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. 1985 Nov 15;232(1):43–47. doi: 10.1042/bj2320043

The effects of phorbol ester, diacylglycerol, phospholipase C and Ca2+ ionophore on protein phosphorylation in human and sheep erythrocytes.

P J Raval, D Allan
PMCID: PMC1152836  PMID: 4084238

Abstract

Treatment of human or sheep erythrocytes with PMA (phorbol myristate acetate) enhanced [32P]phosphate labelling of membrane polypeptides of approx. 100, 80 and 46 kDa. The 80 kDa and 46 kDa polypeptides coincided with bands 4.1 and 4.9 respectively on Coomassie-Blue-stained gels. Similar but smaller effects were obtained by treating human cells with 1-oleoyl-2-acetyl-rac-glycerol (OAG), exogenous bacterial phospholipase C or ionophore A23187 + Ca2+, each of which treatments would be expected to raise the concentration of membrane diacylglycerol. In contrast, sheep cells, which do not increase their content of diacylglycerol when treated with phospholipase C or A23187 + Ca2+, only showed enhanced phosphorylation with OAG. Neither human nor sheep cells showed any enhanced [32P]phosphate labelling of phosphoproteins when treated with 1-mono-oleoyl-rac-glycerol. It is concluded that diacylglycerol from a variety of sources can activate erythrocyte protein kinase C, but that the most effective diacylglycerol is that derived from endogenous polyphosphoinositides. In contrast with bacterial phospholipase C and A23187, which stimulate synthesis of phosphatidate by increasing the cell-membrane content of diacylglycerol in human erythrocytes, PMA, OAG or 1-mono-oleoyl-rac-glycerol caused no change in phospholipid metabolism.

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Selected References

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  1. Allan D., Low M. G., Finean J. B., Michell R. H. Changes in lipid metabolism and cell morphology following attack by phospholipase C (Clostridium perfringens) on red cells or lymphocytes. Biochim Biophys Acta. 1975 Dec 1;413(2):309–316. doi: 10.1016/0005-2736(75)90116-9. [DOI] [PubMed] [Google Scholar]
  2. Allan D., Michell R. H. A calcium-activated polyphosphoinositide phosphodiesterase in the plasma membrane of human and rabbit erythrocytes. Biochim Biophys Acta. 1978 Apr 4;508(2):277–286. doi: 10.1016/0005-2736(78)90330-9. [DOI] [PubMed] [Google Scholar]
  3. Allan D., Michell R. H. Calcium ion-dependent diacylglycerol accumulation in erythrocytes is associated with microvesiculation but not with efflux of potassium ions. Biochem J. 1977 Sep 15;166(3):495–499. doi: 10.1042/bj1660495. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Allan D., Thomas P. Ca2+-induced biochemical changes in human erythrocytes and their relation to microvesiculation. Biochem J. 1981 Sep 15;198(3):433–440. doi: 10.1042/bj1980433. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Allan D., Thomas P., Limbrick A. R. The isolation and characterization of 60 nm vesicles ('nanovesicles') produced during ionophore A23187-induced budding of human erythrocytes. Biochem J. 1980 Jun 15;188(3):881–887. doi: 10.1042/bj1880881. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Allan D., Watts R., Michell R. H. Production of 1,2-diacylglycerol and phosphatidate in human erythrocytes treated with calcium ions and ionophore A23187. Biochem J. 1976 May 15;156(2):225–232. doi: 10.1042/bj1560225. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Anderson F. S., Murphy R. C. Isocratic separation of some purine nucleotide, nucleoside, and base metabolites from biological extracts by high-performance liquid chromatography. J Chromatogr. 1976 Jun 23;121(2):251–262. doi: 10.1016/s0021-9673(00)85021-9. [DOI] [PubMed] [Google Scholar]
  8. Berridge M. J. Inositol trisphosphate and diacylglycerol as second messengers. Biochem J. 1984 Jun 1;220(2):345–360. doi: 10.1042/bj2200345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Cockcroft S., Barrowman M. M., Gomperts B. D. Breakdown and synthesis of polyphosphoinositides in fMetLeuPhe-stimulated neutrophils. FEBS Lett. 1985 Feb 25;181(2):259–263. doi: 10.1016/0014-5793(85)80271-4. [DOI] [PubMed] [Google Scholar]
  10. Ganong B. R., Bell R. M. Transmembrane movement of phosphatidylglycerol and diacylglycerol sulfhydryl analogues. Biochemistry. 1984 Oct 9;23(21):4977–4983. doi: 10.1021/bi00316a023. [DOI] [PubMed] [Google Scholar]
  11. Gilman A. G. G proteins and dual control of adenylate cyclase. Cell. 1984 Mar;36(3):577–579. doi: 10.1016/0092-8674(84)90336-2. [DOI] [PubMed] [Google Scholar]
  12. Goodman S. R., Shiffer K. The spectrin membrane skeleton of normal and abnormal human erythrocytes: a review. Am J Physiol. 1983 Mar;244(3):C121–C141. doi: 10.1152/ajpcell.1983.244.3.C121. [DOI] [PubMed] [Google Scholar]
  13. Kaibuchi K., Takai Y., Sawamura M., Hoshijima M., Fujikura T., Nishizuka Y. Synergistic functions of protein phosphorylation and calcium mobilization in platelet activation. J Biol Chem. 1983 Jun 10;258(11):6701–6704. [PubMed] [Google Scholar]
  14. Kikkawa U., Takai Y., Minakuchi R., Inohara S., Nishizuka Y. Calcium-activated, phospholipid-dependent protein kinase from rat brain. Subcellular distribution, purification, and properties. J Biol Chem. 1982 Nov 25;257(22):13341–13348. [PubMed] [Google Scholar]
  15. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  16. Ling E., Sapirstein V. Phorbol ester stimulates the phosphorylation of rabbit erythrocyte band 4.1. Biochem Biophys Res Commun. 1984 Apr 16;120(1):291–298. doi: 10.1016/0006-291x(84)91447-5. [DOI] [PubMed] [Google Scholar]
  17. Nishizuka Y. The role of protein kinase C in cell surface signal transduction and tumour promotion. Nature. 1984 Apr 19;308(5961):693–698. doi: 10.1038/308693a0. [DOI] [PubMed] [Google Scholar]
  18. Steck T. L. The organization of proteins in the human red blood cell membrane. A review. J Cell Biol. 1974 Jul;62(1):1–19. doi: 10.1083/jcb.62.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Taylor M. V., Metcalfe J. C., Hesketh T. R., Smith G. A., Moore J. P. Mitogens increase phosphorylation of phosphoinositides in thymocytes. 1984 Nov 29-Dec 5Nature. 312(5993):462–465. doi: 10.1038/312462a0. [DOI] [PubMed] [Google Scholar]
  20. Thomas P., Limbrick A. R., Allan D. Limited breakdown of cytoskeletal proteins by an endogenous protease controls Ca2+-induced membrane fusion events in chicken erythrocytes. Biochim Biophys Acta. 1983 May 5;730(2):351–358. doi: 10.1016/0005-2736(83)90352-8. [DOI] [PubMed] [Google Scholar]
  21. de Chaffoy de Courcelles D., Roevens P., Van Belle H. 1-Oleoyl-2-acetyl-glycerol (OAG) stimulates the formation of phosphatidylinositol 4-phosphate in intact human platelets. Biochem Biophys Res Commun. 1984 Sep 17;123(2):589–595. doi: 10.1016/0006-291x(84)90270-5. [DOI] [PubMed] [Google Scholar]
  22. de Chaffoy de Courcelles D., Roevens P., van Belle H. 12-O-Tetradecanoylphorbol 13-acetate stimulates inositol lipid phosphorylation in intact human platelets. FEBS Lett. 1984 Aug 6;173(2):389–393. doi: 10.1016/0014-5793(84)80811-x. [DOI] [PubMed] [Google Scholar]

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