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Lowering apolipoprotein CIII delays onset of type 1 diabetes

Holmberg, Rebecka (author)
Refai, Essam (author)
Karolinska Institutet
Höög, Anders (author)
Karolinska Institutet
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Crooke, Rosanne M (author)
Graham, Mark (author)
Olivecrona, Gunilla (author)
Umeå universitet,Fysiologisk kemi
Berggren, Per-Olof (author)
Karolinska Institutet
Juntti-Berggren, Lisa (author)
Karolinska Institutet
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 (creator_code:org_t)
2011-06-13
2011
English.
In: Proceedings of the National Academy of Sciences of the United States of America. - : National Academy of Sciences. - 0027-8424 .- 1091-6490. ; 108:26, s. 10685-10689
  • Journal article (peer-reviewed)
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  • Serum levels of apolipoprotein CIII (apoCIII) are increased in type 1 diabetic patients, and when β cells are exposed to these diabetic sera, apoptosis occurs, an effect abolished by an antibody against apoCIII. We have investigated the BB rat, an animal model that develops a human-like type 1 diabetes, and found that apoCIII was also increased in sera from prediabetic rats. This increase in apoCIII promoted β-cell death. The endogenous levels of apoCIII were reduced by treating prediabetic animals with an antisense against this apolipoprotein, resulting in a significantly delayed onset of diabetes. ApoCIII thus serves as a diabetogenic factor, and intervention with this apolipoprotein in the prediabetic state can arrest disease progression. These findings suggest apoCIII as a target for the treatment of type 1 diabetes.

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