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The development of lymphoid and nonlymphoid cells in Peyer's patches (PP) of the rat was investigated using light microscopical methods (routine histological techniques, enzyme histochemistry and immunohistochemistry). In newborn rats PP were mainly populated by T lymphocytes and Ia-positive nonlymphoid cells, which most likely are interdigitating cells. At about 12 days after birth the B and T cells were localized in defined regions, the follicular (FA) and interfollicular area (IFA), respectively. Compartmentalization within the FA started about 14 days after birth. The first signs of the development of secondary follicles were seen from about 18 days onward. PP obtained their mature structure at about 4 weeks after birth. It is suggested that after PP had developed fully, cells having cytoplasmic IgA migrate via the high endothelial venules (HEV) to the lamina propria of the intestine; cIgM and IgG cells seem to develop locally within the FA.
Anat Rec 1983 Oct
PMID:Ontogeny of Peyer's patches of the rat. 665 Aug 63

Three mouse strains, NZBxW, BXSB, and MRL/lpr have well documented congenital lymphoproliferative syndromes and lupus-like disease. We studied the ultrastructures of the marrows of these mice searching for a model for intramedullary lymphopoiesis. In MRL/lpr, the strain with the most severe disease, the marrow was largely populated by large lymphocytes associated with dark branching stromal cells. These stromal cells are apparently of a recently recognized cell type which has been associated with extremely accelerated eosinophilopoiesis and erythropoiesis. They did not appear in the lymph nodes and spleens of the MRL/lpr mice or in the marrows of the other strains. BXSB marrows showed some non-proliferant lymphocytic infiltrates and heightened erythropoiesis while NZBxW marrows resembled controls. We suggest that the dark stromal cells in the MRL/lpr marrows were important in supporting the production or differentiation of lymphoid precursor cells.
Anat Rec 1983 Nov
PMID:Ultrastructure of the bone marrow in three murine strains with non-malignant lymphoproliferative syndromes NZBxW, BXSB, and MRL/lpr. 665 Aug 75

We have studied the lymphoid development and structure of Meckel's diverticulum (MD). The lymphoid accumulation began about 2 weeks of age. Between 2 and 5 weeks of age the longitudinal folds were filled with lymphoid tissue. The intensive germinal center formation occurred between 5 and 7 weeks of age. Germinal center formation was associated with the presence of secretory cells. The absence of the secretory cells in the germinal centers was followed by germinal center inactivity which was indicated by the lack of lymphoblasts and the high number of tingible body macrophages. The lymphoid tissue of MD seemed to be fully developed by 10 weeks of age and remained lymphoid at least until 21 months of age. Meckel's diverticulum produced large numbers of plasma cells which were comparable to those of the gland of Harder. We may regard MD as the third pouch of the intestine and suggest that it may be a novel lymphoepithelial organ in the chicken.
Anat Rec 1984 Feb
PMID:Meckel's diverticulum. II. A novel lymphoepithelial organ in the chicken. 670 41

Incubation of skin in 2 N sodium bromide allows separation of dermal and epidermal layers leaving an intact basal lamina covering the dermal portion. Examination of the surface of the dermis by SEM shows cells migrating through the basal lamina. By scanning and transmission electron microscopy, these cells have the characteristics of lymphocytes. The migrating lymphocytes produce a sequence of basal lamina deformations including dome formation, effacement of corrugations, and central fenestrations with hole formation allowing lymphocyte passage. Following passage there is reestablishment of a relatively smooth basal lamina in the crater base, effacement of the crater rim, and finally reformation of basal lamina corrugations. This deformability of the basal lamina supports the hypothesis that basal lamina is thixotropic. This study is the first demonstration in three dimensions of lymphocyte traffic across the basal lamina, an important component of skin-associated lymphoid tissue (SALT).
Anat Rec 1984 Mar
PMID:Migration of lymphocytes through the cutaneous basal lamina in normal skin: an ultrastructural study. 672 Dec 30

Pure cultures of an isolate of Campylobacter fetus subspecies intestinalis obtained from the congested small intestinal mucosa of a two-week-old calf were used to infect three milk-fed calves and three ruminating calves in two separate controlled experiments. Inoculated animals all developed clinical signs which included fever (to 40 degrees C) and diarrhoea with excess clear mucus containing occasional spots of blood. C fetus subspecies intestinalis was isolated from the faeces of all infected animals in the two experiments but not from those of the five control animals. Changes in the enteric tract were most marked in the ileum which was thickened and mildly inflamed with accumulations of lymphoid cells and crypts filled with inflammatory cells in all six infected animals. The mesenteric lymph nodes were pale and enlarged. C fetus subspecies intestinalis was recovered from the jejunum, ileum, caecum and colon of the infected animals and less frequently from the abomasum, mesenteric lymph nodes, liver and gall bladder. It was never isolated from the control animals. Antibody to the inocular strain of C fetus subspecies intestinalis was demonstrated, at titres of at least 1 in 320, in the serum of all inoculated animals and was absent from all the control sera. The findings were considered to indicate that C fetus subspecies intestinalis caused the syndrome described above and that the syndrome produced differed only in minor details from that produced in calves by infection with C jejuni.
Vet Rec 1983 Jan 15
PMID:Production of enteritis in calves by the oral inoculation of pure cultures of Campylobacter fetus subspecies intestinalis. 683 83

We have observed by light and transmission electron microscopy lymphoid accumulations (LA) in the chicken located along the posterior tibial-popliteal and lower femoral veins. Three types of LA were characterized: 1) LA on the wall of the lymphatic, 2) LA with germinal center, and 3) well-developed LA possessing germinal centers and an intricate lymphatic sinus system. The latter will be termed a lymph node and is perhaps the structure responding to foot-pad injection of antigen and/or phytohemagglutinin (PHA). After the injection of PHA into the foot-pad, the lymph node enlarged and revealed the intermingling of two distinct groups of cells consisting of either small lymphocytes or medium lymphocytes and lymphoblasts. Because our earlier immunological paper proved the presence of T and B cells in the node, the two histologically distinct groups of cells appearing after PHA injection could reflect compartmentalization of T and B cells in the avian lymph node. Lymphoid and adipose tissues are in the same compartment. After PHA or antigen injection into the foot pad, the lymphoid tissue proliferates and the amount of the adipose tissue rapidly decreases. This suggests that lymphoid and adipose tissue form a special complex which is separated from the surrounding tissue by delicate connective tissue capsule. The relationship of the lymphoid and adipose tissue is comparable with that of myeloid and adipose tissue in the bone marrow. The majority of the sinuses shows smooth endothelial lining while others contain "hairy" macrophages attached to the endothelium. The germinal centers are located at the periphery of the node, but a few occur inside. The cellular content of the germinal centers is not unusual except for the presence of plasma cells.
Anat Rec 1983 Mar
PMID:Avian lymph node: light and electron microscopic study. 683 43

Administration of androgens produces damage in lymphoid tissue and in the bursa of Fabricius. After IM administration of 5 mg of testosterone propionate (TP) beginning at hatching and continued during the following 4 days, a significant reduction in the bursal weights is observed. Histologically, an increase in the connective tissue is observed and cystic formations are also found. In all cysts examined, there is continuity of the cystic lumen with the free surface. The follicle-associated epithelial (FAE) cells are on the bottom of the pseudocysts and form a separation between the pseudocystic cavity and the lymphoid tissue which is still further inwards. These cells do not lose their esterase activity, even though they are often flattened. Furthermore, they disappear in the pseudocysts deprived of lymphoid tissue. A new hypothesis is advanced that the FAE cells originate from the mesenchyme with differentiation in the histiocytic line.
Anat Rec 1983 Feb
PMID:The behavior of bursal lymphoid follicle-associated cells after treatment with testosterone. 684 68

The production of lymphoid cells in the pig spleen was studied autoradiographically after selective labeling of the spleen using an extracorporeal perfusion circuit. Tritiated thymidine was added as a DNA precursor. One to 4 days after local labeling of the spleen the relative and absolute number of spleen-derived lymphocytes were determined in the following organs: mesenteric, cervical and inguinal lymph nodes, thymus, bone marrow, Peyer's patches, tonsils, three different parts of the gut, lung, liver, and blood. The labeled lymphocytes which migrated to these organs were all small lymphocytes, except for some large cells in the lamina propria. In the bone marrow, however, a considerable number of the spleen-derived immigrants were transformed into plasma cells. The total number of labeled lymphocytes decreased dramatically from Day 1 to Day 4 after labeling, indicating a high percentage of short-lived cells. Within the spleen, plasma cells had the highest labeling index of about 30% at Day 1 but this dropped to only 1.5% on Day 3. The organ distribution of the splenic emigrants changed from Day 1 to Day 4 with a relative increase in lymphocytes found in lymph nodes and a decrease in the lung and intestinal wall. The newly formed splenic lymphocytes migrated to T-and B-cell areas in lymph nodes, Peyer's patches and tonsils. In the intestinal wall labeled lymphocytes were found in the lamina propria and also as intraepithelial lymphocytes. There was no obvious redistribution between organ compartments with time after labeling of the spleen. The spleen produces large numbers of lymphocytes, which show typical organ distribution and homing to areas in lymphoid and nonlymphoid organs.
Anat Rec 1982 Jan
PMID:Organ distribution and fate of newly formed splenic lymphocytes in the pig. 705 22

A simultaneous morphological and quantitative profile was obtained of the cells of blood, thoracic duct, and renal hilar lymph in the dog. Monolayer cytocentrifuged preparations were used to determine the number, type, and size of cells in the three compartments. The cell count of renal lymph was not related to that of blood or thoracic duct lymph. There was a greater percentage of lymphoid cells in the afferent lymph than could be accounted for by the random movement of cells from the blood to the lymph. Thus, there appeared to be a selective transit of cells from blood to lymph. Monocytes and neutrophils were largely absent from the thoracic duct lymph; however, eosinophils were present. Cells were observed in hilar lymph that were characteristic of cells subjected to antigenic stimulation. It was concluded that lymphocytes have a preferential pathway from blood to lymphatic and in the course of this pathway they undergo a change which is consistent with an active immunological role.
Anat Rec 1980 Oct
PMID:A simultaneous comparison of the cells of blood, renal hilar and thoracic duct lymph in the dog. 721 9

Morphology of guinea-pig thymic fragments was studied sequentially during in vitro organ culture by using light and electron microscopy and 3H-thymidine autoradiography. In culture the fragments became alymphoid. Thymic lymphocytes started to disappear first at the corticomedullary border, which gradually broadened, giving rise to the alymphoid epithelial fragments. As the lymphoid cells disappeared the thymic epithelium began to transform into a keratinized squamous epithelium. The keratinization started in the cells surrounding the Hassall's corpuscles, causing the enlargement of the corpuscles and finally total keratinization of the cultured epithelial fragments. In autoradiographic studies cell proliferation could be observed in uncultured thymuses at the cortical pericapsular area. In cultured alymphoid fragments labelled cells were distributed diffusely in the epithelium. Later labelling was concentrated to epithelial cells transforming to keratinized epithelium. Ultrastructural studies similarly showed transformation of the epithelial cells to squamous keratinized epithelium. The observation support the view that Hassall's corpuscles are derived from the keratinized thymic epithelium and that their existence is connected to the normal function of the epithelium.
Anat Rec 1981 Aug
PMID:Thymic morphology during in vitro culture. 730 14


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