Wnt signaling regulates pancreatic [beta] cell proliferation

There is widespread interest in defining factors and mechanisms that stimulate proliferation of pancreatic islet cells. Wnt signaling is an important regulator of organ growth and cell fates, and genes encoding Wnt-signaling factors are expressed in the pancreas. However, it is unclear whether Wnt signaling regulates pancreatic islet proliferation and differentiation. Here we provide evidence that Wnt signaling stimulates islet [beta] cell proliferation. The addition of purified Wnt3a protein to cultured [beta] cells or islets promoted expression of Pitx2, a direct target of Wnt signaling, and Cyclin D2, an essential regulator of [beta] cell cycle progression, and led to increased [beta] cell proliferation in vitro. Conditional pancreatic [beta] cell expression of activated [beta]-catenin, a crucial Wnt signal transduction protein, produced similar phenotypes in vivo, leading to [beta] cell expansion, increased insulin production and serum levels, and enhanced glucose handling. Conditional [beta] cell expression of Axin, a potent negative regulator of Wnt signaling, led to reduced Pitx2 and Cyclin D2 expression by [beta] cells, resulting in reduced neonatal [beta] cell expansion and mass and impaired glucose tolerance. Thus, Wnt signaling is both necessary and sufficient for islet [beta] cell proliferation, and our study provides previously unrecognized evidence of a mechanism governing endocrine pancreas growth and function. Cyclin D2 | diabetes mellitus | islets of Langerhans | pancreas | Pitx2