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

Vasculogenesis of the bursa cloacalis (bursa of Fabricius) was examined in 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.

[1]  Gretchen L. Humason,et al.  Animal Tissue Techniques , 1974 .

[2]  H. Cottier,et al.  The bursa of Fabricius: a central organ providing for contact between the lymphoid system and intestinal content. , 1974, Cellular immunology.

[3]  F. C. Mcduffie,et al.  Role of the bursa of Fabricius in IgG and IgM production in the chicken: evidence for the role of a non-bursal site in the development of humoral immunity. , 1971, Journal of immunology.

[4]  M. Cooper,et al.  Development and Function of the Immunoglobulin-Producing System , 1969, The Journal of Immunology.

[5]  N. S. Fechheimer,et al.  Cell Transport and the Bursa of Fabricius , 1966, Nature.

[6]  J. Owen,et al.  Experimental studies on the development of the bursa of Fabricius. , 1966, Developmental biology.

[7]  R. K. Meyer,et al.  EFFECT OF THYMECTOMY AND BURSECTOMY ON PRECIPITIN AND NATURAL HEMAGGLUTININ PRODUCTION IN THE CHICKEN. , 1963, Journal of immunology.

[8]  F. B. Adamstone,et al.  Phase contrast study of structural changes in terminal epithelial cells of villi of rat intestine , 1963 .

[9]  F. Burnet,et al.  The Influence of Testosterone Treatment on the Development of the Bursa of Fabricius in the Chick Embryo , 1961 .

[10]  R. K. Meyer,et al.  Precipitin production in chickens. XXI. Antibody production in bursectomized chickens and in chickens injected with 19-nortestosterone on the fifth day of incubasion. , 1960, Journal of immunology.

[11]  R. K. Meyer,et al.  Inhibition of the development of the bursa of Fabricius in the embryos of the common fowl by 19-nortestosterone. , 1959, Endocrinology.

[12]  A. R. Winter,et al.  The Significance of the Bursa of Fabricius of Chickens in Antibody Production 3. Resistance to Salmonella Typhimurium Infection , 1957 .

[13]  B. Glick,et al.  The Bursa of Fabricius and Antibody Production , 1956 .

[14]  R. A. Goff Development of the mesodermal constituents of feather germs of chick embryos , 1949, Journal of morphology.

[15]  R. Watterson Development of the glycogen body of the chick spinal cord. I. Normal morphogenesis, vasculogenesis and anatomical relationships , 1949, Journal of morphology.

[16]  R. Watterson,et al.  The development of the vascular pattern within the walls of the central nervous system of the chick embryo , 1946, Journal of morphology.

[17]  James F. Feenet The Rapid Preparation of Celloidin Serial Sections Following India Ink Injections , 1944 .