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Changes in the surface morphologies of the cells in the bursa cloacalis (bursa of Fabricius) and thymus during ontogeny of the chick embryo.

Slices or sections through the bursa cloacalis and thymus of chick embryos at 7-21 days of incubation were observed by light and electron microscopy to determine whether major differences existed in the surface morphologies of lymphoid cells in these organs, and whether the surface morphologies of these cells changed during ontogeny. These organs were fixed concurrently and identically at each stage. The thymus was packed at all stages with spherical cells having fine structures characteristic of those of lymphoid cells. Many irregularly shaped, epithelial cell processes were present between lymphoid cells. The bursa contained many irregularly shaped stromal cells as well as spherical cells. The latter were few in number during early development, but became the predominant type of cell near the end of incubation. Spherical cells in the bursa consisted of three types based on fine structure: lymphoid cells, granulocytic cells, and cells which were probably precursors of granulocytic cells. Spherical cells in the bursa could not be classified into these three types by their surface morphologies, however, because the latter at any one stage of development were similar. At 7-8 days of incubation, spherical cells in the bursa could not be differentiated consistently from neighboring stromal cells by scanning electron microscopy alone, but by 9 days, spherical cells could be identified routinely by this method. At 9-10 days of incubation, only minor differences existed in the surface morphologies of the spherical cells in the bursa and thymus: Bursal cells displayed long, ridgelike processes, whereas thymic cells exhibited fine surface undulations and large blebs. At 11 days, the surfaces of the spherical cells in the bursa were covered by numerous short microvilli, but the surfaces of thymic cells were unchanged. Bursal cells retained their microvilli through 14 days of incubation, but between 15 and 21 days progressively lost their microvilli, becoming essentially bald near the end of this period. Likewise, thymic cells gradually lost their surface wrinkles and blebs. Near the time of hatching, both types of cells were smooth-surfaced and tightly packed, with individual cells assuming polyhedral configurations.

Animals↗

The bursa cloacae (Fabricii) of Struthioniforms in comparison with the bursa of other birds.

The late embryonic and postembryonic genesis of the bursa cloacae (Fabricii) of struthioniforms and other birds is described and discussed. The bursa of ostrich and emu is a wall organ of the caudal cloacal chamber. The bursa of rhea is, like the bursa of Gallus, a cranial appendix of the proctodeum. Lobuli bursales of struthioniforms are composed of a peripheral pars lymphoepithelialis (PLE) and a central pars lymphoreticularis (PLR). By contrast, lobuli bursales of Gallus are composed of a peripheral PLR and a central PLE. The fine structure of the bursa of struthioniforms is described. Other than in Gallus, the apical cell association of the PLE of struthioniforms shows secretory granules. This study thus far does not answer in detail the question of how the imprinting mechanism of the B-lymphocytes operates. It is assumed that they are imprinted in the PLE. Postcapillary venules in the PLR are responsible for the transport of B-lymphocytes. Hormonal bursectomies have been made to get information about the involution of the bursa of struthioniforms. In these species, involution means a gradual metaplasia while in Gallus it means a complete degeneration of the bursa.

Animals↗

The anatomy of the cloacal bursa (bursa of Fabricius) in the helmeted guinea fowl (Numida meleagris galeata).

The cloacal bursa (bursa of Fabricius) in the guinea fowls appeared either as an oval blind sac with a short thick stalk in one group or had a pointed cranial blind end with a slightly bulging middle part that was followed by a thick caudal stalk in the other group. Both groups of bursae originated from the proctodeal wall of the cloaca and were placed dorsal to the rectum. The average length of the bursa was 18 mm while the average width at the mid section was 15 mm. The internal surface showed about 12-14 primary folds. Histologically, the outline of the bursa was well established by day 18 of incubation. The primary folds had also been formed. Lymphocytes had already been encountered within the framework of the bursa at this day. The epithelium bordering the tunica propria was composed principally of two layers of cuboidal cells. Epithelial buds had also formed and some were already detached from the epithelial lining. The blood vessels present were positioned just beneath the outer covering. At day 19 of incubation, most of the epithelial buds had two layers of cells arranged in a circumscribed manner while a few had three layers of cells. Blood vessels had increased in number and were deeper placed inside the bursa than previously. At day 20, the cells of the upper layer of the epithelium were dorsoventrally flattened and stained paler than the cells of the lower layer. It was possible to distinguish the cortex from the medulla and the basement lining between both zones was distinct. Tiny vesicles within the cytoplasm of the epithelial cells at the mucosa and follicles were observed. Macrophages were also observed within the gland. At day 21, blood vessels were observed in the cortex of the follicles. The maximum number of primary folds (14) had been formed. At day 22, several follicles had severed connections with the mucosal epithelium. The mucosal lining had dropped to a single layer of cells in some areas. Goblet cells were observed amongst the mucosal cells. A plasma cell had first appeared. By day 25, dead cells had increased quite in number and there was also an increase in number of medium and small-sized lymphocytes within the gland. By day 26, the upper layer of the surface epithelium was composed primarily of tall columnar cells with numerous large vacuoles. Macrophages had suddenly increased within the thin interfollicular spaces and most of them were crowded internally with various sizes of debris.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

Involution of the chicken bursa of Fabricius: a light microscopic study with special reference to transport of colloidal carbon in the involuting bursa.

The involution of the bursa of Fabricius in White Leghorn chickens and the transport of colloidal carbon in the involuting bursa were studied on light microscopy. In chickens, from newly hatched to 23.5 weeks of age, the bursa was weighed, its histology was described, and the mitoses in the cortical and medullary compartments of the lymphoid follicles were counted. Decrease in bursal weight and in the number of mitoses were observed between 10 and 16 weeks of age. During week 17.5, the follicle-associated epithelium began to lose its endocytic capability, and mucin droplets appeared in the follicular medulla initiating the large mucoid cysts that were seen in the later phases of involution. The involutionary process was almost completed by week 23.5, when the bursa appeared as a fibrotic residue without intact lymphoepithelial structures. The particulate tracer used, colloidal carbon, was not observed to be transported to other organs from the bursa. The present study gives further support to the idea that after completing its central immune function in 6 weeks [21] the bursa, as estimated histologically, still possesses capacity to function like a peripheral lymphoid organ until 16 weeks of age.

Animals↗

[The presence of the lymphatic stomata in ovarian bursa of guinea pig and the ultrastructure of ovarian bursa].

In order to explore its structure and speciality of species, the ovary bursa of guinea pig was studied by using dissecting microscopy and scanning electron microscopy. In this paper, the lymphatic stomata on both internal and external layer of the ovary bursa was frist reported in guinea pig. The results suggested that the stomata in bursa not only provided a pathway to connect the bursal cavity with the lymphatic vessels of bursa and the peritoneal cavity, but also may be involved in the reproduction and local immunity of the ovary. The stomata may play an important role in physiological function of the ovary. At the same time, the structural differences were identified in ovary bursa between guinea pig and golden hamster.

Animals↗

Vasculogenesis of the bursa cloacalis (bursa of Fabricius) of the chick embryo.

Vasculogenesis of the bursa cloacalis (bursa of Fabricius) was examined i 10- to 21-day chick embryos and in chicks during the first 5 days post-hatching. The entire circulatory system was injected with India ink, and the bursae were then removed and either cleared for examination in toto or sectioned serially. The bursa was supplied by three pairs of extrinsic blood vessels. At 10 and 11 days of incubation, most intrinsic vessels were arranged in a superficial, hexagonal network. In regions of developing plicae, the hexagonal plexus extended into the core of each plica, forming middle plical vessels. The latter were interconnected across interplical areas by cross-connecting vessels. The middle plical vessels gave rise to small capillary offshoots, which soon increased in complexity, forming delicate loops. Branches extended from these loops through the subepithelial lamina propria to incipient epithelial buds by 12 days of incubation. All epithelial buds were supplied by at least one such branch, and similar branches extended to the basal aspect of the epithelium in areas where epithelial buds had not yet formed. This observation is consistent with the hypothesis that blood vessels induce formation of epithelial buds. At about 15 days of incubation, the cortex and medulla of each developing lymphatic follicle were defined clearly, and an intricate, web-like, capillary network coursed throughout the follicular cortex. The medulla appeared to be devoid of capillaries. The diameters of all intrinsic and extrinsic bursal blood vessels gradually increased throughout development. During post-hatching stages, the diameters of the extrinsic vessels continued to increase, whereas those of the intrinsic vessels were markedly decreased from late pre-hatching stages.

Animals↗

[Growth of the cloacal bursa (bursa of Fabricius) and spleen in ducks].

The growth in weight of both the bursa of Fabricius and the spleen was investigated in different stocks of ducks between hatching and 154 days of age. The data were analysed by fitting the Janoschek growth curve and the allometric formula. Both organs showed rapid growth to their maximum dimensions and early points of inflection. The regression of the cloacal bursa started at about 12 weeks of age in Pekins and Mallards. In the Muscovy, the involution begins beyond the period of investigation. Allometrically, a biphasic relationship was found. Starting with positive allometry, the allometric exponent decreased to negative or isometric (Muscovies) values within the second week of age. If the organ weights are compared on the basis of these allometric relationships, Pekins had bursa weights that were about 30% higher than those in Mallards. For the spleen, there was no difference between wild and domesticated ducks.

Animals↗

Endoscopy of the navicular bursa: a new technique for the treatment of contaminated and septic bursae.

A technique for evaluation of the navicular bursa using a 4 mm 25 degrees inclined view arthroscope is described. This allows examination of the palmar/plantar surface of the navicular bone, the insertions of the navicular suspensory, T and impar ligaments, the bursal synovium and the dorsal surface of the deep digital flexor tendon. The technique was used in 16 horses with punctures of the navicular bursa. Procedures facilitated by the technique were bursal lavage, removal of pannus, synovial resection and debridement of lesions on the palmar/plantar surface of the bone and in the deep digital flexor tendon. Following treatment, 10 animals were sound and returned to their pre-injury use and 6 animals had persistent lameness; 2 of these were salvaged after neurectomy, 1 was retired for use as a broodmare and 2 were destroyed. In contrast to the 'streetnail' procedure, the reported technique is less invasive and post operative care is simpler. The success rate is also better. Endoscopically guided treatment therefore appears to offer an advantage in the treatment of contaminated or septic navicular bursae.

Animals↗

Gastrocnemio-semimembranosus bursa and its relation to the knee joint. III. Pressure measurements in joint and bursa.

Pressure measurements in the knee joint and gastrocnemio-semimembranosus bursa were performed on patients and autopsy cases. A normally occurring closure mechanism between the joint and the bursa was demonstrated and analysed. Two patients were also found to have a partial valvular mechanism in the form of a hindrance to spontaneous passage of fluid from the bursa to the joint but no hindrance in the other direction.

Autopsy↗

Studies on the pathogenesis of Escherichia coli in the bursa of Fabricius (cloacal bursa) of the turkey.

Turkey poults were inoculated with avirulent or virulent strains of Escherichia coli by direct application to anal lips and were killed at postinoculation hours (PIH) 0.1, 2, 5, 10, 24, 48, 72, and 96. Bursae of Fabricius (cloacal bursae) were collected, cultured, and examined by light, fluorescent, and electron microscopy. The virulent strain of E coli was not recovered from the bursae after PIH 24, although the avirulent strain was recovered up to PIH 96. The E coli strains neither localized at nor associated with the bursal fold epithelium, passed through the follicular pad epithelium, nor caused cytopathologic changes in the lymphoid follicle. A mild catarrhal bursitis was observed at PIH 48 with the avirulent strain of E coli.

Animals↗

The effect of anti-bursa serum (ABS) on the intensity of acid phosphatase reaction in bursa-dependent structures of the chicken spleen and on the level of antibodies in the blood serum.

It has been found that administering rabbit anti-bursa serum (ABS) to chickens, like neonatal bursectomy, brings about a decreased acid phosphatase (APh) reaction in germinal centres type I and II, and in the periellipsoidal lymphatic tissue (PEL) of the spleen. It has turned out, that following a stimulation with sheep erythrocytes (SRBC) in the blood serum of the ABS-treated chickens appear traces of specific anti-SRBC agglutinins, while in bursectomized chickens there is only a slight decrease in the titre of those antibodies. The results may serve as a base for further studies on the role and participation of the spleen structures in chicken immunological response.

Acid Phosphatase↗

Endoscopic bursal resection: the olecranon bursa and prepatellar bursa.

We treated 31 cases of olecranon bursitis and 19 cases of prepatellar bursitis. The average duration of symptoms before surgery was 1.1 years with a range of 3 months to 4 years. All patients had had preoperative aspiration and injection of cortisone. Patients underwent an arthroscopic bursal resection, removing all the bursal sack that could be seen. The results indicated that 86% of patients after olecranon bursectomy had no pain whatsoever. In the patients with prepatellar bursitis, 66% had no pain whatsoever, but we did note some residual tenderness in 24% of the patients, and 10% had pain on kneeling. There were 2 recurrences; 1 patient had rheumatoid arthritis and 1 repetitive daily trauma to the knee. There were no significant complications.

Adult↗