SMAD7 enhances adult β-cell proliferation without significantly affecting β-cell function in mice

Abstract

The interplay between the transforming growth factor β (TGF-β) signaling proteins, SMAD family member 2 (SMAD2) and 3 (SMAD3), and the TGF-β-inhibiting SMAD, SMAD7, seems to play a vital role in proper pancreatic endocrine development and also in normal β-cell function in adult pancreatic islets. Here, we generated conditional SMAD7 knockout mice by crossing insulin1^Cre mice with SMAD7^fx/fx mice. We also created a β cell-specific SMAD7-overexpressing mouse line by crossing insulin1^Dre mice with HPRT-SMAD7/RosaGFP mice. We analyzed β-cell function in adult islets when SMAD7 was either absent or overexpressed in β cells. Loss of SMAD7 in β cells inhibited proliferation, and SMAD7 overexpression enhanced cell proliferation. However, alterations in basic glucose homeostasis were not detectable following either SMAD7 deletion or overexpression in β cells. Our results show that both the absence and overexpression of SMAD7 affect TGF-β signaling and modulates β-cell proliferation but does not appear to alter β-cell function. Reversible SMAD7 overexpression may represent an attractive therapeutic option to enhance β-cell proliferation without negative effects on β-cell function.

Keywords: SMAD transcription factor; SMAD7; beta cell; beta cell (B-cell); cell proliferation; cell signaling; diabetes; endocrine development; gene regulation; glucose homeostasis; glucose metabolism; pancreatic islet; transforming growth factor beta (TGF-beta).