The long-term goal of this project is to reveal basic neurobiological mechanisms about how vagal sensory neurons find, innervate, and interact with specific end-organs and tissues during development. Sensory neurons of the vagus nerve detect and transmit diverse signals from internal organs, including ingested nutrients, changes in blood pressure, and mechanical distension of the stomach. Anatomically, it is a uniquely long cranial nerve that emanates from a single pair of ganglia near the hindbrain yet courses through the entire body and innervates a myriad of target tissues. From these ganglia, each vagal sensory neuron sprouts a single pseudounipolar axon that targets a specific internal organ peripherally and a dedicated brainstem circuit centrally. Faithfully establishing this connectivity is essential for neural control of physiological functions such as breathing, heart rate and digestion. Despite its vital role and the emerging importance of brain-viscera communication, it remains largely unknown how the intricate anatomical structure of the vagus nerve forms during development, and whether miswiring of the vagus nerve may contribute to diseases of the autonomic nervous system. This project proposes to leverage novel genetic and advanced imaging techniques to begin addressing the long-term goal by combining anatomical (Aim 1), cellular (Aim 2), and molecular (Aim 3) approaches.
Aim 1 will establish a comprehensive, high-resolution map of vagus nerve development in the context of the whole animal, by utilizing genetic labeling, tissue clearing, and high- resolution microscopy.
Aim 2 will elucidate the interplay between enteric neuron migration and vagal afferent outgrowth, by utilizing cutting- edge mouse genetics tools to selectively manipulate different cell types.
Aim 3 will identify molecular determinants of vagus nerve pathfinding, by combining publicly available data and mouse genetics tools to label and perturb candidate gene expression in vagal sensory neurons. It is becoming increasingly apparent that vagus nerve connectivity plays a role in metabolism and energy homeostasis, with implications in related disorders. Therefore, results of this project will open new lines of inquiry on how viscera-to-brain communication is established and maintained in health and disease.!

Public Health Relevance

Vital autonomic functions, such as breathing and digestion, are under tight neural control. Vagal sensory neurons convey vital information from the gut and other internal organs to the brain, yet how they are wired together during development is little understood. This project will reveal knowledge fundamental to better understanding how viscera-to-brain communication is established and maintained, and how its disruption may contribute to metabolic and digestive disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32DK117798-02
Application #
9767520
Study Section
Special Emphasis Panel (ZDK1)
Program Officer
Castle, Arthur
Project Start
2018-12-01
Project End
2021-11-30
Budget Start
2019-12-01
Budget End
2020-11-30
Support Year
2
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Harvard Medical School
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
047006379
City
Boston
State
MA
Country
United States
Zip Code