Literature DB >> 2579132

Polymorphism and tissue distribution of maternally transmitted antigen defined by cytotoxic T lymphocyte lines.

R Smith, R R Rich.   

Abstract

We have developed cytotoxic T lymphocyte (CTL) lines specific for two determinants of the maternally transmitted antigen (Mta) and have used these CTL lines to study the tissue distribution of Mta. In previous reports, we characterized CTL lines specific for the Mta.1 determinant. Here, we describe CTL lines specific for the newly defined Mta.2 determinant. Mta.2-specific CTL lines lysed target cells from F1 mice of an NZB (Mtf beta) mother but did not lyse target cells from reciprocal F1 mice of any Mtf alpha mother. Backcross mice were used as the source of target cells to demonstrate that the Mta.2-specific CTL were H-2 nonrestricted in their recognition. Mta.-1- and Mta.2-specific CTL lines were used to demonstrate Mta expression on lymphoid cells taken from spleen, thymus, lymph nodes, and bone marrow. In addition, Mta was expressed on cultured cell lines of myeloid, epithelial, and mesenchymal origin. Our results suggest that Mta is not a differentiation marker restricted to lymphocyte subpopulations.

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Year:  1985        PMID: 2579132

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  6 in total

1.  Mitochondrial modulation of maternally transmitted antigen: analysis of cell hybrids.

Authors:  M M Huston; R Smith; R Hull; D P Huston; R R Rich
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

2.  An unexpectedly labile mitochondrially encoded protein is required for Mta expression.

Authors:  A C Han; J R Rodgers; R R Rich
Journal:  Immunogenetics       Date:  1989       Impact factor: 2.846

3.  Unglycosylated Mtaa expresses an Mtab-like determinant.

Authors:  A C Han; J R Rodgers; R R Rich
Journal:  Immunogenetics       Date:  1987       Impact factor: 2.846

Review 4.  Susceptibility genetics of systemic lupus erythematosus.

Authors:  H H Shen; R J Winchester
Journal:  Springer Semin Immunopathol       Date:  1986

5.  Availability of endogenous peptides limits expression of an M3a-Ld major histocompatibility complex class I chimera.

Authors:  J M Vyas; R R Rich; D D Howell; S M Shawar; J R Rodgers
Journal:  J Exp Med       Date:  1994-01-01       Impact factor: 14.307

6.  Specialized functions of MHC class I molecules. I. An N-formyl peptide receptor is required for construction of the class I antigen Mta.

Authors:  S M Shawar; R G Cook; J R Rodgers; R R Rich
Journal:  J Exp Med       Date:  1990-03-01       Impact factor: 14.307

  6 in total

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