System identification of Drosophila olfactory sensory neurons

The lack of a deeper understanding of how olfactory sensory neurons (OSNs) encode odors has hindered the progress in understanding the olfactory signal processing in higher brain centers. Here we employ methods of system identification to investigate the encoding of time-varying odor stimuli and their representation for further processing in the spike domain by Drosophila OSNs. In order to apply system identification techniques, we built a novel low-turbulence odor delivery system that allowed us to deliver airborne stimuli in a precise and reproducible fashion. The system provides a 1% tolerance in stimulus reproducibility and an exact control of odor concentration and concentration gradient on a millisecond time scale. Using this novel setup, we recorded and analyzed the in-vivo response of OSNs to a wide range of time-varying odor waveforms. We report for the first time that across trials the response of OR59b OSNs is very precise and reproducible. Further, we empirically show that the response of an OSN depends not only on the concentration, but also on the rate of change of the odor concentration. Moreover, we demonstrate that a two-dimensional (2D) Encoding Manifold in a concentration-concentration gradient space provides a quantitative description of the neuron’s response. We then use the white noise system identification methodology to construct one-dimensional (1D) and two-dimensional (2D) Linear-Nonlinear-Poisson (LNP) cascade models of the sensory neuron for a fixed mean odor concentration and fixed contrast. We show that in terms of predicting the intensity rate of the spike train, the 2D LNP model performs on par with the 1D LNP model, with a root mean-square error (RMSE) increase of about 5 to 10%. Surprisingly, we find that for a fixed contrast of the white noise odor waveforms, the nonlinear block of each of the two models changes with the mean input concentration. The shape of the nonlinearities of both the 1D and the 2D LNP model appears to be, for a fixed mean of the odor waveform, independent of the stimulus contrast. This suggests that white noise system identification of Or59b OSNs only depends on the first moment of the odor concentration. Finally, by comparing the 2D Encoding Manifold and the 2D LNP model, we demonstrate that the OSN identification results depend on the particular type of the employed test odor waveforms. This suggests an adaptive neural encoding model for Or59b OSNs that changes its nonlinearity in response to the odor concentration waveforms.

[1]  Andrew S. French,et al.  Dynamic properties of Drosophila olfactory electroantennograms , 2008, Journal of Comparative Physiology A.

[2]  Adrienne L. Fairhall,et al.  What Causes a Neuron to Spike? , 2003, Neural Computation.

[3]  R. Kass,et al.  Statistical smoothing of neuronal data. , 2003, Network.

[4]  Getz,et al.  Temporal resolution of general odor pulses by olfactory sensory neurons in American cockroaches , 1997, The Journal of experimental biology.

[5]  Armin J. Hinterwirth,et al.  Olfactory receptors on the cockroach antenna signal odour ON and odour OFF by excitation , 2005, The European journal of neuroscience.

[6]  B. Knight,et al.  The Power Ratio and the Interval Map: Spiking Models and Extracellular Recordings , 1998, The Journal of Neuroscience.

[7]  Ring T. Cardé,et al.  Antennal resolution of pulsed pheromone plumes in three moth species. , 2002, Journal of insect physiology.

[8]  M. J. Korenberg,et al.  The identification of nonlinear biological systems: Wiener and Hammerstein cascade models , 1986, Biological Cybernetics.

[9]  G. Gomez,et al.  Temporal resolution in olfaction III: flicker fusion and concentration-dependent synchronization with stimulus pulse trains of antennular chemoreceptor cells in the American lobster , 1999, Journal of Comparative Physiology A.

[10]  Michael J. Berry,et al.  Selectivity for multiple stimulus features in retinal ganglion cells. , 2006, Journal of neurophysiology.

[11]  William Bialek,et al.  Adaptive Rescaling Maximizes Information Transmission , 2000, Neuron.

[12]  William Bialek,et al.  Real-time performance of a movement-sensitive neuron in the blowfly visual system: coding and information transfer in short spike sequences , 1988, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[13]  Jeanette Kotaleski,et al.  Modelling and sensitivity analysis of the reactions involving receptor, G-protein and effector in vertebrate olfactory receptor neurons , 2009, Journal of Computational Neuroscience.

[14]  A. Yew,et al.  Computational model of the cAMP-mediated sensory response and calcium-dependent adaptation in vertebrate olfactory receptor neurons. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[15]  Julian J. Bussgang,et al.  Crosscorrelation functions of amplitude-distorted gaussian signals , 1952 .

[16]  Vasilis Z. Marmarelis,et al.  Nonlinear Dynamic Modeling of Physiological Systems: Marmarelis/Nonlinear , 2004 .

[17]  J Reidl,et al.  Model of calcium oscillations due to negative feedback in olfactory cilia. , 2006, Biophysical journal.

[18]  R. Shapley,et al.  A method of nonlinear analysis in the frequency domain. , 1980, Biophysical journal.

[19]  K. Naka,et al.  White-Noise Analysis of a Neuron Chain: An Application of the Wiener Theory , 1972, Science.

[20]  Gilles Laurent,et al.  Neural Encoding of Rapidly Fluctuating Odors , 2009, Neuron.

[21]  Vasilis Z. Marmarelis,et al.  Nonlinear Dynamic Modeling of Physiological Systems , 2004 .

[22]  Richard Loftus,et al.  Differential thermal components in the response of the antennal cold receptor of Periplaneta americana to slowly changing temperature , 1969, Zeitschrift für vergleichende Physiologie.

[23]  John R. Carlson,et al.  Odorant response of individual sensilla on theDrosophila antenna , 1997, Invertebrate Neuroscience.

[24]  A. S. French,et al.  A new method for wide frequency range dynamic olfactory stimulation and characterization. , 2007, Chemical senses.

[25]  Liam Paninski,et al.  Noise-driven adaptation: in vitro and mathematical analysis , 2003, Neurocomputing.

[26]  H. Tichy,et al.  Low rates of change enhance effect of humidity on the activity of insect hygroreceptors , 2003, Journal of Comparative Physiology A.

[27]  Eero P. Simoncelli,et al.  How MT cells analyze the motion of visual patterns , 2006, Nature Neuroscience.

[28]  A. Aertsen,et al.  The Spectro-Temporal Receptive Field , 1981, Biological Cybernetics.

[29]  William Bialek,et al.  Analyzing Neural Responses to Natural Signals: Maximally Informative Dimensions , 2002, Neural Computation.

[30]  A. Hodgkin,et al.  A quantitative description of membrane current and its application to conduction and excitation in nerve , 1990 .

[31]  R. Reid,et al.  Predicting Every Spike A Model for the Responses of Visual Neurons , 2001, Neuron.

[32]  Michael J. Berry,et al.  Refractoriness and Neural Precision , 1997, The Journal of Neuroscience.

[33]  B. Lindemann Predicted profiles of ion concentrations in olfactory cilia in the steady state. , 2001, Biophysical journal.

[34]  Adrienne L Fairhall,et al.  Two-Dimensional Time Coding in the Auditory Brainstem , 2005, The Journal of Neuroscience.

[35]  A. S. French,et al.  Dynamic properties of antennal responses to pheromone in two moth species. , 2005, Journal of neurophysiology.

[36]  Yuqiao Gu,et al.  Computational Model of the Insect Pheromone Transduction Cascade , 2009, PLoS Comput. Biol..

[37]  William Bialek,et al.  Statistical properties of spike trains: universal and stimulus-dependent aspects. , 1999, Physical review. E, Statistical, nonlinear, and soft matter physics.

[38]  J. Victor Analyzing receptive fields, classification images and functional images: challenges with opportunities for synergy , 2005, Nature Neuroscience.

[39]  J. Rospars,et al.  Relation between stimulus and response in frog olfactory receptor neurons in vivo , 2003, The European journal of neuroscience.

[40]  L. Paninski Convergence Properties of Some Spike-Triggered Analysis Techniques , 2002 .

[41]  Liam Paninski,et al.  Convergence properties of three spike-triggered analysis techniques , 2003, NIPS.

[42]  Eero P. Simoncelli,et al.  Dimensionality reduction in neural models: an information-theoretic generalization of spike-triggered average and covariance analysis. , 2006, Journal of vision.

[43]  Robert E Kass,et al.  Statistical issues in the analysis of neuronal data. , 2005, Journal of neurophysiology.

[44]  Jonathan W. Pillow,et al.  Likelihood-based approaches to modeling the neural code , 2007 .

[45]  R. Yuste,et al.  Input Summation by Cultured Pyramidal Neurons Is Linear and Position-Independent , 1998, The Journal of Neuroscience.

[46]  N. Wiener,et al.  Nonlinear Problems in Random Theory , 1964 .

[47]  Eero P. Simoncelli,et al.  Spike-triggered neural characterization. , 2006, Journal of vision.

[48]  Armin Hinterwirth,et al.  Olfactory receptor cells on the cockroach antennae: responses to the direction and rate of change in food odour concentration , 2004, The European journal of neuroscience.

[49]  K. Kaissling,et al.  Olfactory perireceptor and receptor events in moths: a kinetic model revised , 2009, Journal of Comparative Physiology A.

[50]  J. Gallant,et al.  Complete functional characterization of sensory neurons by system identification. , 2006, Annual review of neuroscience.

[51]  John R. Carlson,et al.  Odor Coding in the Drosophila Antenna , 2001, Neuron.