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用于紧密神经元 - 电极接触的粘附蛋白。

Adhesion proteins for a tight neuron-electrode contact.

作者信息

Sorribas H, Braun D, Leder L, Sonderegger P, Tiefenauer L

机构信息

Laboratory for Micro- and Nanotechnology, Paul Scherrer Institute, CH-5232 Villigen PSI, Switzerland.

出版信息

J Neurosci Methods. 2001 Jan 15;104(2):133-41. doi: 10.1016/s0165-0270(00)00333-2.

Abstract

The neural cell adhesion molecules axonin-1 and NgCAM have been genetically engineered and covalently immobilized on glass and silicon oxide surfaces in their correct orientation. Surfaces treated with these adhesion molecules were used as substrates for culturing dorsal root ganglion neurons. The cleft between the neuron cell membrane and the surface was determined using fluorescence interference contrast (FLIC) microscopy. For comparison, cell--material distances on laminin, RGDC, polylysine and amino-terminated surfaces were measured. When the neurons grow on axonin-1 the cell--surface distance is at a minimum (37 nm) probably because the glycocalyx hinders a closer contact. A selective treatment of extracellular electrodes with axonin-1 could be used to improve the cell-material contact and thus increase extracellularly recorded signals.

摘要

神经细胞黏附分子轴突蛋白-1和NgCAM已通过基因工程改造,并以正确的方向共价固定在玻璃和氧化硅表面。用这些黏附分子处理过的表面被用作培养背根神经节神经元的底物。利用荧光干涉对比(FLIC)显微镜测定神经元细胞膜与表面之间的间隙。为作比较,还测量了层粘连蛋白、RGDC、聚赖氨酸和氨基末端表面上的细胞-材料距离。当神经元在轴突蛋白-1上生长时,细胞-表面距离最小(37纳米),这可能是因为糖萼阻碍了更紧密的接触。用轴突蛋白-1对细胞外电极进行选择性处理可用于改善细胞与材料的接触,从而增加细胞外记录的信号。

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