Flexible Sensory Representations in Auditory Cortex Driven by Behavioral Relevance

Neuron

Volumn 88, Issue 5, 2015, Pages 1027-1039

  Kato, Hiroyuki K ^a   Gillet, Shea N ^a   Isaacson, Jeffry S ^a  

^a University of California San Diego   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

SOMATOSTATIN; DNA BINDING PROTEIN; EPITHELIAL SODIUM CHANNEL; GLUTAMATE DECARBOXYLASE; GRHL3 PROTEIN, MOUSE; PARVALBUMIN; SCNN1A PROTEIN, MOUSE; TRANSCRIPTION FACTOR; VESICULAR INHIBITORY AMINO ACID TRANSPORTER; VIAAT PROTEIN, MOUSE;

ADULT; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; AUDITORY STIMULATION; BEHAVIOR; COGNITION; CONTROLLED STUDY; FEMALE; HABITUATION; MALE; MOUSE; NEUROMODULATION; NONHUMAN; PRIMARY AUDITORY CORTEX; PRIORITY JOURNAL; PYRAMIDAL NERVE CELL; SENSORY REPRESENTATION; SOUND; STIMULUS RESPONSE; UPREGULATION; ANIMAL; AUDITORY CORTEX; GENETICS; HEARING; METABOLISM; NERVE CELL; NERVE CELL INHIBITION; NERVE CELL NETWORK; PHYSIOLOGY; PSYCHOMOTOR PERFORMANCE; SENSATION; TIME FACTOR; TRANSGENIC MOUSE; WAKEFULNESS;

ACOUSTIC STIMULATION; ANIMALS; AUDITORY CORTEX; AUDITORY PERCEPTION; DNA-BINDING PROTEINS; EPITHELIAL SODIUM CHANNELS; FEMALE; GLUTAMATE DECARBOXYLASE; HABITUATION, PSYCHOPHYSIOLOGIC; MALE; MICE; MICE, TRANSGENIC; NERVE NET; NEURAL INHIBITION; NEURONS; PARVALBUMINS; PSYCHOMOTOR PERFORMANCE; SENSATION; SOUND; TIME FACTORS; TRANSCRIPTION FACTORS; VESICULAR INHIBITORY AMINO ACID TRANSPORT PROTEINS; WAKEFULNESS;

EID: 84949528904     PISSN: 08966273     EISSN: 10974199     Source Type: Journal    
DOI: 10.1016/j.neuron.2015.10.024     Document Type: Article

References (57)

1. Anderson L.A., Christianson G.B., Linden J.F. Stimulus-specific adaptation occurs in the auditory thalamus. J. Neurosci. 2009, 29:7359-7363.
2. Bakin J.S., Weinberger N.M. Induction of a physiological memory in the cerebral cortex by stimulation of the nucleus basalis. Proc. Natl. Acad. Sci. USA 1996, 93:11219-11224.
3. Bakin J.S., South D.A., Weinberger N.M. Induction of receptive field plasticity in the auditory cortex of the guinea pig during instrumental avoidance conditioning. Behav. Neurosci. 1996, 110:905-913.
4. Bandyopadhyay S., Shamma S.A., Kanold P.O. Dichotomy of functional organization in the mouse auditory cortex. Nat. Neurosci. 2010, 13:361-368.
5. Bao S., Chan V.T., Merzenich M.M. Cortical remodelling induced by activity of ventral tegmental dopamine neurons. Nature 2001, 412:79-83.
6. Barkat T.R., Polley D.B., Hensch T.K. A critical period for auditory thalamocortical connectivity. Nat. Neurosci. 2011, 14:1189-1194.
7. Blake D.T., Strata F., Churchland A.K., Merzenich M.M. Neural correlates of instrumental learning in primary auditory cortex. Proc. Natl. Acad. Sci. USA 2002, 99:10114-10119.
8. Boyd A.M., Kato H.K., Komiyama T., Isaacson J.S. Broadcasting of cortical activity to the olfactory bulb. Cell Rep. 2015, 10:1032-1039.
9. Chen T.-W., Wardill T.J., Sun Y., Pulver S.R., Renninger S.L., Baohan A., Schreiter E.R., Kerr R.A., Orger M.B., Jayaraman V., et al. Ultrasensitive fluorescent proteins for imaging neuronal activity. Nature 2013, 499:295-300.
10. Chen N., Sugihara H., Sur M. An acetylcholine-activated microcircuit drives temporal dynamics of cortical activity. Nat. Neurosci. 2015, 18:892-902.
11. Condon C.D., Weinberger N.M. Habituation produces frequency-specific plasticity of receptive fields in the auditory cortex. Behav. Neurosci. 1991, 105:416-430.
12. Desimone R., Duncan J. Neural mechanisms of selective visual attention. Annu. Rev. Neurosci. 1995, 18:193-222.
13. de Villers-Sidani E., Chang E.F., Bao S., Merzenich M.M. Critical period window for spectral tuning defined in the primary auditory cortex (A1) in the rat. J. Neurosci. 2007, 27:180-189.
14. DeWeese M.R., Wehr M., Zador A.M. Binary spiking in auditory cortex. J. Neurosci. 2003, 23:7940-7949.
15. Fritz J., Shamma S., Elhilali M., Klein D. Rapid task-related plasticity of spectrotemporal receptive fields in primary auditory cortex. Nat. Neurosci. 2003, 6:1216-1223.
16. Froemke R.C., Carcea I., Barker A.J., Yuan K., Seybold B.A., Martins A.R.O., Zaika N., Bernstein H., Wachs M., Levis P.A., et al. Long-term modification of cortical synapses improves sensory perception. Nat. Neurosci. 2013, 16:79-88.
17. Glickfeld L.L., Histed M.H., Maunsell J.H.R. Mouse primary visual cortex is used to detect both orientation and contrast changes. J. Neurosci. 2013, 33:19416-19422.
18. Guo W., Chambers A.R., Darrow K.N., Hancock K.E., Shinn-Cunningham B.G., Polley D.B. Robustness of cortical topography across fields, laminae, anesthetic states, and neurophysiological signal types. J. Neurosci. 2012, 32:9159-9172.
19. Haider B., Häusser M., Carandini M. Inhibition dominates sensory responses in the awake cortex. Nature 2013, 493:97-100.
20. Hensch T.K., Fagiolini M., Mataga N., Stryker M.P., Baekkeskov S., Kash S.F. Local GABA circuit control of experience-dependent plasticity in developing visual cortex. Science 1998, 282:1504-1508.
21. 2+ imaging of tonal organization in mouse auditory cortex. Neuron 2014, 83:944-959.
22. Jaramillo S., Zador A.M. The auditory cortex mediates the perceptual effects of acoustic temporal expectation. Nat. Neurosci. 2011, 14:246-251.
23. Kato H.K., Chu M.W., Isaacson J.S., Komiyama T. Dynamic sensory representations in the olfactory bulb: modulation by wakefulness and experience. Neuron 2012, 76:962-975.
24. Kelly J.B., Glazier S.J. Auditory cortex lesions and discrimination of spatial location by the rat. Brain Res. 1978, 145:315-321.
25. Kilgard M.P., Merzenich M.M. Cortical map reorganization enabled by nucleus basalis activity. Science 1998, 279:1714-1718.
26. Lee S., Kruglikov I., Huang Z.J., Fishell G., Rudy B. A disinhibitory circuit mediates motor integration in the somatosensory cortex. Nat. Neurosci. 2013, 16:1662-1670.
27. Luczak A., Bartho P., Harris K.D. Gating of sensory input by spontaneous cortical activity. J. Neurosci. 2013, 33:1684-1695.
28. Lütcke H., Gerhard F., Zenke F., Gerstner W., Helmchen F. Inference of neuronal network spike dynamics and topology from calcium imaging data. Front. Neural Circuits 2013, 7:201.
29. Malmierca M.S., Cristaudo S., Pérez-González D., Covey E. Stimulus-specific adaptation in the inferior colliculus of the anesthetized rat. J. Neurosci. 2009, 29:5483-5493.
30. McGinley M.J., David S.V., McCormick D.A. Cortical membrane potential signature of optimal states for sensory signal detection. Neuron 2015, 87:179-192.
31. Niell C.M., Stryker M.P. Modulation of visual responses by behavioral state in mouse visual cortex. Neuron 2010, 65:472-479.
32. Noreña A.J., Gourévitch B., Aizawa N., Eggermont J.J. Spectrally enhanced acoustic environment disrupts frequency representation in cat auditory cortex. Nat. Neurosci. 2006, 9:932-939.
33. Otazu G.H., Tai L.-H., Yang Y., Zador A.M. Engaging in an auditory task suppresses responses in auditory cortex. Nat. Neurosci. 2009, 12:646-654.
34. Pai S., Erlich J.C., Kopec C., Brody C.D. Minimal impairment in a rat model of duration discrimination following excitotoxic lesions of primary auditory and prefrontal cortices. Front. Syst. Neurosci. 2011, 5:74.
35. Peron S.P., Freeman J., Iyer V., Guo C., Svoboda K. A cellular resolution map of barrel cortex activity during tactile behavior. Neuron 2015, 86:783-799.
36. Petreanu L., Gutnisky D.A., Huber D., Xu N.L., O'Connor D.H., Tian L., Looger L., Svoboda K. Activity in motor-sensory projections reveals distributed coding in somatosensation. Nature 2012, 489:299-303.
37. Pfeffer C.K., Xue M., He M., Huang Z.J., Scanziani M. Inhibition of inhibition in visual cortex: the logic of connections between molecularly distinct interneurons. Nat. Neurosci. 2013, 16:1068-1076.
38. Pi H.-J., Hangya B., Kvitsiani D., Sanders J.I., Huang Z.J., Kepecs A. Cortical interneurons that specialize in disinhibitory control. Nature 2013, 503:521-524.
39. Pinto L., Goard M.J., Estandian D., Xu M., Kwan A.C., Lee S.-H., Harrison T.C., Feng G., Dan Y. Fast modulation of visual perception by basal forebrain cholinergic neurons. Nat. Neurosci. 2013, 16:1857-1863.
40. Polack P.-O., Friedman J., Golshani P. Cellular mechanisms of brain state-dependent gain modulation in visual cortex. Nat. Neurosci. 2013, 16:1331-1339.
41. Polley D.B., Steinberg E.E., Merzenich M.M. Perceptual learning directs auditory cortical map reorganization through top-down influences. J. Neurosci. 2006, 26:4970-4982.
42. Rodgers C.C., DeWeese M.R. Neural correlates of task switching in prefrontal cortex and primary auditory cortex in a novel stimulus selection task for rodents. Neuron 2014, 82:1157-1170.
43. Rothschild G., Nelken I., Mizrahi A. Functional organization and population dynamics in the mouse primary auditory cortex. Nat. Neurosci. 2010, 13:353-360.
44. Rutkowski R.G., Weinberger N.M. Encoding of learned importance of sound by magnitude of representational area in primary auditory cortex. Proc. Natl. Acad. Sci. USA 2005, 102:13664-13669.
45. Schiff M.L., Reyes A.D. Characterization of thalamocortical responses of regular-spiking and fast-spiking neurons of the mouse auditory cortex in vitro and in silico. J. Neurophysiol. 2012, 107:1476-1488.
46. Schneider D.M., Nelson A., Mooney R. A synaptic and circuit basis for corollary discharge in the auditory cortex. Nature 2014, 513:189-194.
47. Schreiner C.E., Froemke R.C., Atencio C. Spectral processing in auditory cortex. The Auditory Cortex 2010, 275-308. Springer. J.A. Winer, C.E. Schreiner (Eds.).
48. Sutter M.L. Shapes and level tolerances of frequency tuning curves in primary auditory cortex: quantitative measures and population codes. J. Neurophysiol. 2000, 84:1012-1025.
49. Talwar S.K., Musial P.G., Gerstein G.L. Role of mammalian auditory cortex in the perception of elementary sound properties. J. Neurophysiol. 2001, 85:2350-2358.
50. Tian L., Hires S.A., Mao T., Huber D., Chiappe M.E., Chalasani S.H., Petreanu L., Akerboom J., McKinney S.A., Schreiter E.R., et al. Imaging neural activity in worms, flies and mice with improved GCaMP calcium indicators. Nat. Methods 2009, 6:875-881.
51. Ulanovsky N., Las L., Nelken I. Processing of low-probability sounds by cortical neurons. Nat. Neurosci. 2003, 6:391-398.
52. Vogelstein J.T., Packer A.M., Machado T.A., Sippy T., Babadi B., Yuste R., Paninski L. Fast nonnegative deconvolution for spike train inference from population calcium imaging. J. Neurophysiol. 2010, 104:3691-3704.
53. Volkov I.O., Galazjuk A.V. Formation of spike response to sound tones in cat auditory cortex neurons: interaction of excitatory and inhibitory effects. Neuroscience 1991, 43:307-321.
54. Wang X., Lu T., Snider R.K., Liang L. Sustained firing in auditory cortex evoked by preferred stimuli. Nature 2005, 435:341-346.
55. Xiong X.R., Liang F., Zingg B., Ji X.-Y., Ibrahim L.A., Tao H.W., Zhang L.I. Auditory cortex controls sound-driven innate defense behaviour through corticofugal projections to inferior colliculus. Nat. Commun. 2015, 6:7224.
56. Zhang L.I., Bao S., Merzenich M.M. Persistent and specific influences of early acoustic environments on primary auditory cortex. Nat. Neurosci. 2001, 4:1123-1130.
57. Zhou M., Liang F., Xiong X.R., Li L., Li H., Xiao Z., Tao H.W., Zhang L.I. Scaling down of balanced excitation and inhibition by active behavioral states in auditory cortex. Nat. Neurosci. 2014, 17:841-850.