Diverse Representations of Olfactory Information in Centrifugal Feedback Projections

Although feedback or centrifugal projections from higher processing centers of the brain to peripheral regions have long been known to play essential functional roles, the anatomical organization of these connections remains largely unknown. Using a virus-based retrograde labeling strategy and 3D whole-brain reconstruction methods, we mapped the spatial organization of centrifugal projections from two olfactory cortical areas, the anterior olfactory nucleus (AON) and the piriform cortex, to the granule cell layer of the main olfactory bulb in the mouse. Both regions are major recipients of information from the bulb and are the largest sources of feedback to the bulb, collectively constituting circuits essential for olfactory coding and olfactory behavior. We found that, although ipsilateral inputs from the AON were uniformly distributed, feedback from the contralateral AON had a strong ventral bias. In addition, we observed that centrifugally projecting neurons were spatially clustered in the piriform cortex, in contrast to the distributed feedforward axonal inputs that these cells receive from the principal neurons of the bulb. Therefore, information carried from the bulb to higher processing structures by anatomically stereotypic projections is likely relayed back to the bulb by organizationally distinct feedback projections that may reflect different coding strategies and therefore different functional roles. SIGNIFICANCE STATEMENT Principles of anatomical organization, sometimes instantiated as “maps” in the mammalian brain, have provided key insights into the structure and function of circuits in sensory systems. Generally, these characterizations focus on projections from early sensory processing areas to higher processing structures despite considerable evidence that feedback or centrifugal projections often constitute major conduits of information flow. Our results identify structure in the organization of centrifugal feedback projections to the olfactory bulb that is fundamentally different from the organization of feedforward circuits. Our study suggests that understanding computations performed in the olfactory bulb, and more generally in the olfactory system, requires understanding interactions between feedforward and feedback “maps” both structurally and functionally.

[1]  J. Isaacson,et al.  Odor Representations in Olfactory Cortex: “Sparse” Coding, Global Inhibition, and Oscillations , 2009, Neuron.

[2]  V. Murthy,et al.  Functional Properties of Cortical Feedback Projections to the Olfactory Bulb , 2012, Neuron.

[3]  Peter C. Brunjes,et al.  A field guide to the anterior olfactory nucleus (cortex) , 2005, Brain Research Reviews.

[4]  T. Cutforth,et al.  Sensory maps in the olfactory cortex defined by long-range viral tracing of single neurons , 2011, Nature.

[5]  P. Brunjes,et al.  The mouse olfactory peduncle , 2011, The Journal of comparative neurology.

[6]  Bert Sakmann,et al.  Reciprocal intraglomerular excitation and intra‐ and interglomerular lateral inhibition between mouse olfactory bulb mitral cells , 2002, The Journal of physiology.

[7]  Liqun Luo,et al.  Monosynaptic Circuit Tracing with Glycoprotein-Deleted Rabies Viruses , 2015, The Journal of Neuroscience.

[8]  T. Powell,et al.  An experimental study of the origin and the course of the centrifugal fibres to the olfactory bulb in the rat. , 1970, Journal of anatomy.

[9]  A. Litwin-Kumar,et al.  Slow dynamics and high variability in balanced cortical networks with clustered connections , 2012, Nature Neuroscience.

[10]  T. Bonhoeffer,et al.  Tuning and Topography in an Odor Map on the Rat Olfactory Bulb , 2001, The Journal of Neuroscience.

[11]  Dan D. Stettler,et al.  Representations of Odor in the Piriform Cortex , 2009, Neuron.

[12]  Magdalena Götz,et al.  Retrograde monosynaptic tracing reveals the temporal evolution of inputs onto new neurons in the adult dentate gyrus and olfactory bulb , 2013, Proceedings of the National Academy of Sciences.

[13]  J. Bekkers,et al.  Inhibitory neurons in the anterior piriform cortex of the mouse: Classification using molecular markers , 2010, The Journal of comparative neurology.

[14]  Gonzalo H. Otazu,et al.  Cortical Feedback Decorrelates Olfactory Bulb Output in Awake Mice , 2015, Neuron.

[15]  Vikrant Kapoor,et al.  Glomerulus-Specific, Long-Latency Activity in the Olfactory Bulb Granule Cell Network , 2006, The Journal of Neuroscience.

[16]  Michael D. Ehlers,et al.  Neural Circuit Mechanisms for Pattern Detection and Feature Combination in Olfactory Cortex , 2011, Neuron.

[17]  W. G. Hall,et al.  New routes to early memories. , 1987, Science.

[18]  L. Haberly,et al.  Association and commissural fiber systems of the olfactory cortex of the rat II. Systems originating in the olfactory peduncle , 1978, The Journal of comparative neurology.

[19]  P. Lledo,et al.  Is adult neurogenesis essential for olfaction? , 2011, Trends in Neurosciences.

[20]  Gilles Laurent,et al.  Olfactory network dynamics and the coding of multidimensional signals , 2002, Nature Reviews Neuroscience.

[21]  Venkatesh N Murthy,et al.  Olfactory maps in the brain. , 2011, Annual review of neuroscience.

[22]  M. T. Shipley,et al.  the connections of the mouse olfactory bulb: A study using orthograde and retrograde transport of wheat germ agglutinin conjugated to horseradish peroxidase , 1984, Brain Research Bulletin.

[23]  S. Itohara,et al.  Innate versus learned odour processing in the mouse olfactory bulb , 2007, Nature.

[24]  M. Bensafi,et al.  Light microscopy (communication arising): Beyond the diffraction limit , 2002, Nature.

[25]  James H. Marshel,et al.  New Rabies Virus Variants for Monitoring and Manipulating Activity and Gene Expression in Defined Neural Circuits , 2011, Neuron.

[26]  J. Mainland,et al.  Odor Coding by a Mammalian Receptor Repertoire , 2009, Science Signaling.

[27]  J. C. Anderson,et al.  Polyneuronal innervation of spiny stellate neurons in cat visual cortex , 1994, The Journal of comparative neurology.

[28]  Rachel I. Wilson,et al.  Receptors, Circuits, and Behaviors: New Directions in Chemical Senses , 2008, The Journal of Neuroscience.

[29]  William F. Eddy,et al.  A novel algorithm for optimal image thresholding of biological data , 2010, Journal of Neuroscience Methods.

[30]  Fumitaka Osakada,et al.  Design and generation of recombinant rabies virus vectors , 2013, Nature Protocols.

[31]  P. Brunjes,et al.  The mouse olfactory peduncle. 3. Development of neurons, glia, and centrifugal afferents , 2014, Front. Neuroanat..

[32]  Christina Zelano,et al.  Olfactory Predictive Codes and Stimulus Templates in Piriform Cortex , 2011, Neuron.

[33]  Richard Axel,et al.  Visualizing an Olfactory Sensory Map , 1996, Cell.

[34]  Gordon M Shepherd,et al.  Viral tracing identifies distributed columnar organization in the olfactory bulb , 2006, Proceedings of the National Academy of Sciences.

[35]  Amiram Grinvald,et al.  Iso-orientation domains in cat visual cortex are arranged in pinwheel-like patterns , 1991, Nature.

[36]  R. Hen,et al.  The participation of cortical amygdala in innate, odor-driven behavior , 2014, Nature.

[37]  Markus Meister,et al.  Precision and diversity in an odor map on the olfactory bulb , 2009, Nature Neuroscience.

[38]  Rafael C. González,et al.  Digital image processing using MATLAB , 2006 .

[39]  M. T. Shipley,et al.  Cholinergic Inputs from Basal Forebrain Add an Excitatory Bias to Odor Coding in the Olfactory Bulb , 2014, The Journal of Neuroscience.

[40]  V. Murthy,et al.  Serotonergic modulation of odor input to the mammalian olfactory bulb , 2009, Nature Neuroscience.

[41]  Ian R. Wickersham,et al.  Retrograde neuronal tracing with a deletion-mutant rabies virus , 2007, Nature Methods.

[42]  S. R. Datta,et al.  Distinct representations of olfactory information in different cortical centres , 2011, Nature.

[43]  Minmin Luo,et al.  Precise Circuitry Links Bilaterally Symmetric Olfactory Maps , 2008, Neuron.

[44]  D. Hubel,et al.  Receptive fields and functional architecture of monkey striate cortex , 1968, The Journal of physiology.

[45]  Dan D. Stettler,et al.  Driving Opposing Behaviors with Ensembles of Piriform Neurons , 2011, Cell.

[46]  Ian R. Wickersham,et al.  Cortical representations of olfactory input by trans-synaptic tracing , 2011, Nature.

[47]  Takaki Komiyama,et al.  Broadcasting of cortical activity to the olfactory bulb. , 2015, Cell reports.

[48]  P. Lledo,et al.  Centrifugal Drive onto Local Inhibitory Interneurons of the Olfactory Bulb , 2009, Annals of the New York Academy of Sciences.

[49]  Jeffry S. Isaacson,et al.  Cortical Feedback Control of Olfactory Bulb Circuits , 2012, Neuron.

[50]  Wolfgang Kelsch,et al.  Genetically Increased Cell-Intrinsic Excitability Enhances Neuronal Integration into Adult Brain Circuits , 2010, Neuron.

[51]  H. Sompolinsky,et al.  Sparseness and Expansion in Sensory Representations , 2014, Neuron.

[52]  Matt Wachowiak,et al.  Why sniff fast? The relationship between sniff frequency, odor discrimination, and receptor neuron activation in the rat. , 2009, Journal of neurophysiology.

[53]  Nathaniel N Urban,et al.  Disrupting information coding via block of 4-AP-sensitive potassium channels. , 2014, Journal of neurophysiology.

[54]  G. Laurent,et al.  Dynamic optimization of odor representations by slow temporal patterning of mitral cell activity. , 2001, Science.