Assistant Professor of Neurobiology
The primary goal of our research is to determine the role(s) that neuromodulators such as acetylcholine, noradrenaline, serotonin, and oxytocin play in specifying functional connectivity across the wired circuitry of the brain, and how this dynamic circuit specification supports flexible behavior.
Key questions we are working on in the lab at the moment include:
- When and how do acetylcholine and serotonin determine which information makes it into the primary visual cortex (V1) from the thalamus. This is a critical question because you’re very limited in the ways that you can make decisions based on visual information if it does not make it into the cortex.
- What is (are?) the ligand(s) for dopamine receptors in V1, given that these receptors are found in all layers, but dopaminergic axons are only found in layers 1 and 6. If the ligand is not dopamine from the ventral tegmental area (VTA), this changes profoundly what dopamine signaling in V1 is likely ‘for’. If it *is* dopamine from the VTA, how does traverse the 1+mm from layer 1 or 6 to receptors in the middle layers of cortex on a time scale relevant for behavior?
- How do oxytocin and acetylcholine modulate feedback into V1 from higher visual areas? How does this modulation modify receptive fields?
- Over what spatial and temporal scale is acetylcholine released into V4 during a visual attention task? And how does this relate to attention-related changes in spiking activity?
Other questions we are interested in include the ways that modulatory systems signal to each other to enable homeostatic control of state-specifying extracellular signals in cortex? And how does the extracellular space influence diffusion of modulators beyond synapses? How do gonadal hormones such as estrogen interact with modulatory systems? What happens to neuromodulatory signaling as we age?
We are a question-driven lab, and so the techniques we employ are diverse: we use a novel biosensor that combines classical electrophysiological recording capabilities with the ability to measure the local chemical environment at high spatial and temporal resolution; we combine electrophysiological recording with pharmacological manipulation to examine causal relationships between neuromodulation, neuronal activity and behavioral performance; and we study the structure of neuromodulatory systems in the neocortex from a comparative perspective at both the light and electron microscopic levels.
Cell and Molecular Biology Training Program awarded by National Institutes of Health (Mentor). 2021 to 2026
RNA-programmable cell type targeting and manipulation across vertebrate nervous systems awarded by National Institutes of Health (Co Investigator). 2021 to 2024
Neurobiology Training Program awarded by National Institutes of Health (Mentor). 2019 to 2024
Bi-directional, task-dependent control of thalamic input gain, in layer 4c of the primary visual cortex, by the cholinergic and serotonergic neuromodulatory systems awarded by National Institutes of Health (Principal Investigator). 2019 to 2024
Muscarinic-type 2 acetylcholine receptor expression and distribution in macaque early vision; evaluating a candidate model species for Alzheimer's Disease awarded by Ruth K. Broad Biomedical Research Foundation (Principal Investigator). 2020 to 2021
Disney, Anita A. “Neuromodulatory Control of Early Visual Processing in Macaque.” Annual Review of Vision Science, vol. 7, Sept. 2021, pp. 181–99. Epmc, doi:10.1146/annurev-vision-100119-125739. Full Text
Hawken, Michael J., et al. “Functional Clusters of Neurons in Layer 6 of Macaque V1.” J Neurosci, vol. 40, no. 12, Mar. 2020, pp. 2445–57. Pubmed, doi:10.1523/JNEUROSCI.1394-19.2020. Full Text
Disney, Anita A., and Michael J. Higley. “Diverse Spatiotemporal Scales of Cholinergic Signaling in the Neocortex.” J Neurosci, vol. 40, no. 4, Jan. 2020, pp. 720–25. Pubmed, doi:10.1523/JNEUROSCI.1306-19.2019. Full Text
Disney, Anita A., and Jason S. Robert. “Translational implications of the anatomical nonequivalence of functionally equivalent cholinergic circuit motifs.” Proc Natl Acad Sci U S A, Dec. 2019. Pubmed, doi:10.1073/pnas.1902280116. Full Text
Krueger, Juliane, and Anita A. Disney. “Structure and function of dual-source cholinergic modulation in early vision.” J Comp Neurol, vol. 527, no. 3, Feb. 2019, pp. 738–50. Pubmed, doi:10.1002/cne.24590. Full Text
Coppola, Jennifer, and Anita Disney. Most calbindin-immunoreactive neurons, but few calretinin-immunoreative neurons, express the m1 acetylcholine receptor in the middle temporal visual area of the macaque monkey. Feb. 2018. Epmc, doi:10.1101/271924. Full Text
MacDougall, Matthew, et al. “Optogenetic manipulation of neural circuits in awake marmosets.” Journal of Neurophysiology, vol. 116, no. 3, American Physiological Society, Sept. 2016, pp. 1286–94. Crossref, doi:10.1152/jn.00197.2016. Full Text
Coppola, Jennifer J., et al. “Modulatory compartments in cortex and local regulation of cholinergic tone.” J Physiol Paris, vol. 110, no. 1–2, Sept. 2016, pp. 3–9. Pubmed, doi:10.1016/j.jphysparis.2016.08.001. Full Text
Disney, Anita A., et al. “A multi-site array for combined local electrochemistry and electrophysiology in the non-human primate brain.” J Neurosci Methods, vol. 255, Nov. 2015, pp. 29–37. Pubmed, doi:10.1016/j.jneumeth.2015.07.009. Full Text
Disney, Anita A., et al. “Muscarinic acetylcholine receptors are expressed by most parvalbumin-immunoreactive neurons in area MT of the macaque.” Brain Behav, vol. 4, no. 3, May 2014, pp. 431–45. Pubmed, doi:10.1002/brb3.225. Full Text