Project Summary/ Abstract The gradual loss of insulin-producing beta cells of the endocrine pancreas is common to all forms of diabetes. Elucidating transcriptional complexes that increase our understanding of underlying mechanisms governing pancreatic beta-cell development and function is critical for the development of novel therapeutics that will improve beta-cell function. Loss- and gain-of-function mouse studies have demonstrated critical roles of transcription factors in regulating the establishment and function of beta cells. Preliminary data from our lab and others suggest Lhx1, a LIM-homeodomain transcription factor, is expressed and functions in the developing and adult pancreas. Over the next three years, I propose to investigate in detail the role of Lhx1 in regulating beta-cell development and function using beta cell lines as well as a newly developed conditional knockout model. I hypothesize that Lhx1 is a regulator of endocrine cell development and function. In Aim 1, I will characterize Lhx1 expression at specific developmental and postnatal stages. In Aim 2, I will determine Lhx1 gene regulatory mechanisms in beta cells. In Aim 3, I will characterize the effects of Lhx1 ablation in the developing and adult pancreas using pancreas-specific cre/lox knockout approaches.

F31DK111181

2017-07-01

2021-06-30