Understanding the mechanisms that regulate pancreatic beta-cell development is critical to the development of novel approaches to enhance regeneration and viability of beta-cells in patients with Type1 Diabetes. Our recent studies suggest key roles for two cell cycle genes, p57kip2 and cyclin D2, in differentiation and proliferation of pancreatic beta-cells during embryonic and postnatal life. Our goal in these collaborative R01 proposals is to explore further the roles of p57 kip2 and cyclin D2 in postnatal a-cell neogenesis and proliferation using novel """"""""gain of function"""""""" approaches.
Our Specific Aims are (1) To determine if postnatal a-cell neogenesis originates from the epithelial cells of the ducts and the role of p57kip2 expression in mediating post-natal beta-cell differentiation; these studies will use the combination of a novel model in which epithelial cells of the pancreatic ducts are derived from the transplanted bone marrow of GFP transgenic mice, and lentiviral vectors to express p57kip2; (2) To determine whether constitutive expression of cyclin D2 is sufficient to induce post natal beta-cell replication; these studies will use both in vitro (viral vector mediated gene expression in islet cultures) and in vivo (inducible expression of cyclin D2 in transgenic mice) models. These collaborative R01 applications bring together three investigators from the fields of developmental biology of the pancreas (Dr. Anil Bhushan), hematopoietic stem cell biology (Dr. Gay Crooks) and gene transfer and expression using viral vectors (Dr. Donald Kohn). The combination of expertise provided by this diverse group of investigators generates a unique opportunity for innovative and synergistic research relevant to Type 1 Diabetes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
1R01DK068719-01
Application #
6826761
Study Section
Special Emphasis Panel (ZDK1-GRB-1 (M1))
Program Officer
Sato, Sheryl M
Project Start
2004-07-05
Project End
2006-06-30
Budget Start
2004-07-05
Budget End
2005-06-30
Support Year
1
Fiscal Year
2004
Total Cost
$228,450
Indirect Cost
Name
Children's Hospital of Los Angeles
Department
Type
DUNS #
052277936
City
Los Angeles
State
CA
Country
United States
Zip Code
90027
Wang, Xiuli; Ge, Shundi; Crooks, Gay M (2009) Fluorescent immunohistochemistry and in situ hybridization analysis of pancreas. Methods Mol Biol 560:191-201
Shaw, K L; Pais, E; Ge, S et al. (2009) Lentiviral vectors with amplified beta cell-specific gene expression. Gene Ther 16:998-1008
Rountree, C Bart; Wang, Xuli; Ge, Shundi et al. (2007) Bone marrow fails to differentiate into liver epithelium during murine development and regeneration. Hepatology 45:1250-60
Wang, Xiuli; Ge, Shundi; Gonzalez, Ignacio et al. (2006) Formation of pancreatic duct epithelium from bone marrow during neonatal development. Stem Cells 24:307-14
Ge, Shundi; Crooks, Gay M; McNamara, George et al. (2006) Fluorescent immunohistochemistry and in situ hybridization analysis of mouse pancreas using low-power antigen-retrieval technique. J Histochem Cytochem 54:843-7