,被预测广泛参与这些反应;然而,之前的报告存在不一致,其功能作用尚未得到很好的理解。

方法/主要发现:在这里,我们显示 PACAP 缺陷小鼠表现出严重的同步功能障碍,呈时间依赖性。在突变小鼠中,异常表现为强度依赖性的相位延迟和强度依赖性的相位提前。敲除小鼠也表现出掩蔽作用减弱,这取决于光照条件,但并未完全丧失。PACAP-38 的输注可恢复突变小鼠的掩蔽功能障碍。相比之下,这些突变小鼠的 PLR 正常。我们检查了突变小鼠的视网膜形态和神经支配,在黑视素免疫反应细胞中没有观察到明显变化。这些数据表明,同步和掩蔽功能障碍是由 PACAP 的缺失引起的,而不是由光输入本身的缺失引起的。此外,PACAP 缺陷小鼠表现出异常早的活动发作,大约在暗期前四个小时,而不影响内源性生物钟的相位。

结论/意义:尽管包括我们在内的一些研究小组报告了 PACAP 和 PAC(1)敲除小鼠在光适应方面的异常,但他们的结果存在不一致。本文描述的 PACAP 敲除小鼠的光适应时间依赖性功能障碍可以整合以前报告中不兼容的数据。PACAP-38 输注可恢复突变小鼠受损掩蔽的作用,这是 PACAP 与掩蔽之间关系的第一个直接证据。这些结果表明,PACAP 通过传递参数光信息(即强度和持续时间)来调节特定的非视觉光反应。本文最初报道的突变小鼠的“早起鸟”表型假设 PACAP 在日常行为模式中也具有关键作用,尤其是在光暗转换期间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bd5/2823792/b37ac46b3b1d/pone.0009286.g001.jpg

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