Department of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Nat Neurosci. 2012 Jun;15(6):871-5. doi: 10.1038/nn.3102.
Fic domains can catalyze the addition of adenosine monophosphate to target proteins. To date, the function of Fic domain proteins in eukaryotic physiology remains unknown. We generated genetic models of the single Drosophila Fic domain–containing protein, Fic. Flies lacking Fic were viable and fertile, but blind. Photoreceptor cells depolarized normally following light stimulation, but failed to activate postsynaptic neurons, as indicated by the loss of ON transients in electroretinograms, consistent with a neurotransmission defect. Functional rescue of neurotransmission required expression of enzymatically active Fic on capitate projections of glia cells, but not neurons, supporting a role in the recycling of the visual neurotransmitter histamine. Histamine levels were reduced in the lamina of Fic null flies, and dietary histamine partially restored ON transients. These findings establish a previously unknown regulatory mechanism in visual neurotransmission and provide, to the best of our knowledge, the first evidence for a role of glial capitate projections in neurotransmitter recycling.
Fic 结构域能够催化单磷酸腺苷添加到靶蛋白上。迄今为止,真核生理学中 Fic 结构域蛋白的功能仍不清楚。我们生成了果蝇中单个 Fic 结构域蛋白 Fic 的遗传模型。缺乏 Fic 的果蝇具有活力和生育能力,但却是盲的。光刺激后,感光细胞正常去极化,但不能激活突触后神经元,正如在视网膜电图中消失的 ON 瞬变所表明的那样,这与神经传递缺陷一致。神经传递的功能挽救需要在神经胶质细胞的毛状突起上表达具有酶活性的 Fic,但不需要在神经元上表达,这支持了 Fic 在视觉神经递质组氨酸再循环中的作用。在 Fic 缺失果蝇的神经纤维层中,组胺水平降低,饮食组胺部分恢复了 ON 瞬变。这些发现确立了视觉神经传递中一个以前未知的调节机制,并提供了据我们所知的第一个证据,证明神经胶质毛状突起在神经递质再循环中的作用。