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Somatic Mutations Detected by Immunofluorescence and Flow Cytometry

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Biological Dosimetry

Abstract

In order to detect the genotoxic effects of living in today’s complex industrialized society, we must devise sensitive ways to measure early subtle changes in human beings that may lead to more pathological effects in longer periods of time. The detection of mutational changes in somatic cells is a possible way of monitoring for effects that could ultimately lead to carcinogenic or heritable lesions. Depending on the lifespan of the somatic cells analyzed, the frequency of mutated somatic cells in an individual may be a measurement of the effects of recent toxic exposure or an indication of cumulative genetic insult.

Work performed under the auspices of the U.S. Department of Energy by the Lawrence Livermore National Laboratory under contract number W-7405-ENG-48, EPA Grant R808642–01, and USPHS Grant No. ROI CA 31549–01 awarded by the National Cancer Institute, DHHS

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References

  1. Papayannopoulou Th, McGuire TC, Lim G, Garzel E, Nute PE, Stamatoyannopoulos G (1976) Identification of Haemoglobin S in red cells and normoblasts, using fluorescent anti-Hb S antibodies. Brit J Haemat 34:25–31

    Article  PubMed  CAS  Google Scholar 

  2. Papayannopoulou Th, Lim G, Mcguire TC, Ahern V, Nute PE, Stamatoyannopoulos G (1977) Use of specific fluorescent antibodies for the identification of Hemoglobin C in erythrocytes. Amer J Hemat 2:105–115

    Article  CAS  Google Scholar 

  3. Bigbee WL, Branscomb EW, Weintraub HB, Papayannopoulou Th, Stamatoyannopoulos G (1981) Cell sorter immunofluorescence detection of human erythrocytes labeled in suspension with antibodies specific for Hemoglobins S and C. J Immunol Meth 45:117–127

    Article  CAS  Google Scholar 

  4. Stamatoyannopoulos G (1979) Possibilities for demonstration point mutations in somatic cells, as illustrated by studies of mutant hemoglobins. In: Berg K (ed) Genetic Damage in Man Caused by Environmental Agents, Academic Press, New York, p 49–62

    Google Scholar 

  5. Wang K, Richards FM (1975) Reaction of dimethyl-3, 3-dithiobispropionimidate with intact human erythrocytes. J Biol Chem 250:6622–6626

    PubMed  CAS  Google Scholar 

  6. Bigbee WL, Branscomb EW, Jensen RH (1983) Detection of mutated erythrocytes in man. In: Individual Susceptibility to Genotoxic Agents in the Human Population. NIEHS (in Press)

    Google Scholar 

  7. Furthmayr H, Metaxas MN, Metaxas-Bühler M (1981) Mutations within the amino-terminal region of glycophorin A. Proc Natl Acad Sci USA 78:631–635

    Article  PubMed  CAS  Google Scholar 

  8. Dahr W, Kordowicz M, Beyreuther K, Krüger J (1981) The amino-acid sequence of the M(c)-specific major red cell membrane sialoglyprotein- an intermediate of the blood group M- and N-active molecules. Hoppe-Seyler’s Z Physiol Chem 362:363–366

    Article  PubMed  CAS  Google Scholar 

  9. Furthmayer H (1978) Structural comparison of glycophorins and immunochemical analysis of genetic variants. Nature 271:519–524

    Article  Google Scholar 

  10. Pious D, Soderland C (1977) HLA variants of cultured human lymphoid cells: Evidence for mutational origin and estimation of mutation rate. Science 197:769–771

    Article  PubMed  CAS  Google Scholar 

  11. Kvathas P, Bach FH, DeMars R (1980) Gamma ray-induced loss of expression of HLA and glyoxalase I alleles in lymphoblastoid cells. Proc Natl Acad Sci USA 77:4251–4255

    Article  Google Scholar 

  12. Edwards PAW (1980) Monoclonal antibodies that bind to the human erythrocyte-membrane glycoproteins Glycophorin A and Band 3. Biochem Soc Trans 8:334–335

    PubMed  CAS  Google Scholar 

  13. Titus JA, Haugland R, Sharrow SQ, Segal DM (1982) Texas red, a hydrophilic red-emitting fluorophore for use with fluorescein in dual parameter flow microfluorometric and fluorescence microscopic studies. J Immunol Meth 50:193–204

    Article  CAS  Google Scholar 

  14. Dean PN, Pinkel D (1978) High resolution dual laser flow cytometry. J Histochem Cytochem 26:622–627

    Article  PubMed  CAS  Google Scholar 

  15. Tanner MJA, Anstee DJ (1976) The membrane change in En(a-) human erythrocytes. Biochem J 153:217–277

    Google Scholar 

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© 1984 Springer-Verlag Berlin Heidelberg

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Jensen, R.H., Bigbee, W., Branscomb, E.W. (1984). Somatic Mutations Detected by Immunofluorescence and Flow Cytometry. In: Eisert, W.G., Mendelsohn, M.L. (eds) Biological Dosimetry. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-69334-2_15

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  • DOI: https://doi.org/10.1007/978-3-642-69334-2_15

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-12790-1

  • Online ISBN: 978-3-642-69334-2

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