A number of mammalian tissues possess regenerative capacity and rely on tissue-specific somatic stem cells cells for renewal. A fundamental question in the aging field is whether there is a functional decline in somatic stem cells with age and whether we can use dietary or therapeutic interventions to decelerate or reverse age-dependent decline of adult stem cell function. In this proposal, we seek to answer these questions using the mammalian intestine, which undergoes age-dependent functional decline and regenerates through pools of Lgr5+ intestinal stem cells (ISC). In preliminary studies we found that: 1) aged crypts have both decreased function and frequency of ISCs; 2) short-term starvation enhanced the capacity of organoid formation from aged crypts and induced strongly a Peroxisome Proliferator-Activated Receptor Delta program in the ISCs; 3) we can recapitulate fasting effects with the highly specific PPAR? agonist GW501516.
In Aim 1 we will use mouse genetics to determine the necessity and sufficiency of PPAR? signaling in mediating the effects of fasting in intestinal stem cells.
In Aim 2 we will utilize LC-MS and Seahorse metabolic assays to determine if mitochondrial metabolism is augmented in aged ICSs. We will also determine if CPT1A mediates augmented ISC function in the fasted state. In the independent phase and Aim3, I will examine the interplay of diet, aging and microbiota by characterizing the function and regulation of the Gasdermin C family of genes in transit-amplifying progenitor (TA) cells.

Public Health Relevance

The adult mammalian intestine is one of the first sites of nutrient sensing and is maintained and regenerated by intestinal stem cells (ISCs). Age-associated decline of intestinal stem cells may impair renewal of the intestinal epithelium and predispose the elderly population to infections, digestive disorders and malabsorption. The work in this proposal aims to understand what role nutrient sensing pathways have on intestinal regeneration and whether pharmacological or dietary interventions have therapeutic applications for intestinal homeostasis in the aging population.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Transition Award (R00)
Project #
5R00AG054760-04
Application #
9791147
Study Section
Special Emphasis Panel (NSS)
Program Officer
Kerr, Candace L
Project Start
2018-09-30
Project End
2021-05-31
Budget Start
2019-06-01
Budget End
2020-05-31
Support Year
4
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Ohio State University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
832127323
City
Columbus
State
OH
Country
United States
Zip Code
43210