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PMID: 8456591 Published · ppublish English Journal Article

Pattern of gene expression following rat tibial marrow ablation.

Suva LJ, Seedor JG, Endo N, Quartuccio HA, Thompson DD, Bab I, Rodan GA

Abstract

Following injury to bone marrow there is a phase of osteogenesis in which bone trabeculae replace the initial blood clot and fill the marrow cavity. The newly formed bone is subsequently fully resorbed by osteoclasts and normal bone marrow is restored. In this study we correlated the morphologic events with the pattern of gene expression that defines this sequence. Following marrow ablation, the trabecular bone volume in the affected section of the marrow cavity increased from control to 27% at day 6, declined to 18% at day 8, and eventually returned to control levels at day 14. Osteoblast number increased up to day 6 and declined substantially by day 8, but the number of osteoclasts peaked between days 8 and 10. Histologic analysis of alkaline phosphatase (AP) and tartrate-resistant acid phosphatase (TRAP) activity correlated with the observed cellular changes. Northern blot analysis of the levels of AP, osteocalcin (OC), and osteopontin (OP) mRNA shows a specific pattern of regulated gene expression, with AP mRNA maximal at day 6, OC mRNA very low until days 6-8, and OP mRNA expressed at very high levels throughout. In addition, procollagen alpha 1(I) and alpha 1(III) mRNAs show a regulated pattern of expression, with procollagen alpha 1(I) maximally expressed between days 4 and 10 and procollagen alpha 1(III) expressed at lower levels between days 4 and 6. The mRNA encoding insulin-like growth factor I (IGF-I) was found to be highly expressed between days 5 and 12; however, transforming growth factor beta 1 (TGF-beta 1) and TGF-beta 3 mRNA were only weakly expressed between days 4 and 10. These data demonstrate a temporal pattern of gene expression consistent with the observed morphologic profile, identify changes in growth factor mRNA that may be related to this repair process, and suggest that this is a suitable model for studying in vivo a synchronized sequence of bone formation and resorption at a well-defined anatomic site.

MeSH Terms
Alkaline Phosphatase/analysis Animals Blotting, Northern Bone Marrow/metabolism Bone Marrow Cells Gene Expression Regulation Insulin-Like Growth Factor I/metabolism Male Osteocalcin/analysis Osteogenesis Osteopontin Procollagen/biosynthesis Rats Rats, Sprague-Dawley Sialoglycoproteins/analysis Transforming Growth Factor beta/metabolism
Chemicals
Procollagen Sialoglycoproteins Spp1 protein, rat Transforming Growth Factor beta Osteocalcin Osteopontin Insulin-Like Growth Factor I Alkaline Phosphatase
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Suva L J
Department of Bone Biology and Osteoporosis Research, Merck Research Laboratories, West Point, Pennsylvania.
Seedor J G
Endo N
Quartuccio H A
Thompson D D
Bab I
Rodan G A
Article Info
Journal
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Abbr.
J Bone Miner Res
ISSN
0884-0431
Published
1993-03-00
Pages
379-88
Language
English
Region
United States
NLM ID
8610640
Subset
IM
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