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Biomedical subjects

E F Potworowski

Publications and source records attributed to E F Potworowski.

At least 73 records · Page 4Linked to original sources

Induction by thymic fractions of T cell subsets capable of modulating GVHR intensity.

Two thymic stromal fractions previously shown to have specific enhancing effects on anatomically distinct T cell populations were tested for their capacity to induce functionally distinct T cell subsets. Parental mice were injected with either soluble thymic fraction (STF) or insoluble thymic fraction (ITF), and their lymphoid cells were harvested 11 days later. It was shown that ITF elicited a splenic corticosensitive T cell subset endowed with enhanced graft-versus-host reaction (GVHR)-inducing capacity. On the other hand, STF increased, mainly in lymph nodes, the number of corticoresistant T cells significantly less active in GVHR. Furthermore, lymphocytes from ITF-treated parental donors could become corticoresistant with reduced GVHR activity after a 1-hr in vitro incubation with STF. We have thus shown that two different elements of the thymic microenvironment could modulate the intensity of the GVHR by modifying the equilibrium between two T cell subsets. These are believed to represent two consecutive differentiation stages.

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Effect of different components of the thymic stroma on the onset of AKR leukaemia.

Spontaneous leukaemia in AKR mice is characterized by an accumulation of thymocyte precursors prior to the onset of the disease. An insoluble thymic fraction (ITF), previously shown to provoke such an accumulation when injected to normal mice, caused a significant acceleration of death by leukaemia when given to pre-leukaemic AKR mice. Conversely, the injection of a soluble thymic factor (STF), believed to further differentiate thymocyte precursors, was shown to markedly delay the onset of leukaemia. These results are interpreted as reflecting the specific immune functions of T cells at different stages of maturation.

AKR murine leukemia virus↗

Thymic microenvironment: selective activities of soluble and insoluble components.

Two components of the thymic microenvironment have been separated, and their biological properties have been studied. The first component, soluble thymic factor (STF), after injection into syngeneic recipients, provoked a temporary decrease in thymic weight on day 7, concomitant with an increase in the level of T cells in lymph nodes (but not in the spleen), followed by a general hypertrophy of lymph nodes peaking on day 21. In contrast, after the injection of the second component, insoluble thymic fraction (ITF), there was an increase in the number of prothymocytes in the thymic subcapsulary cortex, followed by general thymic hypertrophy on days 14 and 21. STF is believed to trigger a selective migration of lymph-node-seeking T cells from the thymus, whereas ITF seems to play a role in the differentiation step preceding that imparted by STF.

Animals↗

[Role of an insoluble thymus fraction in the differentiation of T lymphocytes].

An insoluble thymic fraction, free of both thymocytes and thymic hormone, was injected intraperitoneally to C57B1/6 mice. Following this injection, marked changes were noted in thymocyte populations: these consisted mainly in a significant increase of subcapsular prothymocytes, peaking at day 7. These observations were made by histological examination and confirmed by a study of physical characteristics of thymocyte populations. The possibility that this insoluble thymic fraction might have a biologically active component responsible for prothymocytes recruitment is examined.

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The thymic microenvironment: localization of a biologically active insoluble fraction.

An insoluble component of the thymus, previously shown to be capable of enhancing stem cell immigration into that organ, has been localized by immunofluorescence in perivascular basement membranes of the thymic medulla. It was found to be antigenically distinct from soluble thymic factor and from thymocyte membranes, and is thought to be responsible, in T-cell maturation, for the differentiation step preceding that imparted by thymic hormone.

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Shared antigenicity between chicken brain and bursa of fabricius.

Antisera to chicken brain, thymus and bursa of Fabricius were prepared in rabbits and rendered organ-specific by appropriate absorptions. Brain was shown by immunofluorescence and immune adherence to have common antigenicity with the bursa of Fabricius but not with the thymus.

Absorption↗

Inhibition of T-cell differentiation by an antibody to a soluble thymic factor.

An antiserum to chicken soluble thymic factor (STF) was prepared in rabbits and absorbed with chicken thymocytes until it reacted only with thymic reticuloepithelial cells. When injected into 6-day-old embryonated eggs, this antiserum caused a severe depletion of small lymphocytes in the cortical region of the thymus which was filled with large undifferentiated cells. In addition, reticuloepithelial cells displayed a marked disruption of cytoplasmic elements. The percentage of thymic lymphocytes bearing the T antigen was greatly reduced. It is believed that a factor responsible for differentiation of stem cells into T cells has been inhibited.

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Induction of T-cell differentiation in the Bursa of Fabricius by a soluble thymus factor.

Bursal lymphocytes from White Leghorn chickens of different ages were incubated with a soluble thymus factor (STF), and tested for t-cell characteristics. Immunofluorescence staining with anti-T-cell serum showed a marked increase inthe percentage of bursal T lymphocytes in cell preparations from young chickensincubated with STF. In older chickens (17 weeks) no such effect was observed. Bursal cells treated with STF were also able to elicit splenomegaly showing thatnot only antigenic but also functional T-cell characteristics had been induced in apopulation of bursal cells. The fate of these bursal T-cell precursors is discussed in the context of known migratory patterns.

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