Caubit X, Riou J F, Coulon J, Arsanto J P, Benraiss A, Boucaut J C, Thouveny Y
Institut de Biologie du Développement de Marseille, CNRS-INSERM, Université Aix-Marseille II, France.
Int J Dev Biol. 1994 Dec;38(4):661-72.
Tenascin (Tn) protein and transcripts were analyzed in developing, adult and regenerating caudal spinal cord (SC) of Pleurodeles waltl. A polyclonal antibody (PAb) against Xenopus Tn and a newt Tn cDNA probe were used. In Western blots, anti-Tn PAb recognized Tn polypeptides of 200-220 kDa in tail regenerate extracts, but also the homolog of Tn/Cytotactin/J1 in brain and SC of adult newt. Immunofluorescence studies showed some reactivity around ependymoglial cells and strong labeling in the nervous tracts, in the developing as well as in the regenerating SC or adult SC. Immunogold electron microscopy revealed the presence of Tn throughout the ependymoglial cells, particularly near and along the plasma membrane of radial processes surrounding axons, especially growth cones. Tn could be more precisely found within rough endoplasmic reticulum and Golgi structures, or again in the surrounding extracellular space. This suggested that Tn was at least produced by radial glial profiles forming axonal compartments in which axons grew. Using the DNA probe for Tn, expression of Tn mRNA was also examined by Northern blot and RNAase protection analyses and by in situ hybridization, respectively. The levels of transcripts, barely detectable in adult tail, increased in regenerates from 3 days through 4-8 weeks post-amputation. In situ Tn mRNA were mainly localized in the mesenchyme, especially at the epithelial-mesenchymal interface, and in the developing cartilage, at the early regeneration stages, whereas high amounts of transcripts were seen not only at these stages, but also later, in the regenerating SC. Our main results supported the view that, in the caudal SC of newts, Tn, synthesized by radial ependymoglial cells, was similarly expressed during regeneration as well as larval development, and exhibited a sustained high accumulation level in the adult SC. On the basis of the multifunctional properties of Tn, the putative roles played by Tn as a substrate for neuronal pathfinding and boundary shaping were discussed.
在有尾两栖动物(Pleurodeles waltl)发育、成年和再生的尾脊髓(SC)中,对腱生蛋白(Tn)蛋白和转录本进行了分析。使用了一种针对非洲爪蟾Tn的多克隆抗体(PAb)和一种蝾螈Tn cDNA探针。在蛋白质免疫印迹中,抗Tn PAb在尾部再生提取物中识别出200 - 220 kDa的Tn多肽,同时也识别成年蝾螈脑和脊髓中Tn/Cytotactin/J1的同源物。免疫荧光研究显示,在发育中的、再生的以及成年脊髓的室管膜胶质细胞周围有一些反应性,并且在神经束中有强烈的标记。免疫金电子显微镜显示,Tn存在于整个室管膜胶质细胞中,特别是在围绕轴突(尤其是生长锥)的放射状突起的质膜附近和沿着质膜的位置。Tn更确切地存在于粗面内质网和高尔基体结构中,或者再次出现在周围的细胞外空间。这表明Tn至少是由形成轴突生长的轴突隔室的放射状胶质细胞轮廓产生的。使用Tn的DNA探针,分别通过Northern印迹、RNA酶保护分析和原位杂交来检测Tn mRNA的表达。转录本水平在成年尾部几乎检测不到,在截肢后3天到4 - 8周的再生过程中有所增加。原位Tn mRNA主要定位于间充质,特别是上皮 - 间充质界面,以及早期再生阶段的发育中的软骨,而不仅在这些阶段,而且在再生脊髓的后期也能看到大量的转录本。我们的主要结果支持这样一种观点,即在蝾螈的尾脊髓中,由放射状室管膜胶质细胞合成的Tn在再生以及幼体发育过程中表达相似,并且在成年脊髓中表现出持续的高积累水平。基于Tn的多功能特性,讨论了Tn作为神经元路径寻找和边界塑造底物所起的假定作用。