Abstrakt
Cytokine-induced apoptosis is recognised as a major cause of the decline in β-cell mass that ultimately leads to type 1 diabetes mellitus. Interleukin-1β, interferon-γ and tumour necrosis factor-α in conjunction initiate a series of events that lead to β-cell apoptosis; important among these is NO production. The glycosphingolipid sulfatide is present in β-cells in the secretory granules in varying amounts and is secreted together with insulin. We now investigate whether sulfatide is able to protect insulin-producing cells against the pro-apoptotic effect of interleukin-1β, interferon-γ and tumour necrosis factor-α.
Originalsprog | Engelsk |
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Tidsskrift | Diabetes - Metabolism: Research and Reviews (Print Edition) |
Vol/bind | 26 |
Udgave nummer | 8 |
Sider (fra-til) | 631-8 |
Antal sider | 8 |
ISSN | 1520-7552 |
DOI | |
Status | Udgivet - 1 nov. 2010 |