Identification of protein disulfide isomerase and calreticulin as autoimmune antigens in LEC strain of rats

Long Evans Cinnamon (LEC) rats, showing spontaneous hereditary hepatitis and hepatic carcinoma, were found to possess autoimmune antibodies to liver microsomal proteins, particularly to proteins with the molecular weight of 56kD and 55kD. The anbodies occurred in association with acute lethal hepati...

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Published inBiochimica et biophysica acta Vol. 1158; no. 3; pp. 339 - 344
Main Authors Yokoi, Tsuyoshi, Nagayama, Sekio, Kajiwara, Rieko, Kawaguchi, Yasuro, Horiuchi, Ryuya, Kamataki, Tetsuya
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 28.11.1993
Elsevier
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ISSN0304-4165
0006-3002
1872-8006
DOI10.1016/0304-4165(93)90033-5

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Abstract Long Evans Cinnamon (LEC) rats, showing spontaneous hereditary hepatitis and hepatic carcinoma, were found to possess autoimmune antibodies to liver microsomal proteins, particularly to proteins with the molecular weight of 56kD and 55kD. The anbodies occurred in association with acute lethal hepatitis in the LEC rats in our previous study. Two-dimensional immunoblot analysis of the antigenic proteins revealed that the 56kD and 55kD proteins showed 4.2 and 4.0 pI values and were estimated to be protein disulfide isomerase (PDI) and calreticulin, respectively, from NH 2-terminal amino acid sequence analysis. These proteins were further identified by immunoblot analyses using proteins and specific antibodies. PDI was a major autoimmune antigenic protein.
AbstractList Long Evans Cinnamon (LEC) rats, showing spontaneous hereditary hepatitis and hepatic carcinoma, were found to possess autoimmune antibodies to liver microsomal proteins, particularly to proteins with the molecular weight of 56kD and 55kD. The antibodies occurred in association with acute lethal hepatitis in the LEC rats in our previous study. Two-dimensional immunoblot analysis of the antigenic proteins revealed that the 56kDa and 55kDa proteins showed 4.2 and 4.0 pI values and were estimated to be protein disulfide isomerase (PDI) and calreticulin, respectively, from NH2-terminal amino acid sequence analysis. These proteins were further identified by immunoblot analyses using purified proteins and specific antibodies. PDI was a major autoimmune antigenic protein.
Long Evans Cinnamon (LEC) rats, showing spontaneous hereditary hepatitis and hepatic carcinoma, were found to possess autoimmune antibodies to liver microsomal proteins, particularly to proteins with the molecular weight of 56kD and 55kD. The antibodies occurred in association with acute lethal hepatitis in the LEC rats in our previous study. Two-dimensional immunoblot analysis of the antigenic proteins revealed that the 56kDa and 55kDa proteins showed 4.2 and 4.0 pI values and were estimated to be protein disulfide isomerase (PDI) and calreticulin, respectively, from NH2-terminal amino acid sequence analysis. These proteins were further identified by immunoblot analyses using purified proteins and specific antibodies. PDI was a major autoimmune antigenic protein.Long Evans Cinnamon (LEC) rats, showing spontaneous hereditary hepatitis and hepatic carcinoma, were found to possess autoimmune antibodies to liver microsomal proteins, particularly to proteins with the molecular weight of 56kD and 55kD. The antibodies occurred in association with acute lethal hepatitis in the LEC rats in our previous study. Two-dimensional immunoblot analysis of the antigenic proteins revealed that the 56kDa and 55kDa proteins showed 4.2 and 4.0 pI values and were estimated to be protein disulfide isomerase (PDI) and calreticulin, respectively, from NH2-terminal amino acid sequence analysis. These proteins were further identified by immunoblot analyses using purified proteins and specific antibodies. PDI was a major autoimmune antigenic protein.
Long Evans Cinnamon (LEC) rats, showing spontaneous hereditary hepatitis and hepatic carcinoma, were found to possess autoimmune antibodies to liver microsomal proteins, particularly to proteins with the molecular weight of 56kD and 55kD. The anbodies occurred in association with acute lethal hepatitis in the LEC rats in our previous study. Two-dimensional immunoblot analysis of the antigenic proteins revealed that the 56kD and 55kD proteins showed 4.2 and 4.0 pI values and were estimated to be protein disulfide isomerase (PDI) and calreticulin, respectively, from NH 2-terminal amino acid sequence analysis. These proteins were further identified by immunoblot analyses using proteins and specific antibodies. PDI was a major autoimmune antigenic protein.
Author Yokoi, Tsuyoshi
Kawaguchi, Yasuro
Horiuchi, Ryuya
Nagayama, Sekio
Kamataki, Tetsuya
Kajiwara, Rieko
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Issue 3
Keywords LEC rats
Calreticulin
Autoimmune
Autoantigen
Protein isomerase
Intramolecular oxidoreductases
Rat
Enzyme
Antibody
Liver
Rodentia
Microsome
Vertebrata
Isomerases
Mammalia
Protein disulfide-isomerase
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Snippet Long Evans Cinnamon (LEC) rats, showing spontaneous hereditary hepatitis and hepatic carcinoma, were found to possess autoimmune antibodies to liver microsomal...
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SubjectTerms Amino Acid Sequence
Animals
Antigens - immunology
Antigens - isolation & purification
Autoantibodies - analysis
Autoantibodies - immunology
Autoantigen
Autoimmune
Autoimmunity
Autoimmunity (experimental aspects and models)
Biological and medical sciences
Calcium-Binding Proteins - immunology
Calcium-Binding Proteins - isolation & purification
Calreticulin
Cell Membrane - enzymology
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Hepatitis - immunology
Intracellular Membranes - enzymology
Isomerases - immunology
Isomerases - isolation & purification
LEC rats
Microsomes, Liver - enzymology
Molecular Sequence Data
Protein Disulfide-Isomerases
Protein isomerase
Rats
Rats, Inbred Strains
Ribonucleoproteins - immunology
Ribonucleoproteins - isolation & purification
Title Identification of protein disulfide isomerase and calreticulin as autoimmune antigens in LEC strain of rats
URI https://dx.doi.org/10.1016/0304-4165(93)90033-5
https://www.ncbi.nlm.nih.gov/pubmed/8251535
https://www.proquest.com/docview/76108881
Volume 1158
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