Vaughan L, Weber P, D'Alessandri L, Zisch A H, Winterhalter K H
Laboratorium für Biochemie I, ETH-Zentrum, Zürich, Switzerland.
Perspect Dev Neurobiol. 1994;2(1):43-52.
To understand how the extracellular matrix glycoprotein tenascin modifies cell adhesion and neurite outgrowth, we sought to isolate cellular receptors for tenascin. So far, two completely different cell surface ligands for tenascin have been detected. This we achieved by affinity chromatography of tissue extracts and of isolated proteins over tenascin-Sepharose and by solid-phase assays using the individual proteins. The first receptor, the neuronal cell adhesion molecule contactin/F11, a member of the immunoglobulin superfamily, binds to tenascin via a site in the N-terminal immunoglobulin-like domains. The binding site is within the fibronectin type III homology region at the boundary of the alternatively spliced region of tenascin, requiring that fibronectin type III homology domains 5 and 9 be adjacent, as they are in the 190 kD tenascin isoform. The close similarity in tertiary structure between type III domains and immunoglobulin-like repeats raises the possibility that we are observing a side-by-side interaction between the two molecules in a manner closely analogous to that between paired immunoglobulin domains. The second receptor is the heparan sulfate proteoglycan, glypican, which, similarly to contactin/F11, is anchored to the membrane via glycosylphosphatidylinositol. Glypican bound to a column of tenascin-Sepharose cannot be dissociated by chondroitin sulfate or dermatan sulfate, but elutes in a broad peak with a gradient of heparan sulfate and in a sharper peak with heparin. By means of fusion proteins, we have identified a potential binding site on the fifth fibronectin type III homology domain of tenascin. We are trying to define these sites more closely by means of site-directed mutagenesis. It will be interesting to see whether the interaction between tenascin and cell surface contactin/F11, and possibly cellular heparan sulfate proteoglycans, contributes to the prominent role played by tenascin in pattern formation during development of the nervous system. In a first step, we have examined the distribution of tenascin isoforms and contactin/F11 during retinal development by means of immunohistochemistry and in situ hybridization with tenascin isoform-specific probes. Tenascin isoforms 190/200 along with contactin/F11 are particularly prominent in the inner and outer plexiform layers of embryonic day 8 retina in the chick. This coordinate up-regulation was confirmed both by immunoblots and Northern blots of retinal extracts. A speculative model is presented to suggest how the unique hexabrachion may signal the cell via contactin/F11.
为了解细胞外基质糖蛋白腱生蛋白如何调节细胞黏附和神经突生长,我们试图分离腱生蛋白的细胞受体。到目前为止,已检测到两种完全不同的腱生蛋白细胞表面配体。我们通过用腱生蛋白-琼脂糖对组织提取物和分离的蛋白质进行亲和层析,以及使用单个蛋白质进行固相分析来实现这一点。第一种受体是神经元细胞黏附分子接触蛋白/F11,它是免疫球蛋白超家族的成员,通过N端免疫球蛋白样结构域中的一个位点与腱生蛋白结合。结合位点位于腱生蛋白可变剪接区域边界处的纤连蛋白III型同源区域内,要求纤连蛋白III型同源结构域5和9相邻,就像在190kD腱生蛋白异构体中那样。III型结构域与免疫球蛋白样重复序列在三级结构上的高度相似性增加了一种可能性,即我们正在观察这两种分子之间的并排相互作用,其方式与成对免疫球蛋白结构域之间的相互作用非常相似。第二种受体是硫酸乙酰肝素蛋白聚糖,磷脂酰肌醇蛋白聚糖,它与接触蛋白/F11类似,通过糖基磷脂酰肌醇锚定在膜上。结合到腱生蛋白-琼脂糖柱上的磷脂酰肌醇蛋白聚糖不能被硫酸软骨素或硫酸皮肤素解离,但在硫酸乙酰肝素梯度洗脱时呈宽峰洗脱,在肝素洗脱时呈更尖锐的峰洗脱。通过融合蛋白,我们在腱生蛋白的第五个纤连蛋白III型同源结构域上确定了一个潜在的结合位点。我们正试图通过定点诱变更精确地确定这些位点。看看腱生蛋白与细胞表面接触蛋白/F11以及可能的细胞硫酸乙酰肝素蛋白聚糖之间的相互作用是否有助于腱生蛋白在神经系统发育过程中的模式形成中所起的重要作用,将是很有趣的。第一步,我们通过免疫组织化学和用腱生蛋白异构体特异性探针进行原位杂交,研究了视网膜发育过程中腱生蛋白异构体和接触蛋白/F11的分布。在鸡胚胎第8天视网膜的内、外丛状层中,190/200腱生蛋白异构体与接触蛋白/F11特别突出。视网膜提取物的免疫印迹和Northern印迹均证实了这种协同上调。本文提出了一个推测性模型,以说明独特的六臂体如何通过接触蛋白/F11向细胞发出信号。