New functional roles for non-collagenous domains of basement membrane collagens

被引:168
作者
Ortega, N [1 ]
Werb, Z [1 ]
机构
[1] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
关键词
basement membrane collagens; NC1; fragments; angiogenesis; morphogenesis;
D O I
10.1242/jcs.00106
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Collagens IV, XV and XVIII are major components of various basement membranes. In addition to the collagen-specific triple helix, these collagens are characterized by the presence of several non-collagenous domains. It is clear now that these ubiquitous collagen molecules are involved in more subtle and sophisticated functions than just the molecular architecture of basement membranes, particularly in the context of extracellular matrix degradation. Degradation of the basement membrane collagens occurs during numerous physiological and pathological processes such as embryonic development or tumorigenesis and generates collagen fragments. These fragments are involved in the, regulation of functions differing from those of their original intact molecules. The non-collagenous C-terminal fragment NC1 of collagen IV, XV and XVIII have been recently highlighted in the literature because of their potential in reducing angiogenesis and tumorigenesis, but it is clear that their biological functions are not limited to these processes Proteolytic release of soluble NC1 fragments stimulates migration, proliferation, apoptosis or survival of different cell types and suppresses various morphogenetic events.
引用
收藏
页码:4201 / 4214
页数:14
相关论文
共 151 条
  • [1] IDENTIFICATION OF A NOVEL COLLAGEN CHAIN REPRESENTED BY EXTENSIVE INTERRUPTIONS IN THE TRIPLE-HELICAL REGION
    ABE, N
    MURAGAKI, Y
    YOSHIOKA, H
    INOUE, H
    NINOMIYA, Y
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 196 (02) : 576 - 582
  • [2] The NC1/endostatin domain of Caenorhabditis elegans type XVIII collagen affects cell migration and axon guidance
    Ackley, BD
    Crew, JR
    Elamaa, H
    Pihlajaniemi, T
    Kuo, CJ
    Kramer, JM
    [J]. JOURNAL OF CELL BIOLOGY, 2001, 152 (06) : 1219 - 1232
  • [3] The angiogenesis induced by HIV-1 Tat protein is mediated by the Flk-1/KDR receptor on vascular endothelial cells
    Albini, A
    Soldi, R
    Giunciuglio, D
    Giraudo, E
    Benelli, R
    Primo, L
    Noonan, D
    Salio, M
    Camussi, G
    Rockl, W
    Bussolino, F
    [J]. NATURE MEDICINE, 1996, 2 (12) : 1371 - 1375
  • [4] ALBINI A, 1985, EUR J CELL BIOL, V36, P104
  • [5] THE EXTRACELLULAR-MATRIX OF CARTILAGE IN THE GROWTH PLATE BEFORE AND DURING CALCIFICATION - CHANGES IN COMPOSITION AND DEGRADATION OF TYPE-II COLLAGEN
    ALINI, M
    MATSUI, Y
    DODGE, GR
    POOLE, AR
    [J]. CALCIFIED TISSUE INTERNATIONAL, 1992, 50 (04) : 327 - 335
  • [6] The angiogenesis inhibitor, endostatin, does not affect murine cutaneous wound healing
    Berger, AC
    Feldman, AL
    Gnant, MFX
    Kruger, EA
    Sim, BKL
    Hewitt, S
    Figg, WD
    Alexander, HR
    Libutti, SK
    [J]. JOURNAL OF SURGICAL RESEARCH, 2000, 91 (01) : 26 - 31
  • [7] Effects of angiogenesis inhibitors on multistage carcinogenesis in mice
    Bergers, G
    Javaherian, K
    Lo, KM
    Folkman, J
    Hanahan, D
    [J]. SCIENCE, 1999, 284 (5415) : 808 - 812
  • [8] Systemic inhibition of tumor growth and tumor metastases by intramuscular administration of the endostatin gene
    Blezinger, P
    Wang, JJ
    Gondo, M
    Quezada, A
    Mehrens, D
    French, M
    Singhal, A
    Sullivan, S
    Rolland, A
    Ralston, R
    Min, W
    [J]. NATURE BIOTECHNOLOGY, 1999, 17 (04) : 343 - 348
  • [9] Bloch W, 2000, FASEB J, V14, P2373
  • [10] BLUMBERG B, 1987, J BIOL CHEM, V262, P5947