Functions of the conserved thrombospondin carboxy-terminal cassette in cell-extracellular matrix interactions and signaling

被引:51
作者
Adams, JC [1 ]
机构
[1] Cleveland Clin Fdn, Lerner Res Inst, Dept Cell Biol, Cleveland, OH 44195 USA
关键词
thrombospondin; calcium-binding; red motif; cell adhesion; cell signalling;
D O I
10.1016/j.biocel.2004.01.022
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
Thrombospondins (TSPs) are extracellular, multidomain, calcium-binding glycoproteins that function at cell surfaces, in extracellular matrix (ECM) and as bridging molecules in cell-cell interactions. TSPs are multifunctional and modulate cell behavior during development, wound-healing, immune response, tumor growth and in the homeostasis of adult tissues. TSPs are assembled as oligomers that are composed of homologous polypeptides. In all the TSP polypeptides, the most highly-conserved region is the carboxyl-region, which contains a characteristic set of domains comprising EGF domains, TSP type 3 repeats and a globular carboxy-terminal domain. This large region is termed here the thrombospondin carboxy-terminal cassette (TSP-CTC). The strong conservation of the TSP-CTC suggests that it may mediate ancestral functions that are shared by all TSPs. This review summarizes the current knowledge of the TSP-CTC and areas of future interest. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1102 / 1114
页数:13
相关论文
共 84 条
  • [71] 2-2
  • [72] DISULFIDES MODULATE RGD-INHIBITABLE CELL ADHESIVE ACTIVITY OF THROMBOSPONDIN
    SUN, X
    SKORSTENGAARD, K
    MOSHER, DF
    [J]. JOURNAL OF CELL BIOLOGY, 1992, 118 (03) : 693 - 701
  • [73] Cartilage oligomeric matrix protein-deficient mice have normal skeletal development
    Svensson, L
    Aszódi, A
    Heinegård, D
    Hunziker, EB
    Reinholt, FP
    Fässler, R
    Oldberg, Å
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (12) : 4366 - 4371
  • [74] TARABOLETTI G, 1992, LAB INVEST, V67, P566
  • [75] Mutations in cartilage oligomeric matrix protein causing pseudoachondroplasia and multiple epiphyseal dysplasia affect binding of calcium and collagen I, II, and IX
    Thur, J
    Rosenberg, K
    Nitsche, DP
    Pihlajamaa, T
    Ala-Kokko, L
    Heinegård, D
    Paulsson, M
    Maurer, P
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (09) : 6083 - 6092
  • [76] Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction
    Topol, EJ
    McCarthy, J
    Gabriel, S
    Moliterno, DJ
    Rogers, WJ
    Newby, LK
    Freedman, M
    Metivier, J
    Cannata, R
    O'Donnell, CJ
    Kottke-Marchant, K
    Murugesan, G
    Plow, EF
    Stenina, O
    Daley, GQ
    [J]. CIRCULATION, 2001, 104 (22) : 2641 - 2644
  • [77] C-terminal peptide of thrombospondin-1 induces platelet aggregation through the Fc receptor γ-chain-associated signaling pathway and by agglutination
    Tulasne, D
    Judd, BA
    Johanson, M
    Asazuma, N
    Best, D
    Brown, EJ
    Kahn, M
    Koretzky, GA
    Watson, SP
    [J]. BLOOD, 2001, 98 (12) : 3346 - 3352
  • [78] Pseudoachondroplasia and multiple epiphyseal dysplasia: New etiologic developments
    Unger, S
    Hecht, JT
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 106 (04): : 244 - 250
  • [79] van der Pluijm G, 1997, LAB INVEST, V77, P665
  • [80] Control of von Willebrand factor multimer size by thrombospondin-1
    Xie, LJ
    Chesterman, CN
    Hogg, PJ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (12) : 1341 - 1349