Jeremy N. Kay
Associate Professor of Neurobiology
We study how neural circuits devoted to specific visual processing tasks arise during development of the retina, and the consequences for circuit function when development goes wrong. The tools of mouse genetics are central to our approach, and we draw on a wide range of molecular, genetic, and imaging methods.
Current Appointments & Affiliations
- Associate Professor of Neurobiology, Neurobiology, Basic Science Departments 2020
- Associate Professor in Ophthalmology, Ophthalmology, Clinical Science Departments 2020
- Associate Professor in Cell Biology, Cell Biology, Basic Science Departments 2021
- Associate of the Duke Initiative for Science & Society, Duke Science & Society, Initiatives 2017
- Affiliate of the Duke Regeneration Center, Regeneration Next Initiative, Basic Science Departments 2021
Contact Information
- 2351 Erwin Rd, Aeri 5004, Durham, NC 27705
- Box 3802, Duec, Durham, NC 27710
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jeremy.kay@duke.edu
(919) 660-7432
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Kay Lab
- Background
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Education, Training, & Certifications
- Ph.D., University of California - San Francisco 2004
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Previous Appointments & Affiliations
- Assistant Professor in Cell Biology, Cell Biology, Basic Science Departments 2019 - 2021
- Assistant Professor in Ophthalmology, Ophthalmology, Clinical Science Departments 2012 - 2020
- Assistant Professor of Neurobiology, Neurobiology, Basic Science Departments 2012 - 2020
- Investigator Duke Institute for Brain Sciences, Duke Institute for Brain Sciences, University Institutes and Centers 2012 - 2016
- Recognition
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In the News
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AUG 8, 2022 -
SEP 21, 2021 Office of Faculty Advancement -
JUN 24, 2014 -
FEB 18, 2014
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Awards & Honors
- Expertise
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Subject Headings
- Research
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Selected Grants
- Training Program in Developmental and Stem Cell Biology awarded by National Institutes of Health 2001 - 2027
- Cell and Molecular Biology Training Program awarded by National Institutes of Health 2021 - 2026
- Genetic and Genomics Training Grant awarded by National Institutes of Health 2020 - 2025
- Precise assembly of retinal circuitry through rejection of inappropriate synaptic partners awarded by National Institutes of Health 2021 - 2024
- Neurobiology Training Program awarded by National Institutes of Health 2019 - 2024
- Bridging gap in comparative biology using the tree shrew visual system awarded by National Institutes of Health 2021 - 2023
- Astrocyte-specific Molecular Cues in Retinal Angiogensis awarded by Hartwell Foundation 2021 - 2023
- Duke CTSA (TL1) Year 5 awarded by National Institutes of Health 2018 - 2023
- Evaluation of CRB1-B AAV therapyin preventing photoreceptor death in murine models awarded by Vedere Bio II, Inc. 2021 - 2023
- Molecular and cellular strategies to rescue visual impairment in CRB1 disease awarded by Foundation Fighting Blindness, Inc 2019 - 2022
- Mechanisms of naturally-occurring astrocyte death during development awarded by National Institutes of Health 2019 - 2022
- Repulsive mechanisms for spatial segregation of developing neural circuits awarded by National Institutes of Health 2017 - 2020
- Muller glial dysfunction in retinal edema awarded by National Institutes of Health 2016 - 2020
- Organization and Function of Cellular Structure awarded by National Institutes of Health 1975 - 2020
- Molecular control of neuronal position during retinal development awarded by National Institutes of Health 2014 - 2019
- Molecular cues for visual circuit assembly in developing retina awarded by Pew Charitable Trusts 2014 - 2019
- Molecular & cellular cues for circuit assembly in mouse retina awarded by National Institutes of Health 2016 - 2019
- Basic predoctoral training in neuroscience awarded by National Institutes of Health 1992 - 2018
- Cell-cell recognition mechanisms for neural circuit wiring in the retina awarded by Alfred P. Sloan Foundation 2014 - 2016
- NEI Mentored Clinical Scientist Development Program Award (K12) awarded by National Institutes of Health 2004 - 2016
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External Relationships
- Opus Genetics
- Rejuvitas
- Vedere Bio II
- Publications & Artistic Works
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Selected Publications
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Academic Articles
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Wang, Yuchen, et al. “Adhesion GPCR Latrophilin 3 regulates synaptic function of cone photoreceptors in a trans-synaptic manner.” Proc Natl Acad Sci U S A, vol. 118, no. 45, Nov. 2021. Pubmed, doi:10.1073/pnas.2106694118.Full Text Link to Item
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Paisley, Caitlin E., and Jeremy N. Kay. “Seeing stars: Development and function of retinal astrocytes.” Dev Biol, vol. 478, Oct. 2021, pp. 144–54. Pubmed, doi:10.1016/j.ydbio.2021.07.007.Full Text Link to Item
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Perelli, Robin M., et al. “Environmental oxygen regulates astrocyte proliferation to guide angiogenesis during retinal development.” Development, vol. 148, no. 9, May 2021. Pubmed, doi:10.1242/dev.199418.Full Text Link to Item
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Ray, Thomas A., et al. “Comprehensive identification of mRNA isoforms reveals the diversity of neural cell-surface molecules with roles in retinal development and disease.” Nat Commun, vol. 11, no. 1, July 2020, p. 3328. Pubmed, doi:10.1038/s41467-020-17009-7.Full Text Link to Item
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Luo, Lin, et al. “Optimizing Nervous System-Specific Gene Targeting with Cre Driver Lines: Prevalence of Germline Recombination and Influencing Factors.” Neuron, vol. 106, no. 1, Apr. 2020, pp. 37-65.e5. Pubmed, doi:10.1016/j.neuron.2020.01.008.Full Text Link to Item
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Peng, Yi-Rong, et al. “Binary Fate Choice between Closely Related Interneuronal Types Is Determined by a Fezf1-Dependent Postmitotic Transcriptional Switch.” Neuron, vol. 105, no. 3, Feb. 2020, pp. 464-474.e6. Pubmed, doi:10.1016/j.neuron.2019.11.002.Full Text Link to Item
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Puñal, Vanessa M., et al. “Large-scale death of retinal astrocytes during normal development is non-apoptotic and implemented by microglia.” Plos Biol, vol. 17, no. 10, Oct. 2019, p. e3000492. Pubmed, doi:10.1371/journal.pbio.3000492.Full Text Link to Item
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O’Koren, Emily G., et al. “Microglial Function Is Distinct in Different Anatomical Locations during Retinal Homeostasis and Degeneration.” Immunity, vol. 50, no. 3, Mar. 2019, pp. 723-737.e7. Pubmed, doi:10.1016/j.immuni.2019.02.007.Full Text Link to Item
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Ray, Thomas A., et al. “The Enigma of CRB1 and CRB1 Retinopathies.” Adv Exp Med Biol, vol. 1185, 2019, pp. 251–55. Pubmed, doi:10.1007/978-3-030-27378-1_41.Full Text Link to Item
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Prigge, Cameron L., and Jeremy N. Kay. “Dendrite morphogenesis from birth to adulthood.” Curr Opin Neurobiol, vol. 53, Dec. 2018, pp. 139–45. Pubmed, doi:10.1016/j.conb.2018.07.007.Full Text Link to Item
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Ray, Thomas A., et al. “Formation of retinal direction-selective circuitry initiated by starburst amacrine cell homotypic contact.” Elife, vol. 7, Apr. 2018. Pubmed, doi:10.7554/eLife.34241.Full Text Open Access Copy Link to Item
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O’Sullivan, Matthew L., et al. “Astrocytes follow ganglion cell axons to establish an angiogenic template during retinal development.” Glia, vol. 65, no. 10, Oct. 2017, pp. 1697–716. Pubmed, doi:10.1002/glia.23189.Full Text Link to Item
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Wang, Jingjing, et al. “Anatomy and spatial organization of Müller glia in mouse retina.” J Comp Neurol, vol. 525, no. 8, June 2017, pp. 1759–77. Pubmed, doi:10.1002/cne.24153.Full Text Link to Item
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Kay, Jeremy N. “Radial migration: Retinal neurons hold on for the ride.” J Cell Biol, vol. 215, no. 2, Oct. 2016, pp. 147–49. Pubmed, doi:10.1083/jcb.201609135.Full Text Link to Item
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Redmond, Stephanie A., et al. “Somatodendritic Expression of JAM2 Inhibits Oligodendrocyte Myelination.” Neuron, vol. 91, no. 4, Aug. 2016, pp. 824–36. Pubmed, doi:10.1016/j.neuron.2016.07.021.Full Text Link to Item
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Visser, Jasper J., et al. “An extracellular biochemical screen reveals that FLRTs and Unc5s mediate neuronal subtype recognition in the retina.” Elife, vol. 4, Dec. 2015, p. e08149. Pubmed, doi:10.7554/eLife.08149.Full Text Link to Item
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Lefebvre, Julie L., et al. “Development of dendritic form and function.” Annu Rev Cell Dev Biol, vol. 31, 2015, pp. 741–77. Pubmed, doi:10.1146/annurev-cellbio-100913-013020.Full Text Link to Item
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Whitney, Irene E., et al. “Sox2 regulates cholinergic amacrine cell positioning and dendritic stratification in the retina.” J Neurosci, vol. 34, no. 30, July 2014, pp. 10109–21. Pubmed, doi:10.1523/JNEUROSCI.0415-14.2014.Full Text Link to Item
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Ford, Kevin J., et al. “A role for TREK1 in generating the slow afterhyperpolarization in developing starburst amacrine cells.” J Neurophysiol, vol. 109, no. 9, May 2013, pp. 2250–59. Pubmed, doi:10.1152/jn.01085.2012.Full Text Link to Item
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Kay, Jeremy N., et al. “MEGF10 and MEGF11 mediate homotypic interactions required for mosaic spacing of retinal neurons.” Nature, vol. 483, no. 7390, Mar. 2012, pp. 465–69. Pubmed, doi:10.1038/nature10877.Full Text Link to Item
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Kay, Jeremy N., et al. “Neurod6 expression defines new retinal amacrine cell subtypes and regulates their fate.” Nat Neurosci, vol. 14, no. 8, July 2011, pp. 965–72. Pubmed, doi:10.1038/nn.2859.Full Text Link to Item
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Kay, Jeremy N., et al. “Retinal ganglion cells with distinct directional preferences differ in molecular identity, structure, and central projections.” J Neurosci, vol. 31, no. 21, May 2011, pp. 7753–62. Pubmed, doi:10.1523/JNEUROSCI.0907-11.2011.Full Text Link to Item
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Voinescu, P. Emanuela, et al. “Birthdays of retinal amacrine cell subtypes are systematically related to their molecular identity and soma position.” J Comp Neurol, vol. 517, no. 5, Dec. 2009, pp. 737–50. Pubmed, doi:10.1002/cne.22200.Full Text Link to Item
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Muto, A., et al. “Forward genetic analysis of visual behavior in zebrafish.” Plos Genetics, vol. 1, no. 5, Dec. 2005, pp. 575–88.
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Kay, Jeremy N., et al. “Staggered cell-intrinsic timing of ath5 expression underlies the wave of ganglion cell neurogenesis in the zebrafish retina.” Development, vol. 132, no. 11, June 2005, pp. 2573–85. Pubmed, doi:10.1242/dev.01831.Full Text Link to Item
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Kay, Jeremy N., et al. “Transient requirement for ganglion cells during assembly of retinal synaptic layers.” Development, vol. 131, no. 6, Mar. 2004, pp. 1331–42. Pubmed, doi:10.1242/dev.01040.Full Text Link to Item
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Kay, J. N., et al. “Retinal ganglion cell genesis requires lakritz, a Zebrafish atonal Homolog.” Neuron, vol. 30, no. 3, June 2001, pp. 725–36. Pubmed, doi:10.1016/s0896-6273(01)00312-9.Full Text Link to Item
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Kay, J. N., and M. Blum. “Differential response of ventral midbrain and striatal progenitor cells to lesions of the nigrostriatal dopaminergic projection.” Dev Neurosci, vol. 22, no. 1–2, 2000, pp. 56–67. Pubmed, doi:10.1159/000017427.Full Text Link to Item
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Kay, J. N., et al. “Trophic effects of androgen: development and hormonal regulation of neuron number in a sexually dimorphic vocal motor nucleus.” J Neurobiol, vol. 40, no. 3, Sept. 1999, pp. 375–85.Link to Item
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Book Sections
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Kay, Jeremy N., and Joshua R. Sanes. “Development of Retinal Arbors and Synapses.” NEW VISUAL NEUROSCIENCES, 2014, pp. 1291–304.Link to Item
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Other Articles
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Ray, Thomas, et al. Formation of retinal direction-selective circuitry initiated by starburst amacrine cell homotypic contact. 18 Dec. 2017. Epmc, doi:10.1101/235978.Full Text
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Ray, Thomas A., and Jeremy N. Kay. “Following directions from the retina to the brain.” Neuron, vol. 86, no. 4, 20 May 2015, pp. 855–57. Pubmed, doi:10.1016/j.neuron.2015.05.017.Full Text Link to Item
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Voinescu, P. E., et al. “Birthdays of retinal amacrine cell subtypes are systematically related to their molecular identity and soma position (The Journal of Comparative Neurology (2009) 517, (737-750)).” Journal of Comparative Neurology, vol. 518, no. 2, 15 Jan. 2010, p. 254. Scopus, doi:10.1002/cne.22253.Full Text
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Kay, Jeremy N., and Herwig Baier. “Out-foxing fate; molecular switches create neuronal diversity in the retina.” Neuron, vol. 43, no. 6, 16 Sept. 2004, pp. 759–60. Pubmed, doi:10.1016/j.neuron.2004.09.001.Full Text Link to Item
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Conference Papers
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Kay, Jeremy N., and Megan Stogsdill. “Starburst amacrine cells orchestrate assembly of retinal direction-selective circuitry.” Investigative Ophthalmology & Visual Science, vol. 56, no. 7, ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2015.Link to Item
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- Teaching & Mentoring
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Recent Courses
- NEUROBIO 393: Research Independent Study 2023
- NEUROBIO 790S: Student Seminar (Topics) 2023
- NEUROBIO 393: Research Independent Study 2022
- NEUROBIO 790S: Student Seminar (Topics) 2022
- NEUROSCI 391: Neuroscience Independent Scholarship 1: Advanced Topics 2022
- NEUROSCI 493: Research Independent Study 1 2022
- UPGEN 778D: University Program in Genetics and Genomics Biological Solutions Module IV 2022
- NEUROBIO 393: Research Independent Study 2021
- NEUROBIO 790S: Student Seminar (Topics) 2021
- NEUROBIO 793: Research in Neurobiology 2021
- UPGEN 778B: University Program in Genetics and Genomics Biological Solutions Module Il 2021
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