Kawasaki T, Oka S
Department of Biological Chemistry, Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, 606-8501 Japan.
Nihon Shinkei Seishin Yakurigaku Zasshi. 2001 Sep;21(3):95-9.
The HNK-epitope, 3-sulfo-glucuronyl residue is expressed specifically on a series of cell adhesion molecules and on some glycolipids in the nervous system over a wide range of species, and its expression is spatially and temporally regulated during the development of the nervous system. To study the biological functions of the epitope, we have cloned the enzymes that are involved in the biosynthesis of the epitope, glucuronyltransferase (GlcAT-P and GlcAT-S) and sulfotransferase (Sulf-T), A Northern blot analysis of GlcAT mRNAs in various rat tissues indicated that GlcAT-P and -S are the brain-specific or neural-specific enzymes. Upon transfection of the full length GlcAT-P cDNA into COS-1 cells, which do not express the HNK-lepitope, cells were transformed into HNK-1 positive cells. These cells showed dramatic changes of the cell architecture. They had long and branched processes with irregular shapes and several micro spikes on the soma and processes. Another function of the HNK-1 epitope is the inhibition of cell-cell aggregation. Thus control COS-1 cells formed huge aggregates after incubation at room temperature for 90 min, and most of the HNK-1 positive cells remained as free single cells.
HNK抗原表位,即3-磺酸葡糖醛酸残基,在多种物种的一系列细胞黏附分子及神经系统中的一些糖脂上特异性表达,并且其表达在神经系统发育过程中受到时空调控。为研究该抗原表位的生物学功能,我们克隆了参与该抗原表位生物合成的酶,即葡糖醛酸基转移酶(GlcAT-P和GlcAT-S)和磺基转移酶(Sulf-T)。对大鼠各种组织中GlcAT mRNA的Northern印迹分析表明,GlcAT-P和-S是脑特异性或神经特异性酶。将全长GlcAT-P cDNA转染到不表达HNK抗原表位的COS-1细胞中后,细胞转变为HNK-1阳性细胞。这些细胞显示出细胞结构的显著变化。它们具有长且分支的突起,形状不规则,在胞体和突起上有多个微刺。HNK-1抗原表位的另一个功能是抑制细胞间聚集。因此,对照COS-1细胞在室温下孵育90分钟后形成巨大聚集体,而大多数HNK-1阳性细胞仍为游离单细胞。