Tourovskaia Anna, Li Nianzhen, Folch Albert
Department of Bioengineering, University of Washington, Seattle, Washington, USA.
Biophys J. 2008 Sep 15;95(6):3009-16. doi: 10.1529/biophysj.107.128173. Epub 2008 May 23.
Agrin is a proteoglycan secreted by the motor neuron's growing axon terminal upon contact with the muscle during embryonic development. It was long thought that agrin's role was to trigger the clustering of acetylcholine receptors (AChRs) to nascent synapse sites. However, agrin-predating, protosynaptic AChR clusters are present well before innervation in the embryo and in myotube cultures, yet no role has been conclusively ascribed to agrin. We used a microfluidic device to focally deliver agrin to protosynaptic AChR clusters in micropatterned myotube cultures. The distribution of AChRs labeled with fluorescent bungarotoxin was imaged at various time points over >24 h. We find that a 4-h focal application of agrin (100 nM) preferentially reduces AChR loss at agrin-exposed clusters by 17% relative to the agrin-deprived clusters on the same myotube. In addition, the focal application increases the addition of AChRs preferentially at the clusters by 10% relative to the agrin-exposed, noncluster areas. Taken together, these findings suggest that a focal agrin stimulus can play a key stabilizing role in the aggregation of AChRs at the early stages of synapse formation. This methodology is generally applicable to various developmental processes and cell types, including neurons and stem cells.
聚集蛋白是一种蛋白聚糖,在胚胎发育过程中,运动神经元生长的轴突末端与肌肉接触时由其分泌。长期以来,人们一直认为聚集蛋白的作用是触发乙酰胆碱受体(AChRs)在新生突触部位的聚集。然而,在胚胎和肌管培养物中,早在神经支配之前就存在先于聚集蛋白的原突触AChR簇,但聚集蛋白尚未被明确赋予任何作用。我们使用微流控装置将聚集蛋白局部递送至微图案化肌管培养物中的原突触AChR簇。在超过24小时的不同时间点对用荧光银环蛇毒素标记的AChRs的分布进行成像。我们发现,相对于同一肌管上未接触聚集蛋白的簇,局部应用4小时的聚集蛋白(100 nM)可使接触聚集蛋白的簇处的AChR损失率降低17%。此外,相对于接触聚集蛋白的非簇区域,局部应用使簇处的AChRs添加量增加10%。综上所述,这些发现表明局部聚集蛋白刺激在突触形成早期AChRs的聚集中可发挥关键的稳定作用。这种方法通常适用于各种发育过程和细胞类型,包括神经元和干细胞。