Mouse models for extracellular matrix diseases

被引:27
作者
Aszódi, A [1 ]
Pfeifer, A
Wendel, M
Hiripi, L
Fässler, R
机构
[1] Max Planck Inst Biochem, D-82152 Martinsried, Germany
[2] Tech Univ Munich, Inst Pharmakol & Toxikol, D-80802 Munich, Germany
[3] Agr Biotechnol Ctr, Inst Anim Sci, H-2101 Godollo, Hungary
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 1998年 / 76卷 / 3-4期
关键词
extracellular matrix; gene targeting; transgenic mice; mouse models; human diseases;
D O I
10.1007/s001090050214
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mutations of a number of genes encoding for extracellular matrix (ECM) proteins in mice have provided new insights regarding their role during development and disease, Many mouse strains have helped to verify the link between mutation and disease in humans, and others have produced unexpected phenotypes and identified new functions for ECM proteins. Finally, some null mutations in ECM genes provide no phenotypic alterations in mice, confronting the scientific community with a new challenge to search for their functions. This review lists all mouse strains with spontaneous and experimentally induced mutations in ECM genes. The phenotypes of these mice are discussed in comparison with the human diseases.
引用
收藏
页码:238 / 252
页数:15
相关论文
共 132 条
[91]   KNIEST DYSPLASIA IS CHARACTERIZED BY AN APPARENT ABNORMAL PROCESSING OF THE C-PROPEPTIDE OF TYPE-II CARTILAGE COLLAGEN RESULTING IN IMPERFECT FIBRIL ASSEMBLY [J].
POOLE, AR ;
PIDOUX, I ;
REINER, A ;
ROSENBERG, L ;
HOLLISTER, D ;
MURRAY, L ;
RIMOIN, D .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (02) :579-589
[92]  
PREISSNER KT, 1991, ANNU REV CELL BIOL, V7, P275, DOI 10.1146/annurev.cb.07.110191.001423
[93]   COLLAGENS - MOLECULAR-BIOLOGY, DISEASES, AND POTENTIALS FOR THERAPY [J].
PROCKOP, DJ ;
KIVIRIKKO, KI .
ANNUAL REVIEW OF BIOCHEMISTRY, 1995, 64 :403-434
[94]   HERITABLE DISEASES OF COLLAGEN [J].
PROCKOP, DJ ;
KIVIRIKKO, KI .
NEW ENGLAND JOURNAL OF MEDICINE, 1984, 311 (06) :376-386
[95]   Marrow stromal cells as steam cells for nonhematopoietic tissues [J].
Prockop, DJ .
SCIENCE, 1997, 276 (5309) :71-74
[96]  
RITTENHOUSE E, 1978, J EMBRYOL EXP MORPH, V43, P71
[97]   NORMAL LONG-BONE GROWTH AND DEVELOPMENT IN TYPE-X COLLAGEN NULL MICE [J].
ROSATI, R ;
HORAN, GSB ;
PINERO, GJ ;
GAROFALO, S ;
KEENE, DR ;
HORTON, WA ;
VUORIO, E ;
DECROMBRUGGHE, B ;
BEHRINGER, RR .
NATURE GENETICS, 1994, 8 (02) :129-135
[98]  
Rosenbloom J, 1995, CIBA F SYMP, V192, P59
[99]   MICE DEVELOP NORMALLY WITHOUT TENASCIN [J].
SAGA, Y ;
YAGI, T ;
IKAWA, Y ;
SAKAKURA, T ;
AIZAWA, S .
GENES & DEVELOPMENT, 1992, 6 (10) :1821-1831
[100]  
SCHNAPER HW, 1993, DIS KIDNEY