The anatomy of organogenesis: Novel solutions to old problems

被引:6
作者
Davies, Jamie A. [1 ]
Armstrong, Jane E. [1 ]
机构
[1] Heidelberg Univ, Stiftung Orthopad Klin, Sekt Expt Orthopadie, D-69118 Heidelberg, Germany
关键词
green fluorescent protein; GFP; optical projection tomography; OPT; RNAi; RNA interference; branching; organ development;
D O I
10.1016/j.proghi.2006.02.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Osteoarthritis (OA) is a disease of high ethical and economical importance. In advanced stages, the patients suffer from severe pain and restriction of mobility. The consequence in many cases is an inability to work and often the substitution of the diseased joint with an artificial implant becomes inevitable. As cartilage tissue itself has only very limited capacities of self-renewing, the development of this disorder is chronic and progressive. Generally, OA is diagnosed in more advanced stages, when clinical and radiographic signs become evident. At this time point the options for therapeutic intervention without surgery are limited. It is, therefore, crucial to know about the basic incidents in the course of OA and especially in early stages to develop new diagnostic and therapeutic strategies. Numerous studies on human osteoarthritic tissue and in animal models have addressed various aspects of OA progression to get a better understanding of the pathophysiology of this disease. This review presents an overview on different aspects of OA research and the cellular and molecular alterations in degenerating cartilage. (c) 2006 Elsevier GmbH. All rights reserved.
引用
收藏
页码:165 / 176
页数:12
相关论文
共 46 条
[1]   Architectural patterns in branching morphogenesis in the kidney [J].
Al-Awqati, Q ;
Goldberg, MR .
KIDNEY INTERNATIONAL, 1998, 54 (06) :1832-1842
[2]   THE EXPRESSION OF THE WILMS-TUMOR GENE, WT1, IN THE DEVELOPING MAMMALIAN EMBRYO [J].
ARMSTRONG, JF ;
PRITCHARDJONES, K ;
BICKMORE, WA ;
HASTIE, ND ;
BARD, JBL .
MECHANISMS OF DEVELOPMENT, 1993, 40 (1-2) :85-97
[3]  
Bertram JF, 1995, INT REV CYTOL, V161, P111
[4]   Talking about a revolution: The impact of site-specific recombinases on genetic analyses in mice [J].
Branda, CS ;
Dymecki, SM .
DEVELOPMENTAL CELL, 2004, 6 (01) :7-28
[5]  
Bryson-Richardson RJ, 2004, METHOD CELL BIOL, V76, P37
[6]   ISOLATION, CHARACTERIZATION, AND EXPRESSION OF THE MURINE WILMS-TUMOR GENE (WT1) DURING KIDNEY DEVELOPMENT [J].
BUCKLER, AJ ;
PELLETIER, J ;
HABER, DA ;
GLASER, T ;
HOUSMAN, DE .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (03) :1707-1712
[7]   Exogenous BMP-4 amplifies asymmetric ureteric branching in the developing mouse kidney in vitro [J].
Cain, JE ;
Nion, T ;
Jeulin, D ;
Bertram, JF .
KIDNEY INTERNATIONAL, 2005, 67 (02) :420-431
[8]  
Campbell TN, 2005, CURR ISSUES MOL BIOL, V7, P1
[9]   GREEN FLUORESCENT PROTEIN AS A MARKER FOR GENE-EXPRESSION [J].
CHALFIE, M ;
TU, Y ;
EUSKIRCHEN, G ;
WARD, WW ;
PRASHER, DC .
SCIENCE, 1994, 263 (5148) :802-805
[10]   Nephron number, renal function, and arterial pressure in aged GDNF heterozygous mice [J].
Cullen-McEwen, LA ;
Kett, MM ;
Dowling, J ;
Anderson, WP ;
Bertram, JF .
HYPERTENSION, 2003, 41 (02) :335-340