Abstract
We isolated osteoclasts from neonatal rat bone and assessed the effects of prostaglandins (PGs) I2, E1 and E2 on osteoclastic spreading. We found that although the PGs and dibutyryl cyclic AMP (DB-cAMP) acted as direct inhibitors of osteoclastic spreading, if osteoblasts and osteoclasts were co-cultured, the addition of PGs or DB-cAMP caused a considerable increase in spreading. This suggests that the PGs and DB-cAMP induce osteoblasts to stimulate osteoclasts. Osteoblasts are known to produce PGs, and thus possess the capacity to either inhibit (through PGs) or stimulate osteoclasts. Our results suggest that the balance between stimulation and inhibition of osteoclasts by osteoblasts may be determined by osteoblastic cyclic AMP levels.
Full text
PDF









Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Aubin J. E., Heersche J. N., Merrilees M. J., Sodek J. Isolation of bone cell clones with differences in growth, hormone responses, and extracellular matrix production. J Cell Biol. 1982 Feb;92(2):452–461. doi: 10.1083/jcb.92.2.452. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bianco C., Eden A., Cohn Z. A. The induction of macrophage spreading: role of coagulation factors and the complement system. J Exp Med. 1976 Dec 1;144(6):1531–1544. doi: 10.1084/jem.144.6.1531. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chambers T. J., Magnus C. J. Calcitonin alters behaviour of isolated osteoclasts. J Pathol. 1982 Jan;136(1):27–39. doi: 10.1002/path.1711360104. [DOI] [PubMed] [Google Scholar]
- Chambers T. J. Osteoblasts release osteoclasts from calcitonin-induced quiescence. J Cell Sci. 1982 Oct;57:247–260. doi: 10.1242/jcs.57.1.247. [DOI] [PubMed] [Google Scholar]
- Davies P., Fox R. I., Polyzonis M., Allison A. C., Haswell A. D. The inhibition of phagocytosis and facilitation of exocytosis in rabbit polymorphonuclear leukocytes by cytochalasin B. Lab Invest. 1973 Jan;28(1):16–22. [PubMed] [Google Scholar]
- Heersche J. N., Heyboer M. P., Ng B. Hormone-specific suppression of adenosine 3',5'-monophosphate responses in bone in vitro during prolonged incubation with parathyroid hormone, prostaglandin E1, and calcitonin. Endocrinology. 1978 Aug;103(2):333–340. doi: 10.1210/endo-103-2-333. [DOI] [PubMed] [Google Scholar]
- Kallio D. M., Garant P. R., Minkin C. Ultrastructural effects of calcitonin on osteoclasts in tissue culture. J Ultrastruct Res. 1972 May;39(3):205–216. doi: 10.1016/s0022-5320(72)90017-2. [DOI] [PubMed] [Google Scholar]
- Kent G. N., Jilka R. L., Cohn D. V. Homologous and heterologous control of bone cell adenosine 3',5'-monophosphate response to hormones by parathoromone, prostaglandin E2, calcitonin, and 1,25-dihydroxycholecalciferol. Endocrinology. 1980 Nov;107(5):1474–1481. doi: 10.1210/endo-107-5-1474. [DOI] [PubMed] [Google Scholar]
- Klein D. C., Raisz L. G. Prostaglandins: stimulation of bone resorption in tissue culture. Endocrinology. 1970 Jun;86(6):1436–1440. doi: 10.1210/endo-86-6-1436. [DOI] [PubMed] [Google Scholar]
- Loutit J. F., Nisbet N. W. Resorption of bone. Lancet. 1979 Jul 7;2(8132):26–27. doi: 10.1016/s0140-6736(79)90186-7. [DOI] [PubMed] [Google Scholar]
- Luben R. A., Cain C. D., Chen M. C., Rosen D. M., Adey W. R. Effects of electromagnetic stimuli on bone and bone cells in vitro: inhibition of responses to parathyroid hormone by low-energy low-frequency fields. Proc Natl Acad Sci U S A. 1982 Jul;79(13):4180–4184. doi: 10.1073/pnas.79.13.4180. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lucht U. Effects of calcitonin on osteoclasts in vivo. An ultrastructural and histochemical study. Z Zellforsch Mikrosk Anat. 1973 Nov 23;145(1):75–87. doi: 10.1007/BF00307190. [DOI] [PubMed] [Google Scholar]
- Raisz L. G., Vanderhoek J. Y., Simmons H. A., Kream B. E., Nicolaou K. C. Prostaglandin synthesis by fetal rat bone in vitro: evidence for a role of prostacyclin. Prostaglandins. 1979 Jun;17(6):905–914. doi: 10.1016/0090-6980(79)90061-3. [DOI] [PubMed] [Google Scholar]
- Rodan G. A., Bourret L. A., Harvey A., Mensi T. Cyclic AMP and cyclic GMP: mediators of the mechanical effects on bone remodeling. Science. 1975 Aug 8;189(4201):467–469. doi: 10.1126/science.168639. [DOI] [PubMed] [Google Scholar]
- Rodan S. B., Rodan G. A., Simmons H. A., Walenga R. W., Feinstein M. B., Raisz L. G. Bone resorptive factor produced by osteosarcoma cells with osteoblastic features is PGE2. Biochem Biophys Res Commun. 1981 Oct 30;102(4):1358–1365. doi: 10.1016/s0006-291x(81)80161-1. [DOI] [PubMed] [Google Scholar]
- Somjen D., Binderman I., Berger E., Harell A. Bone remodelling induced by physical stress is prostaglandin E2 mediated. Biochim Biophys Acta. 1980 Jan 3;627(1):91–100. doi: 10.1016/0304-4165(80)90126-9. [DOI] [PubMed] [Google Scholar]
- Vaes G. On the mechanisms of bone resorption. The action of parathyroid hormone on the excretion and synthesis of lysosomal enzymes and on the extracellular release of acid by bone cells. J Cell Biol. 1968 Dec;39(3):676–697. doi: 10.1083/jcb.39.3.676. [DOI] [PMC free article] [PubMed] [Google Scholar]


