iDISCO+ for the Study of Neuroimmune Architecture of the Rat Auditory Brainstem

The lower stations of the auditory system display a complex anatomy. The inner ear labyrinth is composed of several interconnecting membranous structures encased in cavities of the temporal bone, and the cerebellopontine angle contains fragile structures such as meningeal folds, the choroid plexus (CP), and highly variable vascular formations. For this reason, most histological studies of the auditory system have either focused on the inner ear or the CNS by physically detaching the temporal bone from the brainstem. However, several studies of neuroimmune interactions have pinpointed the importance of structures such as meninges and CP; in the auditory system, an immune function has also been suggested for inner ear structures such as the endolymphatic duct (ED) and sac. All these structures are thin, fragile, and have complex 3D shapes. In order to study the immune cell populations located on these structures and their relevance to the inner ear and auditory brainstem in health and disease, we obtained a clarified-decalcified preparation of the rat hindbrain still attached to the intact temporal bone. This preparation may be immunolabeled using a clearing protocol (based on iDISCO+) to show location and functional state of immune cells. The observed macrophage distribution suggests the presence of CP-mediated communication pathways between the inner ear and the cochlear nuclei.

[1]  G. Lomberk,et al.  Resolution of Cochlear Inflammation: Novel Target for Preventing or Ameliorating Drug-, Noise- and Age-related Hearing Loss , 2017, Front. Cell. Neurosci..

[2]  J. Alvarado,et al.  The Role of Glia in the Peripheral and Central Auditory System Following Noise Overexposure: Contribution of TNF-α and IL-1β to the Pathogenesis of Hearing Loss , 2017, Frontiers in neuroanatomy.

[3]  M. Harrington,et al.  Cranial dural permeability of inflammatory nociceptive mediators: Potential implications for animal models of migraine , 2017, Cephalalgia : an international journal of headache.

[4]  O. Lindvall,et al.  Choroid plexus-cerebrospinal fluid route for monocyte-derived macrophages after stroke , 2017, Journal of Neuroinflammation.

[5]  Guido Gerig,et al.  User-guided 3D active contour segmentation of anatomical structures: Significantly improved efficiency and reliability , 2006, NeuroImage.

[6]  Hiroki R Ueda,et al.  Whole-body and Whole-Organ Clearing and Imaging Techniques with Single-Cell Resolution: Toward Organism-Level Systems Biology in Mammals. , 2016, Cell chemical biology.

[7]  M. Nedergaard,et al.  Understanding the functions and relationships of the glymphatic system and meningeal lymphatics. , 2017, The Journal of clinical investigation.

[8]  A. Rivas,et al.  3D model of frequency representation in the cochlear nucleus of the CBA/J mouse , 2013, The Journal of comparative neurology.

[9]  H. Okano,et al.  Inflammatory and immune responses in the cochlea: potential therapeutic targets for sensorineural hearing loss , 2014, Front. Pharmacol..

[10]  C. C. Law,et al.  ParaView: An End-User Tool for Large-Data Visualization , 2005, The Visualization Handbook.

[11]  Steffen Jung,et al.  Recruitment of beneficial M2 macrophages to injured spinal cord is orchestrated by remote brain choroid plexus. , 2013, Immunity.

[12]  H. Barendregt,et al.  The regulation of brain states by neuroactive substances distributed via the cerebrospinal fluid; a review , 2010, Cerebrospinal Fluid Research.

[13]  Alec N. Salt,et al.  Communication pathways to and from the inner ear and their contributions to drug delivery , 2017, Hearing Research.

[14]  L. Trussell,et al.  Microcircuits of the Dorsal Cochlear Nucleus , 2018 .

[15]  J. Palha,et al.  The choroid plexus in health and in disease: dialogues into and out of the brain , 2017, Neurobiology of Disease.

[16]  Johannes E. Schindelin,et al.  Fiji: an open-source platform for biological-image analysis , 2012, Nature Methods.

[17]  J. Ghersi-Egea,et al.  Physiology of blood-brain interfaces in relation to brain disposition of small compounds and macromolecules. , 2013, Molecular pharmaceutics.

[18]  M. Prinz,et al.  Ontogeny and homeostasis of CNS myeloid cells , 2017, Nature Immunology.

[19]  Witold Konopka,et al.  Light-sheet microscopy imaging of a whole cleared rat brain with Thy1-GFP transgene , 2016, Scientific Reports.

[20]  Marc Flajolet,et al.  Three-Dimensional Study of Alzheimer's Disease Hallmarks Using the iDISCO Clearing Method. , 2016, Cell reports.

[21]  B. Edgerton,et al.  Physical effects of the choroid plexus on the cochlear nuclei in man. , 1985, Acta oto-laryngologica.

[22]  Cheuk Y. Tang,et al.  Mapping of Brain Activity by Automated Volume Analysis of Immediate Early Genes , 2016, Cell.

[23]  I. Chung,et al.  Variability of the Surgical Anatomy of the Neurovascular Complex of the Cerebellopontine Angle , 1990, The Annals of otology, rhinology, and laryngology.