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AbstractAbstract
[en] Objective: To investigate the inhibitive effect of Interferon-γ (γ-IFN) of Chinese genotype on proliferation of human lung fibroblast (HLF) induced by radiation, and examine its possible mechanism and role in prevention and treatment of radiation pulmonary fibrosis. Methods: The proliferation of HLF was determined by MTT assay, the expression of γ-smooth muscle actin (αa-SMA) and the synthesis of collagen type IV by immunocytochemistry assays. Results: Chinese α-IFN was observed to inhibit, proportionally to irradiation dose, the proliferation of HLF induced by 60Co γ-irradiation. The expression of γ-SMA was remarkable in cytoplasmic matrix after the irradiation, suggesting that irradiation could induce the transformation from fibroblast (FB) to myofibroblast (MFB). The expression of collagen IV was increased with irradiation. Compared with the irradiated group, the expression of collagen IV was lower when γ-IFN was administered before being irradiated. Conclusion: 60Co γ irradiation can induce pulmonary fibrosis by promoting the proliferation of HLF, inducing the transformation from FB to MFB, and increasing the excreting of collagen type IV. γ-IFN can prevent pulmonary fibrosis by effectively inhibiting the abnormal proliferation of HLF and the excessive synthesis of collagen IV after irradiation. (authors)
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Source
4 figs., 10 refs.
Record Type
Journal Article
Journal
Chinese Journal of Radiological Medicine and Protection; ISSN 0254-5098;
; v. 26(2); p. 144-147

Country of publication
ANIMAL CELLS, ASIA, BETA DECAY RADIOISOTOPES, BETA-MINUS DECAY RADIOISOTOPES, BIOASSAY, BIOCHEMISTRY, BODY, CHEMISTRY, COBALT ISOTOPES, CONNECTIVE TISSUE CELLS, ELECTROMAGNETIC RADIATION, GROWTH FACTORS, INTERMEDIATE MASS NUCLEI, INTERNAL CONVERSION RADIOISOTOPES, IONIZING RADIATIONS, ISOMERIC TRANSITION ISOTOPES, ISOTOPES, LYMPHOKINES, MEDICINE, MINUTES LIVING RADIOISOTOPES, MITOGENS, NUCLEI, ODD-ODD NUCLEI, ORGANIC COMPOUNDS, ORGANS, PATHOLOGICAL CHANGES, PROTEINS, RADIATIONS, RADIOISOTOPES, RESPIRATORY SYSTEM, SCLEROPROTEINS, SOMATIC CELLS, YEARS LIVING RADIOISOTOPES
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