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PMID: 8567980 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Imogen 38: a novel 38-kD islet mitochondrial autoantigen recognized by T cells from a newly diagnosed type 1 diabetic patient.

The Journal of clinical investigation ·Vol. 97 ·No. 2 ·1996-01-15 ·Pages 551-61

Arden SD, Roep BO, Neophytou PI, Usac EF, Duinkerken G, de Vries RR, Hutton JC

Abstract

Cell-mediated autoimmune attack directed against islet proteins of approximately 38 kD in size has been associated with type 1 diabetes. A novel murine cDNA encoding an antigen of this size was cloned using a screening procedure based on the proliferative response of a human diabetic T cell clone (1C6) to a recombinant antigen epitope library. Membrane preparations from COS 7 cells transfected with the full-length 1,267-bp cDNA elicited a proliferative response from the reporter T cells comparable to that of the defined peptide epitope and native insulinoma antigen. In vitro translation and transfection experiments suggested that the protein is initially synthesized as a 44-kD protein and then processed to the native 38-kD form through the proteolytic removal of a 54-aa NH2-terminal mitochondrial targeting sequence. Differential centrifugation, Percoll density gradient centrifugation, and immunofluorescence studies confirmed localization of the antigen to mitochondria. Northern blot, Western blot, and 1C6 T cell proliferation assays showed that, although imogen 38 was more highly expressed in beta cell than alpha cell lines, it was also present in other tissues. It is concluded that imogen 38 may be a target for bystander autoimmune attack in diabetes rather than a primary autoantigen.

MeSH Terms
Amino Acid Sequence Animals Autoantigens/chemistry,genetics,immunology Base Sequence Cells, Cultured Cloning, Molecular DNA, Complementary/genetics Diabetes Mellitus, Type 1/immunology Fluorescent Antibody Technique, Indirect Humans Insulinoma/genetics Islets of Langerhans/immunology Lymphocyte Activation Mice Mitochondria/immunology Molecular Sequence Data Protein Processing, Post-Translational Rats Ribosomal Proteins Subcellular Fractions/chemistry T-Lymphocytes/immunology
Chemicals
Autoantigens DNA, Complementary MRPS31 protein, human Mrps31 protein, mouse Ribosomal Proteins
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Arden S D
Department of Clinical Biochemistry, University of Cambridge, Addenbrooke's Hospital, United Kingdom.
Roep B O
Neophytou P I
Usac E F
Duinkerken G
de Vries R R
Hutton J C
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Article Info
Journal
The Journal of clinical investigation
Abbr.
J Clin Invest
ISSN
0021-9738
Published
1996-01-15
Pages
551-61
Language
English
Region
United States
NLM ID
7802877
PMCID
PMC507050
Subset
IM
Grants
Wellcome Trust · United Kingdom
Databases
GENBANK
Z46966
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