Novel interactions of perlecan: Unraveling perlecan's role in angiogenesis

被引:78
作者
Bix, Gregory [1 ]
Iozzo, Renato V. [1 ,2 ]
机构
[1] Thomas Jefferson Univ, Dept Pathol Anat & Cellular Biol, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Kimmel Canc Ctr, Cellular Biol & Signaling Program, Philadelphia, PA 19107 USA
关键词
endorepellin; heparan sulfate proteoglycan; extracellular matrix; alpha; 2; beta; 1; integrin;
D O I
10.1002/jemt.20562
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 [人体解剖与组织胚胎学];
摘要
Perlecan, a highly conserved and ubiquitous basement membrane heparan sulfate proteoglycan, is essential for life, inasmuch as its absence results in embryonic lethality in mice and C. elegans, and neonatal lethality in humans. Perlecan plays an essential role in vasculogenesis and chondrogenesis, as well as in pathological states where these processes are maladapted. Although a large body of evidence supports a pro-angiogenic role for perlecan, recent findings suggests that portions of the perlecan protein core can be antiangiogenic, requiring a further evaluation of the functioning of this complex molecule. This review is focused on the genetics of mammalian and nonmammalian perlecan, the elucidation of its novel interacting partners and its role in angiogenesis. By more fully understanding perlecan's functioning in angiogenesis, we may gain invaluable insight that could lead to therapeutic interventions in cancer and other pathologic states.
引用
收藏
页码:339 / 348
页数:10
相关论文
共 138 条
[1]
KERATINOCYTE GROWTH-FACTOR - A FIBROBLAST GROWTH-FACTOR FAMILY MEMBER WITH UNUSUAL TARGET-CELL SPECIFICITY [J].
AARONSON, SA ;
BOTTARO, DP ;
MIKI, T ;
RON, D ;
FINCH, PW ;
FLEMING, TP ;
AHN, J ;
TAYLOR, WG ;
RUBIN, JS .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1991, 638 :62-77
[2]
Suppression of invasive behavior of melanoma cells by stable expression of anti-sense perlecan cDNA [J].
Adatia, R ;
Albini, A ;
Carlone, S ;
Giunciuglio, D ;
Benelli, R ;
Santi, L ;
Noonan, DM .
ANNALS OF ONCOLOGY, 1997, 8 (12) :1257-1261
[3]
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
[4]
Absence of acetylcholinesterase at the neuromuscular junctions of perlecan-null mice [J].
Arikawa-Hirasawa, E ;
Rossi, SG ;
Rotundo, RL ;
Yamada, Y .
NATURE NEUROSCIENCE, 2002, 5 (02) :119-123
[5]
Dyssegmental dysplasia, Silverman-Handmaker type: Unexpected role of perlecan in cartilage development [J].
Arikawa-Hirasawa, E ;
Wilcox, WR ;
Yamada, Y .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 106 (04) :254-257
[6]
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
[7]
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
[8]
Thrombospondins 1 and 2 function as inhibitors of angiogenesis [J].
Armstrong, LC ;
Bornstein, P .
MATRIX BIOLOGY, 2003, 22 (01) :63-71
[9]
Suppression of autocrine and paracrine functions of basic fibroblast growth factor by stable expression of perlecan antisense cDNA [J].
Aviezer, D ;
Iozzo, RV ;
Noonan, DM ;
Yayon, A .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (04) :1938-1946
[10]
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