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Also, the adenylate cyclase activator forskolin (10 µM) did not affect oxygen consumption in mouse islets (data not shown).
Similar results were observed in mouse islets (data not shown).
INS-1 cells express Tcf19 protein at a level that is similar to the mouse β-cell line MIN6, and both cell lines have moderately increased Tcf19 protein relative to mouse islets (data not shown).
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In agreement with the immunofluorescence data from mouse islets, IGF-1R protein was present in β- but not α-cell lines (Figure 3C).
Application of the workflow for analysis of the mouse islet RNA-Seq data resulted in a splice junction database containing approximately 32,000 (B6) and 20,000 (CAST) splice junction polypeptides.
By contrast, we have previously detected Pask mRNA in mouse islets and MIN6 cells [ 18], data recently confirmed by others [ 20].
Our data also revealed that in mouse islets, Etv1 was strongly expressed in α-cells and Mlxipl was strongly expressed in β-cells.
In the pancreas samples of the Tg(RIP-luc) mice, luciferase-positive cells were only detected in islets (data not shown).
Similar results were obtained with 50 nmol/l wortmannin in MIN6 cells, pseudoislets and mouse islets, whereas 1 μmol/l wortmannin was required to obtain inhibition in human islets (data not shown).
In mouse islets hypoglycemia but not hyperglycemia increased the Bax/Bcl-2 ratio (p<0.01) (data not shown).
These data further suggest that those observed phenotypes in FGF21-KO mouse islets are due, at least in part, to the removal of FGF21 inhibition on islet GH signaling.
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