Correspondences between retinotopic areas and myelin maps in human visual cortex

We generated probabilistic area maps and maximum probability maps (MPMs) for a set of 18 retinotopic areas previously mapped in individual subjects (Georgieva et al., 2009 and Kolster et al., 2010) using four different inter-subject registration methods. The best results were obtained using a recent...

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Vydáno v:NeuroImage (Orlando, Fla.) Ročník 99; číslo 100; s. 509 - 524
Hlavní autoři: Abdollahi, Rouhollah O., Kolster, Hauke, Glasser, Matthew F., Robinson, Emma C., Coalson, Timothy S., Dierker, Donna, Jenkinson, Mark, Van Essen, David C., Orban, Guy A.
Médium: Journal Article
Jazyk:angličtina
Vydáno: Amsterdam Elsevier Inc 01.10.2014
Elsevier
Elsevier Limited
Academic Press
Témata:
Adult
Biological and medical sciences
Brain
Brain Mapping
Databases, Factual
Eye and associated structures. Visual pathways and centers. Vision
Female
Fundamental and applied biological sciences. Psychology
Humans
Magnetic Resonance Imaging
Male
Methods
Models, Neurological
Myelin Sheath - physiology
NMR
Nuclear magnetic resonance
Retina
Studies
Vertebrates: nervous system and sense organs
Visual Cortex - physiology
Visual Pathways - physiology
Human
Visual cortex
Visual pathway
Myelin
Central nervous system
Encephalon
ISSN:1053-8119, 1095-9572, 1095-9572
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Abstract We generated probabilistic area maps and maximum probability maps (MPMs) for a set of 18 retinotopic areas previously mapped in individual subjects (Georgieva et al., 2009 and Kolster et al., 2010) using four different inter-subject registration methods. The best results were obtained using a recently developed multimodal surface matching method. The best set of MPMs had relatively smooth borders between visual areas and group average area sizes that matched the typical size in individual subjects. Comparisons between retinotopic areas and maps of estimated cortical myelin content revealed the following correspondences: (i) areas V1, V2, and V3 are heavily myelinated; (ii) the MT cluster is heavily myelinated, with a peak near the MT/pMSTv border; (iii) a dorsal myelin density peak corresponds to area V3D; (iv) the phPIT cluster is lightly myelinated; and (v) myelin density differs across the four areas of the V3A complex. Comparison of the retinotopic MPM with cytoarchitectonic areas, including those previously mapped to the fs_LR cortical surface atlas, revealed a correspondence between areas V1–3 and hOc1–3, respectively, but little correspondence beyond V3. These results indicate that architectonic and retinotopic areal boundaries are in agreement in some regions, and that retinotopy provides a finer-grained parcellation in other regions. The atlas datasets from this analysis are freely available as a resource for other studies that will benefit from retinotopic and myelin density map landmarks in human visual cortex. •Maximum probability maps for 18 retinotopic areas were generated.•Multimodal surface matching was used to compare with myelin and cytoarchitectonic maps.•Early areas V1–3 areas are heavily myelinated, as are V3D and most of areas MT/pMSTv.•The phPIT cluster is lightly myelinated compared to other retinotopic areas.•Early areas V1–3 correspond to areas hOc1–3, with little correspondence beyond V3.
AbstractList We generated probabilistic area maps and maximum probability maps (MPMs) for a set of 18 retinotopic areas previously mapped in individual subjects (Georgieva et al., 2009 and Kolster et al., 2010) using four different inter-subject registration methods. The best results were obtained using a recently developed multimodal surface matching method. The best set of MPMs had relatively smooth borders between visual areas and group average area sizes that matched the typical size in individual subjects. Comparisons between retinotopic areas and maps of estimated cortical myelin content revealed the following correspondences: (i) areas V1, V2, and V3 are heavily myelinated; (ii) the MT cluster is heavily myelinated, with a peak near the MT/pMSTv border; (iii) a dorsal myelin density peak corresponds to area V3D; (iv) the phPIT cluster is lightly myelinated; and (v) myelin density differs across the four areas of the V3A complex. Comparison of the retinotopic MPM with cytoarchitectonic areas, including those previously mapped to the fs_LR cortical surface atlas, revealed a correspondence between areas V1–3 and hOc1–3, respectively, but little correspondence beyond V3. These results indicate that architectonic and retinotopic areal boundaries are in agreement in some regions, and that retinotopy provides a finer-grained parcellation in other regions. The atlas datasets from this analysis are freely available as a resource for other studies that will benefit from retinotopic and myelin density map landmarks in human visual cortex. •Maximum probability maps for 18 retinotopic areas were generated.•Multimodal surface matching was used to compare with myelin and cytoarchitectonic maps.•Early areas V1–3 areas are heavily myelinated, as are V3D and most of areas MT/pMSTv.•The phPIT cluster is lightly myelinated compared to other retinotopic areas.•Early areas V1–3 correspond to areas hOc1–3, with little correspondence beyond V3.
We generated probabilistic area maps and maximum probability maps (MPMs) for a set of 18 retinotopic areas previously mapped in individual subjects (Georgieva et al., 2009 and Kolster et al., 2010) using four different inter-subject registration methods. The best results were obtained using a recently developed multimodal surface matching method. The best set of MPMs had relatively smooth borders between visual areas and group average area sizes that matched the typical size in individual subjects. Comparisons between retinotopic areas and maps of estimated cortical myelin content revealed the following correspondences: (i) areas V1, V2, and V3 are heavily myelinated; (ii) the MT cluster is heavily myelinated, with a peak near the MT/pMSTv border; (iii) a dorsal myelin density peak corresponds to area V3D; (iv) the phPIT cluster is lightly myelinated; and (v) myelin density differs across the four areas of the V3A complex. Comparison of the retinotopic MPM with cytoarchitectonic areas, including those previously mapped to the fs_LR cortical surface atlas, revealed a correspondence between areas V1-3 and hOc1-3, respectively, but little correspondence beyond V3. These results indicate that architectonic and retinotopic areal boundaries are in agreement in some regions, and that retinotopy provides a finer-grained parcellation in other regions. The atlas datasets from this analysis are freely available as a resource for other studies that will benefit from retinotopic and myelin density map landmarks in human visual cortex.
We generated probabilistic area maps and maximum probability maps (MPMs) for a set of 18 retinotopic areas previously mapped in individual subjects (Georgieva et al., 2009 and Kolster et al., 2010) using four different inter-subject registration methods. The best results were obtained using a recently developed multimodal surface matching method. The best set of MPMs had relatively smooth borders between visual areas and group average area sizes that matched the typical size in individual subjects. Comparisons between retinotopic areas and maps of estimated cortical myelin content revealed the following correspondences: (i) areas V1, V2, and V3 are heavily myelinated; (ii) the MT cluster is heavily myelinated, with a peak near the MT/pMSTv border; (iii) a dorsal myelin density peak corresponds to area V3D; (iv) the phPIT cluster is lightly myelinated; and (v) myelin density differs across the four areas of the V3A complex. Comparison of the retinotopic MPM with cytoarchitectonic areas, including those previously mapped to the fs_LR cortical surface atlas, revealed a correspondence between areas V1-3 and hOc1-3, respectively, but little correspondence beyond V3. These results indicate that architectonic and retinotopic areal boundaries are in agreement in some regions, and that retinotopy provides a finer-grained parcellation in other regions. The atlas datasets from this analysis are freely available as a resource for other studies that will benefit from retinotopic and myelin density map landmarks in human visual cortex.We generated probabilistic area maps and maximum probability maps (MPMs) for a set of 18 retinotopic areas previously mapped in individual subjects (Georgieva et al., 2009 and Kolster et al., 2010) using four different inter-subject registration methods. The best results were obtained using a recently developed multimodal surface matching method. The best set of MPMs had relatively smooth borders between visual areas and group average area sizes that matched the typical size in individual subjects. Comparisons between retinotopic areas and maps of estimated cortical myelin content revealed the following correspondences: (i) areas V1, V2, and V3 are heavily myelinated; (ii) the MT cluster is heavily myelinated, with a peak near the MT/pMSTv border; (iii) a dorsal myelin density peak corresponds to area V3D; (iv) the phPIT cluster is lightly myelinated; and (v) myelin density differs across the four areas of the V3A complex. Comparison of the retinotopic MPM with cytoarchitectonic areas, including those previously mapped to the fs_LR cortical surface atlas, revealed a correspondence between areas V1-3 and hOc1-3, respectively, but little correspondence beyond V3. These results indicate that architectonic and retinotopic areal boundaries are in agreement in some regions, and that retinotopy provides a finer-grained parcellation in other regions. The atlas datasets from this analysis are freely available as a resource for other studies that will benefit from retinotopic and myelin density map landmarks in human visual cortex.
We generated probabilistic area maps and maximum probability maps (MPMs) for a set of 18 retinotopic areas previously mapped in individual subjects (Georgieva et al., 2009 and Kolster et al., 2010) using four different inter-subject registration methods. The best results were obtained using a recently developed multimodal surface matching method. The best set of MPMs had relatively smooth borders between visual areas and group average area sizes that matched the typical size in individual subjects. Comparisons between retinotopic areas and maps of estimated cortical myelin content revealed the following correspondences: (i) areas V1, V2, and V3 are heavily myelinated; (ii) the MT cluster is heavily myelinated, with a peak near the MT/pMSTv border; (iii) a dorsal myelin density peak corresponds to area V3D; (iv) the phPIT cluster is lightly myelinated; and (v) myelin density differs across the four areas of the V3A complex. Comparison of the retinotopic MPM with cytoarchitectonic areas, including those previously mapped to the fs_LR cortical surface atlas, revealed a correspondence between areas V1–3 and hOc1–3, respectively, but little correspondence beyond V3. These results indicate that architectonic and retinotopic areal boundaries are in agreement in some regions, and that retinotopy provides a finer-grained parcellation in other regions. The atlas datasets from this analysis are freely available as a resource for other studies that will benefit from retinotopic and myelin density map landmarks in human visual cortex. • Maximum probability maps for 18 retinotopic areas were generated. • Multimodal surface matching was used to compare with myelin and cytoarchitectonic maps. • Early areas V1–3 areas are heavily myelinated, as are V3D and most of areas MT/pMSTv. • The phPIT cluster is lightly myelinated compared to other retinotopic areas. • Early areas V1–3 correspond to areas hOc1–3, with little correspondence beyond V3.
Author Dierker, Donna
Abdollahi, Rouhollah O.
Jenkinson, Mark
Robinson, Emma C.
Glasser, Matthew F.
Kolster, Hauke
Coalson, Timothy S.
Orban, Guy A.
Van Essen, David C.
AuthorAffiliation b Department of Anatomy and Neurobiology, Washington University School of Medicine, St Louis, MO, USA
c Centre for Functional Magnetic Resonance Imaging of the Brain (FMRIB), University of Oxford, Oxford, UK
a Laboratorium voor Neuro-en Psychofysiologie, KU Leuven, Leuven, Belgium
d Department of Neuroscience, University of Parma, Parma, Italy
AuthorAffiliation_xml – name: a Laboratorium voor Neuro-en Psychofysiologie, KU Leuven, Leuven, Belgium
– name: c Centre for Functional Magnetic Resonance Imaging of the Brain (FMRIB), University of Oxford, Oxford, UK
– name: d Department of Neuroscience, University of Parma, Parma, Italy
– name: b Department of Anatomy and Neurobiology, Washington University School of Medicine, St Louis, MO, USA
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  givenname: Rouhollah O.
  surname: Abdollahi
  fullname: Abdollahi, Rouhollah O.
  organization: Laboratorium voor Neuro-en Psychofysiologie, KU Leuven, Leuven, Belgium
– sequence: 2
  givenname: Hauke
  surname: Kolster
  fullname: Kolster, Hauke
  organization: Laboratorium voor Neuro-en Psychofysiologie, KU Leuven, Leuven, Belgium
– sequence: 3
  givenname: Matthew F.
  surname: Glasser
  fullname: Glasser, Matthew F.
  organization: Department of Anatomy and Neurobiology, Washington University School of Medicine, St Louis, MO, USA
– sequence: 4
  givenname: Emma C.
  surname: Robinson
  fullname: Robinson, Emma C.
  organization: Centre for Functional Magnetic Resonance Imaging of the Brain (FMRIB), University of Oxford, Oxford, UK
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  givenname: Timothy S.
  orcidid: 0000-0002-2105-7896
  surname: Coalson
  fullname: Coalson, Timothy S.
  organization: Department of Anatomy and Neurobiology, Washington University School of Medicine, St Louis, MO, USA
– sequence: 6
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  surname: Dierker
  fullname: Dierker, Donna
  organization: Department of Anatomy and Neurobiology, Washington University School of Medicine, St Louis, MO, USA
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  surname: Jenkinson
  fullname: Jenkinson, Mark
  organization: Centre for Functional Magnetic Resonance Imaging of the Brain (FMRIB), University of Oxford, Oxford, UK
– sequence: 8
  givenname: David C.
  surname: Van Essen
  fullname: Van Essen, David C.
  organization: Department of Anatomy and Neurobiology, Washington University School of Medicine, St Louis, MO, USA
– sequence: 9
  givenname: Guy A.
  surname: Orban
  fullname: Orban, Guy A.
  email: guy.orban@med.kuleuven.be
  organization: Laboratorium voor Neuro-en Psychofysiologie, KU Leuven, Leuven, Belgium
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28701147$$DView record in Pascal Francis
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ContentType Journal Article
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Copyright © 2014 Elsevier Inc. All rights reserved.
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– notice: 2015 INIST-CNRS
– notice: Copyright © 2014 Elsevier Inc. All rights reserved.
– notice: Copyright Elsevier Limited Oct 1, 2014
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Issue 100
Keywords Human
Visual cortex
Visual pathway
Myelin
Central nervous system
Encephalon
Language English
License http://creativecommons.org/licenses/by-nc-nd/3.0
CC BY 4.0
Copyright © 2014 Elsevier Inc. All rights reserved.
This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
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Contributed equally.
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Snippet We generated probabilistic area maps and maximum probability maps (MPMs) for a set of 18 retinotopic areas previously mapped in individual subjects (Georgieva...
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SubjectTerms Adult
Biological and medical sciences
Brain
Brain Mapping
Databases, Factual
Eye and associated structures. Visual pathways and centers. Vision
Female
Fundamental and applied biological sciences. Psychology
Humans
Magnetic Resonance Imaging
Male
Methods
Models, Neurological
Myelin Sheath - physiology
NMR
Nuclear magnetic resonance
Retina
Studies
Vertebrates: nervous system and sense organs
Visual Cortex - physiology
Visual Pathways - physiology
Title Correspondences between retinotopic areas and myelin maps in human visual cortex
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https://dx.doi.org/10.1016/j.neuroimage.2014.06.042
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