Literature DB >> 5419273

Surface alloantigens of plasma cells.

T Takahashi, L J Old, E A Boyse.   

Abstract

A serological study of immunoglobulin-forming cells of the mouse, normal and malignant, shows that they lack all known surface differentiation antigens of the thymocyte-lymphocyte axis: TL, theta, Ly-A, Ly-B, and MSLA. Two systems of normal alloantigens are expressed on these cells, H-2 and a new system named PC. The gene Pca (Plasma cell antigen) which specifies PC.1 alloantigen segregates as a mendelian dominant not closely linked with H-2. This cell surface antigen is absent from thymocytes, leukemias, and very probably from thymus-derived lymphocytes also; it is present on cells of the liver, kidney, brain, and lymph nodes as well as on hemolytic plaque-forming cells of the spleen, and on myelomas. So PC.1 is properly classified as a differentiation alloantigen. The strain distribution of PC.1 does not conform to that of any known immunoglobulin allotype or cell surface alloantigen previously described. Thus the cell surface antigens of immunoglobulin-producing cells are clearly different from those of cells belonging to the thymocyte-lymphocyte axis. Each family of cells has distinctive alloantigens, and the two families share alloantigens of only one known system, H-2. This implies that either immunoglobulin-producing cells are not derived from thymic lymphocytes, or if they are, the program responsible for the transition must include extensive revision of cell surface structure.

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Year:  1970        PMID: 5419273      PMCID: PMC2138842          DOI: 10.1084/jem.131.6.1325

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


  18 in total

1.  Recent developments in peptic ulcer.

Authors:  J B KIRSNER
Journal:  Ann N Y Acad Sci       Date:  1962-02-28       Impact factor: 5.691

Review 2.  Role of the thymus and other central lymphoid tissues in immunological disease.

Authors:  M D Cooper; A E Gabrielsen; R A Good
Journal:  Annu Rev Med       Date:  1967       Impact factor: 13.739

3.  Ly-A and Ly-B: two systems of lymphocyte isoantigens in the mouse.

Authors:  E A Boyse; M Miyazawa; T Aoki; L J Old
Journal:  Proc R Soc Lond B Biol Sci       Date:  1968-06-11

4.  The G (Gross) leukemia antigen.

Authors:  L J Old; E A Boyse; E Stockert
Journal:  Cancer Res       Date:  1965-07       Impact factor: 12.701

5.  Preparation of lymphocyte-specific antibody from anti-lymphocyte serum.

Authors:  N Shigeno; U Hämmerling; C Arpels; E A Boyse; L J Old
Journal:  Lancet       Date:  1968-08-10       Impact factor: 79.321

6.  Cytolysis of mouse lymph node cells by alloantibody: a comparison of guinea-pig and rabbit complements.

Authors:  G Haughton; M P McGehee
Journal:  Immunology       Date:  1969-04       Impact factor: 7.397

7.  Use of an antiglobulin serum to detect cells producing antibody with low haemolytic efficiency.

Authors:  D W Dresser; D H Wortis
Journal:  Nature       Date:  1965-11-27       Impact factor: 49.962

Review 8.  Antigens of tumors and leukemias induced by viruses.

Authors:  L J Old; E A Boyse
Journal:  Fed Proc       Date:  1965 Sep-Oct

9.  Cytokinetics of antibody formation.

Authors:  G Sainte-Marie
Journal:  J Cell Physiol       Date:  1966-06       Impact factor: 6.384

10.  Autoradiographic studies on the immune response.I. The kinetics of plasma cell proliferation.

Authors:  G J NOSSAL; O MAKELA
Journal:  J Exp Med       Date:  1962-01-01       Impact factor: 14.307

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  84 in total

1.  Ontogeny of murine B lymphocytes: sequence of B-cell differentiation from surface-immunoglobulin-negative precursors to plasma cells.

Authors:  U Hämmerling; A F Chin; J Abbott
Journal:  Proc Natl Acad Sci U S A       Date:  1976-06       Impact factor: 11.205

2.  Differentiation of lymphoid cells: the non-mitogenic induction of immunoglobulin production by thymus cell extract and thymus cell culture filtrate.

Authors:  N Shinohara; K Okumura; M Kern
Journal:  Immunology       Date:  1976-09       Impact factor: 7.397

3.  Plasma cell membrane glycoprotein gene Pca-1 (alkaline phosphodiesterase I) is linked to the proto-oncogene Myb on mouse chromosome 10.

Authors:  M F Buckley; J W Goding
Journal:  Immunogenetics       Date:  1992       Impact factor: 2.846

4.  Identification of nucleotide pyrophosphatase/alkaline phosphodiesterase I activity associated with the mouse plasma cell differentiation antigen PC-1.

Authors:  N F Rebbe; B D Tong; E M Finley; S Hickman
Journal:  Proc Natl Acad Sci U S A       Date:  1991-06-15       Impact factor: 11.205

5.  Regulation of purified hepatic PC-1 (phosphodiesterase-I/nucleotide pyrophosphatase) by threonine auto(de)phosphorylation and by binding of acidic fibroblast growth factor.

Authors:  M Uriarte; W Stalmans; S Hickman; M Bollen
Journal:  Biochem J       Date:  1995-02-15       Impact factor: 3.857

Review 6.  Subline divergence within L.C. Strong's C3H and CBA inbred mouse strains. A review.

Authors:  A C Whitmore; S P Whitmore
Journal:  Immunogenetics       Date:  1985       Impact factor: 2.846

7.  Differentiation of lymphoid cells: evidence for a B-cell specific serum suppressor.

Authors:  M Kern
Journal:  Immunology       Date:  1978-07       Impact factor: 7.397

8.  Involvement of a surface concanavalin A-binding glycoprotein in the adhesion of Trichomonas vaginalis to substrates.

Authors:  P Cappuccinelli; I Cagliani; G Cavallo
Journal:  Experientia       Date:  1975-10-15

9.  Phosphorylation and nucleotide-dependent dephosphorylation of hepatic polypeptides related to the plasma cell differentiation antigen PC-1.

Authors:  M Uriarte; W Stalmans; S Hickman; M Bollen
Journal:  Biochem J       Date:  1993-07-01       Impact factor: 3.857

10.  Adherence of Trichomonas vaginalis to cell culture monolayers.

Authors:  M G Martinotti; P Martinetto; D Savoia
Journal:  Eur J Clin Microbiol       Date:  1986-06       Impact factor: 3.267

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