A study of modified lymphatics in the deep cortex of ruminant lymph nodes.

Ruminant lymph nodes, except when very small, were found to have a system of smooth-walled channels in the periphery of the 'deep cortical units' defined by Bélisle & Sainte-Marie (1981 a,b). Each channel originated with many 'blind' branches in the subnodular layer of the cortex and ended by joining a medullary sinus. The wall consisted of a continuous endothelial lining, a sometimes thin or discontinuous basement membrane without a basal lamina, and at least one layer of flattened reticular fibroblasts.

Ontogeny of reticular cells in the ileal Peyer's patch of sheep and goats.

The ontogeny of reticular cells in the ileal Peyer's patch of sheep from 70 days gestational age was studied by light and electron microscopy and by enzyme histochemistry. Small to medium-sized lymphocytes were seen in the lamina propria at 97 days, when the stroma was essentially still mesenchymal. By 110 days, the stromal cells in the dome/follicle primordia had differentiated into reticular fibroblasts, whose processes and fibers were seen to surround groups of lymphocytes.

The intestinal habitat for organized lymphoid tissues in ruminants; comparative aspects of structure, function and development.

Unlike the Peyer's patches of rats and mice, which are considered to be secondary lymphoid organs, the ileal Peyer's patch of sheep is thought to be responsible for the primary generation of B cells, like the bursa of Fabricius of birds. The ileal Peyer's patch of sheep shows prenatal maturation, antigen-independent lymphopoiesis, a rate of lymphocyte production larger than that of the thymus, and involution at a young age. Follicles contain few T cells and have an IgM+, relatively immature B lymphocyte population, as judged by B-cell differentiation markers.

Ontogeny, distribution and structure of aggregated lymphoid follicles in the large intestine of sheep.

Aggregates of lymphocytes were demonstrated from 70 days gestation (term 150 days in sheep) in the proximal colon and rectum. Immunoperoxidase staining for 5'-bromo-2'-deoxyuridine incorporation and IgM, indicated that the lymphocyte population of lymphoid follicles in fetal sheep colon was actively dividing and surface IgM positive. Enzyme histochemistry for 5'-nucleotidase showed that the lymphocytes developed in a meshwork of positive reticular cells, suggestive of developing follicles.

Organization of ruminant Peyer's patches as seen with enzyme histochemical markers of stromal and accessory cells.

Five enzyme histochemical reactions were used to characterize calf, goat kid and lamb Peyer's patches. 5'-nucleotidase and acid phosphatase gave a reticular pattern of staining in follicular and interfollicular regions, respectively. Different subpopulations of fibroblastic reticulum cells were suggested for the T cell area, the dome/corona region, and the follicle capsule.

Transfer of carbonic anhydrase-positive particles from the follicle-associated epithelium to lymphocytes of Peyer's patches in foetal sheep and lambs.

Carbonic anhydrase cytochemistry of the ileal Peyer's patch in foetal and neonatal lambs has indicated secretion from the follicle-associated epithelium to the follicles. Reaction for carbonic anhydrase in the follicle-associated epithelium was found in the luminal plasma membrane, in cytoplasmic vesicles, and in vacuoles containing 50-nm membrane-bounded particles that seemed to be shed to the intercellular space. The lateral plasma membrane was negative for carbonic anhydrase, indicating that formation of carbonic anhydrase-positive particles was restricted to vacuoles.

Ultrastructure of the uterotubal junction in preovulatory pigs.

The ultrastructure of the surface epithelia from the uterotubal junction (UTJ), and the adjacent tubal isthmic and endometrial regions, was studied in preovulatory oestrus gilts, either unmated or inseminated 12 h before with fresh boar semen. The simple columnar epithelium of the UTJ consisted of non-ciliated (secretory) and ciliated cells. Secretory vesicles occurred in the secretory cells, especially in inseminated gilts.

Carbonic anhydrase--a marker for particles shed from the epithelium to the lymphoid follicles of the ileal Peyer's patch in goat kids and lambs.

Carbonic anhydrase (CA) was found to be a marker for 50 nanometer membrane-bounded particles shed from the lateral cell border of follicle-associated epithelial cells (FAE) in the ileal Peyer's patch (PP) of pre- and post-natal lambs and goat kids. The CA-positive particles seemed to filter into the underlying lymphoid tissue where they formed part of the matrix embedding the cells of the follicle centre.

Early effects of efferent ductule ligation on the proximal segment of the rat epididymis.

The effects on the proximal caput epididymidis of efferent ductule ligation were studied. After 6 h there was a slight increase in autophagocytosis in the initial segment proper (1A). After 12 h this segment showed cell death and cytoplasmic regression and after 24 h large amounts of necrotic cells and focal degeneration in the epithelium, and desquamated cells and débris in the lumen.

Ultrastructural observations suggesting merocrine secretion in the initial segment of the mammalian epididymis.

Principal cells in the initial segment of the epididymis in horses, cattle, pigs, sheep, dogs, cats, and rabbits have an abundant, partly rough, endoplasmic reticulum and a large Golgi complex. Small vacuoles with opaque content seem to be formed by the Golgi complex and move to the cell apex, where they empty their contents into the lumen by a merocrine mechanism.

Influence of thawing diluents on vitality, acrosome morphology, ultrastructure and enzyme release of deep frozen boar spermatozoa.

The present investigation was performed to study the effect of freezing and thawing on boar spermatozoa. Thirty-one ejaculates from four boars were investigated after thawing in three different thawing diluents (seminal plasma, OLEP, isotonic glucose solution). From each ejaculate one sample of 1 × 10 spermatozoa was thawed in each of the thawing diluents.