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J E Coggle

Publications and source records attributed to J E Coggle.

At least 37 records · Page 2Linked to original sources

Nonstochastic effects of different energy beta emitters on the mouse skin.

The effect of irradiating varying areas of mouse skin from 860 down to 0.8 mm2 with different energy beta emitters was studied to clarify protection problems of localized doses to the skin. Both 90Sr and 170Tm sources show area effects for dose-response curves. The 90Sr doses that produced moist desquamation in 50% of irradiated fields (MD-50 doses) were 22, 42, 70, and 1000 Gy for 400-, 95-, 20-, and 0.8-mm2 sources. The MD-50 doses for 170Tm were 50, 54, 90, and 170 Gy for 860-, 64-, 20-, and 3.1-mm2 sources. Thus for the larger 170Tm sources there is much less area effect. There was no significant difference in effect between the different energy 90Sr and 170Tm sources for moist desquamation. A simple hypothesis based upon the repopulation of epithelial cells from the edges of the irradiated field and/or from surviving follicle basal cells can explain these area and energy effects in the mouse and in parallel pig skin experiments. The doses needed for 50% of the mice to show ulceration after 64-, 20-, and 3.1-mm2 170Tm sources were 260, 550, and 8300 Gy, respectively, while those for 90-, 20-, and 0.8-mm2 90Sr sources were 150, 210, and 3100 Gy. Thus there is a definite area and energy effect for these sources for this deep dermal damage. The steep rise in dose needed to produce given skin reactions for the smallest area (0.8 mm2) should reassure those faced with assessing the hazard of sub-millimeter-sized particles in/on human skin.

Animals↗

Cell kinetics of pulmonary alveolar macrophages in the mouse.

The study of pulmonary alveolar macrophages (PAMs) involves two techniques, one following the migration of a cohort of labelled PAMs from the lung and the other involves the use of a continuous labelling method with [3H]TdR. In both studies, strikingly similar, probably biphasic curves are obtained that can be interpreted as indicating the existence of two proliferating cell populations with turnover times of approximately 10 days and approximately 35 days. It is suggested that one of these compartments is an intra-alveolar PAM population whilst the other probably represents a precursor population. It is also possible to interpret the data as indicating a single, and probably solely intra-alveolar, PAM population with a very skewed distribution of cell cycle times.

Animals↗

Evidence for the pulmonary origin of alveolar macrophages.

This paper supports the hypothesis that some form of pulmonary alveolar macrophage (PAM) production occurs within the lung in the normal steady state. The study involved monitoring the change in number of labelled PAMs following two modes of irradiation--the first with the thorax being irradiated and the rest of the mouse shielded, the second with the thorax shielded and the body irradiated. Also measurements of monocyte and PAM numbers after a single bone marrow irradiation were carried out. Finally, the labelling indices of monocytes in both control and thorax irradiated mice were measured. Both the number of monocytes and PAMs, along with the labelling indices of monocytes and PAMs after irradiation, indicate the independence of PAMs from a monocyte precursor population, and also provide evidence for a pulmonary origin of PAMs.

Animals↗

The effects of negative pions on spermatogonial survival in the mouse.

A study of the radiation effects of pi-mesons on the testes of the mouse has been carried out using the pion beam at the SRC Rutherford Laboratory. The cell killing effects on type B and intermediate spermatogonia have been assessed and compared with the effects of 20-0 kVp X rays, delivered at the same dose rate. It was found that not only did irradiation of the testes not disturb the kinetics of spermatogenesis, but also the RBE for pions measured in the Bragg peak and on the plateau was not significantly different from unity. The comparison of this result with those of others using other pion beams is discussed.

Animals↗

Some long-term effects of negative pions in mice exposed to partial body irradiation.

The long-term effects of partial body exposure of one-day-old mice given either 60Co gamma rays or negative pions have been studied. Both radiations produced considerable life-shortening; for pions 6.8 +/- 1.5% of life is lost per 100 rad and for gamma rays the value is 5.7 +/- 0.5% per 100 rad. The RBE of pions for ten weeks of life-shortening is about 1.3 compared with 60Co gamma rays, although at lower doses the RBE may be higher reaching about two for six weeks of life shortening. The incidence rate of tumours at any particular age was greater in mice irradiated with pions at the peak and in those given higher doses of gamma rays than in the controls.

Age Factors↗

Some in vivo effects of pi mesons in mice.

The effect of 70 MeV pi mesons was studied to determine the effectivness of such beams aginst normal tissues in vivo. The end points included thymic weight loss, oocyte and bone marrow CFU-S survival and the induction of macroscopid lens opacities. The results indicate that pi mesons are not signifacantly more effective for these end-points than more conventional radiation sources such as 60Co gama rays, 220 kVp X rays, and 14 MeV X rays and electrons. Nor was there any detectable difference in RBE between the peak and plateau regions of the pi meson beam. The significance of these findings is discussed in relation of the the published pi meson RBE values of between 1 therefore 4 and 5 therefore 0.

Animals↗

Anaemia and the induction of myeloid leukaemia in RFM mice.

The results from short term experiments provide little support for the idea that the anaemic stress produced by phlebotomy acts as a trigger for myeloid leukaemia in mice genetically prone to the development of the disease. Longer term investigation has also failed to reveal any difference between bled and control mice and at this time (16 months after bleeding) no animals have died from myeloid leukaemia. These observations are in contrast to the recently reported effect of phlebotomy as a trigger for myeloid leukaemia in unirradiated RFM mice and in irradiated rats. The results given in this paper are discussed in relation to the haemopoietic stem cell compartment in leukaemogenesis and the relationship between these cells and the mature cells in the peripheral blood.

Anemia↗

Age-related changes in the bone marrow and spleen of SAS/4 mice.

The total number of nucleated cells in the bone marrow of SAS/4 mice increase some twofold between 1 and 24 months of age but when related to body weight remains essentially constant over a wide range of ages. The concentration of CFU-S in femoral marrow is also constant with age and since other bones containing marrow appear, at least in young mice, to have the same CFU-S concentration as the femur it is concluded that the CFU-S compartment size of the whole bone marrow is independent of age when expressed on a body weight basis, In contrast, both the absolute number and the concentration of exogenous CFU-S in the spleen decline markedly in old mice. Smilary there is a decline in the number of endogenous colony-forming cells and the spleens of 24-month-old mice seem virtually devoid of such colonies. Not only were older mice less capable of supporting the growth of endogenous colonies, but their spleens also appear to provide a poorer environment for exogenous colony growth when compared with growth in younger recipient spleens.

Aging↗

Quantitative measurements on the haemopoietic systems of three strains of mice.

Quantitative measurements on the haemopoiedic systems of SAS/4, 3H and RFM mice have been used to calculate the distribution and population sizes of haemopoietic cells in the bone marrow, spleen and peripheral blood. Considerable strain differences have been found in the sizes of haemopioetic stem cell populations and in the distribution of these cells within the haemopioetic system, although the incidence of CFU-S was shown to be uniform throughout skeletal sites of haemopioesis. The seeding efficiency of colony forming cells in the spleen, measured by the 'f" factor 24 hours after irradiation and transplantation, also differs between strains and between the bone marrow and spleen of the strains investigated.

Animals↗