A major challenge for the development of mechanism-based therapeutic strategies to treat FXS is the diversity of FMRP target mRNAs, which encode proteins with a large variety of different functions in the neuron. Our recent work suggests that FMRP directly regulates intracellular signaling and protein synthesis through the PI3K/mT0R pathway, which is downstream of mGlu1/5 and other receptors, by limiting the translation and synaptic localization of pi 10p, a catalytic subunit of PI3K. The overall goal of this project is to provide experimental support for our hypothesis that dysregulated activity of the PI3K catalytic subunit p110 beta is a promising therapeutic target in FXS. These studies motivate aim 1 to investigate whether the selective genetic reduction or pharmacologic inhibition of p110 beta can rescue FX-associated phenotypes, as a novel therapeutic strategy acting at a key signaling molecule downstream of cell surface receptors. To reduce p110 beta activity, we, will (1) cross Fm1l knockout mice with mice heterozygous for p110 beta, and (2) use p110 beta selective antagonists. Since p110 beta selective inhibitors are in current clinical trials for cancers resulting from overactive PI3K, the proposed research may repurpose these available drugs for FXS. We will analyze the effect of p110 beta inhibition on FXS-associated molecular and cellular dysfunctions, and, in collaboration with Eric Klann (EAB Core), on impaired synaptic plasticity and behavior. To test the applicability of a p110 beta-based strategy in patients, we will analyze the effect of p110 beta selective inhibitors on PI3K activity and protein synthesis in induced pluripotent stem cells from FXS patients (aim 3). By integration with projects and rescue strategies from the Klann and Richter labs, and associated cores, we will employ genome wide ribosome profiling and bioinformatic analysis to test the hypothesis that inhibition/reduction of P110 beta (Bassell), S6K1 (Klann) and CPEB (Richter) reduces excess mRNA translation by correction of ribosome occupancy defects in Fmr1 KO mice (aim 2) and human iPSC-derived neurons from FXS patients (aim 3). This integrated and multidisciplinary approach will provide new insight into converging mechanisms of FMRP biology to reveal novel strategies to rescue FXS-associated phenotypes and lead to new therapeutic approaches.

Public Health Relevance

This research will elucidate a critical role for p110 beta as a mediator of dysregulated signaling and protein synthesis in fragile x syndrome (FXS), and advanced use of a novel class of p110 beta subunit selective inhibitors to correct FXS-associated phenotypes. This research will also facilitate development of PI3K signaling-targeted therapies in a broader range of brain disorders.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
1U54HD082013-01
Application #
8795362
Study Section
Special Emphasis Panel (ZHD1-DSR-Y (53))
Project Start
2014-09-22
Project End
2019-05-31
Budget Start
2014-09-22
Budget End
2015-05-31
Support Year
1
Fiscal Year
2014
Total Cost
$438,075
Indirect Cost
$16,875
Name
University of Massachusetts Medical School Worcester
Department
Type
DUNS #
603847393
City
Worcester
State
MA
Country
United States
Zip Code
01655