Low doses and high doses of heparin have different effects on osteoblast‐like Saos‐2 cells in vitro
- 25 February 2004
- journal article
- research article
- Published by Wiley in Journal of Cellular Biochemistry
- Vol. 91 (5) , 1062-1073
- https://doi.org/10.1002/jcb.20007
Abstract
Long‐term treatment with heparin has been associated with an increased risk of osteoporosis. Given the importance of heparan sulfate proteoglycans for bone metabolism, it can be anticipated that heparin due to its structural similarity with heparan sulfate chains somehow interferes with the biological activities of these cell surface‐ and extracellular matrix‐associated molecules. Initially in order to study the effect(s) of heparin on osteoblasts that possibly contribute to the development of heparin‐induced osteoporosis, we treated osteoblast‐like Saos‐2 cells in monolayer culture for different periods of time with different concentrations of heparin. None of the heparin concentrations tested led to an inhibition of osteoblast proliferation during the early proliferative phase. After longer incubation times, however, cultures treated with higher concentrations of heparin (≥5 μg/ml) exhibited a reduction in cell number as well as an inhibition of matrix deposition and mineralization. These effects could not be observed with lower heparin concentrations. On the contrary, low concentrations of heparin (5–500 ng/ml) even promoted matrix deposition and its subsequent mineralization. Apparently, heparin has a biphasic effect on osteoblast‐like Saos‐2 cells, being inhibitory at high concentrations but stimulatory at low concentrations. These results imply that heparin at concentrations well below those used for antithrombotic therapy might eventually turn out to be beneficial for bone formation.Keywords
This publication has 33 references indexed in Scilit:
- Heparin acts synergistically with interleukin-11 to induce STAT3 activation and in vitro osteoclast formationBlood, 2002
- Cbfa1-independent decrease in osteoblast proliferation, osteopenia, and persistent embryonic eye vascularization in mice deficient in Lrp5, a Wnt coreceptorThe Journal of cell biology, 2002
- A Mutation in the LDL Receptor–Related Protein 5 Gene Results in the Autosomal Dominant High–Bone-Mass TraitAmerican Journal of Human Genetics, 2002
- Anabolic or Catabolic Responses of MC3T3-E1 Osteoblastic Cells to Parathyroid Hormone Depend on Time and Duration of TreatmentJournal of Bone and Mineral Research, 1999
- Functions of Cell Surface Heparan Sulfate ProteoglycansAnnual Review of Biochemistry, 1999
- Heparan Sulfate Proteoglycan Modulates Keratinocyte Growth Factor Signaling through Interaction with both Ligand and ReceptorBiochemistry, 1999
- Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndromeNature Genetics, 1996
- Biphasic response of complement to heparin: Fluid-phase generation of neoantigens in human serum and in a reconstituted alternative pathway amplification cycleAmerican Journal of Hematology, 1995
- Rapidly Forming Apatitic Mineral in an Osteoblastic Cell Line (UMR 106—01 BSP)Journal of Biological Chemistry, 1995
- Biphasic effects of low-molecular-weight and conventional heparins on chylomicron clearance in rats.Arteriosclerosis and Thrombosis: A Journal of Vascular Biology, 1993