Hikino Megumi, Mikami Tadahisa, Faissner Andreas, Vilela-Silva Ana-Cristina E S, Pavão Mauro S G, Sugahara Kazuyuki
Department of Biochemistry, Kobe Pharmaceutical University, Higashinada-ku, Kobe 658-8558, Japan.
J Biol Chem. 2003 Oct 31;278(44):43744-54. doi: 10.1074/jbc.M308169200. Epub 2003 Aug 12.
Brain-specific chondroitin sulfate (CS) proteoglycan (PG) DSD-1-PG/6B4-PG/phosphacan isolated from neonatal mouse brains exhibits neurite outgrowth-promoting activity toward embryonic rat and mouse hippocampal neurons in vitro through the so-called DSD-1 epitope embedded in its glycosaminoglycan side chains. Oversulfated CS variants, CS-D from shark cartilage and CS-E from squid cartilage, also possess similar activities. We have proposed that the neuritogenic property of the DSD-1 epitope may be attributable to a distinct CS structure characterized by the disulfated D disaccharide unit [GlcUA(2S)-GalNAc(6S)]. In this study, we assessed neuritogenic potencies of various oversulfated dermatan sulfate (DS) preparations purified from hagfish notochord, the bodies of two kinds of ascidians and embryonic sea urchin, which are characterized by the predominant disulfated disaccharide units of [IdoUA-GalNAc(4S,6S)] (68%), [IdoUA(2S)-GalNAc(4S)] (66%) plus [IdoUA(2S)-GalNAc(6S)] (5%), [IdoUA(2S)-GalNAc (6S)] (>90%), and [IdoUA-GalNAc(4S,6S)] (74%), respectively. They exerted marked neurite outgrowth-promoting activities, resulting in distinct morphological features depending on the individual structural features. Such activities were not observed for a less sulfated DS preparation derived from porcine skin, which has a monosulfated disaccharide unit [IdoUA-Gal-NAc(4S)] as a predominant unit. The neurite outgrowth-promoting activities of these oversulfated DS preparations and DSD-1-PG were eliminated by the specific enzymatic cleavage of GalNAc-IdoUA linkages characteristic of DS using chondroitinase B. In addition, chemical analysis of the glycosaminoglycan side chains of DSD-1-PG revealed the DS-type structures. These observations suggest potential novel neurobiological functions of oversulfated DS structures and may reflect the physiological neuritogenesis during brain development by mammalian oversulfated DS structures exemplified by the DSD-1 epitope.
从新生小鼠大脑中分离出的脑特异性硫酸软骨素(CS)蛋白聚糖(PG)DSD-1-PG/6B4-PG/phosphacan,通过其糖胺聚糖侧链中嵌入的所谓DSD-1表位,在体外对胚胎大鼠和小鼠海马神经元表现出促进神经突生长的活性。过度硫酸化的CS变体,鲨鱼软骨中的CS-D和鱿鱼软骨中的CS-E,也具有类似的活性。我们提出,DSD-1表位的促神经突生长特性可能归因于一种独特的CS结构,其特征在于二硫酸化的D二糖单元[GlcUA(2S)-GalNAc(6S)]。在本研究中,我们评估了从盲鳗脊索、两种海鞘的身体和胚胎海胆中纯化的各种过度硫酸化的硫酸皮肤素(DS)制剂的促神经突生长能力,它们分别以[IdoUA-GalNAc(4S,6S)](68%)、[IdoUA(2S)-GalNAc(4S)](66%)加[IdoUA(2S)-GalNAc(6S)](5%)、[IdoUA(2S)-GalNAc(6S)](>90%)和[IdoUA-GalNAc(4S,6S)](74%)的主要二硫酸化二糖单元为特征。它们表现出显著的促进神经突生长的活性,根据各自的结构特征导致不同的形态特征。对于源自猪皮的硫酸化程度较低的DS制剂未观察到这种活性,该制剂以单硫酸化二糖单元[IdoUA-Gal-NAc(4S)]作为主要单元。使用硫酸软骨素酶B对DS特有的GalNAc-IdoUA键进行特异性酶切后,这些过度硫酸化的DS制剂和DSD-1-PG的促进神经突生长的活性被消除。此外,对DSD-1-PG糖胺聚糖侧链的化学分析揭示了DS型结构。这些观察结果表明过度硫酸化的DS结构具有潜在的新的神经生物学功能,并且可能反映了以DSD-1表位为代表的哺乳动物过度硫酸化的DS结构在大脑发育过程中的生理神经突形成。