Literature DB >> 6198384

Antibodies from patients with mixed connective tissue disease react with heterogeneous nuclear ribonucleoprotein or ribonucleic acid (hnRNP/RNA) of the nuclear matrix.

M J Fritzler, R Ali, E M Tan.   

Abstract

The sera of patients with mixed connective tissue disease (MCTD) have high titers of antibodies directed against nuclear U1-ribonucleoprotein (U1-RNP). This antigen is easily extracted from nuclear preparations with physiologic saline and from tissue sections with 0.1 HCl, leaving the nucleic acids and nuclear matrix behind. When U1-RNP is extracted from HEp-2 cells with 0.1 N HCl, the sera of 32/32 patients with MCTD react with another antigen that is exposed by the extraction procedure. This antigen is not destroyed by trypsin and deoxyribonuclease 1 treatment but is sensitive to both purified ribonuclease A and purified micrococcal nuclease. Absorption studies showed that the antibody reacting with this antigen cannot be absorbed by sheep red blood cells coated with extracts of rabbit thymus that contain U1-RNP. Radioimmunoassay showed that the reaction of the unadsorbed antibody was with heterogeneous nuclear ribonucleoprotein or ribonucleic acid (hnRNP/RNA) and not with transfer RNA or ribosomal RNA. The hnRNP/RNA antigen is demonstrated as discrete particles in the internucleolar chromatin of interphase cells, but in metaphase cells the antigen is diffusely dispersed. The distribution, solubility, and biochemical characteristics suggest that the antigenic moiety is part of the nuclear matrix. Therefore, MCTD sera contain antibodies that react with at least two species of nuclear RNP: small nuclear RNP (snRNP), as described by others, and a high m.w. hnRNP/RNA bound to the nuclear matrix.

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Year:  1984        PMID: 6198384

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


  8 in total

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Authors:  J Craft; T Mimori; T L Olsen; J A Hardin
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2.  Autoantibodies to purified nuclear proteins related to DNA metabolism during ageing and in SLE patients.

Authors:  G C Astaldi Ricotti; M Pazzaglia; A M Martelli; A Cerino; M Bestagno; A Caprelli; S Riva; M A Pedrini; A Facchini
Journal:  Immunology       Date:  1987-07       Impact factor: 7.397

Review 3.  Oxygen free radicals and systemic autoimmunity.

Authors:  H Ahsan; A Ali; R Ali
Journal:  Clin Exp Immunol       Date:  2003-03       Impact factor: 4.330

4.  Purification and partial sequencing of the nuclear autoantigen RA33 shows that it is indistinguishable from the A2 protein of the heterogeneous nuclear ribonucleoprotein complex.

Authors:  G Steiner; K Hartmuth; K Skriner; I Maurer-Fogy; A Sinski; E Thalmann; W Hassfeld; A Barta; J S Smolen
Journal:  J Clin Invest       Date:  1992-09       Impact factor: 14.808

Review 5.  Diversity and origin of rheumatologic autoantibodies.

Authors:  M J Fritzler; M Salazar
Journal:  Clin Microbiol Rev       Date:  1991-07       Impact factor: 26.132

6.  Purification of hnRNP from HeLa cells with a monoclonal antibody and its application in ELISA: detection of autoantibodies.

Authors:  C Gelpi; J L Rodriguez-Sanchez; J A Hardin
Journal:  Clin Exp Immunol       Date:  1988-02       Impact factor: 4.330

7.  Autoantibodies to the URNP particles: relationship to clinical diagnosis and nephritis.

Authors:  M Reichlin; W J Van Venrooij
Journal:  Clin Exp Immunol       Date:  1991-02       Impact factor: 4.330

8.  Quantitation of anti-RNP and anti-Sm antibodies in MCTD and SLE patients by immunoblotting.

Authors:  W J Habets; D J de Rooij; M H Hoet; L B van de Putte; W J van Venrooij
Journal:  Clin Exp Immunol       Date:  1985-02       Impact factor: 4.330

  8 in total

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