Literature DB >> 308984

Adaptive differentiation of murine lymphocytes. I. Both T and B lymphocytes differentiating in F1 transplanted to parental chimeras manifest preferential cooperative activity for partner lymphocytes derived from the same parental type corresponding to the chimeric host.

D H Katz, B J Skidmore, L R Katz, C A Bogowitz.   

Abstract

The concept of adaptive (selective) differentiation preducts that early differentiation of lymphocytes is conditioned by the environment in which such differentiation takes place. These processes appear to involve selection of lymphocytes according to their self-recognition between interacting lymphocytes is, at least in part, controlled by major histocompatibility complex-linked genes, then adaptive differentiation is also controlled by these genes. In these studies, we have tested the capacities of helper T lymphocytes and hapten-specific B lymphocytes primed in the environments of various combinations of bone marrow chimeras prepared between two parental strains (i.e. A/J and BALB/c) and their corresponding F1 hybrid (CAF1) to interact with primed B and T lymphocytes derived from conventional parent and F1 donors as well as all of the corresponding bone marrow chimera combinations. The results demonstrate clearly that (a) F1 transplanted to F1 chimeric lymphocytes display no restriction in terms of cooperative activity with all of the various partner cell combinations; (b) parent transplanted to F1 chimeric lymphocytes manifest effective cooperative activity only for partner cells from F) or parental donors corresponding to the haplotype of the original bone marrow donor, thereby behaving phenotypically just like conventional parental lymphocytes; and (c) F1 transplanted to parent chimeric lymphocytes display restricted haplotype preference in cooperating best with partner lymphocytes sharing the H-2 haplotype, either entirely or codomimantly, of the parental chimeric host. The implications of these findings for understanding certain controlling mechanisms for lymphocyte differentiation are discussed.

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Year:  1978        PMID: 308984      PMCID: PMC2184998          DOI: 10.1084/jem.148.3.727

Source DB:  PubMed          Journal:  J Exp Med        ISSN: 0022-1007            Impact factor:   14.307


  36 in total

1.  In a radiation chimaera, host H-2 antigens determine immune responsiveness of donor cytotoxic cells.

Authors:  M J Bevan
Journal:  Nature       Date:  1977-09-29       Impact factor: 49.962

2.  Cooperation of nonsyngeneic tolerant lymphocytes: genetic restriction.

Authors:  M Marusić; J W Goodman; S G Shinpock
Journal:  Cell Immunol       Date:  1977-09       Impact factor: 4.868

3.  The role of the histocompatibilty gene complex in lymphocyte defferetiation.

Authors:  D H Katz
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1977

Review 4.  Functional specificity of thymus- dependent lymphocytes.

Authors:  W E Paul; B Benacerraf
Journal:  Science       Date:  1977-03-25       Impact factor: 47.728

5.  The role of the histocompatibility gene complex in lymphocyte differentiation.

Authors:  D H Katz
Journal:  Transplant Proc       Date:  1976-09       Impact factor: 1.066

6.  Cell interactions between histoincompatible T an B lymphocytes. IX. The failure of histoincompatible cells is not due to suppression and cannot be circumvented by carrier-priming T cells with allogeneic macrophages.

Authors:  D H Katz; N Chiorazzi; J McDonald; L R Katz
Journal:  J Immunol       Date:  1976-11       Impact factor: 5.422

Review 7.  Conditions determining the generation and expression of T helper cells.

Authors:  H Waldmann
Journal:  Immunol Rev       Date:  1977       Impact factor: 12.988

8.  The lymphoreticular system in triggering virus plus self-specific cytotoxic T cells: evidence for T help.

Authors:  R M Zinkernagel; G N Callahan; A Althage; S Cooper; J W Streilein; J Klein
Journal:  J Exp Med       Date:  1978-03-01       Impact factor: 14.307

9.  On the thymus in the differentiation of "H-2 self-recognition" by T cells: evidence for dual recognition?

Authors:  R M Zinkernagel; G N Callahan; A Althage; S Cooper; P A Klein; J Klein
Journal:  J Exp Med       Date:  1978-03-01       Impact factor: 14.307

10.  Allotype-specific analysis of anti-(Tyr,Glu)-Ala-Lys antibodies produced by Ir-1A high and low responder chimeric mice.

Authors:  J L Press; H O McDevitt
Journal:  J Exp Med       Date:  1977-12-01       Impact factor: 14.307

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  26 in total

1.  Idiotypic and anti-idiotypic B-B cell interaction is controlled by major histocompatibility complex-restricted regulation.

Authors:  S Bitoh; S Fujimoto; H Yamamoto
Journal:  Immunology       Date:  1989-04       Impact factor: 7.397

2.  Major histocompatibility complex-restricted recognition by B lymphocytes and accessory cells.

Authors:  R J Hodes; K S Hathcock; A Singer
Journal:  Surv Immunol Res       Date:  1983

3.  Self Ia-recognizing T cells undergo an ordered series of interactions with Ia-bearing substrate cells of defined function during their development: a model.

Authors:  C A Janeway; M E Katz
Journal:  Surv Immunol Res       Date:  1984

4.  H-2 restriction as a consequence of intentional priming: T cells of fully allogeneic chimeric mice as well as of normal mice respond to foreign antigens in the context of H-2 determinants not encountered on thymic epithelial cells.

Authors:  H Stockinger; K Pfizenmaier; C Hardt; H Rodt; M Röllinghoff; H Wagner
Journal:  Proc Natl Acad Sci U S A       Date:  1980-12       Impact factor: 11.205

Review 5.  T cell recognition of antigen in vivo: role of the H-2 complex.

Authors:  J Sprent; R Korngold; K Molnar-Kimber
Journal:  Springer Semin Immunopathol       Date:  1980-08

6.  Genetic control of the immune response to collagen. II. Antibody responses produced in fetal liver restored radiation chimeras and thymus reconstituted F1 hybrid nude mice.

Authors:  S M Hedrick; J Watson
Journal:  J Exp Med       Date:  1979-09-19       Impact factor: 14.307

7.  Analysis of contact sensitivity to 2,4-dinitrofluorobenzene (DNFB) in allogeneic bone marrow chimaera in mice.

Authors:  R Yasumizu; K Onoé; K Iwabuchi; M Ogasawara; L Geng; K Morikawa
Journal:  Immunology       Date:  1985-01       Impact factor: 7.397

8.  Immunization with SV40-transformed cells yields mainly MHC-restricted monoclonal antibodies.

Authors:  B G Froscher; N R Klinman
Journal:  J Exp Med       Date:  1986-07-01       Impact factor: 14.307

9.  Antigen recognition. V. Requirement for histocompatibility between antigen-presenting cell and B cell in the response to a thymus-dependent antigen, and lack of allogeneic restriction between T and B cells.

Authors:  E Nisbet-Brown; B Singh; E Diener
Journal:  J Exp Med       Date:  1981-09-01       Impact factor: 14.307

10.  Murine syngeneic mixed lymphocyte response. I. Target antigens are self Ia molecules.

Authors:  L H Glimcher; D L Longo; I Green; R H Schwartz
Journal:  J Exp Med       Date:  1981-11-01       Impact factor: 14.307

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