Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1994 May 24;91(11):4897–4901. doi: 10.1073/pnas.91.11.4897

Membrane-derived second messenger regulates x-ray-mediated tumor necrosis factor alpha gene induction.

D E Hallahan 1, S Virudachalam 1, J Kuchibhotla 1, D W Kufe 1, R R Weichselbaum 1
PMCID: PMC43896  PMID: 8197153

Abstract

Cells adapt to adverse environmental conditions through a wide range of responses that are conserved throughout evolution. Physical agents such as ionizing radiation are known to initiate a stress response that is triggered by the recognition of DNA damage. We have identified a signaling pathway involving the activation of phospholipase A2 and protein kinase C in human cells that confers x-ray induction of the tumor necrosis factor alpha gene. Treatment of human cells with ionizing radiation or H2O2 was associated with the production of arachidonic acid. Inhibition of phospholipase A2 abolished radiation-mediated arachidonate production as well as the subsequent activation of protein kinase C and tumor necrosis factor alpha gene expression. These findings demonstrate that ionizing radiation-mediated gene expression in human cells is regulated in part by extranuclear signal transduction. One practical application of phospholipase A2 inhibitors is to ameliorate the adverse effects of radiotherapy associated with tumor necrosis factor alpha production.

Full text

PDF
4899

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Au A. M., Chan P. H., Fishman R. A. Stimulation of phospholipase A2 activity by oxygen-derived free radicals in isolated brain capillaries. J Cell Biochem. 1985;27(4):449–453. doi: 10.1002/jcb.240270413. [DOI] [PubMed] [Google Scholar]
  2. Bell R. M., Hannun Y., Loomis C. Mixed micelle assay of protein kinase C. Methods Enzymol. 1986;124:353–359. doi: 10.1016/0076-6879(86)24027-6. [DOI] [PubMed] [Google Scholar]
  3. Bianco J. A., Appelbaum F. R., Nemunaitis J., Almgren J., Andrews F., Kettner P., Shields A., Singer J. W. Phase I-II trial of pentoxifylline for the prevention of transplant-related toxicities following bone marrow transplantation. Blood. 1991 Sep 1;78(5):1205–1211. [PubMed] [Google Scholar]
  4. Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem. 1987 Apr;162(1):156–159. doi: 10.1006/abio.1987.9999. [DOI] [PubMed] [Google Scholar]
  5. Cole G. M., Schild D., Lovett S. T., Mortimer R. K. Regulation of RAD54- and RAD52-lacZ gene fusions in Saccharomyces cerevisiae in response to DNA damage. Mol Cell Biol. 1987 Mar;7(3):1078–1084. doi: 10.1128/mcb.7.3.1078. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Datta R., Hallahan D. E., Kharbanda S. M., Rubin E., Sherman M. L., Huberman E., Weichselbaum R. R., Kufe D. W. Involvement of reactive oxygen intermediates in the induction of c-jun gene transcription by ionizing radiation. Biochemistry. 1992 Sep 8;31(35):8300–8306. doi: 10.1021/bi00150a025. [DOI] [PubMed] [Google Scholar]
  7. Eldor A., Vlodavsky I., Fuks Z., Matzner Y., Rubin D. B. Arachidonic metabolism and radiation toxicity in cultures of vascular endothelial cells. Prostaglandins Leukot Essent Fatty Acids. 1989 Jun;36(4):251–258. doi: 10.1016/0952-3278(89)90137-3. [DOI] [PubMed] [Google Scholar]
  8. Enoch T., Carr A. M., Nurse P. Fission yeast genes involved in coupling mitosis to completion of DNA replication. Genes Dev. 1992 Nov;6(11):2035–2046. doi: 10.1101/gad.6.11.2035. [DOI] [PubMed] [Google Scholar]
  9. Fan X. T., Huang X. P., Da Silva C., Castagna M. Arachidonic acid and related methyl ester mediate protein kinase C activation in intact platelets through the arachidonate metabolism pathways. Biochem Biophys Res Commun. 1990 Jun 29;169(3):933–940. doi: 10.1016/0006-291x(90)91983-y. [DOI] [PubMed] [Google Scholar]
  10. Godfrey R. W., Johnson W. J., Hoffstein S. T. Recombinant tumor necrosis factor and interleukin-1 both stimulate human synovial cell arachidonic acid release and phospholipid metabolism. Biochem Biophys Res Commun. 1987 Jan 15;142(1):235–241. doi: 10.1016/0006-291x(87)90476-1. [DOI] [PubMed] [Google Scholar]
  11. Godson C., Weiss B. A., Insel P. A. Differential activation of protein kinase C alpha is associated with arachidonate release in Madin-Darby canine kidney cells. J Biol Chem. 1990 May 25;265(15):8369–8372. [PubMed] [Google Scholar]
  12. Gross N. J. Radiation pneumonitis in mice. Some effects of corticosteroids on mortality and pulmonary physiology. J Clin Invest. 1980 Sep;66(3):504–510. doi: 10.1172/JCI109881. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Gustafson C., Lindahl M., Tagesson C. Hydrogen peroxide stimulates phospholipase A2-mediated arachidonic acid release in cultured intestinal epithelial cells (INT 407). Scand J Gastroenterol. 1991 Mar;26(3):237–247. doi: 10.3109/00365529109025037. [DOI] [PubMed] [Google Scholar]
  14. Hahn G. L., Menconi M. J., Cahill M., Polgar P. The influence of gamma radiation on arachidonic acid release and prostacyclin synthesis. Prostaglandins. 1983 Jun;25(6):783–791. doi: 10.1016/0090-6980(83)90003-5. [DOI] [PubMed] [Google Scholar]
  15. Hallahan D. E., Spriggs D. R., Beckett M. A., Kufe D. W., Weichselbaum R. R. Increased tumor necrosis factor alpha mRNA after cellular exposure to ionizing radiation. Proc Natl Acad Sci U S A. 1989 Dec;86(24):10104–10107. doi: 10.1073/pnas.86.24.10104. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Hallahan D. E., Sukhatme V. P., Sherman M. L., Virudachalam S., Kufe D., Weichselbaum R. R. Protein kinase C mediates x-ray inducibility of nuclear signal transducers EGR1 and JUN. Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2156–2160. doi: 10.1073/pnas.88.6.2156. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Hallahan D. E., Virudachalam S., Schwartz J. L., Panje N., Mustafi R., Weichselbaum R. R. Inhibition of protein kinases sensitizes human tumor cells to ionizing radiation. Radiat Res. 1992 Mar;129(3):345–350. [PubMed] [Google Scholar]
  18. Hallahan D. E., Virudachalam S., Sherman M. L., Huberman E., Kufe D. W., Weichselbaum R. R. Tumor necrosis factor gene expression is mediated by protein kinase C following activation by ionizing radiation. Cancer Res. 1991 Sep 1;51(17):4565–4569. [PubMed] [Google Scholar]
  19. Han J., Thompson P., Beutler B. Dexamethasone and pentoxifylline inhibit endotoxin-induced cachectin/tumor necrosis factor synthesis at separate points in the signaling pathway. J Exp Med. 1990 Jul 1;172(1):391–394. doi: 10.1084/jem.172.1.391. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Herrlich P., Ponta H., Rahmsdorf H. J. DNA damage-induced gene expression: signal transduction and relation to growth factor signaling. Rev Physiol Biochem Pharmacol. 1992;119:187–223. doi: 10.1007/3540551921_7. [DOI] [PubMed] [Google Scholar]
  21. Holler E., Kolb H. J., Möller A., Kempeni J., Liesenfeld S., Pechumer H., Lehmacher W., Ruckdeschel G., Gleixner B., Riedner C. Increased serum levels of tumor necrosis factor alpha precede major complications of bone marrow transplantation. Blood. 1990 Feb 15;75(4):1011–1016. [PubMed] [Google Scholar]
  22. House C., Kemp B. E. Protein kinase C contains a pseudosubstrate prototope in its regulatory domain. Science. 1987 Dec 18;238(4834):1726–1728. doi: 10.1126/science.3686012. [DOI] [PubMed] [Google Scholar]
  23. Jones J. S., Prakash L. Transcript levels of the Saccharomyces cerevisiae DNA repair gene RAD18 increase in UV irradiated cells and during meiosis but not during the mitotic cell cycle. Nucleic Acids Res. 1991 Feb 25;19(4):893–898. doi: 10.1093/nar/19.4.893. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Kastan M. B., Zhan Q., el-Deiry W. S., Carrier F., Jacks T., Walsh W. V., Plunkett B. S., Vogelstein B., Fornace A. J., Jr A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia-telangiectasia. Cell. 1992 Nov 13;71(4):587–597. doi: 10.1016/0092-8674(92)90593-2. [DOI] [PubMed] [Google Scholar]
  25. Khan W., el Touny S., Hannun Y. A. Arachidonic and cis-unsaturated fatty acids induce selective platelet substrate phosphorylation through activation of cytosolic protein kinase C. FEBS Lett. 1991 Nov 4;292(1-2):98–102. doi: 10.1016/0014-5793(91)80843-r. [DOI] [PubMed] [Google Scholar]
  26. Lester D. S., Collin C., Etcheberrigaray R., Alkon D. L. Arachidonic acid and diacylglycerol act synergistically to activate protein kinase C in vitro and in vivo. Biochem Biophys Res Commun. 1991 Sep 30;179(3):1522–1528. doi: 10.1016/0006-291x(91)91745-x. [DOI] [PubMed] [Google Scholar]
  27. Lognonne J. L., Ducousso R., Rocquet G., Kergonou J. F. Influence of whole-body gamma irradiation upon arachidonic acid metabolism in rat platelets. Biochimie. 1985 Sep;67(9):1015–1021. doi: 10.1016/s0300-9084(85)80296-0. [DOI] [PubMed] [Google Scholar]
  28. McPhail L. C., Clayton C. C., Snyderman R. A potential second messenger role for unsaturated fatty acids: activation of Ca2+-dependent protein kinase. Science. 1984 May 11;224(4649):622–625. doi: 10.1126/science.6231726. [DOI] [PubMed] [Google Scholar]
  29. Murakami K., Chan S. Y., Routtenberg A. Protein kinase C activation by cis-fatty acid in the absence of Ca2+ and phospholipids. J Biol Chem. 1986 Nov 25;261(33):15424–15429. [PubMed] [Google Scholar]
  30. Neta R., Oppenheim J. J., Schreiber R. D., Chizzonite R., Ledney G. D., MacVittie T. J. Role of cytokines (interleukin 1, tumor necrosis factor, and transforming growth factor beta) in natural and lipopolysaccharide-enhanced radioresistance. J Exp Med. 1991 May 1;173(5):1177–1182. doi: 10.1084/jem.173.5.1177. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Nishizuka Y. Intracellular signaling by hydrolysis of phospholipids and activation of protein kinase C. Science. 1992 Oct 23;258(5082):607–614. doi: 10.1126/science.1411571. [DOI] [PubMed] [Google Scholar]
  32. Peppelenbosch M. P., Tertoolen L. G., Hage W. J., de Laat S. W. Epidermal growth factor-induced actin remodeling is regulated by 5-lipoxygenase and cyclooxygenase products. Cell. 1993 Aug 13;74(3):565–575. doi: 10.1016/0092-8674(93)80057-l. [DOI] [PubMed] [Google Scholar]
  33. Peters-Golden M., McNish R. W., Sporn P. H., Balazovich K. Basal activation of protein kinase C in rat alveolar macrophages: implications for arachidonate metabolism. Am J Physiol. 1991 Dec;261(6 Pt 1):L462–L471. doi: 10.1152/ajplung.1991.261.6.L462. [DOI] [PubMed] [Google Scholar]
  34. Phillips T. L., Wharam M. D., Margolis L. W. Modification of radiation injury to normal tissues by chemotherapeutic agents. Cancer. 1975 Jun;35(6):1678–1684. doi: 10.1002/1097-0142(197506)35:6<1678::aid-cncr2820350629>3.0.co;2-k. [DOI] [PubMed] [Google Scholar]
  35. Rao G. N., Lasségue B., Griendling K. K., Alexander R. W., Berk B. C. Hydrogen peroxide-induced c-fos expression is mediated by arachidonic acid release: role of protein kinase C. Nucleic Acids Res. 1993 Mar 11;21(5):1259–1263. doi: 10.1093/nar/21.5.1259. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Rossignol L., Plantavid M., Chap H., Douste-Blazy L. Effects of two methylxanthines, pentoxifylline and propentofylline, on arachidonic acid metabolism in platelets stimulated by thrombin. Biochem Pharmacol. 1988 Sep 1;37(17):3229–3236. doi: 10.1016/0006-2952(88)90632-6. [DOI] [PubMed] [Google Scholar]
  37. Sevanian A., Muakkassah-Kelly S. F., Montestruque S. The influence of phospholipase A2 and glutathione peroxidase on the elimination of membrane lipid peroxides. Arch Biochem Biophys. 1983 Jun;223(2):441–452. doi: 10.1016/0003-9861(83)90608-2. [DOI] [PubMed] [Google Scholar]
  38. Shasby D. M., Winter M., Shasby S. S. Oxidants and conductance of cultured epithelial cell monolayers: inositol phospholipid hydrolysis. Am J Physiol. 1988 Dec;255(6 Pt 1):C781–C788. doi: 10.1152/ajpcell.1988.255.6.C781. [DOI] [PubMed] [Google Scholar]
  39. Sherman M. L., Datta R., Hallahan D. E., Weichselbaum R. R., Kufe D. W. Regulation of tumor necrosis factor gene expression by ionizing radiation in human myeloid leukemia cells and peripheral blood monocytes. J Clin Invest. 1991 May;87(5):1794–1797. doi: 10.1172/JCI115199. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Sporn P. H., Marshall T. M., Peters-Golden M. Differential dependence on protein kinase C of arachidonic acid metabolism stimulated by hydrogen peroxide and by zymosan in the alveolar macrophage. Biochim Biophys Acta. 1990 Nov 12;1047(2):187–191. doi: 10.1016/0005-2760(90)90046-z. [DOI] [PubMed] [Google Scholar]
  41. Spriggs D. R., Sherman M. L., Imamura K., Mohri M., Rodriguez C., Robbins G., Kufe D. W. Phospholipase A2 activation and autoinduction of tumor necrosis factor gene expression by tumor necrosis factor. Cancer Res. 1990 Nov 15;50(22):7101–7107. [PubMed] [Google Scholar]
  42. Strieter R. M., Remick D. G., Ward P. A., Spengler R. N., Lynch J. P., 3rd, Larrick J., Kunkel S. L. Cellular and molecular regulation of tumor necrosis factor-alpha production by pentoxifylline. Biochem Biophys Res Commun. 1988 Sep 30;155(3):1230–1236. doi: 10.1016/s0006-291x(88)81271-3. [DOI] [PubMed] [Google Scholar]
  43. Uckun F. M., Tuel-Ahlgren L., Song C. W., Waddick K., Myers D. E., Kirihara J., Ledbetter J. A., Schieven G. L. Ionizing radiation stimulates unidentified tyrosine-specific protein kinases in human B-lymphocyte precursors, triggering apoptosis and clonogenic cell death. Proc Natl Acad Sci U S A. 1992 Oct 1;89(19):9005–9009. doi: 10.1073/pnas.89.19.9005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Walker G. C. Inducible DNA repair systems. Annu Rev Biochem. 1985;54:425–457. doi: 10.1146/annurev.bi.54.070185.002233. [DOI] [PubMed] [Google Scholar]
  45. Ward H. E., Kemsley L., Davies L., Holecek M., Berend N. The effect of steroids on radiation-induced lung disease in the rat. Radiat Res. 1993 Oct;136(1):22–28. [PubMed] [Google Scholar]
  46. Ward H. E., Kemsley L., Davies L., Holecek M., Berend N. The pulmonary response to sublethal thoracic irradiation in the rat. Radiat Res. 1993 Oct;136(1):15–21. [PubMed] [Google Scholar]
  47. Wright T. M., Rangan L. A., Shin H. S., Raben D. M. Kinetic analysis of 1,2-diacylglycerol mass levels in cultured fibroblasts. Comparison of stimulation by alpha-thrombin and epidermal growth factor. J Biol Chem. 1988 Jul 5;263(19):9374–9380. [PubMed] [Google Scholar]
  48. Yasuda I., Kishimoto A., Tanaka S., Tominaga M., Sakurai A., Nishizuka Y. A synthetic peptide substrate for selective assay of protein kinase C. Biochem Biophys Res Commun. 1990 Feb 14;166(3):1220–1227. doi: 10.1016/0006-291x(90)90996-z. [DOI] [PubMed] [Google Scholar]
  49. Yatvin M. B., Gipp J. J., Dennis W. H. Influence of unsaturated fatty acids, membrane fluidity and oxygenation on the survival of an E. coli fatty acid auxotroph following gamma-irradiation. Int J Radiat Biol Relat Stud Phys Chem Med. 1979 Jun;35(6):539–548. doi: 10.1080/09553007914550651. [DOI] [PubMed] [Google Scholar]
  50. Zhou Z., Elledge S. J. Isolation of crt mutants constitutive for transcription of the DNA damage inducible gene RNR3 in Saccharomyces cerevisiae. Genetics. 1992 Aug;131(4):851–866. doi: 10.1093/genetics/131.4.851. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES