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Biomedical subjects

B Glick

Publications and source records attributed to B Glick.

At least 145 records · Page 8Linked to original sources
PubMed1978

Nylon wool column separation of chicken thymic-derived (T) and bursal-derived (B) lymphocytes.

Since the original work of Julius et al. (1973), the nylon wool technique has become a standard laboratory procedure for separating cell populations and obtaining relatively pure populations of T and B cells. While this technique has been applied to a number of different animal systems, it had, to our knowledge, neither been qualitated nor quantitated in the chicken. One passage of chicken splenic lymphocytes through a nylon wool column yields an enriched T cell population in the effluent fraction and an enriched B cell population in the column fraction. As in the murine system, we found fractionation of chicken splenic cells by nylon wool to be a rapid method for enrichment of both T and B cell populations. It is emphasized, however, that each passage should be monitored to check the relative purity of the two cell populations.

Animals↗
PubMed1978

A scanning electron microscope study of the caecal tonsil: the identification of a bacterial attachment to the villi of the caecal tonsil and the possible presence of lymphatics in the caecal tonsil.

A scanning electron microscope (SEM) was used to compare the proximal region (PR) and distal region (DR) of the caecum. The caecal tonsil (CT) occupied the initial 4-10 mm of the PR. Villi were present in the PR and absent from the DR. Segmented structures were attached to the surface of PR. Transmission electron microscopy (TEM) revealed these structures to be bacteria. No difference in surface morphology could be discerned between the CT and the remainder of the PR. Lymphatic vessels were observed in the CT by employing TEM.

Animals↗
PubMed1978

The number and size of the follicular epithelium (FE) and follicles in the bursa of Fabricius.

In a four-week-old chicken .1 ml carbon solution was deposited on the vent. The carbon was sucked into the lumen of the bursa and absorbed by the follicular epithelium which appeared as black dots on the surface of the folds. The number of black dots on the surface of a fold represents the number of follicles per fold. The average number of follicles per fold was 820. Since the number of folds per bursa ranges between 10--15, we were able to calculate 8000--12000 follicles per bursa. The volumetric mathematical analysis of the follicles and folds confirmed our calculated number of follicles. On a stereomicrograph from a randomly selected area of a fold surface, a trapezoid was outlined and measured. The surface analysis of the black dots within a trapezoid area revealed that about 10% of the bursal surface was covered by follicular epithelium which is immunologically oriented.

Animals↗
PubMed1977

Contact sites between lymphoid cells of the bursa of Fabricius, in vivo and in vitro.

Contact sites between lymphocytes and between lymphocytes and macrophages were demonstrated by electron microscopy in the lymphoid follicles of the bursa of Fabricius. When compared with nonspecialized regions of the cell membranes, these contact sites were characterized by a decreased intercellular distance, subplasmalemmal densities and coated pits. Microfilaments, microtubules and coated vesicles of the subjacent cytoplasm were frequently associated with these contact sites. When the same cells were isolated and introduced into culture, they formed cluster-like assemblies in which cells were closely approximated along broadly contacting surfaces. The morphology of the sites appeared to involve primarily the plasma membrane (including coated pits) and the cell coat. These observations indicated that the same cells of a given lymphoid tissue can form one type of contact site in vivo and another, dissimilar type of contact site, in vitro.

Animals↗
PubMed1977

The production of a lymphocyte inhibitory factor (LyIF) by bursal and thymic lymphocytes.

In this study the migration and migration inhibition of different lymphoid cell populations from immunized and control birds were evaluated. Bursal, thymic, and splenic cells migrated in a capillary tube with thymic cells forming the characteristic cone of cells within 4 hours of culture. Both thymic and bursal cell populations from birds sensitized by Mycobacterium tuberculosis produced a lymphocyte inhibitory factor (LyIF) when stimulated by specific antigen in vitro. The ability of bursal cells to release LyIF declined subsequent to 10 weeks of age while LyIF was not apparent in thymic lymphocytes until 9 weeks of age and remained high until 27 weeks of age. The active material generated in specifically stimulated cultures from sensitized bursal cells appeared to be antigen dependent whereas thymic cell mediator is antigen independent. The production of LyIF in chickens, while correlating with delayed type hypersensitivity, does not solely reflect T-cell function but B-cell response as well.

Age Factors↗
PubMed1977

Brain-associated thymic antigen in chickens.

Sera were produced in rabbits against a saline extract of chicken embryo brain (CBE). The rabbit anti-chicken brain (RACB) sera revealed, in micro-Ouchterlony studies, brain-associated antigens in extracts from the thymus, bursa, spleen and kidney. Absorption of the sera with normal serum (ns) and kidney (K), (RACBns, K), removed all reactivity with tissues other than brain. However, cytotoxic studies demonstrated that the kidney-absorbed serum was toxic to lymphocytes from thymus, bursa and spleen. Proper dilution of the RACBns, K produced a serum which was more cytotoxic for thymic lymphocytes than bursal lymphocytes. This study indicates the presence of brain-associated thymic antigens in the chicken.

Animals↗
PubMed1977

Effect of cold exposure on the immune response of chickens.

The effect of various environmental temperature changes on the antibody production of chickens were examined. Chronic cold exposure significantly increased the antibody titers. Birds exposed to 32.2 degrees C. and above had significantly depressed agglutinin levels. Short term cold exposures 2 or 4 times following the antigen injection enhanced the agglutinin and hemolysin response. Thirty minute cold exposures for 2 or 4 times significantly increased IgM antibody production and markedly reduced the IgG antibody. The data suggest the elevation of antibody titers are in relation to time of the cold treatment and antigen injection. Observed differences of antibody production may be due to cold induced changes in the metabolic activity of antigen reactive cells and antibody producing cells.

Agglutinins↗
PubMed1976

Cellular composition of the bone marrow in the chicken. I. Identification of cells.

Incorporation of Fe55 in vivo was used for verifying on radioautographs the identity of chicken bone marrow cells that are in the process of hemesyntheses. Under the experimental conditions all labeled cells may be considered to be linked with erythroid differentiation. They were classified into five maturational stages according to their morphology and capacity for DNA synthesis. Granulocytes were identified by the presence of specific granules. All mononuclear cells were classified as lymphocytes which had a pachychromatic nucleus, a high nucleocytoplasmic ratio, lacked the capacity for DNA synthesis, and resembled small lymphocytes of the bursa, spleen and bone marrow that bound, in vitro, anti-chicken gamma globulins labeled with I125. Radioautography with H3TdR was used to identify proliferating and non-proliferating members of each cell population.

Animals↗
PubMed1975

The function of the preoptic, mammilaris lateralis and ruber nuclei in normal and sexually inactive male chickens.

Male chickens were lesioned and canulated at five weeks of age. Lesions were located in the mammilaris lateralis (ML) and Ruber (Ru) nuclei. Cannulas filled with testosterone propionate (TP) were positioned in the praeopticus paraventricularis magnocellularis (PPM) area of the hypothalamus. The mating behavior of lesioned birds was tested at maturity while mating behavior of cannulated birds was evaluated at eight weeks of age. Males hatched from eggs dipped in 2 g% TP were designated TP birds. The TP birds exhibited a marked decrease in their sexual behavior responses and lesioning did not alter this effect. TP birds with cannulas in the PPM nuclei were stimulated to attempt to mate. These data indicate that TP birds failed to mate because of an interference in the development of the PPM nuclei. Bilateral lesions in the ML nuclei did not significantly influence sexual behavior while lesions in the Ru nuclei increased the sexual response. Therefore, the mammilaris region in the chicken's hypothalamus does not inhibit mating behavior while the Ru nucleus may be an inhibitory center for mating behavior in the chicken.

Animals↗
PubMed1975

Antibody and cell-mediated immunity in phytohemagglutinin-treated chickens.

The effects of phytohemagglutinin (PHA) on humoral and homograft immunity in young chickens were studied. Intravenous (IV) injections of PHA stimulated the antibody production while intraperitoneal (IP) injections suppressed the antibody production. IP injected PHA failed to prolong the survival of the homografts. The route and time of PHA administration must be considered when evaluating the influence which PHA exerts on homograft survival and hemagglutinin production in the chiicken. The results obtained in this study suggest that there may be two different target cell lines involved in PHA's action. The reduced antibody production following IP injections of PHA may be due to its interference with the peritoneal macrophages and T cells and in the case ov IV administration PHA may be activating both macrophages and T cells. Possibly, there may be a difference in the effective PHA concentration after IP versus IV administration to account for different responses observed.

Animals↗