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Novel pancreatic beta cell-specific proteins : Antibody-based proteomics for identification of new biomarker candidates

Lindskog, Cecilia (author)
Uppsala universitet,Molekylär och morfologisk patologi,Science for Life Laboratory, SciLifeLab
Korsgren, Olle (author)
Uppsala universitet,Klinisk immunologi,Science for Life Laboratory, SciLifeLab
Pontén, Fredrik (author)
Uppsala universitet,Molekylär och morfologisk patologi,Science for Life Laboratory, SciLifeLab
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Eriksson, Jan W (author)
Department of Molecular and Clinical Medicine, Sahlgrenska University Hospital, Gothenburg, Sweden
Johansson, Lars (author)
Uppsala universitet,Enheten för radiologi,Institutionen för immunologi, genetik och patologi,Science for Life Laboratory, SciLifeLab
Danielsson, Angelika (author)
Uppsala universitet,Enheten för radiologi,Klinisk immunologi,Science for Life Laboratory, SciLifeLab
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 (creator_code:org_t)
Elsevier BV, 2012
2012
English.
In: Journal of Proteomics. - : Elsevier BV. - 1874-3919 .- 1876-7737. ; 75:9, s. 2611-2620
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Beta cell-specific surface targets are required for non-invasive monitoring of beta cell mass, which could be used for evaluation of new diabetes treatments as well as to help unravel pathogenic mechanisms underlying beta cell dysfunction. By antibody-based proteomics, we have identified and explored a set of islet cell-specific proteins. A search algorithm in the Human Protein Atlas was set up for identification of islet-specific proteins that yielded 27 hits, of which twelve showed a clear membranous expression pattern or had predicted transmembrane regions. The specificity of the identified proteins was investigated by immunohistochemical staining of pancreas sections from diabetic and non-diabetic subjects. No expression of these antigens could be detected in the exocrine pancreas. Colocalization with insulin and glucagon was further determined by confocal microscopy using isolated human islets. All antibodies specifically stained human islets and colocalization analysis revealed that four proteins were exclusively expressed in beta cells. Importantly, these antibodies were negative in sections from subjects with long-standing type 1 diabetes. In the present study, we present four proteins; DGCR2, GBF1, GPR44 and SerpinB10, the expression of which has not previously been described in beta cells.

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