Bursztajn S, Vincent S, Brodsky F M, Benes F, Morris S A
Psychiatry Department (Neuroscience), Harvard Medical School, Belmont, Massachusetts 02178, USA.
J Cell Biochem. 1998 Mar 15;68(4):457-71.
Monoclonal antibodies were generated to vesicular membranes of clathrin coated vesicles enriched for acetylcholinesterase (AChE). One of these, C172, recognizes vesicles which accumulate in muscle cells around nuclei associated with acetylcholine receptor AChR clusters. Immunoblots of muscle extracts and brain purified clathrin coated vesicles show that C172 recognizes a 100 kd band in muscle, but a 180 kd band in brain. Western blots of purified AP180 protein stained with the two antibodies AP180.1 and C172 displayed the same staining pattern. Tryptic digests probed with peptide antibodies (PS26 and PS27) generated to known sequences of AP180 were used to map the epitope for C172 within the brain AP180 sequence. On immunoblots of digested AP180, all AP180 antibodies and C172 recognized a 100 kd tryptic fragment, however only C172 recognized a smaller 60 kd. Our results suggest that the C172 epitope is located within amino acids 305-598 of the AP180 sequence. Confocal fluorescence microscopy of myoblasts and myotubes stained with the C172 antibody gives a punctate immunofluorescence pattern. Myoblasts stained with C172 revealed a polarized distribution of vesicles distinct from that observed when cells are stained with gamma adaptin antibody which is known to localize to trans Golgi network. Myotubes stained with C172 antibody reveal a linear array of vesicular staining. Quantitative analysis of C172 reactive vesicles revealed a significant increase in number of vesicles present around the nuclei associated with the acetylcholine receptor clusters. These vesicles did not colocalize with the Golgi cisternae. These results indicate that a protein with homology to the neuron-specific coated vesicle protein AP180, is present in muscle cells associated with vesicles showing significant concentration around postsynaptic nuclei present in close proximity to AChR clusters.
制备了针对富含乙酰胆碱酯酶(AChE)的网格蛋白包被囊泡的囊泡膜的单克隆抗体。其中一种抗体C172可识别在与乙酰胆碱受体AChR簇相关的细胞核周围的肌肉细胞中积累的囊泡。肌肉提取物和脑纯化的网格蛋白包被囊泡的免疫印迹显示,C172在肌肉中识别一条100kd的条带,但在脑中识别一条180kd的条带。用两种抗体AP180.1和C172对纯化的AP180蛋白进行的蛋白质印迹显示出相同的染色模式。用针对AP180已知序列产生的肽抗体(PS26和PS27)探测胰蛋白酶消化物,以在脑AP180序列中定位C172的表位。在消化的AP180的免疫印迹上,所有AP180抗体和C172都识别一个100kd的胰蛋白酶片段,然而只有C172识别一个较小的60kd片段。我们的结果表明,C172表位位于AP180序列的305-598氨基酸内。用C172抗体染色的成肌细胞和肌管的共聚焦荧光显微镜检查给出点状免疫荧光模式。用C172染色的成肌细胞显示出囊泡的极化分布,这与用已知定位于反式高尔基体网络的γ衔接蛋白抗体染色细胞时观察到的分布不同。用C172抗体染色的肌管显示出囊泡染色的线性排列。对C172反应性囊泡的定量分析显示,与乙酰胆碱受体簇相关的细胞核周围存在的囊泡数量显著增加。这些囊泡不与高尔基池共定位。这些结果表明,与神经元特异性包被囊泡蛋白AP180具有同源性的一种蛋白质存在于肌肉细胞中,这些细胞中的囊泡在紧邻AChR簇的突触后核周围显示出明显的聚集。