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Ma Xiangrui; Wang Tao; Wang Hongyun
China Nuclear Information Centre, Beijing, BJ (China)1991
China Nuclear Information Centre, Beijing, BJ (China)1991
AbstractAbstract
[en] Kinetics and radiosensitivity of human lymphocytes were studied by the techniques of monolayer agar culture and liquid culture in vitro. In the experiments of lymphocyte kinetics, PHA was designated as a motogen for T lymphocyte. LPS, MEBC and BSA were chosen as mitogens for B lymphocyte. The data from thses experiments showed that under the alone or combination stimulation of LPS, MRBC and BSA, B lymphocytes developed to form colonies in agar culture (0.3%) with the same manner. The stimulation of LPS to B lymphocytes was most significant. By the day 6 after seeding, the numbers of colonies in agar culture were maximal. Whereas the numbers decreased significantly by the day 8. The number of T lymphocyte colonies increased with culture time within 12 days. The peak of 3H-TdR incorporation into T lymphocytes in liquid culture occured at 5th day after seeding. The data above-mentioned demonstrated that the kinetics of lymphocytes cultured in two kinds of environments were different. The studies of the radiosensitivity of T lymphocytes showed that the decreasing in the number of colonies and rate of 3H-TdR incorporation varied in different dose ranges. In the range of 0∼1.0 Gy, r = -0.96, D0 value was 1.71 Gy for TL-CFC in agar culture, r = -.96, D0 value was 4.34 Gy for the proliferation T lymphocytes in liquid culture. In the range of 1.0∼6.0 Gy, r were -0.99 and -0.98, the D0 were 5.88 and 7.36 Gy respectively. The declining tendency in colonies formed by BL-CFC was the same as that of TL-CFC, r = -0.97, for the range of 0∼1.0 Gy, r = -0.97, for the range of 1.0∼3.0, the D0 values were 1.35 and 4.36 Gy respectively. The results from these experiments shown that the colony technique was a good method for the study in radiosensitivity
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Jul 1991; 9 p; SMC--0065; ISBN 7-5022-0545-4;
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Report
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ANIMAL CELLS, AZINES, BETA DECAY RADIOISOTOPES, BETA-MINUS DECAY RADIOISOTOPES, BIOLOGICAL MATERIALS, BLOOD, BLOOD CELLS, BODY FLUIDS, CONNECTIVE TISSUE CELLS, HETEROCYCLIC COMPOUNDS, HYDROGEN ISOTOPES, ISOTOPES, LEUKOCYTES, LIGHT NUCLEI, MATERIALS, NUCLEI, NUCLEOSIDES, NUCLEOTIDES, ODD-EVEN NUCLEI, ORGANIC COMPOUNDS, ORGANIC NITROGEN COMPOUNDS, PYRIMIDINES, RADIOISOTOPES, RIBOSIDES, SOMATIC CELLS, YEARS LIVING RADIOISOTOPES
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