Immunoglobulin G levels in fetal and newborn tammar wallabies (Macropus eugenii)

1990 ◽  
Vol 2 (4) ◽  
pp. 369 ◽  
Author(s):  
EM Deane ◽  
DW Cooper ◽  
MB Renfree
Keyword(s):  
Immunoglobulin G ◽  
Tammar Wallaby ◽  
Yolk Sac ◽  
Acquired Immunity ◽  
High Concentration ◽  
Macropus Eugenii ◽  
Route Of Transmission ◽  
Fetal Serum ◽  
Fetus And Neonate ◽  
Yolk Sac Placenta

Immunoglobulin G (IgG) was measured in fetal, neonatal and colostral samples from the tammar wallaby (Macropus eugenii) in order to study the possibility of passively acquired immunity. Samples were obtained from young at a known stage of gestation and at known times (to the minute) after birth. IgG was present (in increasing levels of concentration) in fetal serum, neonatal serum and colostrum. Since the fetus and neonate are probably unable to make immunoglobulin (Ig), it is hypothesized that transplacental and trans-gut transmission takes place from mother to offspring. The vascular yolk sac placenta has a high concentration of IgG, and is the most likely route of transmission from mother to young. Some observations were made of IgA which was found only in colostrum. No Ig of either kind was found in yolk sac fluid.

STEROID METABOLISM IN THE YOLK SAC PLACENTA AND ENDOMETRIUM OF THE TAMMAR WALLABY, MACROPUS EUGENII

1980 ◽  
Vol 87 (3) ◽  
pp. 339-349 ◽  
Author(s):  
R. B. HEAP ◽  
M. B. RENFREE ◽  
R. D. BURTON
Keyword(s):  
Tammar Wallaby ◽  
Yolk Sac ◽  
Endometrial Tissue ◽  
Steroid Synthesis ◽  
Metabolizing Enzymes ◽  
Macropus Eugenii ◽  
Progesterone Synthesis ◽  
Histological Appearance ◽  
Steroid Conjugates ◽  
Yolk Sac Placenta

Yolk sac and endometrial tissue were obtained from tammar wallabies between 11 and 25 days after the removal of pouch young. Tissues were examined histologically and steroid-metabolizing enzymes were identified by incubation for 3 h at 37 °C in Medium 199 containing labelled steroid precursors. Yolk sac membrane (YSM) incubated with labelled pregnenolone produced a small amount of progesterone and pregnanediols; 80·5 ± 8·4 (s.e.m.) % of the original substrate remained unmetabolized. Labelled androstenedione was metabolized to 5α-androstane-3,17-dione and androsterone, and only 5·8 ± 3·8% of the original substrate remained at the end of incubation. Incorporation of androstenedione or dehydroepiandrosterone (DHA) into phenolic compounds was low (0·5 ± 0·1%). There was no evidence for the enzymes, arylsulphatase or sulphotransferase, in YSM. Endometrial tissue from the same animals metabolized pregnenolone, DHA and androstenedione, converted progesterone to androstenedione, and produced aqueous-soluble steroid conjugates. The results demonstrated that YSM contains enzymes associated predominantly with steroid catabolism and with incipient progesterone synthesis. The findings are discussed in relation to the histological appearance of the tissues and compared with placental steroid synthesis in eutherian mammals.

Development of the lymphoid tissues of the tammar wallaby Macropus eugenii

1997 ◽  
Vol 9 (2) ◽  
pp. 243 ◽  
Author(s):  
K. Basden ◽  
D. W. Cooper ◽  
E. M. Deane
Keyword(s):  
Lymph Nodes ◽  
Immunoglobulin G ◽  
Lymphoid Tissue ◽  
Post Partum ◽  
Tammar Wallaby ◽  
Didelphis Virginiana ◽  
Lymphoid Tissues ◽  
Macropus Eugenii ◽  
Germinal Centres

A study has been made of the development of four lymphoid tissues from birth to maturity in the tammar wallaby Macropus eugenii —the cervical and thoracic thymus, lymph nodes and gut-associated lymphoid tissue (GALT). The development of these tissues in the tammar wallaby is similar to that in two other marsupials, the quokka Setonix brachyurus and the Virginian opossum Didelphis virginiana. Lymphocytes were first detected in the cervical thymus of the tammar at Day 2 post partum and in the thoracic thymus at Day 6. They were subsequently detected in lymph nodes at Day 4 and in the spleen by Day 12 but were not apparent in the GALT until around Day 90 post partum. By Day 21, the cervical thymus had developed distinct areas of cortex and medulla and Hassall’s corpuscles were apparent. The maturation of other tissues followed with Hassall’s corpuscles in the thoracic thymus by Day 30 and nodules and germinal centres in the lymph nodes by Day 90. Measurement of immunoglobulin G concentrations in the serum of young animals indicated a rise in titre around Day 90 post partum, correlating with the apparent maturation of the lymphoid tissues.

Visualization of Antibody Transport in Rat Visceral Yolk-Sac Placenta

1982 ◽  
Vol 40 ◽  
pp. 246-247
Author(s):  
William P. Jollie
Keyword(s):  
Phosphate Buffer ◽  
Yolk Sac ◽  
Female Rats ◽  
Thin Sections ◽  
Visceral Yolk Sac ◽  
Antibody Complex ◽  
Cytochemical Reaction ◽  
Hind Foot ◽  
Antigen Antibody ◽  
Yolk Sac Placenta

A technique has been developed for visualizing antibody against horseradish peroxidase (HRP) in rat visceral yolk sac, the placental membrane across which passive immunity previously has been shown to be transferred from mother to young just prior to birth. Female rats were immunized by injecting both hind foot pads with 1 mg HRP emulsified in complete Freund's adjuvant. They were given a booster of 0.5mg HRP in 0.1 ml normal saline i.v. after one week, then bred and autopsied at selected stages of pregnancy, viz., 12, 1 7 and 22 days post coitum, receiving a second booster, injected as above, five days before autopsy. Yolk sacs were removed surgically and fixed immediately in 2% paraformaldehye, 1% glutaraldehye in 0.1 M phosphate buffer with 0.01% CaCl2 at pH 7.4, room temperature, for 3 hr, rinsed 3X in 0.1 M phosphate buffer plus 5% sucrose, then exposed to 1 mg HRP in 1 ml 0.1 M phosphate buffer at pH 7.4 for 1 hr. They were refixed in aldehydes, as above, for 1 5 min (to assure binding of antigen-antibody complex). Following buffer washes, the tissues were incubated in 3 mg diaminobenzidine tetrahydrochloride and 0.01% H2O2 in 0.05 M Tris-HCl buffer for 30 min. After brief buffer washes, they were postfixed in 2% OsO4. in phosphate buffer at pH 7.4, 4°C for 2 hr, dehydrated through a graded series of ethanols, and embedded in Durcupan. Thin sections were observed and photographed without contrast-enhancement with heavy metals. Cytochemical reaction product marked the site of HRP (i.e., antigen) which, in turn, was present only where it was bound with anti-HRP antibody.

Structure of the paraplacenta and the yolk sac placenta of the viviparous Australian sharpnose shark, Rhizoprionodon taylori

Placenta ◽  
2021 ◽  
Vol 108 ◽  
pp. 11-22
Author(s):  
Alice L. Buddle ◽  
James U. Van Dyke ◽  
Michael B. Thompson ◽  
Colin A. Simpfendorfer ◽  
Christopher R. Murphy ◽  
...  
Keyword(s):  
Yolk Sac ◽  
Yolk Sac Placenta
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