Age-related inhibitory activity of rat bone marrow supernatant on osteoblast proliferation

Citation
D. Egrise et al., Age-related inhibitory activity of rat bone marrow supernatant on osteoblast proliferation, J BONE MIN, 14(12), 1999, pp. 2099-2106
Citations number
42
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
JOURNAL OF BONE AND MINERAL RESEARCH
ISSN journal
08840431 → ACNP
Volume
14
Issue
12
Year of publication
1999
Pages
2099 - 2106
Database
ISI
SICI code
0884-0431(199912)14:12<2099:AIAORB>2.0.ZU;2-5
Abstract
Because histomorphometric indices of bone formation (osteoblastic index, te tracyclin-labeled perimeter) are deeply depressed in aged rats, while in vi tro proliferation of trabecular bone cells was found increased, we hypothes ized that a signal to proliferate, correctly induced by increased strains o n scarce bone, could be opposed in vivo by an inhibitor present in the bone marrow extracellular medium. Thus, we tested the effect of bone marrow ext racellular fluid (BM supernatant) of rat femoral diaphysis on cultures of p rimary osteoblasts and osteoblastic cell lines and found that it inhibited bone cell proliferation, In a group of 69 female rats aged 4, 12, and 15/21 months, there was a stepwise increase in the inhibitory activity of the BM supernatant, The double reciprocal plots relating inhibition power of the medium to BM supernatant dilution suggest that we deal with a simple system and that the kinetics of the phenomenon are the same in older and younger animals. Moreover, proliferation inhibition by BM supernatant and trabecula r bone surface measured by histomorphometry in the distal femoral metaphysi s were inversely correlated. Because the extracellular fluid of bone marrow is also the medium surrounding the osteoblasts and their precursor cells, our results suggest that the bone marrow negatively regulates osteogenic ce lls and that this inhibition could contribute to the inability of older ani mals to supply osteoblasts to bone in proportion to the demand, Preliminary biochemical characterization of the inhibitor suggests it to be a protein of 30-40 kDa with an isoelectric point (pI) of about 6.5.