Chondroitin sulfate/dermatan sulfate hybrid chains from embryonic pig brain, which contain a higher proportion of L-iduronic acid than those from adult pig brain, exhibit neuritogenic and growth factor binding activities

被引:96
作者
Bao, XF
Nishimura, S
Mikami, T
Yamada, S
Itoh, N
Sugahara, K
机构
[1] Kobe Pharmaceut Univ, Dept Biochem, Higashinada Ku, Kobe, Hyogo 6588558, Japan
[2] Kyoto Univ, Grad Sch Pharmaceut Sci, Dept Biochem Genet, Kyoto 6068501, Japan
关键词
D O I
10.1074/jbc.M310877200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have shown that over-sulfated chondroitin sulfate/ dermatan sulfate (CS/DS) chains from various marine organisms exhibit growth factor binding activities and neurite outgrowth-promoting activities in embryonic mouse hippocampal neurons in vitro. In this study we demonstrated that CS/DS hybrid chains purified from embryonic pig brain displayed marked neuritogenic activity and growth factor binding activities toward fibroblast growth factor 2 (FGF2), FGF10, FGF18, pleiotrophin, and midkine, all of which exhibit neuroregulatory activities in the brain. In contrast, the CS/DS preparation from adult pig brain showed considerably less activity to bind these growth factors and no neuritogenic activity. Structural analysis indicated that the average size of the CS/DS chains was similar ( 40 kDa) between these two preparations, but the disaccharide compositions differed considerably, with a significant proportion of L-iduronic acid (IdoUA)-containing disaccharides ( 8 similar to 9%) in the CS/DS chains from embryos but not in those from adults (< 1%). Interestingly, both neurite out-growth-promoting activity and growth factor binding activities of the CS/DS chains from embryos were abolished by digestion not only with chondroitinase ABC but also with chondroitinase B, suggesting that the IdoUA-containing motifs are essential for these activities. These findings imply that the temporal expression of CS/DS hybrid structures containing both GlcUA and IdoUA and binding activities toward various growth factors play important roles in neurogenesis in the early stages of the development of the brain.
引用
收藏
页码:9765 / 9776
页数:12
相关论文
共 59 条
[1]   Proteoglycans in the developing brain: New conceptual insights for old proteins [J].
Bandtlow, CE ;
Zimmermann, DR .
PHYSIOLOGICAL REVIEWS, 2000, 80 (04) :1267-1290
[2]  
BAO X, 2003, SEIKAGAKU, V75, P908
[3]   Endocan is a novel chondroitin sulfate/dermatan sulfate proteoglycan that promotes hepatocyte growth factor/scatter factor mitogenic activity [J].
Béchard, D ;
Gentina, T ;
Delehedde, M ;
Scherpereel, A ;
Lyon, M ;
Aumercier, M ;
Vazeux, R ;
Richet, C ;
Degand, P ;
Jude, B ;
Janin, A ;
Fernig, DG ;
Tonnel, AB ;
Lassalle, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (51) :48341-48349
[4]   A MODIFIED URONIC ACID CARBAZOLE REACTION [J].
BITTER, T ;
MUIR, HM .
ANALYTICAL BIOCHEMISTRY, 1962, 4 (04) :330-&
[5]   Chondroitinase ABC promotes functional recovery after spinal cord injury [J].
Bradbury, EJ ;
Moon, LDF ;
Popat, RJ ;
King, VR ;
Bennett, GS ;
Patel, PN ;
Fawcett, JW ;
McMahon, SB .
NATURE, 2002, 416 (6881) :636-640
[6]  
CASU B, 1988, TRENDS BIOCHEM SCI, V13, P747
[7]   Chondroitin sulfate E promotes neurite outgrowth of rat embryonic day 18 hippocampal neurons [J].
Clement, AM ;
Sugahara, K ;
Faissner, A .
NEUROSCIENCE LETTERS, 1999, 269 (03) :125-128
[8]   The DSD-1 carbohydrate epitope depends on sulfation, correlates with chondroitin sulfate D motifs, and is sufficient to promote neurite outgrowth [J].
Clement, AM ;
Nadanaka, S ;
Masayama, K ;
Mandl, C ;
Sugahara, K ;
Faissner, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (43) :28444-28453
[9]   Specific molecular interactions of oversulfated chondroitin sulfate E with various heparin-binding growth factors - Implications as a physiological binding partner in the brain and other tissues [J].
Deepa, SS ;
Umehara, Y ;
Higashiyama, S ;
Itoh, N ;
Sugahara, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (46) :43707-43716
[10]   Neurogenesis in the adult human hippocampus [J].
Eriksson, PS ;
Perfilieva, E ;
Björk-Eriksson, T ;
Alborn, AM ;
Nordborg, C ;
Peterson, DA ;
Gage, FH .
NATURE MEDICINE, 1998, 4 (11) :1313-1317