Microarray analysis of gene expression during the inflammation and endochondral bone formation stages of rat femur fracture repair

被引:113
作者
Rundle, CH
Wang, HL
Yu, HR
Chadwick, RB
Davis, EI
Wergedal, JE
Lau, KHW
Mohan, S
Ryaby, JT
Baylink, DJ
机构
[1] Jerry L Pettis Mem Vet Adm Med Ctr, Musculoskeletal Dis Ctr 151, Loma Linda, CA 92357 USA
[2] Loma Linda Univ, Dept Med, Loma Linda, CA 92354 USA
[3] Loma Linda Univ, Dept Biochem, Loma Linda, CA 92354 USA
[4] Orthol Corp, Res & Dev, Tempe, AZ 85281 USA
关键词
fracture healing; microarray; inflammation; endochondral; scarless;
D O I
10.1016/j.bone.2005.09.015
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Microarray analysis of gene expression was performed in the healing femur fractures of 13-week-old male rats during the inflammatory stage of repair, at 3 days post-fracture, and the endochondral bone formation stage of repair, at 11 days post-fracture. Multiple replicate pairs of fracture tissues paired with unfractured tissues, and Unfractured control bones that had the stabilizing K-wire were introduced. This approach normalized the marrow contributions to the RNA repertoire. We identified 6555 genes with significant changes in expression in fracture tissues at 3 days and 11 days healing. The repertoire of growth factor genes expressed was also Surprisingly restricted at both post-fracture intervals. The large number of Expressed Sequence Tags (ESTs) expressed at both post-fracture times indicates that several molecular pathways yet to be identified regulate fracture repair. The number of genes expressed during immune responses and inflammatory processes was restricted with higher expression largely during the early post-fracture analysis. Several of the genes identified in this study have been associated with regulation of cell and extracellular matrix interactions during scarless healing of fetal skin wounds. These observations suggest that these genes might also regulate the scarless healing characteristic of bone regeneration by similar mechanisms. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:521 / 529
页数:9
相关论文
共 48 条
[1]
ANDREW JG, 1995, BONE, V16, P455
[2]
INSULIN-LIKE GROWTH-FACTOR GENE-EXPRESSION IN HUMAN FRACTURE CALLUS [J].
ANDREW, JG ;
HOYLAND, J ;
FREEMONT, AJ ;
MARSH, D .
CALCIFIED TISSUE INTERNATIONAL, 1993, 53 (02) :97-102
[3]
The matrix metalloproteinase-14 (MMP-14) gene is structurally distinct from other MMP genes and is co-expressed with the TIMP-2 gene during mouse embryogenesis [J].
Apte, SS ;
Fukai, N ;
Beier, DR ;
Olsen, BR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (41) :25511-25517
[4]
Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[5]
Growth factor regulation of fracture repair [J].
Barnes, GL ;
Kostenuik, PJ ;
Gerstenfeld, LC ;
Einhorn, TA .
JOURNAL OF BONE AND MINERAL RESEARCH, 1999, 14 (11) :1805-1815
[6]
THE ACUTE-PHASE RESPONSE [J].
BAUMANN, H ;
GAULDIE, J .
IMMUNOLOGY TODAY, 1994, 15 (02) :74-80
[7]
Beasley Leslie S., 2000, P311
[8]
BOLANDER ME, 1992, P SOC EXP BIOL MED, V200, P165
[9]
BONNARENS F, 1984, Journal of Orthopaedic Research, V2, P97, DOI 10.1002/jor.1100020115
[10]
Fetal wound healing: Current biology [J].
Bullard, KM ;
Longaker, MT ;
Lorenz, HP .
WORLD JOURNAL OF SURGERY, 2003, 27 (01) :54-61