Characterization of Inhibitory and Projection Specific Neurons of the Presubiculum

Total Page:16

File Type:pdf, Size:1020Kb

Characterization of Inhibitory and Projection Specific Neurons of the Presubiculum Aus dem Institut für Integrative Neuroanatomie der Medizinischen Fakultät Charité – Universitätsmedizin Berlin DISSERTATION Characterization of inhibitory and projection specific neurons of the presubiculum zur Erlangung des akademischen Grades Doctor medicinae (Dr. med.) vorgelegt der Medizinischen Fakultät Charité – Universitätsmedizin Berlin von Roxanne Lofredi Aus Frankfurt am Main Datum der Promotion: 10.03.2017.................................. TABLE OF CONTENTS DATUM DER PROMOTION: .................................. ................................................................. 1 ABSTRACT (ENGLISH) ............................................................................................................. 4 ABSTRACT (DEUTSCH) ............................................................................................................ 5 LIST OF ABBREVIATIONS ....................................................................................................... 6 LIST OF FIGURES ...................................................................................................................... 8 1. INTRODUCTION ................................................................................................................. 9 1.1 ANATOMY OF THE PRESUBICULUM ....................................................................................... 9 1.2 FUNCTION OF THE PRESUBICULUM ..................................................................................... 14 1.2.1 The sense of orientation ............................................................................................ 14 1.2.2 The head direction signal .......................................................................................... 15 1.3 INFORMATION PROCESSING IN THE PRESUBICULUM ............................................................ 19 1.3.1 Excitatory microcircuit .............................................................................................. 20 1.3.2 Inhibitory microcircuit .............................................................................................. 23 1.4 MAIN QUESTIONS OF THE PRESENT STUDY .......................................................................... 27 2. METHODS AND MATERIALS ........................................................................................ 28 2.1 ANIMALS ............................................................................................................................ 28 2.2 IMMUNOHISTOCHEMISTRY ................................................................................................. 28 2.3 ANALYSIS AND QUANTIFICATION OF NEURONAL DENSITY .................................................. 30 2.4 ANALYSIS AND QUANTIFICATION OF LABELED INTERNEURONS .......................................... 32 2.5 RETROGRADE TRACING ...................................................................................................... 33 2.6 STEREOTACTIC SURGERY ................................................................................................... 34 2.7 VERIFICATION OF INJECTION SITE ....................................................................................... 34 2.8 ELECTROPHYSIOLOGICAL RECORDINGS .............................................................................. 35 2.9 ELECTROPHYSIOLOGICAL ANALYSIS .................................................................................. 36 2.10 3D RECONSTRUCTION OF RECORDED NEURONS .............................................................. 37 2.11 STATISTICS ......................................................................................................................... 38 3. RESULTS ............................................................................................................................. 39 3.1 STRUCTURES AND BOUNDARIES OF THE PRESUBICULUM .................................................... 39 3.2 INTERNEURONS OF THE PRESUBICULUM ............................................................................. 41 3.2.1 Layer distribution of presubicular GABAergic and non-GABAergic neurons ......... 41 3.2.2 Labeling of GABAergic neurons in the presubiculum using molecular markers ..... 45 3.2.3 GABAergic neurons of the presubiculum express different molecular markers ...... 47 3.2.4 Double-labeling of GABAergic neurons ................................................................... 52 3.3 PROJECTION SPECIFIC NEURONAL SUBPOPULATIONS IN THE PRESUBICULUM ...................... 54 3.3.1 Animals ..................................................................................................................... 54 3.3.2 Laminar distribution of LMN and ADN projecting neurons .................................... 54 3.3.3 LMN projecting neurons ........................................................................................... 56 3.3.4 ADN projecting neurons ........................................................................................... 58 4. DISCUSSION ...................................................................................................................... 61 4.1 INTERNEURONS OF THE PRESUBICULUM ............................................................................. 61 4.1.1 Evaluation of chosen methods – Cell counting ......................................................... 62 4.1.2 Neuronal density in the presubiculum ....................................................................... 64 4.1.3 Specific distribution of interneurons in the presubiculum ........................................ 65 2 4.1.4 Colocalization of GABA and marker proteins in the presubiculum ......................... 66 4.1.5 Molecular subtypes of presubicular interneurons ..................................................... 67 4.1.6 Double labeling reveals additional subtypes ............................................................. 70 4.1.7 Functional relevance of the findings ......................................................................... 71 4.1.8 Prospects .................................................................................................................... 74 4.2 PROJECTION- SPECIFIC NEURONAL SUBPOPULATIONS IN THE PRESUBICULUM ..................... 75 4.2.1 Evaluation of chosen methods ................................................................................... 75 4.2.2 Functional role of presubicular projections to subcortical nuclei ............................. 76 4.2.3 Prospects .................................................................................................................... 77 REFERENCES ............................................................................................................................ 79 EIDESSTATTLICHE VERSICHERUNG ............................................................................... 89 PUBLIKATIONSLISTE ............................................................................................................ 90 LEBENSLAUF ............................................................................................................................ 91 DANKSAGUNG .......................................................................................................................... 93 3 ABSTRACT (English) Presubiculum (PrS) is a transitional cortical area of the parahippocampal formation in the temporal lobe, close to hippocampus and entorhinal cortex. PrS is involved in spatial navigation processing by encoding an animal’s head direction (HD). The HD signal is most likely generated in lateral mammillary nucleus (LMN) and relayed in anterodorsal thalamus (ADN) before being processed in the PrS. PrS is thought to be crucial for updating the HD signal with visual landmark information as it receives direct projections of visual cortex and projects back to downstream ADN and LMN. The aim of my work has been twofold. First, I examined the GABAergic neurons of the PrS. GABAergic interneurons are the source of inhibitory activity that is essential for local signal generation. I quantified the total number of presubicular interneurons in the GAD67-GFP transgenic mouse and investigated morphological properties and layer specific distribution of interneuron subtypes. The proportion of interneurons in the PrS was 11% of all neurons. To identify neurochemical subpopulations, I performed double immunolabeling with combinations of Parvalbumin (PV), Calretinin (CR), Calbindin (CB), Somatostatin (SOM), Vasointestinal Peptide (VIP) and Neuropeptide Y (NPY). Largest population of presubicular interneurons was PV+ (36%). CR, CB and SOM interneurons contributed evenly to the population (~18%), while there were less VIP+ interneurons (9%). Double labeling experiments revealed a small subpopulation of presubicular interneurons positive for PV and SOM, a co-expression pattern seen in the hippocampal formation but usually absent in neocortical regions. Indeed, the PrS displays a unique expression pattern of inhibitory cells, and their functional role within the presubicular microcircuit will have to be investigated in future studies. The second part of my work focused on projection-specific neurons of the PrS targeting LMN and ADN. To reveal their morphological and electrophysiological identity, I injected retrogradely transported fluorescent beads into LMN or ADN which allowed assessing the laminar origin of projection neurons. While LMN projecting neurons were exclusively seen in layer IV, ADN projecting neurons were restricted to deep layers. Patch
Recommended publications
  • Toward a Common Terminology for the Gyri and Sulci of the Human Cerebral Cortex Hans Ten Donkelaar, Nathalie Tzourio-Mazoyer, Jürgen Mai
    Toward a Common Terminology for the Gyri and Sulci of the Human Cerebral Cortex Hans ten Donkelaar, Nathalie Tzourio-Mazoyer, Jürgen Mai To cite this version: Hans ten Donkelaar, Nathalie Tzourio-Mazoyer, Jürgen Mai. Toward a Common Terminology for the Gyri and Sulci of the Human Cerebral Cortex. Frontiers in Neuroanatomy, Frontiers, 2018, 12, pp.93. 10.3389/fnana.2018.00093. hal-01929541 HAL Id: hal-01929541 https://hal.archives-ouvertes.fr/hal-01929541 Submitted on 21 Nov 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. REVIEW published: 19 November 2018 doi: 10.3389/fnana.2018.00093 Toward a Common Terminology for the Gyri and Sulci of the Human Cerebral Cortex Hans J. ten Donkelaar 1*†, Nathalie Tzourio-Mazoyer 2† and Jürgen K. Mai 3† 1 Department of Neurology, Donders Center for Medical Neuroscience, Radboud University Medical Center, Nijmegen, Netherlands, 2 IMN Institut des Maladies Neurodégénératives UMR 5293, Université de Bordeaux, Bordeaux, France, 3 Institute for Anatomy, Heinrich Heine University, Düsseldorf, Germany The gyri and sulci of the human brain were defined by pioneers such as Louis-Pierre Gratiolet and Alexander Ecker, and extensified by, among others, Dejerine (1895) and von Economo and Koskinas (1925).
    [Show full text]
  • The Structural Model: a Theory Linking Connections, Plasticity, Pathology, Development and Evolution of the Cerebral Cortex
    Brain Structure and Function https://doi.org/10.1007/s00429-019-01841-9 REVIEW The Structural Model: a theory linking connections, plasticity, pathology, development and evolution of the cerebral cortex Miguel Ángel García‑Cabezas1 · Basilis Zikopoulos2,3 · Helen Barbas1,3 Received: 11 October 2018 / Accepted: 29 January 2019 © Springer-Verlag GmbH Germany, part of Springer Nature 2019 Abstract The classical theory of cortical systematic variation has been independently described in reptiles, monotremes, marsupials and placental mammals, including primates, suggesting a common bauplan in the evolution of the cortex. The Structural Model is based on the systematic variation of the cortex and is a platform for advancing testable hypotheses about cortical organization and function across species, including humans. The Structural Model captures the overall laminar structure of areas by dividing the cortical architectonic continuum into discrete categories (cortical types), which can be used to test hypotheses about cortical organization. By type, the phylogenetically ancient limbic cortices—which form a ring at the base of the cerebral hemisphere—are agranular if they lack layer IV, or dysgranular if they have an incipient granular layer IV. Beyond the dysgranular areas, eulaminate type cortices have six layers. The number and laminar elaboration of eulaminate areas differ depending on species or cortical system within a species. The construct of cortical type retains the topology of the systematic variation of the cortex and forms the basis for a predictive Structural Model, which has successfully linked cortical variation to the laminar pattern and strength of cortical connections, the continuum of plasticity and stability of areas, the regularities in the distribution of classical and novel markers, and the preferential vulnerability of limbic areas to neurodegenerative and psychiatric diseases.
    [Show full text]
  • Cortical Connections Position Primate Area 25 As a Keystone for Interoception, Emotion, and Memory
    The Journal of Neuroscience, February 14, 2018 • 38(7):1677–1698 • 1677 Systems/Circuits Cortical Connections Position Primate Area 25 as a Keystone for Interoception, Emotion, and Memory X Mary Kate P. Joyce1,2 and XHelen Barbas1,2 1Graduate Program in Neuroscience, Boston University and School of Medicine, Boston, Massachusetts 02215, and 2Neural Systems Laboratory, Department of Health Sciences, Boston University, Boston, Massachusetts 02215 The structural and functional integrity of subgenual cingulate area 25 (A25) is crucial for emotional expression and equilibrium. A25 has a key role in affective networks, and its disruption has been linked to mood disorders, but its cortical connections have yet to be systematically or fully studied. Using neural tracers in rhesus monkeys, we found that A25 was densely connected with other ventrome- dial and posterior orbitofrontal areas associated with emotions and homeostasis. A moderate pathway linked A25 with frontopolar area 10, an area associated with complex cognition, which may regulate emotions and dampen negative affect. Beyond the frontal lobe, A25 was connected with auditory association areas and memory-related medial temporal cortices, and with the interoceptive-related anterior insula. A25 mostly targeted the superficial cortical layers of other areas, where broadly dispersed terminations comingled with modula- tory inhibitory or disinhibitory microsystems, suggesting a dominant excitatory effect. The architecture and connections suggest that A25 is the consummate feedback system in the PFC. Conversely, in the entorhinal cortex, A25 pathways terminated in the middle-deep layers amid a strong local inhibitory microenvironment, suggesting gating of hippocampal output to other cortices and memory storage. The graded cortical architecture and associated laminar patterns of connections suggest how areas, layers, and functionally distinct classes of inhibitory neurons can be recruited dynamically to meet task demands.
    [Show full text]
  • Ontology and Nomenclature
    TECHNICAL WHITE PAPER: ONTOLOGY AND NOMENCLATURE OVERVIEW Currently no “standard” anatomical ontology is available for the description of human brain development. The main goal behind the generation of this ontology was to guide specific brain tissue sampling for transcriptome analysis (RNA sequencing) and gene expression microarray using laser microdissection (LMD), and to provide nomenclatures for reference atlases of human brain development. This ontology also aimed to cover both developing and adult human brain structures and to be mostly comparable to the nomenclatures for non- human primates. To reach these goals some structure groupings are different from what is traditionally put forth in the literature. In addition, some acronyms and structure abbreviations also differ from commonly used terms in order to provide unique identifiers across the integrated ontologies and nomenclatures. This ontology follows general developmental stages of the brain and contains both transient (e.g., subplate zone and ganglionic eminence in the forebrain) and established brain structures. The following are some important features of this ontology. First, four main branches, i.e., gray matter, white matter, ventricles and surface structures, were generated under the three major brain regions (forebrain, midbrain and hindbrain). Second, different cortical regions were named as different “cortices” or “areas” rather than “lobes” and “gyri”, due to the difference in cortical appearance between developing (smooth) and mature (gyral) human brains. Third, an additional “transient structures” branch was generated under the “gray matter” branch of the three major brain regions to guide the sampling of some important transient brain lamina and regions. Fourth, the “surface structures” branch mainly contains important brain surface landmarks such as cortical sulci and gyri as well as roots of cranial nerves.
    [Show full text]
  • Differences in Functional Connectivity Along the Anterior-Posterior Axis of Human Hippocampal Subfields
    bioRxiv preprint doi: https://doi.org/10.1101/410720; this version posted February 21, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Differences in functional connectivity along the anterior-posterior axis of human hippocampal subfields Marshall A. Dalton, Cornelia McCormick, Eleanor A. Maguire* Wellcome Centre for Human Neuroimaging, Queen Square Institute of Neurology, University College London, UK *Corresponding author: Wellcome Centre for Human Neuroimaging, Queen Square Institute of Neurology, University College London, 12 Queen Square, London, WC1N 3AR, UK T: +44-20-34484362; F: +44-20-78131445; E: [email protected] (E.A. Maguire) Highlights High resolution resting state functional MRI scans were collected We investigated functional connectivity (FC) of human hippocampal subfields We specifically examined FC along the anterior-posterior axis of subfields FC between subfields extended beyond the canonical tri-synaptic circuit Different portions of subfields showed different patterns of FC with neocortex 1 bioRxiv preprint doi: https://doi.org/10.1101/410720; this version posted February 21, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Abstract There is a paucity of information about how human hippocampal subfields are functionally connected to each other and to neighbouring extra-hippocampal cortices.
    [Show full text]
  • Neuronal Properties and Synaptic Connectivity in Rodent Presubiculum Jean Simonnet
    Neuronal properties and synaptic connectivity in rodent presubiculum Jean Simonnet To cite this version: Jean Simonnet. Neuronal properties and synaptic connectivity in rodent presubiculum. Neurons and Cognition [q-bio.NC]. Université Pierre et Marie Curie - Paris VI, 2014. English. NNT : 2014PA066435. tel-02295014 HAL Id: tel-02295014 https://tel.archives-ouvertes.fr/tel-02295014 Submitted on 24 Sep 2019 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. THÈSE DE DOCTORAT DE L’UNIVERSITÉ PIERRE ET MARIE CURIE Spécialité Neurosciences École doctorale Cerveau – Cognition – Comportement Présentée par : Jean Simonnet Pour obtenir le grade de DOCTEUR DE L’UNIVERSITÉ PIERRE ET MARIE CURIE Sujet de la thèse : Neuronal properties and synaptic connectivity in rodent presubiculum Soutenue le 23.09.2014 devant le jury composé de : Dr Jean-Christophe Poncer Président Dr Dominique Debanne Rapporteur Dr Maria Cecilia Angulo Rapportrice Pr Hannah Monyer Examinatrice Dr Bruno Cauli Examinateur Dr Desdemona Fricker Directrice de thèse Université Pierre & Marie Curie - Paris 6 Tél. Secrétariat : 01 42 34 68 35 Bureau d’accueil, inscription des doctorants Fax : 01 42 34 68 40 et base de données Tél. pour les étudiants de A à EL : 01 42 34 68 41 Esc.
    [Show full text]
  • History, Anatomical Nomenclature, Comparative Anatomy and Functions of the Hippocampal Formation
    Bratisl Lek Listy 2006; 107 (4): 103106 103 TOPICAL REVIEW History, anatomical nomenclature, comparative anatomy and functions of the hippocampal formation El Falougy H, Benuska J Institute of Anatomy, Faculty of Medicine, Comenius University, Bratislava, [email protected] Abstract The complex structures in the cerebral hemispheres is included under one term, the limbic system. Our conception of this system and its special functions rises from the comparative neuroanatomical and neurophysiological studies. The components of the limbic system are the hippocampus, gyrus parahippocampalis, gyrus dentatus, gyrus cinguli, corpus amygdaloideum, nuclei anteriores thalami, hypothalamus and gyrus paraterminalis Because of its unique macroscopic and microscopic structure, the hippocampus is a conspicuous part of the limbic system. During phylogenetic development, the hippocampus developed from a simple cortical plate in amphibians into complex three-dimensional convoluted structure in mammals. In the last few decades, structures of the limbic system were extensively studied. Attention was directed to the physi- ological functions and pathological changes of the hippocampus. Experimental studies proved that the hippocampus has a very important role in the process of learning and memory. Another important functions of the hippocampus as a part of the limbic system is its role in regulation of sexual and emotional behaviour. The term hippocampal formation is defined as the complex of six structures: gyrus dentatus, hippocampus proprius, subiculum proprium, presubiculum, parasubiculum and area entorhinalis In this work we attempt to present a brief review of knowledge about the hippocampus from the point of view of history, anatomical nomenclature, comparative anatomy and functions (Tab. 1, Fig. 2, Ref.
    [Show full text]
  • Behavioral Neuroanatomy: Large-Scale Networks, Association
    M. - MAR S E L M E SU LAM Faced with an anatomical fact proven beyond doubt, any physiological result that stands in contradiction to it loses all its meaning. ... So, first anatomy and then physiology; but if first physiology, then not without ana tomy. —BERNHARD VON GUDDEN(1824-1886), QUOTED BY KORBINIAN BRODMANN, IN LAU RENCE GAREY ‘S TRANSLATION I. INTRODUCTION The human brain displays marked regional variations in architecture, connectivity, neurochemistrv, and physiology. This chapter explores the relevance of these re- gional variations to cognition and behavior. Some topics have been included mostly for the sake of completeness and continuity. Their coverage is brief, either because the available information is limited or because its relevance to behavior and cog- nition is tangential. Other subjects, such as the processing of visual information, are reviewed in extensive detail, both because a lot is known and also because the information helps to articulate general principles relevant to all other domains of behavior. Experiments on laboratory primates will receive considerable emphasis, espe- cially in those areas of cerebral connectivity and physiology where relevant infor- mation is not yet available in the human. Structural homologies across species are always incomplete, and many complex behaviors, particularly those that are of greatest interest to the clinician and cognitive neuroscientist, are either rudimentary or absent in other animals. Nonetheless, the reliance on animal data in this chapter is unlikely to be too misleading since the focus will be on principles rather than specifics and since principles of organization are likely to remain relatively stable across closely related species.
    [Show full text]
  • Neuroimage 192 (2019) 38–51
    NeuroImage 192 (2019) 38–51 Contents lists available at ScienceDirect NeuroImage journal homepage: www.elsevier.com/locate/neuroimage Differences in functional connectivity along the anterior-posterior axis of human hippocampal subfields Marshall A. Dalton, Cornelia McCormick, Eleanor A. Maguire * Wellcome Centre for Human Neuroimaging, UCL Queen Square Institute of Neurology, University College London, UK ARTICLE INFO ABSTRACT Keywords: There is a paucity of information about how human hippocampal subfields are functionally connected to each Hippocampus other and to neighbouring extra-hippocampal cortices. In particular, little is known about whether patterns of fi Hippocampal sub elds functional connectivity (FC) differ down the anterior-posterior axis of each subfield. Here, using high resolution Functional connectivity structural MRI we delineated the hippocampal subfields in healthy young adults. This included the CA fields, Pre/parasubiculum separating DG/CA4 from CA3, separating the pre/parasubiculum from the subiculum, and also segmenting the Uncus uncus. We then used high resolution resting state functional MRI to interrogate FC. We first analysed the FC of each hippocampal subfield in its entirety, in terms of FC with other subfields and with the neighbouring regions, namely entorhinal, perirhinal, posterior parahippocampal and retrosplenial cortices. Next, we analysed FC for different portions of each hippocampal subfield along its anterior-posterior axis, in terms of FC between different parts of a subfield, FC with other subfield portions, and FC of each subfield portion with the neighbouring cortical regions of interest. We found that intrinsic functional connectivity between the subfields aligned generally with the tri-synaptic circuit but also extended beyond it. Our findings also revealed that patterns of functional con- nectivity between the subfields and neighbouring cortical areas differed markedly along the anterior-posterior axis of each hippocampal subfield.
    [Show full text]
  • Topographically Specific Hippocampal Projections Target Functionally Distinct Prefrontal Areas in the Rhesus Monkey
    HIPPOCAMPUS 5:511-533 (1995) Topographically Specific Hippocampal Projections Target Functionally Distinct Prefrontal Areas in the Rhesus Monkey Helen Barbas1r2and Gene J. Blatt2 [Department of Health Sciences, Boston University and lJ2Departmentof Anatomy and Neurobiology, Boston University School of Medicine, Boston, Massachusetts ABSTRACT: The sources of ipsilateral projections from the hippocam- KEY WORDS: medial prefrontal cortex, orbitofrontal pal formation, the presubiculum, area 29a-c, and parasubiculum to me- cortex, memory, CA1, subiculum, .presubiculum, area dial, orbital, and lateral prefrontal cortices were studied with retrograde 29, lateral prefrontal cortex, working memory tracers in 27 rhesus monkeys. labeled neurons within the hippocampal formation (CA1, CA1’, prosubiculum, and subiculum) were found ros- trally, although some were noted throughout the entire rostrocaudal ex- tent of the hippocampal formation. Most labeled neurons in the hip- pocampal formation projected to medial prefrontal cortices, followed by orbital areas. In addition, there were differences in the topography of af- ferent neurons projecting to medial when compared with orbital cortices. Labeled neurons innervating medial cortices were found mainly in the The prefrontal cortex in the rhesus monkey is a large CA1’ and CA1 fields rostrally, but originated in the subicular fields cau- cortical cxpanse associated with complex cognitive, dally. In contrast, labeled neurons which innervated orbital cortices were mnemonic, and emotional processes (for rcvicws, see considerably more focal, emanating from the same relative position within Fuster, 1989; Barbas, 1995a). The functions of pre- a field throughout the rostrocaudal extent of the hippocampal formation. frontal areas are likely to depend on their connections In marked contrast to the pattern of projection to medial and orbital prefrontal cortices, lateral prefrontal areas received projections from only with other cortical and subcortical structures.
    [Show full text]
  • NIH Public Access Author Manuscript Neuroimage
    NIH Public Access Author Manuscript Neuroimage. Author manuscript; available in PMC 2014 January 01. Published in final edited form as: Neuroimage. 2013 January 1; 64C: 32–42. doi:10.1016/j.neuroimage.2012.08.071. Predicting the Location of Human Perirhinal Cortex, Brodmann's area 35, from MRI $watermark-text $watermark-text $watermark-text Jean C. Augustinacka,#, Kristen E. Hubera, Allison A. Stevensa, Michelle Roya, Matthew P. Froschb, André J.W. van der Kouwea, Lawrence L. Walda, Koen Van Leemputa,f, Ann McKeec, Bruce Fischla,d,e, and The Alzheimer's Disease Neuroimaging Initiative* aAthinoula A Martinos Center, Dept. of Radiology, MGH, 149 13th Street, Charlestown MA 02129 USA bC.S. Kubik Laboratory for Neuropathology, Pathology Service, MGH, 55 Fruit St., Boston MA 02115 USA cDepartment of Pathology, Boston University School of Medicine, Bedford Veterans Administration Medical Center, MA 01730 USA dMIT Computer Science and AI Lab, Cambridge MA 02139 USA eMIT Division of Health Sciences and Technology, Cambridge MA 02139 USA fDepartment of Informatics and Mathematical Modeling, Technical University of Denmark, Copenhagen, Denmark Abstract The perirhinal cortex (Brodmann's area 35) is a multimodal area that is important for normal memory function. Specifically, perirhinal cortex is involved in detection of novel objects and manifests neurofibrillary tangles in Alzheimer's disease very early in disease progression. We scanned ex vivo brain hemispheres at standard resolution (1 mm × 1 mm × 1 mm) to construct pial/white matter surfaces in FreeSurfer and scanned again at high resolution (120 μm × 120 μm × 120 μm) to determine cortical architectural boundaries. After labeling perirhinal area 35 in the high resolution images, we mapped the high resolution labels to the surface models to localize area 35 in fourteen cases.
    [Show full text]
  • Layer Pattern in Presubiculum, Parasubiculum and Entorhinal Cortex. a Review
    REVIEW published: 04 October 2017 doi: 10.3389/fnana.2017.00084 The Human Periallocortex: Layer Pattern in Presubiculum, Parasubiculum and Entorhinal Cortex. A Review Ricardo Insausti 1*, Mónica Muñoz-López 1, Ana M. Insausti 2 and Emilio Artacho-Pérula 1 1Human Neuroanatomy Laboratory, School of Medicine, University of Castilla-La Mancha, Albacete, Spain, 2Department of Health Sciences, Physical Therapy School, Public University of Navarra, Tudela, Spain The cortical mantle is not homogeneous, so that three types of cortex can be distinguished: allocortex, periallocortex and isocortex. The main distinction among those three types is based on morphological differences, in particular the number of layers, overall organization, appearance, etc., as well as its connectivity. Additionally, in the phylogenetic scale, this classification is conserved among different mammals. The most primitive and simple cortex is the allocortex, which is characterized by the presence of three layers, with one cellular main layer; it is continued by the periallocortex, which presents six layers, although with enough differences in the layer pattern to separate three different fields: presubiculum (PrS), parasubiculum (PaS), and entorhinal cortex (EC). The closest part to the allocortex (represented by the subiculum) is the PrS, which shows outer (layers I–III) and inner (V–VI) principal layers (lamina principalis externa and lamina principalis interna), both separated by a cell poor band, parallel to the pial surface (layer IV or lamina dissecans). This layer organization is present throughout the anterior- posterior axis. The PaS continues the PrS, but its rostrocaudal extent is shorter than the PrS. The organization of the PaS shows the layer pattern more clearly than in the Edited by: PrS.
    [Show full text]