Cellular and Developmental Neuroscience
Ball State University
Department of Biology
OUR RESEARCH
Serotonin neurons regulate many behavioral functions such as mood, appetite, sleep, and cognition. Abnormalities in the morphology of these neurons have recently been implicated as contributing factors in behavioral disorders, yet the cellular mechanisms underlying these abnormalities are unclear. The powerful genetic tools available in Drosophila allow us to manipulate cellular and molecular function of these specific neurons during development. Together with a variety of emerging techniques such as Brainbow circuit analysis, Expansion Microscopy, and live-cell imaging, we seek to take an exciting new look at the developing nervous system in the hope of understanding how abnormalities in the serotonin system arise.
PROJECTS
SEROTONIN AUTOREGULATION OF SEROTONERGIC AXON MORPHOLOGY
In vivo circuit analysis
In addition to its established role as a neurotransmitter, serotonin signaling via autoreceptors is believed to affect axon branch morphology during development. We are currently using genetic and pharmacological methods to tune serotonin levels during development. Doing so in Brainbow flies will allow us to reconstruct how these manipulations affect the final morphology of serotonergic axons.
SEROTONIN AUTOREGULATION OF SEROTONERGIC AXON MORPHOLOGY
In vitro intracellular analysis
While current methods for primary neuronal culture of Drosophila neurons are valuable for studying general cellular and molecular mechanisms of function, they often require the plating of neuroblasts or unidentified neuronal types. In order to tease apart the cellular mechanisms of serotonin autoregulation, however, we need to ensure neurons of interest are true serotonergic neurons. We are therefore developing methods that can yield differentiated serotonergic neurons in culture from the developing Drosophila embryo and/or larva.
SPATIAL PATTERNING OF SEROTONERGIC NEURONS
In vivo circuit analysis
Work by others suggests that serotonergic neurons use cell-autonomous mechanisms to establish their regions of innervation in the target neuropil, yet the mechanisms are as yet unidentified. We are combining Expansion Microscopy with Brainbow labeling in mutant flies to examine the genetic basis for axonal patterning in the Drosophila ventral nerve cord.
OUR APPROACH
See the following publications for further details of our methods
MULTISPECTRAL TRACING IN DENSELY LABELED MOUSE BRAIN WITH NTRACER
Roossien DH, Sadis BV*, Yan Y*, Webb JM*, Min LY, Dizaji AS, Bogart LJ, Mazuski C, Huth RS, Stecher JS, Akula S, Shen F, Xiao T, Vandenbrink M, Lichtman JW, Hensch TK, Herzog ED, Cai D Bioinformatics 2019;35:3544-3546
IMAGING NEURAL ARCHITECTURE IN BRAINBOW SAMPLES
Roossien DH, Cai D Methods in Molecular Biology 2017;1642:211-228
DROSOPHILA GROWTH CONES ADVANCE BY FORWARD TRANSLOCATION OF THE NEURONAL CYTOSKELETAL MESHWORK IN VIVO.
DH Roossien, P Lamoureux, D Van Vactor, KE Miller - PLoS One, 2013
Please navigate here to see a full list of publications.
GET IN TOUCH
Contact Roossien Lab to discuss their published work, teaching, collaboration opportunities or for any other inquiries.