| Literature DB >> 12941769 |
Xiaopei Cao1, Zhiyong Gao, Claudia E Robert, Scott Greene, Gang Xu, Weizhen Xu, Ewan Bell, Don Campbell, Yuan Zhu, Robert Young, Matteo Trucco, James F Markmann, Ali Naji, Bryan A Wolf.
Abstract
PANDER (PANcreatic DERived factor, FAM3B), a newly discovered secreted cytokine, is specifically expressed at high levels in the islets of Langerhans of the endocrine pancreas. To evaluate the role of PANDER in beta-cell function, we investigated the effects of PANDER on rat, mouse, and human pancreatic islets; the beta-TC3 cell line; and the alpha-TC cell line. PANDER protein was present in alpha- and beta-cells of pancreatic islets, insulin-secreting beta-TC3 cells, and glucagon-secreting alpha-TC cells. PANDER induced islet cell death in rat and human islets. Culture of beta-TC3 cells with recombinant PANDER had a dose-dependent inhibitory effect on cell viability. This effect was also time-dependent. PANDER caused apoptosis of beta-cells as assessed by electron microscopy, annexin V fluorescent staining, and flow-cytometric terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling assay. PANDER did not affect cytosolic Ca(2+) levels or nitric oxide levels. However, PANDER activated caspase-3. Hence, PANDER may have a role in the process of pancreatic beta-cell apoptosis.Entities:
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Year: 2003 PMID: 12941769 DOI: 10.2337/diabetes.52.9.2296
Source DB: PubMed Journal: Diabetes ISSN: 0012-1797 Impact factor: 9.461