Heparan sulfate chains of perlecan are indispensable in the lens capsule but not in the kidney

被引:180
作者
Rossi, M
Morita, H
Sormunen, R
Airenne, S
Kreivi, M
Wang, L
Fukai, N
Olsen, BR
Tryggvason, K
Soininen, R [1 ]
机构
[1] Univ Oulu, Bioctr Oulu, Dept Med Biochem & Mol Biol, FIN-90014 Oulu, Finland
[2] Univ Oulu, Bioctr Oulu, Dept Pathol, FIN-90014 Oulu, Finland
[3] Univ Oulu, Bioctr Oulu, Dept Biochem, FIN-90014 Oulu, Finland
[4] Karolinska Inst, Dept Med Biochem & Biophys, Div Matrix Biol, S-17177 Stockholm, Sweden
[5] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
关键词
basement membranes; collagen XVIII; congenital cataract; heparan sulfate; perlecan;
D O I
10.1093/emboj/cdg019
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
Mice lacking exon 3 of perlecan (Hspg2) gene were generated by gene targeting. Exon deletion does not alter the expression or the reading frame but causes loss of attachment sites for three heparan sulfate (HS) side chains. Hspg2(Delta3/Delta3) mice are viable and fertile but have small eyes. Apoptosis and leakage of cellular material through the lens capsule are observed in neonatal lenses, and lenses degenerate within 3 weeks of birth. Electron microscopy revealed altered structure of the lens capsule through which cells had formed extensions. No kidney malfunction, such as proteinuria, was detected in Hspg2(Delta3/Delta3) mutant mice, nor were ultrastructural changes observed in the glomerular basement membranes (BMs). To achieve further depletion in the HS content of the BMs, Hspg2(Delta3/Delta3) mice were bred with collagen XVIII null mice. Lens defects were more severe in the newborn Col18a1(-/-) x Hspg2(Delta3/Delta3) mice and degeneration proceeded faster than in Hspg2(Delta3/Delta3) mice. The results suggest that in the lens capsule, HS chains have a structural function and are essential in the insulation of the lens from its environment and in regulation of incoming signals.
引用
收藏
页码:236 / 245
页数:10
相关论文
共 33 条
[1]   Perlecan is essential for cartilage and cephalic development [J].
Arikawa-Hirasawa, E ;
Watanabe, H ;
Takami, H ;
Hassell, JR ;
Yamada, Y .
NATURE GENETICS, 1999, 23 (03) :354-358
[2]   Dyssegmental dysplasia, Silverman-Handmaker type, is caused by functional null mutations of the perlecan gene [J].
Arikawa-Hirasawa, E ;
Wilcox, WR ;
Le, AH ;
Silverman, N ;
Govindraj, P ;
Hassell, JR ;
Yamada, Y .
NATURE GENETICS, 2001, 27 (04) :431-434
[3]   PERLECAN, BASAL LAMINA PROTEOGLYCAN, PROMOTES BASIC FIBROBLAST GROWTH FACTOR-RECEPTOR BINDING, MITOGENESIS, AND ANGIOGENESIS [J].
AVIEZER, D ;
HECHT, D ;
SAFRAN, M ;
EISINGER, M ;
DAVID, G ;
YAYON, A .
CELL, 1994, 79 (06) :1005-1013
[4]   BASEMENT-MEMBRANE HEPARAN-SULFATE PROTEOGLYCAN BINDS TO LAMININ BY ITS HEPARAN-SULFATE CHAINS AND TO NIDOGEN BY SITES IN THE PROTEIN CORE [J].
BATTAGLIA, C ;
MAYER, U ;
AUMAILLEY, M ;
TIMPL, R .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 208 (02) :359-366
[5]  
BATTAGLIA C, 1993, EUR J CELL BIOL, V61, P92
[6]   MACROMOLECULAR ORGANIZATION OF BOVINE LENS CAPSULE [J].
CAMMARATA, PR ;
CANTUCROUCH, D ;
OAKFORD, L ;
MORRILL, A .
TISSUE & CELL, 1986, 18 (01) :83-97
[7]   STRUCTURAL CHARACTERIZATION OF THE COMPLETE HUMAN PERLECAN GENE AND ITS PROMOTER [J].
COHEN, IR ;
GRASSEL, S ;
MURDOCH, AD ;
IOZZO, RV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (21) :10404-10408
[8]   Perlecan maintains the integrity of cartilage and some basement membranes [J].
Costell, M ;
Gustafsson, E ;
Aszódi, A ;
Mörgelin, M ;
Bloch, W ;
Hunziker, E ;
Addicks, K ;
Timpl, R ;
Fässler, R .
JOURNAL OF CELL BIOLOGY, 1999, 147 (05) :1109-1122
[9]   Identification of sites in domain I of perlecan that regulate heparan sulfate synthesis [J].
Dolan, M ;
Horchar, T ;
Rigatti, B ;
Hassell, JR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (07) :4316-4322
[10]   ASSIGNMENT OF CONGENITAL CATARACT VOLKMANN TYPE (CCV) TO CHROMOSOME 1P36 [J].
EIBERG, H ;
LUND, AM ;
WARBURG, M ;
ROSENBERG, T .
HUMAN GENETICS, 1995, 96 (01) :33-38