[PAST EVENT] Nikolas Vann, Applied Science - Ph.D. Dissertation Defense
LocationISC3 (Integrated Science Center), Room 1280
540 Landrum Dr
Williamsburg, VA 23185Map this location
Access & Features
- Open to the public
Title: "Role of Dbx1-derived pre-B?tzinger complex interneurons in breathing behaviors of adult mice."
Abstract: Breathing is a rhythmic motor behavior essential to sustain homeostasis and life itself in humans and all terrestrial mammals. A specialized neuronal network is responsible for generating and controlling the rhythm and pattern for breathing. The core rhythm-generating microcircuit in particular is located within a site dubbed the preB?tzinger complex (preB?tC). The preB?tC is a heterogeneous region containing neurons with both respiratory and non-respiratory activity that express excitatory and inhibitory transmitters, peptide transmitters, and peptide receptors. More recently, preB?tC neurons have been characterized by molecular genetics. The excitatory transmitter phenotype, and peptide and peptide receptors, commonly used to define the respiratory core oscillator within the preB?tC are properties associated with neurons whose precursors express the embryonic transcription factor, developing brain homeobox 1 (Dbx1). Our lab, and our French colleagues, hypothesized that neurons derived from the Dbx1-expressing precursor cells (Dbx1 neurons) form the core microcircuit for inspiration breathing rhythm, that is, the Dbx1 core hypothesis. Evidence from many labs supports the Dbx1 core hypothesis at embryonic and neonatal stages of development. However, the role of Dbx1 neurons in adult animals remains incompletely understood. Furthermore, contemporary data suggests the portfolio of functions for brainstem Dbx1 neurons includes premotor and arousal-related functions, which casts doubt on the veracity of the Dbx1 core hypothesis. Here I investigate the role of Dbx1 neurons in adult animals with intact sensorimotor integration systems using intersectional mouse genetics to express light-responsive membrane proteins to excite or depress Dbx1 neurons while simultaneous measuring breathing. Using these light-sensitive proteins to manipulate Dbx1 neuron function to depress or stop breathing, enhance breathing, and alter the precise timing of inspiratory breaths, I offer evidence that affirms the Dbx1 core hypothesis. I conclude that Dbx1 preB?tC neurons are essential for breathing and form the respiratory core oscillator in adult mice. Knowing the cellular point of origin for breathing behavior gives us a target to study the cellular and synaptic mechanisms to this key physiological behavior and provides general insight into rhythmic networks and physiological brain function.
Bio: Nikolas Vann was raised in Chesterfield, Virginia. He earned a B.S. in Physics from Longwood University in Farmville, Virginia in 2012. He the began his graduate study in William & Mary in the fall of 2012 under the direction of Dr. Christopher Del Negro. His research focused on understanding the of role neurons derived from the Dbx1 gene in forming the pattern and rhythm of breathing.