Maintenance of body homeostasis is critical to survival; animals must detect and correct chemical and thermal imbalances as well as eliminate toxic compounds. Internal sensory neurons innervate various internal organs and provide information about internal physiological state to the nervous system. Internal sensory neurons are conserved across species and yet are poorly understood compared to external sensory neurons. In particular, there is a large gap in knowledge of the internal sensory neural circuitry and the underlying molecular mechanisms for detecting internal state. These gaps in our knowledge may be due to the relative complexity and genetic inaccessibility of specific subpopulations of neurons in these circuits. To overcome these challenges, we propose to combine powerful anatomic, genetic, and functional methods and provide an entry point into studying internal sensory circuits in the Drosophila nervous system. In this proposal we will build on state-of-the-art serial electron microscopy that has identified synaptic connectivity of internal sensory neuron circuits and further propose to (a) use genetically-encoded indicators of neural activity to assess activity in deep, hard-to-access internal sensory neuron populations, and (b) use powerful Drosophila genetic tools to elucidate the molecular mechanisms that mediate sensory transduction of internal sensory neurons, as well as to manipulate activity of specific subcomponents of the neural circuit to elucidate their role in maintaining physiological homeostasis.

Public Health Relevance

Homeostatic control of internal physiological state is essential for health and survival. However, the neural detection and control of internal physiology is poorly understood. We propose to characterize principles of action of a sensory-neuropeptide circuit for sensing and modulation of internal state to maintain body homeostasis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21NS105507-01A1
Application #
9616404
Study Section
Neurotransporters, Receptors, and Calcium Signaling Study Section (NTRC)
Program Officer
Churn, Severn Borden
Project Start
2018-07-01
Project End
2020-06-30
Budget Start
2018-07-01
Budget End
2019-06-30
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Physiology
Type
Schools of Medicine
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032