How do tissues respond to damage at the cellular level? The role of cytokines in irradiated tissues.

The capacity of ionizing radiation to affect tissue function, control tumor growth and elicit pathological sequelae has been attributed in great part to its effects on cellular DNA, which, as the transmitter of genetic information, can both register damage and perpetuate it. Nonetheless, multicellular organisms function as the result of the cooperation of many cell types. What then occurs when individual cells are damaged by ionizing radiation? Is tissue response a sum of cellular effects such as cell death and DNA damage? Or does the tissue respond as a coherent unit to the damage of its parts? In this paper, data in support of the latter model that indicate a role for cytokines, in particular transforming growth factor beta1, as critical components of extracellular signaling pathways that mediate tissue response to radiation will be reviewed. The key to manipulating the consequences of radiation exposure lies in understanding the complex interplay of events initiated at the cellular level, but acting on the tissue.

[1]  R. Miskin,et al.  Plasminogen activator: Induction of synthesis by DNA damage , 1980, Cell.

[2]  C. Nathan,et al.  Production of large amounts of hydrogen peroxide by human tumor cells. , 1991, Cancer research.

[3]  S. Albelda,et al.  Integrins and other cell adhesion molecules , 1990, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[4]  J. Kehrl Transforming growth factor-beta: an important mediator of immunoregulation. , 1991, International journal of cell cloning.

[5]  B. Fanburg,et al.  Enhanced rate of H2O2 release from bovine pulmonary artery endothelial cells induced by TGF-beta 1. , 1993, The American journal of physiology.

[6]  H. Rubin Cancer as a dynamic developmental disorder. , 1985, Cancer research.

[7]  C. Daniel,et al.  Glycosaminoglycans in the basal lamina and extracellular matrix of the developing mouse mammary duct. , 1982, Developmental biology.

[8]  E. Kohn,et al.  Anchorage-independent growth-conferring factor production by rat mammary tumor cells. , 1982, Cancer research.

[9]  M. Bissell,et al.  Wounding and its role in RSV-mediated tumor formation. , 1985, Science.

[10]  L. Liotta,et al.  Differential response to growth factor by rat mammary epithelium plated on different collagen substrata in serum-free medium. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[11]  I. K. Cohen,et al.  Transforming growth factor beta (TGF-β) induces fibrosis in a fetal wound model , 1988 .

[12]  M. Sporn,et al.  Transforming growth factor-,B: possible roles incarcinogenesis* , 1988 .

[13]  B. Lucchesi Free radicals and tissue injury , 1998 .

[14]  M. Stack,et al.  Modulation of murine B16F10 melanoma plasminogen activator production by a synthetic peptide derived from the laminin A chain. , 1993, Cancer research.

[15]  G. Woloschak,et al.  Differential modulation of specific gene expression following high- and low-LET radiations. , 1990, Radiation research.

[16]  S. Kondo Altruistic cell suicide in relation to radiation hormesis. , 1988, International journal of radiation biology and related studies in physics, chemistry, and medicine.

[17]  R. Derynck,et al.  Expression of transforming growth factor alpha (TGF alpha) in differentiated rat mammary tumors: estrogen induction of TGF alpha production. , 1987, Molecular endocrinology.

[18]  E. Kruithof,et al.  Human Co115 colon carcinoma cells potentiate the degradation of laminin mediated by tissue‐type plasminogen activator , 1994, Journal of cellular physiology.

[19]  H. van den Berghe,et al.  Collagen metabolism and basement membrane formation in cultures of mouse mammary epithelial cells. Induction of 'assembly' on fibrillar type I collagen substrata. , 1987, Experimental cell research.

[20]  M. Martin,et al.  Coactivation of AP-1 activity and TGF-β1 gene expression in the stress response of normal skin cells to ionizing radiation , 1997, Oncogene.

[21]  K. Kamiya,et al.  Evidence that carcinogenesis involves an imbalance between epigenetic high-frequency initiation and suppression of promotion. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[22]  G. T. Bowden,et al.  Biological and molecular aspects of radiation carcinogenesis in mouse skin. , 1990, Radiation research.

[23]  L. Liotta,et al.  Effects of inhibition of basement membrane collagen deposition on rat mammary gland development. , 1980, Developmental biology.

[24]  D. Rifkin,et al.  Basic fibroblast growth factor-induced activation of latent transforming growth factor beta in endothelial cells: regulation of plasminogen activator activity , 1992, The Journal of cell biology.

[25]  K. Miyazono,et al.  Role of the latent TGF-beta binding protein in the activation of latent TGF-beta by co-cultures of endothelial and smooth muscle cells , 1993, The Journal of cell biology.

[26]  R. Hynes,et al.  Fibronectins: multifunctional modular glycoproteins , 1982, The Journal of cell biology.

[27]  M. Anscher,et al.  Transforming Growth Factor β as a Predictor of Liver and Lung Fibrosis after Autologous Bone Marrow Transplantation for Advanced Breast Cancer , 1993 .

[28]  Georg Bauer,et al.  Stimulatory role of transforming growth factors in multistage skin carcinogenesis: Possible explanation for the tumor‐inducing effect of wounding in initiated nmri mouse skin , 1989, International journal of cancer.

[29]  M. Sporn,et al.  Expression and secretion of type beta transforming growth factor by activated human macrophages. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[30]  J. Foidart,et al.  Fibroblasts induce the assembly of the macromolecules of the basement membrane. , 1988, The Journal of investigative dermatology.

[31]  H. Withers,et al.  Induction of acute phase gene expression by brain irradiation. , 1995, International journal of radiation oncology, biology, physics.

[32]  M. A. Tanner,et al.  Assessment of radiogenic cancer initiation frequency per clonogenic rat mammary cell in vivo. , 1986, Cancer research.

[33]  M. Meyers,et al.  Enhanced induction of tissue-type plasminogen activator in normal human cells compared to cancer-prone cells following ionizing radiation. , 1992, International journal of radiation oncology, biology, physics.

[34]  R. Chiquet‐Ehrismann,et al.  Tenascin: an extracellular matrix protein involved in tissue interactions during fetal development and oncogenesis , 1986, Cell.

[35]  S. Wahl,et al.  Transforming growth factor beta: the good, the bad, and the ugly , 1994, The Journal of experimental medicine.

[36]  B. Fanburg,et al.  Modulation of transforming growth factor-beta 1 antiproliferative effects on endothelial cells by cysteine, cystine, and N-acetylcysteine. , 1992, The Journal of clinical investigation.

[37]  W. Ward,et al.  Plasminogen activator activity in lung and alveolar macrophages of rats exposed to graded single doses of gamma rays to the right hemithorax. , 1985, Radiation research.

[38]  D. Rifkin,et al.  Characterization of the activation of latent TGF-beta by co-cultures of endothelial cells and pericytes or smooth muscle cells: a self- regulating system , 1990, The Journal of cell biology.

[39]  M. Ferguson Skin wound healing: transforming growth factor beta antagonists decrease scarring and improve quality. , 1994, Journal of interferon research.

[40]  Riley Pa Free Radicals in Biology: Oxidative Stress and the Effects of Ionizing Radiation , 1994 .

[41]  M. Terzaghi-Howe Interactions between cell populations influence expression of the transformed phenotype in irradiated rat tracheal epithelial cells. , 1990, Radiation research.

[42]  D. Penney,et al.  Cell-cell matrix interactions in induced lung injury. I. The effects of X-irradiation on basal laminar proteoglycans. , 1984, Radiation research.

[43]  T. Dix,et al.  Redox-mediated activation of latent transforming growth factor-beta 1. , 1996, Molecular endocrinology.

[44]  B. Fanburg,et al.  Regulation of Cu,Zn‐superoxide dismutase in bovine pulmonary artery endothelial cells , 1992, Journal of cellular physiology.

[45]  L. Liotta,et al.  Induction of tissue‐type plasminogen activator and 72‐kDa type‐IV collagenase by ionizing radiation in rat astrocytes , 1994, International journal of cancer.

[46]  K. Muldrew,et al.  A semiquantitative probe for radiation-induced normal tissue damage at the molecular level. , 1986, Radiation research.

[47]  W. Ward,et al.  Acute radiation effects on the content and release of plasminogen activator activity in cultured aortic endothelial cells. , 1985, Radiation research.

[48]  H. Kleinman,et al.  Laminin, a multidomain protein. The A chain has a unique globular domain and homology with the basement membrane proteoglycan and the laminin B chains. , 1988, The Journal of biological chemistry.

[49]  Z. Werb,et al.  Mammary gland tumor formation in transgenic mice overexpressing stromelysin-1. , 1995, Seminars in cancer biology.

[50]  P. Powers-Risius,et al.  Tumorigenic potential of high-Z, high-LET charged-particle radiations. , 1993, Radiation research.

[51]  B. Fanburg,et al.  TGF-beta 1 produces a "prooxidant" effect on bovine pulmonary artery endothelial cells in culture. , 1991, The American journal of physiology.

[52]  C. Daniel,et al.  Reversible inhibition of mammary gland growth by transforming growth factor-beta. , 1987, Science.

[53]  D. Hallahan,et al.  The role of cytokines in radiation oncology. , 1993, Important advances in oncology.

[54]  R. Ullrich The rate of progression of radiation-transformed mammary epithelial cells is enhanced after low-dose-rate neutron irradiation. , 1986, Radiation research.

[55]  G. Bauer,et al.  Reactive oxygen species act at both TGF-beta-dependent and -independent steps during induction of apoptosis of transformed cells by normal cells. , 1996, Experimental cell research.

[56]  J. Folkman,et al.  Endothelial cell-derived basic fibroblast growth factor: synthesis and deposition into subendothelial extracellular matrix. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[57]  N. Kyprianou,et al.  Expression of transforming growth factor-β in the rat ventral prostate during castration-induced programmed cell death , 1989 .

[58]  M. Martin,et al.  Temporal modulation of TGF-beta 1 and beta-actin gene expression in pig skin and muscular fibrosis after ionizing radiation. , 1993, Radiation research.

[59]  M. Benito,et al.  Apoptosis induced by transforming growth factor-beta in fetal hepatocyte primary cultures: involvement of reactive oxygen intermediates. , 1996, The Journal of biological chemistry.

[60]  R. Tarnuzzer,et al.  Estrogen accelerates cutaneous wound healing associated with an increase in TGF-β1 levels , 1997, Nature Medicine.

[61]  P. Canney,et al.  Transforming growth factor beta: a promotor of late connective tissue injury following radiotherapy? , 1990, The British journal of radiology.

[62]  R. Ullrich,et al.  Influence of gamma irradiation on the development of neoplastic disease in mice. III. Dose-rate effects. , 1979, Radiation research.

[63]  D. Hallahan,et al.  Mechanisms of X-ray-mediated protooncogene c-jun expression in radiation-induced human sarcoma cell lines. , 1991, International journal of radiation oncology, biology, physics.

[64]  K. Ang,et al.  Elevated levels of plasminogen activators in the pathogenesis of delayed radiation damage in rat cervical spinal cord in vivo. , 1994, Radiation research.

[65]  D. Foreman,et al.  Control of scarring in adult wounds by neutralising antibody to transforming growth factor β , 1992, The Lancet.

[66]  Trump Bf,et al.  INFLAMMATION AND OXIDATIVE STRESS IN CARCINOGENESIS , 1993 .

[67]  Sandra R. Smith,et al.  An activated form of transforming growth factor beta is produced by cocultures of endothelial cells and pericytes. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[68]  S. Sheela,et al.  Radiation-induced anchorage-independent growth and collagenase production in diploid human fibroblasts. , 1986, Carcinogenesis.

[69]  P. Herrlich,et al.  Transcriptional and post-transcriptional responses to DNA-damaging agents. , 1994, Current opinion in cell biology.

[70]  H. Moses,et al.  Mechanism of activation of latent recombinant transforming growth factor beta 1 by plasmin , 1990, The Journal of cell biology.

[71]  D. Hallahan,et al.  Increased tumor necrosis factor alpha mRNA after cellular exposure to ionizing radiation. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[72]  M. E. van der Rest,et al.  Collagen family of proteins , 1991, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[73]  M. Hauer-Jensen,et al.  Expression of fibrogenic cytokines in rat small intestine after fractionated irradiation. , 1994, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

[74]  Gary R. Grotendorst,et al.  Production of transforming growth factor beta by human peripheral blood monocytes and neutrophils , 1989, Journal of cellular physiology.

[75]  D. Rifkin,et al.  The extracellular regulation of growth factor action. , 1992, Molecular biology of the cell.

[76]  M. Bissell The differentiated state of normal and malignant cells or how to define a "normal" cell in culture. , 1981, International review of cytology.

[77]  P. Rubin,et al.  Molecular biology mechanisms in the radiation induction of pulmonary injury syndromes: interrelationship between the alveolar macrophage and the septal fibroblast. , 1992, International journal of radiation oncology, biology, physics.

[78]  T. Sakakura,et al.  Tenascin in mammary gland development: from embryogenesis to carcinogenesis. , 1991, Cancer treatment and research.

[79]  N. Kyprianou,et al.  Effect of Transforming Growth Factor-β1 on Proliferation and Death of Rat Prostatic Cells* , 1990 .

[80]  M. Kusakabe,et al.  Epithelial induction of stromal tenascin in the mouse mammary gland: from embryogenesis to carcinogenesis. , 1988, Developmental biology.

[81]  Y. Matsuzawa,et al.  Suppression of antioxidative enzyme expression by transforming growth factor-beta 1 in rat hepatocytes. , 1994, The Journal of biological chemistry.

[82]  G. Bauer,et al.  Direct transforming activity of TGF‐β on rat fibroblasts , 1995 .

[83]  D. Boothman,et al.  Identification and characterization of X-ray-induced proteins in human cells. , 1989, Cancer research.

[84]  G. Bauer Elimination of transformed cells by normal cells: a novel concept for the control of carcinogenesis. , 1996, Histology and histopathology.

[85]  B. Fanburg,et al.  Reduction of glutathione is associated with growth restriction and enlargement of bovine pulmonary artery endothelial cells produced by transforming growth factor-beta 1. , 1992, American journal of respiratory cell and molecular biology.

[86]  P. Rubin,et al.  Early alterations in extracellular matrix and transforming growth factor beta gene expression in mouse lung indicative of late radiation fibrosis. , 1994, International journal of radiation oncology, biology, physics.

[87]  E. Farber,et al.  Pre-cancerous steps in carcinogenesis. Their physiological adaptive nature. , 1984, Biochimica et biophysica acta.

[88]  G. Panayotou,et al.  Tenascin: a modulator of cell growth. , 1992, European journal of biochemistry.

[89]  M. Barcellos-Hoff Radiation-induced transforming growth factor beta and subsequent extracellular matrix reorganization in murine mammary gland. , 1993, Cancer research.

[90]  S. Wahl,et al.  Reversal of acute and chronic synovial inflammation by anti- transforming growth factor beta , 1993, The Journal of experimental medicine.

[91]  M. Ferguson,et al.  Immunohistochemical localization of growth factors in fetal wound healing. , 1991, Developmental biology.

[92]  M. Bissell,et al.  The Influence of Extracellular Matrix on Gene Expression: Is Structure the Message? , 1987, Journal of Cell Science.

[93]  E. Gillette,et al.  Immunohistochemical evidence of rapid extracellular matrix remodeling after iron-particle irradiation of mouse mammary gland. , 1996, Radiation research.

[94]  S. Coleman,et al.  Epithelium-dependent extracellular matrix synthesis in transforming growth factor-beta 1-growth-inhibited mouse mammary gland , 1990, The Journal of cell biology.

[95]  K. Nose,et al.  Production of hydrogen peroxide by transforming growth factor-beta 1 and its involvement in induction of egr-1 in mouse osteoblastic cells , 1994, The Journal of cell biology.

[96]  K. Miyazono,et al.  Latent forms of TGF-beta: molecular structure and mechanisms of activation. , 1991, Ciba Foundation symposium.

[97]  K. Nose,et al.  Release of H2O2 and phosphorylation of 30 kilodalton proteins as early responses of cell cycle-dependent inhibition of DNA synthesis by transforming growth factor beta 1. , 1991, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.

[98]  P. Fox,et al.  Effects of ionizing radiation and beta-adrenergic stimulation on the expression of early response genes in rat parotid glands. , 1992, Radiation research.

[99]  P. Nettesheim,et al.  Dynamics of neoplastic development in carcinogen-exposed tracheal mucosa. , 1979, Cancer research.

[100]  N. Marceau,et al.  TGFβ gene transcription in normal and neoplastic liver growth , 1989 .

[101]  M J Bissell,et al.  Functional differentiation and alveolar morphogenesis of primary mammary cultures on reconstituted basement membrane. , 1989, Development.

[102]  M. Terzaghi-Howe Changes in response to, and production of, transforming growth factor type beta during neoplastic progression in cultured rat tracheal epithelial cells. , 1989, Carcinogenesis.

[103]  J. Massagué,et al.  Transforming growth factor-beta stimulates the expression of fibronectin and collagen and their incorporation into the extracellular matrix. , 1986, The Journal of biological chemistry.

[104]  J. Little,et al.  Relationship between x-ray exposure and malignant transformation in C3H 10T1/2 cells. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[105]  D. Salomon,et al.  Substratum modulation of epidermal growth factor receptor expression by normal mouse mammary cells. , 1988, Journal of dairy science.

[106]  D. Penney,et al.  Cell-cell matrix interactions in induced lung injury. II. X-irradiation mediated changes in specific basal laminar glycosaminoglycans. , 1985, International journal of radiation oncology, biology, physics.

[107]  M. Sporn,et al.  Transforming growth factor type beta: rapid induction of fibrosis and angiogenesis in vivo and stimulation of collagen formation in vitro. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[108]  M. Anscher,et al.  Transforming growth factor-beta 1 expression in irradiated liver. , 1990, Radiation research.

[109]  M. Barcellos-Hoff,et al.  Immunohistochemical Localization of Transforming Growth Factor β and Tumor Necrosis Factor α in the Lungs of Fibrosis-Prone and "Non-Fibrosing" Mice during the Latent Period and Early Phase after Irradiation , 1997 .

[110]  R. Shenkar,et al.  Anti-transforming growth factor-beta monoclonal antibodies prevent lung injury in hemorrhaged mice. , 1994, American journal of respiratory cell and molecular biology.

[111]  M. Bernfield,et al.  Collagen reduces glycosaminoglycan degradation by cultured mammary epithelial cells: possible mechanism for basal lamina formation. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[112]  B. Fanburg,et al.  Activation of an H2O2-generating NADH Oxidase in Human Lung Fibroblasts by Transforming Growth Factor β1 (*) , 1995, The Journal of Biological Chemistry.

[113]  J. Isner,et al.  Expression of transforming growth factor-beta 1 is increased in human vascular restenosis lesions. , 1992, The Journal of clinical investigation.

[114]  M. Bissell,et al.  Interaction of mouse mammary epithelial cells with collagen substrata: regulation of casein gene expression and secretion. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[115]  P. Lambin,et al.  Hypersensitivity to very-low single radiation doses: its relationship to the adaptive response and induced radioresistance. , 1996, Mutation research.