Fadool J M, Linser P J
Whitney Laboratory, University of Florida, St. Augustine 32086.
Dev Dyn. 1993 Apr;196(4):252-62. doi: 10.1002/aja.1001960406.
In continuing efforts to identify cell-surface molecules involved in cell-cell interactions in the developing avian retina, we identified a monoclonal antibody, the 5A11 antibody, which possessed the ability to interfere with contact-dependent glial cell maturation in vitro. We sought to determine the molecular and biochemical identity of the glycoprotein recognized by this antibody, and using additional criteria, establish whether the 5A11 antigen is indeed a cell-recognition molecule in the developing retina. Immunohistochemical analyses demonstrate that in the hatchling chick retina and in live cultures of embryonic retina cells, the 5A11 antigen is predominantly associated with Müller glial cells whereas little is observed on neuronal elements. Microsequencing of the major component isolated by immunoaffinity chromatography identifies the HT7 antigen (Seulberger et al.: EMBO Journal 9:2151-2158, 1990), a unique member of the immunoglobulin super gene family (IGSF), as a homologous if not identical protein to the 5A11 antigen. The HT7 antibody, furthermore, recognizes affinity purified 5A11 antigen, and both the HT7 antibody and additional probes generated against the 5A11 antigen recognize a major polypeptide of 45.5 kDa and a minor band of 69 kDa on Western blots of membrane preparations from neural retina. To verify that the 5A11 antigen mediates cell-cell recognition events in the developing neural retina, we examined the consequences of adding antibody to monolayer cultures of dissociated embryonic retina cells and to dissociated retina cells in rotation-mediated suspension culture. Addition of the 5A11 antibody to monolayer cultures results in alteration in the development of the stereotypic arrangement of neurons and glia characterized by a reduction in the number and complexity of neural extensions upon the glial-derived flat cells. Similarly, addition of antibodies generated against the 5A11 antigen to dissociated cells in rotation cultures significantly reduces retina cell reaggregation as monitored by computer-assisted image analysis of cell aggregate size. These data and the identification of the 5A11 antigen as a member of the IGSF establish a role for the 5A11 antigen as a novel recognition molecule in the developing neural retina.
为了持续努力鉴定参与发育中的鸟类视网膜细胞间相互作用的细胞表面分子,我们鉴定出一种单克隆抗体,即5A11抗体,它具有在体外干扰接触依赖性神经胶质细胞成熟的能力。我们试图确定被该抗体识别的糖蛋白的分子和生化特性,并利用其他标准来确定5A11抗原在发育中的视网膜中是否确实是一种细胞识别分子。免疫组织化学分析表明,在雏鸡视网膜和胚胎视网膜细胞的活培养物中,5A11抗原主要与米勒神经胶质细胞相关,而在神经元成分上观察到的很少。通过免疫亲和层析分离的主要成分的微量测序确定HT7抗原(Seulberger等人:《欧洲分子生物学组织杂志》9:2151 - 2158,1990),免疫球蛋白超基因家族(IGSF)的一个独特成员,是与5A11抗原同源(如果不是完全相同)的蛋白质。此外,HT7抗体识别亲和纯化的5A11抗原,并且HT7抗体和针对5A11抗原产生的其他探针在来自神经视网膜的膜制剂的蛋白质印迹上识别一条45.5 kDa的主要多肽带和一条69 kDa的次要条带。为了验证5A11抗原在发育中的神经视网膜中介导细胞间识别事件,我们检查了向解离的胚胎视网膜细胞单层培养物和旋转介导的悬浮培养中的解离视网膜细胞添加抗体的后果。向单层培养物中添加5A11抗体导致神经元和神经胶质细胞刻板排列发育的改变,其特征是神经胶质来源的扁平细胞上神经突起的数量和复杂性减少。同样,通过计算机辅助图像分析细胞聚集体大小监测,向旋转培养中的解离细胞添加针对5A11抗原产生的抗体显著降低视网膜细胞再聚集。这些数据以及将5A11抗原鉴定为IGSF的成员确立了5A11抗原作为发育中的神经视网膜中一种新型识别分子的作用。