Abstract
The terminal differentiation of Ob1771 pre-adipose cells induced by arachidonic acid in serum-free hormone-supplemented medium containing insulin, transferrin, growth hormone, tri-iodothyronine and fetuin (5F medium) was strongly diminished in the presence of inhibitors of prostaglandin synthesis, namely aspirin or indomethacin. Carbaprostacyclin, a stable analogue of prostacyclin (prostaglandin I2) known to be synthesized by pre-adipocytes and adipocytes, behaved as an efficient activator of cyclic AMP production and was able, when added to 5F medium, to mimic the adipogenic effect of arachidonic acid. Prostaglandins E2, F2 alpha and D2, unable to affect the cyclic AMP production, failed to substitute for carbaprostacyclin. However, prostaglandin F2 alpha, which is another metabolite of arachidonic acid in pre-adipose and adipose cells, able to promote inositol phospholipid breakdown and protein kinase C activation, potentiated the adipogenic effect of carbaprostacyclin. In addition, carbaprostacyclin enhanced both a limited proliferation and terminal differentiation of adipose precursor cells isolated from rodent and human adipose tissues maintained in primary culture. These results demonstrate the critical role of prostacyclin and prostaglandin F2 alpha on adipose conversion in vitro and suggest a paracrine/autocrine role of both prostanoids in the development of adipose tissue in vivo.
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- Aiken J. W., Shebuski R. J. Comparison in anesthetized dogs of the anti-aggregatory and hemodynamic effects of prostacyclin and a chemically stable prostacyclin analog, 6a-carba-PGI2 (carbacyclin). Prostaglandins. 1980 Apr;19(4):629–643. doi: 10.1016/s0090-6980(80)80011-6. [DOI] [PubMed] [Google Scholar]
- Amri E. Z., Dani C., Doglio A., Etienne J., Grimaldi P., Ailhaud G. Adipose cell differentiation: evidence for a two-step process in the polyamine-dependent Ob1754 clonal line. Biochem J. 1986 Aug 15;238(1):115–122. doi: 10.1042/bj2380115. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Amri E. Z., Dani C., Doglio A., Grimaldi P., Ailhaud G. Coupling of growth arrest and expression of early markers during adipose conversion of preadipocyte cell lines. Biochem Biophys Res Commun. 1986 Jun 13;137(2):903–910. doi: 10.1016/0006-291x(86)91165-4. [DOI] [PubMed] [Google Scholar]
- Axelrod L., Levine L. Prostacyclin production by isolated adipocytes. Diabetes. 1981 Feb;30(2):163–167. doi: 10.2337/diab.30.2.163. [DOI] [PubMed] [Google Scholar]
- Axelrod L., Minnich A. K., Ryan C. A. Stimulation of prostacyclin production in isolated rat adipocytes by angiotensin II, vasopressin, and bradykinin: evidence for two separate mechanisms of prostaglandin synthesis. Endocrinology. 1985 Jun;116(6):2548–2553. doi: 10.1210/endo-116-6-2548. [DOI] [PubMed] [Google Scholar]
- Axelrod L., Ryan C. A., Shaw J. L., Kieffer J. D., Ausiello D. A. Prostacyclin production by isolated rat adipocytes: evidence for cyclic adenosine 3',5'-monophosphate-dependent and independent mechanisms and for a selective effect of insulin. Endocrinology. 1986 Nov;119(5):2233–2239. doi: 10.1210/endo-119-5-2233. [DOI] [PubMed] [Google Scholar]
- Catalioto R. M., Négrel R., Gaillard D., Ailhaud G. Growth-promoting activity in serum-free medium of kallikreinlike arginylesteropeptidases from rat submaxillary gland. J Cell Physiol. 1987 Mar;130(3):352–360. doi: 10.1002/jcp.1041300307. [DOI] [PubMed] [Google Scholar]
- Claesson H. E. Prostaglandin I2 synthesis and elevation of cyclic AMP levels in 3T3 fibroblasts. Biochim Biophys Acta. 1980 Jun 23;618(3):399–406. doi: 10.1016/0005-2760(80)90258-1. [DOI] [PubMed] [Google Scholar]
- Cook J. R., Kozak L. P. Sn-glycerol-3-phosphate dehydrogenase gene expression during mouse adipocyte development in vivo. Dev Biol. 1982 Aug;92(2):440–448. doi: 10.1016/0012-1606(82)90189-0. [DOI] [PubMed] [Google Scholar]
- Deslex S., Negrel R., Ailhaud G. Development of a chemically defined serum-free medium for differentiation of rat adipose precursor cells. Exp Cell Res. 1987 Jan;168(1):15–30. doi: 10.1016/0014-4827(87)90412-5. [DOI] [PubMed] [Google Scholar]
- Djian P., Grimaldi P., Négrel R., Ailhaud G. Adipose conversion of OB17 preadipocytes. Relationships between cell division and fat cell cluster formation. Exp Cell Res. 1982 Dec;142(2):273–281. doi: 10.1016/0014-4827(82)90368-8. [DOI] [PubMed] [Google Scholar]
- Dutta-Roy A. K., Sinha A. K. Purification and properties of prostaglandin E1/prostacyclin receptor of human blood platelets. J Biol Chem. 1987 Sep 15;262(26):12685–12691. [PubMed] [Google Scholar]
- Gaillard D., Ailhaud G., Négrel R. Fetuin modulates growth and differentiation of Ob17 preadipose cells in serum-free hormone-supplemented medium. Biochim Biophys Acta. 1985 Jul 30;846(1):185–191. doi: 10.1016/0167-4889(85)90125-9. [DOI] [PubMed] [Google Scholar]
- Gaillard D., Négrel R., Lagarde M., Ailhaud G. Requirement and role of arachidonic acid in the differentiation of pre-adipose cells. Biochem J. 1989 Jan 15;257(2):389–397. doi: 10.1042/bj2570389. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gaillard D., Négrel R., Serrero-Davé G., Cermolacce C., Ailhaud G. Growth of preadipocyte cell lines and cell strains from rodents in serum-free hormone-supplemented medium. In Vitro. 1984 Feb;20(2):79–88. doi: 10.1007/BF02626647. [DOI] [PubMed] [Google Scholar]
- Gorman R. R., Hamilton R. D., Hopkins N. K. Stimulation of human foreskin fibroblast adenosine 3':5'-cyclic monophosphate levels by prostacyclin (prostaglandin I2). J Biol Chem. 1979 Mar 10;254(5):1671–1676. [PubMed] [Google Scholar]
- Green H., Kehinde O. Spontaneous heritable changes leading to increased adipose conversion in 3T3 cells. Cell. 1976 Jan;7(1):105–113. doi: 10.1016/0092-8674(76)90260-9. [DOI] [PubMed] [Google Scholar]
- Hopkins N. K., Gorman R. R. Regulation of 3T3-L1 fibroblast differentiation by prostacyclin (prostaglandin I2). Biochim Biophys Acta. 1981 Feb 23;663(2):457–466. doi: 10.1016/0005-2760(81)90174-0. [DOI] [PubMed] [Google Scholar]
- Hyman B. T., Stoll L. L., Spector A. A. Prostaglandin production by 3T3-L1 cells in culture. Biochim Biophys Acta. 1982 Nov 12;713(2):375–385. doi: 10.1016/0005-2760(82)90256-9. [DOI] [PubMed] [Google Scholar]
- Marcus A. J., Weksler B. B., Jaffe E. A. Enzymatic conversion of prostaglandin endoperoxide H2 and arachidonic acid to prostacyclin by cultured human endothelial cells. J Biol Chem. 1978 Oct 25;253(20):7138–7141. [PubMed] [Google Scholar]
- Mitchell M. D., Cleland W. H., Smith M. E., Simpson E. R., Mendelson C. R. Inhibition of prostaglandin biosynthesis in human adipose tissue by glucocorticosteroids. J Clin Endocrinol Metab. 1983 Oct;57(4):771–776. doi: 10.1210/jcem-57-4-771. [DOI] [PubMed] [Google Scholar]
- Nishizuka Y. Perspectives on the role of protein kinase C in stimulus-response coupling. J Natl Cancer Inst. 1986 Mar;76(3):363–370. [PubMed] [Google Scholar]
- Négrel R., Ailhaud G. Metabolism of arachidonic acid and prostaglandin synthesis in the preadipocyte clonal line ob17. Biochem Biophys Res Commun. 1981 Feb 12;98(3):768–777. doi: 10.1016/0006-291x(81)91178-5. [DOI] [PubMed] [Google Scholar]
- Négrel R., Grimaldi P., Ailhaud G. Establishment of preadipocyte clonal line from epididymal fat pad of ob/ob mouse that responds to insulin and to lipolytic hormones. Proc Natl Acad Sci U S A. 1978 Dec;75(12):6054–6058. doi: 10.1073/pnas.75.12.6054. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Négrel R., Grimaldi P., Forest C., Ailhaud G. Establishment and characterization of fibroblast-like cell lines derived from adipocytes with the capacity to redifferentiate into adipocyte-like cells. Methods Enzymol. 1985;109:377–385. doi: 10.1016/0076-6879(85)09103-0. [DOI] [PubMed] [Google Scholar]
- Parham E. S., King S. L., Bedell M. L., Martersteck S. Weight control content of women's magazines: bias and accuracy. Int J Obes. 1986;10(1):19–27. [PubMed] [Google Scholar]
- Pilgrim C. DNA synthesis and differentiation in developing white adipose tissue. Dev Biol. 1971 Sep;26(1):69–76. doi: 10.1016/0012-1606(71)90108-4. [DOI] [PubMed] [Google Scholar]
- Richelsen B. Factors regulating the production of prostaglandin E2 and prostacyclin (prostaglandin I2) in rat and human adipocytes. Biochem J. 1987 Oct 15;247(2):389–394. doi: 10.1042/bj2470389. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smith W. L., Lands W. E. Stimulation and blockade of prostaglandin biosynthesis. J Biol Chem. 1971 Nov;246(21):6700–6702. [PubMed] [Google Scholar]
- Tateson J. E., Moncada S., Vane J. R. Effects of prostacyclin (PGX) on cyclic AMP concentrations in human platelets. Prostaglandins. 1977 Mar;13(3):389–397. doi: 10.1016/0090-6980(77)90019-3. [DOI] [PubMed] [Google Scholar]
- Yamashita T., Tsuda T., Hamamori Y., Takai Y. Possible involvement of cyclic AMP and calcium ion in prostaglandin E1-induced elevation of c-myc mRNA levels in Swiss 3T3 fibroblasts. J Biol Chem. 1986 Dec 25;261(36):16878–16882. [PubMed] [Google Scholar]


