Joliot A, Triller A, Volovitch M, Prochiantz A
Développement et Evolution du Système nerveux, C.N.R.S., U.R.A. 1414, Ecole normale supérieure, Paris, France.
C R Acad Sci III. 1992;314(9 Suppl):59-63.
In a previous study we demonstrated that the homeobox peptide pAntp was able to penetrate into rat embryonic neurons in culture thus provoking their morphological differentiation [1]. In the present work we have started to analyse the process of penetration of the homeobox peptide. As illustrated in Figure 1 pAntp migrating as a homogeneous 7 kDa band could be recovered in the nuclear fraction 2 hrs. only after its addition to cultured embryonic neurons (lane 2). Penetration and nuclear targeting were quantitatively blocked by preincubating pAntp with its cognate recognition sequence present in the promoter of Hox-1.3 (lane 3) or by incubating the cells with an antibody directed against the NCAM-specific alpha 2-8 polysialic acid (lane 4). Similar inhibitions were observed when the peptide was incubated with double stranded DNA or added to cells deprived of alpha 2-8 polysialic acid by EndoN treatment (not shown). As illustrated in Figure 2, the strong pAntp-induced neurite growth was antagonized when pAntp internalization was prevented by the EndoN removal of PSA. This effect of EndoN was not due to the enzyme itself since morphological differentiation was not inhibited if EndoN was added after pAntp penetration (Fig. 2B). Polysialic acid is composed of long chains of neuraminic acids, each pyranose ring carrying a negatively charged carboxylic group linked to carbon in position 1. NMR studies of the molecule in solution have demonstrated that the alpha 2-8 link between each pyranose ring allows specific and stable helical conformation [2].(ABSTRACT TRUNCATED AT 250 WORDS)
在先前的一项研究中,我们证明了同源异型盒肽pAntp能够穿透培养的大鼠胚胎神经元,从而引发其形态分化[1]。在本研究中,我们开始分析同源异型盒肽的穿透过程。如图1所示,作为一条均一的7 kDa条带迁移的pAntp,仅在添加到培养的胚胎神经元2小时后,才能在核组分中回收(泳道2)。通过将pAntp与其在Hox-1.3启动子中存在的同源识别序列预孵育(泳道3),或通过用针对NCAM特异性α2-8多唾液酸的抗体孵育细胞(泳道4),穿透和核靶向被定量阻断。当该肽与双链DNA孵育或添加到经内切酶N处理而缺失α2-8多唾液酸的细胞中时,观察到类似的抑制作用(未显示)。如图2所示,当通过内切酶N去除PSA阻止pAntp内化时,pAntp诱导的强烈神经突生长受到拮抗。内切酶N的这种作用不是由于酶本身,因为如果在pAntp穿透后添加内切酶N,则形态分化不会受到抑制(图2B)。多唾液酸由神经氨酸的长链组成,每个吡喃糖环带有一个连接到1位碳的带负电荷的羧基。对溶液中该分子的核磁共振研究表明,每个吡喃糖环之间的α2-8连接允许特定且稳定的螺旋构象[2]。(摘要截断于250字)