Basement membrane assembly, stability and activities observed through a developmental lens

被引:291
作者
Yurchenco, PD
Amenta, PS
Patton, BL
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Pathol & Lab Med, Piscataway, NJ 08854 USA
[2] Oregon Hlth & Sci Univ, Ctr Res Occupat & Environm Toxicol, Portland, OR 97239 USA
关键词
basement membrane; laminins; mutagenesis;
D O I
10.1016/j.matbio.2003.10.006
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
Basement membranes are cell surface associated extracellular matrices containing laminins, type IV collagens, nidogens, perlecan, agrin, and other macromolecules. Biochemical and ultrastructural studies have suggested that basement membrane assembly and integrity is provided through multiple component interactions consisting of self-polymerizations, inter-component binding, and cell surface adhesions. Mutagenesis in vertebrate embryos and embryoid bodies have led to revisions of this model, providing evidence that laminins are essential for the formation of an initial polymeric scaffold of cell-attached matrix which matures in stability, ligand diversity, and functional complexity as additional matrix components are integrated into the scaffold. These studies also demonstrate that basement membrane components differentially promote cell polarization, organize and compartmentalize developing tissues, and maintain adult tissue function. (C) 2003 Elsevier B.V./International Society of Matrix Biology. All rights reserved.
引用
收藏
页码:521 / 538
页数:18
相关论文
共 165 条
[1]  
Ackley BD, 2003, J NEUROSCI, V23, P3577
[2]   The NC1/endostatin domain of Caenorhabditis elegans type XVIII collagen affects cell migration and axon guidance [J].
Ackley, BD ;
Crew, JR ;
Elamaa, H ;
Pihlajaniemi, T ;
Kuo, CJ ;
Kramer, JM .
JOURNAL OF CELL BIOLOGY, 2001, 152 (06) :1219-1232
[3]   Binding of fibulin-1 to nidogen depends on its C-terminal globular domain and a specific array of calcium-binding epidermal growth factor-like (EG) modules [J].
Adam, S ;
Gohring, W ;
Wiedemann, H ;
Chu, ML ;
Timpl, R ;
Kostka, G .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 272 (02) :226-236
[4]   Analysis of heparin, α-dystroglycan and sulfatide binding to the G domain of the laminin α1 chain by site-directed mutagenesis [J].
Andac, Z ;
Sasaki, T ;
Mann, K ;
Brancaccio, A ;
Deutzmann, R ;
Timpl, R .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 287 (02) :253-264
[5]  
Anderson R, 1999, DEVELOPMENT, V126, P1655
[6]   Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia [J].
Arikawa-Hirasawa, E ;
Le, AH ;
Nishino, I ;
Nonaka, I ;
Ho, NC ;
Francomano, CA ;
Govindraj, P ;
Hassell, JR ;
Devaney, JM ;
Spranger, J ;
Stevenson, RE ;
Iannaccone, S ;
Dalakas, MC ;
Yamada, Y .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (05) :1368-1375
[7]   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
[8]   NIDOGEN MEDIATES THE FORMATION OF TERNARY COMPLEXES OF BASEMENT-MEMBRANE COMPONENTS [J].
AUMAILLEY, M ;
BATTAGLIA, C ;
MAYER, U ;
REINHARDT, D ;
NISCHT, R ;
TIMPL, R ;
FOX, JW .
KIDNEY INTERNATIONAL, 1993, 43 (01) :7-12
[9]   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
[10]   ABNORMALITIES OF PERIPHERAL-NERVES IN MURINE MUSCULAR-DYSTROPHY [J].
BRADLEY, WG ;
JENKISON, M .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1973, 18 (02) :227-247