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Apolipoprotein CIII promotes Ca2+-dependent beta cell death in type 1 diabetes.
Juntti-Berggren, Lisa; Refai, Essam; Appelskog, Ioulia; Andersson, Mats; Imreh, Gabriela; Dekki, Nancy; Uhles, Sabine; Yu, Lina; Griffiths, William J; Zaitsev, Sergei; Leibiger, Ingo; Yang, Shao-Nian; Olivecrona, Gunilla; Jörnvall, Hans; Berggren, Per-Olof.
Afiliação
  • Juntti-Berggren L; Department of Molecular Medicine, Rolf Luft Center for Diabetes Research, Karolinska Institutet, SE-171 76 Stockholm, Sweden. lisa.juntti-berggren@molmed.ki.se
Proc Natl Acad Sci U S A ; 101(27): 10090-4, 2004 Jul 06.
Article em En | MEDLINE | ID: mdl-15210953
ABSTRACT
In type 1 diabetes (T1D), there is a specific destruction of the insulin secreting pancreatic beta cell. Although the exact molecular mechanisms underlying beta cell destruction are not known, sera from T1D patients have been shown to promote Ca(2+)-induced apoptosis. We now demonstrate that apolipoprotein CIII (apoCIII) is increased in serum from T1D patients and that this serum factor both induces increased cytoplasmic free intracellular Ca(2+) concentration ([Ca(2+)](i)) and beta cell death. The apoCIII-induced increase in [Ca(2+)](i) reflects an activation of the voltage-gated L-type Ca(2+) channel. Both the effects of T1D sera and apoCIII on the beta cell are abolished in the presence of antibody against apoCIII. Increased serum levels of apoCIII can thus account for the increase in beta cell [Ca(2+)](i) and thereby beta cell apoptosis associated with T1D.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Apolipoproteínas C / Cálcio / Ilhotas Pancreáticas / Apoptose / Diabetes Mellitus Tipo 1 Limite: Adult / Animals / Female / Humans / Male Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2004 Tipo de documento: Article País de afiliação: Suécia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Apolipoproteínas C / Cálcio / Ilhotas Pancreáticas / Apoptose / Diabetes Mellitus Tipo 1 Limite: Adult / Animals / Female / Humans / Male Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2004 Tipo de documento: Article País de afiliação: Suécia
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