Department of Molecular Neurobiology, Max Planck Institute for Medical Research, 69120 Heidelberg, Germany.
J Biol Chem. 2010 Nov 5;285(45):34589-96. doi: 10.1074/jbc.M110.168880. Epub 2010 Sep 2.
The lifetime of nicotinic acetylcholine receptors (AChRs) in neuromuscular junctions (NMJs) is increased from <1 day to >1 week during early postnatal development. However, the exact timing of AChR stabilization is not known, and its correlation to the concurrent embryonic to adult AChR channel conversion, NMJ remodeling, and neuromuscular diseases is unclear. Using a novel time lapse in vivo imaging technology we show that replacement of the entire receptor population of an individual NMJ occurs end plate-specifically within hours. This makes it possible to follow directly in live animals changing stabilities of end plate receptors. In three different, genetically modified mouse models we demonstrate that the metabolic half-life values of synaptic AChRs increase from a few hours to several days after postnatal day 6. Developmental stabilization is independent of receptor subtype and apparently regulated by an intrinsic muscle-specific maturation program. Myosin Va, an F-actin-dependent motor protein, is also accumulated synaptically during postnatal development and thus could mediate the stabilization of end plate AChR.
在出生后的早期发育过程中,神经肌肉接头 (NMJ) 中的烟碱型乙酰胆碱受体 (AChR) 的寿命从 <1 天延长到 >1 周。然而,AChR 稳定的确切时间尚不清楚,其与同时发生的胚胎到成年 AChR 通道转换、NMJ 重塑以及神经肌肉疾病的相关性也不清楚。我们使用一种新的活体延时成像技术,显示 NMJ 中整个受体群体的替换是在数小时内特异性地发生在终板上。这使得我们可以直接在活体动物中跟踪终板受体稳定性的变化。在三种不同的基因修饰小鼠模型中,我们证明突触 AChR 的代谢半衰期值在出生后第 6 天之后从几个小时增加到几天。发育稳定性与受体亚型无关,显然受肌肉特异性内在成熟程序的调节。肌球蛋白 Va 是一种依赖 F-肌动蛋白的运动蛋白,也在出生后发育过程中突触累积,因此可能介导终板 AChR 的稳定。