Recent advances in imaging technology are opening doors to a whole new dimension of study for the neurosciences. Phenomena that were once deuced from in situ, biochemical, and genetic approaches are now being directly observed in the context of native environments, and in real time. The amount of information contained in the 3- and 4-dimensional images obtained by today's technology is enormous, and if extracted, these data can reveal valuable mechanistic insight into a host of neurobiological processes. However, the business of imaging analysis has moved far beyond the days of visual evaluation of 2D photographic print and the skill sets needed to data mine 3 and 4D digital data are often not within the scope of a biologist's available resources and expertise. Indeed, digital imaging analysis of today has become a sophisticated scientific discipline in and of itself, employing principles from mathematics, computer science and physics. Consequently, despite the powerful advancements in imaging capability, the wealth of information contained in images remains untapped in many cases. The purpose of the Quantitative Imaging Core will be to provide training and assistance in methods for quantitative analysis of microscopic images. Because the potential for applying quantitation to microscopic images depends in large part on optimizing experimental design and imaging parameters, providing training in proper image acquisition will be an inherent part of the core's mission. The Core's scope will include, but not be limited to, optimizing analysis strategies for the quantification of identified cells during migration and differentiation, quantification of dendritic spines, 3D reconstruction of intracellularly stained neurons, and quantification of dynamic microscopic data from calcium imaging experiments. As much of the work of our faculty leads to primary data in the form of images or image sequences, we propose to use the core not only to promote the quantitative analysis of imaging data for SNRP-investigators, but will extend our expertise to the general Neurobiology community at UTSA.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
5U54NS060658-05
Application #
8381132
Study Section
Special Emphasis Panel (ZNS1-SRB-P)
Project Start
Project End
2014-07-31
Budget Start
2012-08-01
Budget End
2013-07-31
Support Year
5
Fiscal Year
2012
Total Cost
$69,586
Indirect Cost
$20,253
Name
University of Texas Health Science Center San Antonio
Department
Type
DUNS #
800189185
City
San Antonio
State
TX
Country
United States
Zip Code
78249
Gaval-Cruz, Meriem; Goertz, Richard B; Puttick, Daniel J et al. (2016) Chronic loss of noradrenergic tone produces ?-arrestin2-mediated cocaine hypersensitivity and alters cellular D2 responses in the nucleus accumbens. Addict Biol 21:35-48
Goertz, Richard Brandon; Wanat, Matthew J; Gomez, Jorge A et al. (2015) Cocaine increases dopaminergic neuron and motor activity via midbrain ?1 adrenergic signaling. Neuropsychopharmacology 40:1151-62
Takano-Maruyama, Masumi; Chen, Yiju; Gaufo, Gary O (2012) Differential contribution of Neurog1 and Neurog2 on the formation of cranial ganglia along the anterior-posterior axis. Dev Dyn 241:229-41
Chen, Yiju; Moon, Anne M; Gaufo, Gary O (2012) Influence of mesodermal Fgf8 on the differentiation of neural crest-derived postganglionic neurons. Dev Biol 361:125-36
Ko, D; Wilson, C J; Lobb, C J et al. (2012) Detection of bursts and pauses in spike trains. J Neurosci Methods 211:145-58
Chen, Yiju; Takano-Maruyama, Masumi; Fritzsch, Bernd et al. (2012) Hoxb1 controls anteroposterior identity of vestibular projection neurons. PLoS One 7:e34762
Chen, Yiju; Takano-Maruyama, Masumi; Gaufo, Gary O (2011) Plasticity of neural crest-placode interaction in the developing visceral nervous system. Dev Dyn 240:1880-8
Morikawa, H; Paladini, C A (2011) Dynamic regulation of midbrain dopamine neuron activity: intrinsic, synaptic, and plasticity mechanisms. Neuroscience 198:95-111
Lobb, Collin J; Wilson, Charles J; Paladini, Carlos A (2011) High-frequency, short-latency disinhibition bursting of midbrain dopaminergic neurons. J Neurophysiol 105:2501-11
Ko, Daijin; Windle, Brad (2011) Enriching for correct prediction of biological processes using a combination of diverse classifiers. BMC Bioinformatics 12:189

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