There has been a significant interest in the effects of the gut microbiome on brain function. Reports have linked gut microbes with an array of brain disorders ranging from anorexia to autism. The gut microbe-neuron interface is therefore emerging as an attractive target to treat neurological disorders from the gut surface. Unfortunately, mechanistic explanations of how nerves sense microbes are scant. Here, I propose that enteroendocrine cells serve as sensory transducers of bacterial signals to nerves. Enteroendocrine cells are electrically excitable cells that, unlike nerves, are directly exposed to luminal ligands. Although enteroendocrine cells are commonly recognized for their role in hormone secretion, hence their name, my research team recently discovered that enteroendocrine cells form synaptic-like contacts with neurons. Some of these belong to the vagus nerve. This neural circuit between enteroendocrine cells and vagal neurons is a direct path for sensory transduction from gut to brain. A path through which bacteria signals can modulate brain function. Enteroendocrine cells of the mouse colon express bacterial toll-like receptors. These receptors are membrane proteins that recognize pathogen-associated molecular patterns. Our preliminary data show that these cells express specific members of the toll-like receptor family. Moreover, defined ligands to these receptors trigger current responses in enteroendocrine cells. With the support of a R03 Small Grant Program for NIDDK K01 awardees, our objective is to define if toll-like receptors mediate the transduction of bacterial stimuli from enteroendocrine cells to neurons. We will test the hypothesis in two specific aims: 1) to define if enteroendocrine cells are electrically excitated by toll- like receptor ligands; and 2) to determine if bacterial stimuli are transduced from enteroendocrine cells onto neurons. My laboratory has expertise in electrophysiology and transgenic animals in which enteroendocrine cells of the colon express fluorescence proteins and calcium reporters. Combined with our electrophysiology capabilities, these animal models allow us to interrogate the electrical activity of individual enteroendocrine cells both in vitro and in vivo. This project will be a foundation to unveil a neural path through which the brain senses gut bacteria.

Public Health Relevance

This research-training project is relevant to public health because understanding how gut bacteria is sensed by the brain will be a foundation to develop therapeutic treatments for behavioral disorders. Neurological disorders such as anorexia and autism are linked to gut microbes but the modes of action remain to be described .

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Small Research Grants (R03)
Project #
5R03DK114500-02
Application #
9532835
Study Section
Kidney, Urologic and Hematologic Diseases D Subcommittee (DDK)
Program Officer
Saslowsky, David E
Project Start
2017-08-01
Project End
2019-07-31
Budget Start
2018-08-01
Budget End
2019-07-31
Support Year
2
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Duke University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Liu, Hongbing; Chen, Shaowei; Yao, Xiao et al. (2018) Histone deacetylases 1 and 2 regulate the transcriptional programs of nephron progenitors and renal vesicles. Development 145:
Kaelberer, Melanie Maya; Bohórquez, Diego V (2018) Where the gut meets the brain. Brain Res 1693:127
Kaelberer, Melanie M; Bohórquez, Diego V (2018) The now and then of gut-brain signaling. Brain Res 1693:192-196
Buchanan, Kelly L; Bohórquez, Diego V (2018) You Are What You (First) Eat. Front Hum Neurosci 12:323
Kaelberer, Melanie Maya; Buchanan, Kelly L; Klein, Marguerita E et al. (2018) A gut-brain neural circuit for nutrient sensory transduction. Science 361: