Literature DB >> 6375870

A comparison of low and high dose-rate radiation for recipient mice in spleen-colony studies.

B I Lord, J H Hendry, J P Keene, B W Hodgson, C X Xu, M Rezvani, T J Jordan.   

Abstract

Over the last 15 years, endogenous spleen-colony formation in our mice, following lethal irradiation, has increased to an unacceptable level. It has been found necessary, therefore, to introduce a new method of preparing recipient mice for spleen-colony studies. Irradiation with low dose-rate 60Cobalt gamma rays has been compared with high dose-rate linear accelerator electrons, and their effects on endogenous spleen colony formation compared with earlier X and gamma ray dose-response data. It was found that a large dose (13.5 Gy) of gamma rays results in fewer endogenous colonies than 8.5 Gy of electrons, yet because of its low dose rate (14.1 X 10(-3) Gy/min) it has a marked sparing of the intestinal tissue as measured by the intestinal microcolony technique. This in turn permits better survival and, therefore, a 'healthier' animal for spleen-colony work. Exogenous colony formation is also lower in the low dose-rate, gamma-irradiated recipients and this is shown to be due to a reduced spleen-seeding efficiency. It is concluded that very low dose-rate radiation is preferable for haemopoietic ablation, that a mouse colony requires constant monitoring for changes of endogenous spleen-colony formation and that the spleen-seeding efficiency of CFU-s depends on the irradiation technique used--there is no absolute value for a given strain of mouse.

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Year:  1984        PMID: 6375870     DOI: 10.1111/j.1365-2184.1984.tb00592.x

Source DB:  PubMed          Journal:  Cell Tissue Kinet        ISSN: 0008-8730


  2 in total

1.  Parvovirus infection suppresses long-term repopulating hematopoietic stem cells.

Authors:  José C Segovia; Guillermo Guenechea; Jesús M Gallego; José M Almendral; Juan A Bueren
Journal:  J Virol       Date:  2003-08       Impact factor: 5.103

2.  The cellular specificity of haemopoietic stem cell proliferation regulators.

Authors:  C Tejero; N G Testa; B I Lord
Journal:  Br J Cancer       Date:  1984-09       Impact factor: 7.640

  2 in total

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