Background: Dendritic arbor shape and functional properties emerge from the interaction of many complex developmental processes. It is now accepted that multiple local-level interactions of cytoskeleton elements direct the growth and development of the dendrite arbor. However, the specific mechanisms that control developmental acquisition of final functional dendritic properties are largely unknown. Addressing this fundamental question requires novel data driven systems-biology tools to study developmental and biophysical mechanisms in the same neuronal model. A tightly-knit collaboration between molecular genetics, quantitative morphometry, and mathematical simulation can for the first time enable large-scale studies capable of achieving holistic understanding of the mechanisms underlying emergent features of the arbor. Project Goals: The main neuroscientific goal of this project is to understand how multiple local interactions of cytoskeleton components during differentiation define mature dendritic arbor shape and its functional integrative properties, using Drosophila sensory neurons as a model. The technological goal of this project is to develop a novel investigative approach that integrates and extends previously separate approaches from developmental biology &genetics, in vivo confocal imaging &electrophysiology, computer vision, and neuroanatomical modeling.
Specific Aims : We propose 3 tightly integrated specific aims.
Aim 1 : use genetic manipulations and electrophysiological recordings to model the role of cytoskeletal organization and dynamics as a fundamental determinant of emergent dendrite arbor shape and function.
Aim 2 : Implement advanced 4D multi-parameter imaging protocols and automated algorithms to reconstruct the arbor, and quantify spatial and temporal associations among multiple sub-cellular components.
Aim 3 : using automated reconstructions &measurements from aim 2, statistically characterize the structural and cytoskeletal features of dendrite arbors, and stochastically simulate the growth and electrotonic properties of anatomically realistic virtual neuronal analogues. The data from aim 3 will feed back novel hypotheses to be tested by a subsequent repetition of the (aim 1 - aim 2 - aim 3) cycle. Approach: We will focus on a single model system - Drosophila dendritic arborization (da) sensory neurons. More specifically, we will investigate class I and class IV da neuron arborization based upon their radically distinct dendritic morphologies (simple vs. complex) and underlying cytoskeletal organizations. We will make fusion constructs of cytoskeleton components with spectrally distinct fluorescent proteins. These will be used in transgenic Drosophila in order to quantitatively measure the distribution of F-actin, microtubules, and microtubule polarity within the dendrite arbor throughout its development in vivo using confocal multi-fluor imaging. The resulting images will be processed by automated quantitative computer vision algorithms that will accurately extract the topology of the dendritic arbor, and it changes over time. We will use the resulting maps in neuroanatomical stochastic simulations to establish the links between the emergent morphometrics of the dendrite and specific cytoskeleton features at various developmental stages. Intellectual Merit: From a neurogenetics perspective, this project will pioneer the use of cytoskeletal features as putative fundamental determinants in statistical neuroanatomical models. These determinants will be linked to morphological determinants. From a computational perspective, this project will advance the state of the art in automated algorithms for delineating neuroanatomy (and its morphological dynamics) by deploying core technologies for large-scale multi-parameter studies, and result in an effective interfacing of automated reconstruction and simulation technologies. With this innovation, model predictions can be tested by molecular biological techniques, and findings of statistical models can be used to inform molecular models of dendrite arbor development. Educational Impact: This project will result in a cross-disciplinary training of post-doctoral fellows, graduate students, undergraduate students and high school interns. It will result in practical insight on ways to conduct cutting-edge systems-level scientific research overcoming disciplinary boundaries and using best-available collaborative tools. The trainees from this program will be uniquely positioned to develop the broader field of imaging-driven integrative systems neurobiology. It will expose minority and K-12 students to a new world of trans-disciplinary research that is indicative of the future. Broader Impacts: The combined body of molecular, imaging, and computational tools and datasets from this research will be disseminated widely, and made available to a broad class of investigators for adoption in the study of other major neuroscience problems. This project will serve as a new model for computationally enabled neuroscience research that achieves a long-desired synergy between the wet lab and computation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
7R01NS086082-02
Application #
8697162
Study Section
Special Emphasis Panel (ZRG1-IFCN-B (50))
Program Officer
Liu, Yuan
Project Start
2013-07-15
Project End
2018-06-30
Budget Start
2014-09-01
Budget End
2015-06-30
Support Year
2
Fiscal Year
2014
Total Cost
$333,533
Indirect Cost
$69,563
Name
Georgia State University
Department
Neurosciences
Type
Schools of Arts and Sciences
DUNS #
837322494
City
Atlanta
State
GA
Country
United States
Zip Code
30302