Type III collagen is crucial for collagen I fibrillogenesis and for normal cardiovascular development

被引:461
作者
Liu, X
Wu, H
Byrne, M
Krane, S
Jaenisch, R
机构
[1] MIT,DEPT BIOL,CAMBRIDGE,MA 02142
[2] HARVARD UNIV,SCH MED,DEPT MED,BOSTON,MA 02214
[3] MASSACHUSETTS GEN HOSP,MED SERV,ARTHRITIS UNIT,BOSTON,MA 02214
关键词
gene targeting; Ehlers-Danlos syndrome type IV; aortic rupture;
D O I
10.1073/pnas.94.5.1852
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Type III collagen is a fibrilar forming collagen comprising three alpha 1(III) chains and is expressed in early embryos and throughout embryogenesis. In the adult, type III collagen is a major component of the extracellular matrix in a variety of internal organs and skin, Mutations in the COL3A1 gene have been implicated as a cause of type IV Ehlers-Danlos syndrome, a disease leading to aortic rupture in early adult life. To directly study the role of Col3a1 in development and disease, we have inactivated the Col3a1 gene in embryonic stem cells by homologous recombination, The mutated allele was transmitted through the mouse germ line and homozygous mutant animals were derived from heterozygous intercrosses. About 10% of the homozygous mutant animals survived to adulthood but have a much shorter life span compared with wild-type mice. The major cause of death of mutant mice was rupture of the major blood vessels, similar to patients with type IV Ehlers-Danlos syndrome. Ultrastructural analysis of tissues from mutant mice revealed that type III collagen is essential for normal collagen I fibrillogenesis in the cardiovascular system and other organs.
引用
收藏
页码:1852 / 1856
页数:5
相关论文
共 27 条
[1]   TARGETED MUTATION IN THE COL5A2 GENE REVEALS A REGULATORY ROLE FOR TYPE-V COLLAGEN DURING MATRIX ASSEMBLY [J].
ANDRIKOPOULOS, K ;
LIU, X ;
KEENE, DR ;
JAENISCH, R ;
RAMIREZ, F .
NATURE GENETICS, 1995, 9 (01) :31-36
[2]  
Bancroft J. D., 1984, MANUAL HISTOLOGICAL, P49
[3]   STRUCTURALLY DISTINCT COLLAGEN TYPES [J].
BORNSTEIN, P ;
SAGE, H .
ANNUAL REVIEW OF BIOCHEMISTRY, 1980, 49 :957-1003
[4]  
EPSTEIN EH, 1975, J BIOL CHEM, V250, P9304
[5]   MICE LACKING ALPHA(IX) COLLAGEN DEVELOP NONINFLAMMATORY DEGENERATIVE JOINT DISEASE [J].
FASSLER, R ;
SCHNEGELSBERG, PNJ ;
DAUSMAN, J ;
SHINYA, T ;
MURAGAKI, Y ;
MCCARTHY, MT ;
OLSEN, BR ;
JAENISCH, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (11) :5070-5074
[6]   COLLAGEN FIBRIL FORMATION DURING EMBRYOGENESIS [J].
FLEISCHMAJER, R ;
OLSEN, BR ;
TIMPL, R ;
PERLISH, JS ;
LOVELACE, O .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (11) :3354-3358
[7]   ULTRASTRUCTURAL IDENTIFICATION OF EXTENSION AMINOPROPEPTIDES OF TYPE-I AND TYPE-III COLLAGENS IN HUMAN-SKIN [J].
FLEISCHMAJER, R ;
TIMPL, R ;
TUDERMAN, L ;
RAISHER, L ;
WIESTNER, M ;
PERLISH, JS ;
GRAVES, PN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (12) :7360-7364
[8]   PROCOLLAGEN INTERMEDIATES DURING TENDON FIBRILLOGENESIS [J].
FLEISCHMAJER, R ;
PERLISH, JS ;
TIMPL, R ;
OLSEN, BR .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1988, 36 (11) :1425-1432
[9]  
GELMAN RA, 1979, J BIOL CHEM, V254, P180
[10]   COLLAGEN FIBRILS INVITRO GROW FROM POINTED TIPS IN THE C-TERMINAL TO N-TERMINAL DIRECTION [J].
KADLER, KE ;
HOJIMA, Y ;
PROCKOP, DJ .
BIOCHEMICAL JOURNAL, 1990, 268 (02) :339-343