Wallace B. Thoreson

Dr. Wallace B. Thoreson

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Research Focus & Metrics

Academic Career Length

39Years (1988-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2006 in Developmental Biology
Verified
Journal Article
Closed access
ADAni V. Das
Ani V. Das
KMKavita B. Mallya
Kavita B. Mallya
XZXing Zhao
Xing Zhao
FAFaraz Ahmad
Faraz Ahmad
SBSumitra Bhattacharya
Sumitra Bhattacharya
IAIqbal Ahmad
Iqbal Ahmad

1 September 2012 in Progress in Retinal and Eye Research
Verified
Journal Article
Closed access
WTWallace B. Thoreson
Wallace B. Thoreson
SMStuart C. Mangel
Stuart C. Mangel

1 November 2005 in Progress in Retinal and Eye Research
Verified
Journal Article
Closed access
Ruth HeidelbergerRuth Heidelberger
Ruth Heidelberger
WTWallace B. Thoreson
Wallace B. Thoreson
PWPaul Witkovsky
Paul Witkovsky

1 November 1999 in Progress in Retinal and Eye Research
Verified
Journal Article
Closed access
WTWallace B. Thoreson
Wallace B. Thoreson
PWP Witkovsky
P Witkovsky

1 May 2004 in Neuron
Verified
Journal Article
Closed access
WTWallace B. Thoreson
Wallace B. Thoreson
KRKatalin Rabl
Katalin Rabl
ETEllen Townes-Anderson
Ellen Townes-Anderson
Ruth HeidelbergerRuth Heidelberger
Ruth Heidelberger

24 July 2011 in Nature Neuroscience
Verified
Journal Article
Open access
PDF file
JSJosefin Snellman
Josefin Snellman
BMBhupesh Mehta
Bhupesh Mehta
NBNorbert Babai
Norbert Babai
TBTheodore M Bartoletti
Theodore M Bartoletti
WAWendy Akmentin
Wendy Akmentin
David ZenisekDavid Zenisek
David Zenisek
The authors find that acute disruption of synaptic ribbons reduces both sustained and transient components of neurotransmitter release in mouse bipolar cells and salamander cones. However, this does not affect ribbon ultrastructure or its ability to localize synaptic vesicles to the active zone. In vision, balance and hearing, sensory receptor cells translate sensory stimuli into electrical signals whose amplitude is graded with stimulus intensity. The output synapses of these sensory neurons must provide fast signaling to follow rapidly changing stimuli while also transmitting graded information covering a wide range of stimulus intensity and must be able to sustain this signaling for long time periods. To meet these demands, specialized machinery for transmitter release, the synaptic ribbon, has evolved at the synaptic outputs of these neurons. We found that acute disruption of synaptic ribbons by photodamage to the ribbon markedly reduced both sustained and transient components of neurotransmitter release in mouse bipolar cells and salamander cones without affecting the ultrastructure of the ribbon or its ability to localize synaptic vesicles to the active zone. Our results indicate that ribbons mediate both slow and fast signaling at sensory synapses and support an additional role for the synaptic ribbon in priming vesicles for exocytosis at active zones.