Loss of IDO1 Expression From Human Pancreatic β-Cells Precedes Their Destruction During the Development of Type 1 Diabetes
Author(s) -
Florence Anquetil,
Giada Mondanelli,
Nathaly Gonzalez,
Teresa Rodríguez-Calvo,
Jose Zapardiel Gonzalo,
Lars Krogvold,
Knut DahlJørgensen,
Benoı̂t Van den Eynde,
Ciriana Orabona,
Ursula Grohmann,
Matthias G. von Herrath
Publication year - 2018
Publication title -
diabetes
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.219
H-Index - 330
eISSN - 1939-327X
pISSN - 0012-1797
DOI - 10.2337/db17-1281
Subject(s) - pancreatic islets , autoantibody , demise , type 1 diabetes , diabetes mellitus , insulin , endocrinology , medicine , indoleamine 2,3 dioxygenase , type 2 diabetes , islet , biology , immunology , antibody , biochemistry , tryptophan , amino acid , political science , law
Indoleamine 2,3 dioxygenase-1 (IDO1) is a powerful immunoregulatory enzyme that is deficient in patients with type 1 diabetes (T1D). In this study, we present the first systematic evaluation of IDO1 expression and localization in human pancreatic tissue. Although IDO1 was constitutively expressed in β-cells from donors without diabetes, less IDO1 was expressed in insulin-containing islets from double autoantibody-positive donors and patients with recent-onset T1D, although it was virtually absent in insulin-deficient islets from donors with T1D. Scatter plot analysis suggested that IDO1 decay occurred in individuals with multiple autoantibodies, prior to β-cell demise. IDO1 impairment might therefore contribute to β-cell demise and could potentially emerge as a promising therapeutic target.
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