Persistent differences in the level of chimerism in B versus T cells of freemartin cattle

Developmental and Comparative Immunology

Volumn 28, Issue 1, 2004, Pages 77-87

  Pessa Morikawa, Tiina ^a   Niku, Mikael ^a   Iivanainen, Antti ^a  

^a UNIVERSITY OF HELSINKI   (Finland)

Author keywords

B cell; Cattle; Chimerism; Development; Freemartin; Immunomagnetic cell separation; In situ hybridization; Peyer's patch

Indexed keywords

CD3 ANTIGEN; IMMUNOGLOBULIN M;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; B LYMPHOCYTE; CATTLE; CHIMERA; CONTROLLED STUDY; FEMALE; HEMATOPOIETIC STEM CELL; IMMUNOMAGNETIC SEPARATION; IN SITU HYBRIDIZATION; LYMPHOID TISSUE; MALE; NONHUMAN; PARABIOSIS; PRIORITY JOURNAL; T LYMPHOCYTE; Y CHROMOSOME;

BOS TAURUS; RAPHIA FRATER;

EID: 0042330517     PISSN: 0145305X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0145-305X(03)00104-6     Document Type: Article

References (47)

1. Kondo M., Wagers A., Manz M.G., Prohaska S.S., Scherer D.C., Beilhack G.F., Shizuru J.A., Weissman I.L. Biology of hematopoietic stem cells and progenitors: implications for clinical application. Annu Rev Immunol. 21:2003;759-806.
2. Kondo M., Weissman I.L., Akashi K. Identification of clonogenic common lymphoid progenitors in mouse bone marrow. Cell. 91:1997;661-672.
3. Akashi K., Traver D., Miyamoto T., Weissman I.L. A clonogenic common myeloid progenitor that gives rise to all myeloid lineages. Nature. 404:2000;193-197.
4. Poussier P., Julius M. Thymus independent T cell development and selection in the intestinal epithelium. Annu Rev Immunol. 12:1994;521-553.
5. Griebel P.J., Hein W.R. Expanding the role of Peyer's patches in B-cell ontogeny. Immunol Today. 17:1996;30-39.
6. Reynolds J. The genesis, tutelage and exodus of B cells in the ileal Peyer's patch of sheep. Int Rev Immunol. 15:1997;265-299.
7. Carlens O. Studien über das lymphatische Gewebe des Darmkanals bei einigen Haustieren, mit besonderer Berücksichtigung der embryonalen Entwicklung, der Mengenverhältnisse and der Altersinvolution dieses Gewebes im Dünndarm des Rindes. Z Anat Entwicklungsgesch. 86:1928;393-493.
8. Gerber H.A., Morris B., Trevella W. The role of gut-associated lymphoid tissues in the generation of immunoglobulin-bearing lymphocytes in sheep. Aust J Exp Med Sci. 64:1986;201-213.
9. Reynaud C.A., Mackay C.R., Muller R.G., Weill J.C. Somatic generation of diversity in a mammalian primary lymphoid organ: the sheep ileal Peyer's patches. Cell. 64:1991;995-1005.
10. Reynaud C.A., Garcia C., Hein W.R., Weill J.C. Hypermutation generating the sheep immunoglobulin repertoire is an antigen-independent process. Cell. 80:1995;115-125.
11. Meyer A., Parng C.L., Hansal S.A., Osborne B.A., Goldsby R.A. Immunoglobulin gene diversification in cattle. Int Rev Immunol. 15:1997;165-183.
12. Lucier M.R., Thompson R.E., Waire J., Lin A.W., Osborne B.A., Goldsby R.A. Multiple sites of V lambda diversification in cattle. J Immunol. 161:1998;5438-5444.
13. Lillie F.R. The theory of the free-martin. Science. 43:1916;611-613.
14. Owen R.D. Immunogenetic consequences of vascular anastomoses between bovine twins. Science. 102:1945;400-401.
15. Anderson D., Billingham R.E., Lampkin G.H., Medawar P.B. The use of skin grafting to distinguish between monozygotic and dizygotic twins in cattle. Heredity. 5:1951;379-397.
16. Billingham R.E., Lampkin G.H., Medawar P.B., Williams H.L. Tolerance to homografts, twin diagnosis, and the freemartin condition in cattle. Heredity. 6:1952;201-212.
17. Wilkes P.R., Wijeratne W.V., Munro I.B. Reproductive anatomy and cytogenetics of freemartin heifers. Vet Rec. 108:1981;349-353.
18. Lillie F.R. The free-martin; a study of the action of sex hormones in the foetal life of cattle. J Exp Zool. 23:1917;371-452.
19. Vigier B., Tran D., Legeai L., Bezard J., Josso N. Origin of anti-mullerian hormone in bovine freemartin fetuses. J Reprod Fertil. 70:1984;473-479.
20. Niku M., Pessa-Morikawa T., Andersson L.C., Iivanainen A. Oligoclonal Peyer's patch follicles in the terminal small intestine of cattle. Dev Comp Immunol. 26:2002;689-695.
21. Dulac R.W., Yang T.J. Differential sodium fluoride sensitivity of alpha-naphthyl acetate esterase in human, bovine, canine and murine monocytes and lymphocytes. Exp Hematol. 19:1991;59-62.
22. Dhingra V.K., Gupta R.K.P., Sadana J.R. Demonstration of acid alpha naphtyl acetate esterase activity in bovine lymphocytes and monocytes or macrophages. Res Vet Sci. 33:1982;26-30.
23. Parsons K.R., Sopp P., Jones B.V., Bland P., Howard C.J. Identification of a molecule uniquely expressed on a (gamma)/(delta) TCR+ subset within bovine intestinal intraepithelial lymphocytes. Immunology. 87:1996;64-70.
24. Perret J., Shia Y.C., Fries R., Vassart G., Georges M. A polymorphic satellite sequence maps to the pericentric region of the bovine Y chromosome. Genomics. 6:1990;482-490.
25. Modi W.S., Gallagher D.S., Womack J.E. Molecular organization and chromosomal localization of six highly repeated DNA families in the bovine genome. Anim Biotechnol. 4:1993;143-161.
26. Hopman A.H., Ramaekers F.C., Speel E.J. Rapid synthesis of biotin-, digoxigenin-, trinitrophenyl-, and fluorochrome-labeled tyramides and their application for in situ hybridization using CARD amplification. J Histochem Cytochem. 46:1998;771-777.
27. Duhamel G.E., Bernoco D., Davis W.C., Osburn B.I. Distribution of T and B lymphocytes in mammary dry sections, colostrum and blood of adult dairy cattle. Vet Immunol Immunopathol. 14:1987;101-122.
28. Fossum C., Burny A., Portetelle D., Mammerickx M., Morein B. Detection of B and T cells with lectins or antibodies, in healthy and bovine leukemia virus-infected cattle. Vet Immunol Immunopathol. 18:1988;269-278.
29. Taylor B.C., Stott J.L., Thurmond M.A., Picanso J.P. Alteration in lymphocyte subpopulations in bovine leukosis virus-infected cattle. Vet Immunol Immunopathol. 31:1992;35-47.
30. Hayday A. γδ cells: a right time and right place for a conserved third way of protection. Annu Rev Immunol. 18:2000;975-1026.
31. Rüsse I. Lehrbuch der Embryologie der Haustiere; 1991. Parey, Berlin.
32. Schultz R.D., Dunne H.W., Heist C.E. Ontogeny of the bovine immune response. Infect Immun. 7:1973;981-991.
33. Isono S., Kadota K., Matsubara Y., Agawa H., Matsui N. Immunohistochemical studies on ontogeny of bovine lymphoid tissues. J Vet Med Sci. 53:1991;877-882.
34. Ohno S., Gropp A. Embryological basis for germ cell chimerism in mammals. Cytogenetics. 4:1965;251-261.
35. Marcum J.B., Lasley J.F., Day B.N. Variability of sex-chromosome chimerism in cattle from heterosexual multiple births. Cytogenetics. 11:1972;388-399.
36. Press C.M., Hein W.R., Landsverk T. Ontogeny of leukocyte populations in the spleen of fetal lambs with emphasis on the early prominence of B cells. Immunology. 80:1993;598-604.
37. Press C.M., Reynolds J.D., McClure S.J., Simpson-Morgan M.W., Landsverk T. Fetal lambs are depleted of IgM+ cells following a single injection of an anti-IgM antibody in early gestation. Immunol. 88:1996;28-34.
38. Mebius R.E., Miyamoto T., Christensen J., Domen J., Cupedo T., Weissman I.L., Akashi K. The fetal liver counterpart of adult common lymphoid progenitors gives rise to all lymphoid lineages CD45+CD4+CD3- cells, as well as macrophages. J Immunol. 166:2001;6593-6601.
39. Ohmura K., Kawamoto H., Fujimoto S., Ozaki S., Nakao K., Katsura Y. Emergence of T, B, and myeloid lineage-committed as well as multipotent hemopoietic progenitors in the aorta-gonad-mesonephros region of day 10 fetuses of the mouse. J Immunol. 163:1999;4788-4795.
40. Kawamoto H., Ikawa T., Ohmura K., Fujimoto S., Katsura Y. T cell progenitors emerge earlier than B cell progenitors in the murine fetal liver. Immunity. 12:2000;441-450.
41. Kondo M., Scherer T., Miyamoto T., King A.G., Akashi K., Sugamura K., Weissman I.L. Cell-fate conversion of lymphoid-committed progenitors by instructive actions of cytokines. Nature. 407:2000;383-386.
42. Reynolds J.D. Mitotic rate maturation in the Peyer's patches of fetal sheep and in the bursa of Fabricius of the chick embryo. Eur J Immunol. 17:1987;503-507.
43. Donskoy E., Goldschneider I. Thymocytopoiesis is maintained by blood-borne precursors throughout postnatal life. A study in parabiotic mice. J Immunol. 148:1992;1604-1612.
44. Cunningham C.P., Kimpton W.G., Holder J.E., Cahill R.N. Thymic export in aged sheep: a continuous role for the thymus throughout pre- and postnatal life. Eur J Immunol. 31:2001;802-811.
45. Loder F., Mutschler B., Ray R.J., Paige C.J., Sideras P., Torres R., Lamers M.C., Carsetti R.B. Cell development in the spleen takes place in discrete steps and is determined by the quality of B cell receptor-derived signals. J Exp Med. 190:1999;75-90.
46. Miyasaka M., Morris B. The ontogeny of the lymphoid system and immune responsiveness in sheep. Prog Vet Microbiol Immun. 4:1988;21-55.
47. Niku M, Ilmonen L, Pessa-Morikawa T, Iivanainen A. Limited contribution of circulating cells to the development and maintenance of nonhenatopoietic bovine tissues. Stem cells, in press.