Connectomic reconstruction of the inner plexiform layer in the mouse retina
Comprehensive high-resolution structural maps are central to functional exploration and understanding in biology. For the nervous system, in which high resolution and large spatial extent are both needed, such maps are scarce as they challenge data acquisition and analysis capabilities. Here we pres...
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Published in | Nature (London) Vol. 500; no. 7461; pp. 168 - 174 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group
08.08.2013
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Subjects | |
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Abstract | Comprehensive high-resolution structural maps are central to functional exploration and understanding in biology. For the nervous system, in which high resolution and large spatial extent are both needed, such maps are scarce as they challenge data acquisition and analysis capabilities. Here we present for the mouse inner plexiform layer--the main computational neuropil region in the mammalian retina--the dense reconstruction of 950 neurons and their mutual contacts. This was achieved by applying a combination of crowd-sourced manual annotation and machine-learning-based volume segmentation to serial block-face electron microscopy data. We characterize a new type of retinal bipolar interneuron and show that we can subdivide a known type based on connectivity. Circuit motifs that emerge from our data indicate a functional mechanism for a known cellular response in a ganglion cell that detects localized motion, and predict that another ganglion cell is motion sensitive. |
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AbstractList | Comprehensive high-resolution structural maps are central to functional exploration and understanding in biology. For the nervous system, in which high resolution and large spatial extent are both needed, such maps are scarce as they challenge data acquisition and analysis capabilities. Here we present for the mouse inner plexiform layer--the main computational neuropil region in the mammalian retina--the dense reconstruction of 950 neurons and their mutual contacts. This was achieved by applying a combination of crowd-sourced manual annotation and machine-learning-based volume segmentation to serial block-face electron microscopy data. We characterize a new type of retinal bipolar interneuron and show that we can subdivide a known type based on connectivity. Circuit motifs that emerge from our data indicate a functional mechanism for a known cellular response in a ganglion cell that detects localized motion, and predict that another ganglion cell is motion sensitive. Comprehensive high-resolution structural maps are central to functional exploration and understanding in biology. For the nervous system, in which high resolution and large spatial extent are both needed, such maps are scarce as they challenge data acquisition and analysis capabilities. Here we present for the mouse inner plexiform layer-the main computational neuropil region in the mammalian retina-the dense reconstruction of 950 neurons and their mutual contacts. This was achieved by applying a combination of crowd-sourced manual annotation and machine-learning-based volume segmentation to serial block-face electron microscopy data. We characterize a new type of retinal bipolar interneuron and show that we can subdivide a known type based on connectivity. Circuit motifs that emerge from our data indicate a functional mechanism for a known cellular response in a ganglion cell that detects localized motion, and predict that another ganglion cell is motion sensitive. [PUBLICATION ABSTRACT] |
Author | SEBASTIAN SEUNG, H TURAGA, Srinivas C JAIN, Viren BRIGGMAN, Kevin L HELMSTAEDTER, Moritz DENK, Winfried |
Author_xml | – sequence: 1 givenname: Moritz surname: HELMSTAEDTER fullname: HELMSTAEDTER, Moritz organization: Max-Planck Institute for Medical Research, 69120 Heidelberg, Germany – sequence: 2 givenname: Kevin L surname: BRIGGMAN fullname: BRIGGMAN, Kevin L organization: Max-Planck Institute for Medical Research, 69120 Heidelberg, Germany – sequence: 3 givenname: Srinivas C surname: TURAGA fullname: TURAGA, Srinivas C organization: Department of Brain and Cognitive Sciences, Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States – sequence: 4 givenname: Viren surname: JAIN fullname: JAIN, Viren organization: Department of Brain and Cognitive Sciences, Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States – sequence: 5 givenname: H surname: SEBASTIAN SEUNG fullname: SEBASTIAN SEUNG, H organization: Department of Brain and Cognitive Sciences, Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States – sequence: 6 givenname: Winfried surname: DENK fullname: DENK, Winfried organization: Max-Planck Institute for Medical Research, 69120 Heidelberg, Germany |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27605664$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/23925239$$D View this record in MEDLINE/PubMed |
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Keywords | Cartography Data analysis High resolution Rodentia Exploration Retina Nervous system Interneuron Neuropile Eye Learning Visual system Vertebrata Mammalia Acquisition process Mouse Animal Inner plexiform layer |
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SubjectTerms | Amacrine Cells - cytology Amacrine Cells - physiology Animals Biological and medical sciences Cell Communication Classification Connectome Eye and associated structures. Visual pathways and centers. Vision Fundamental and applied biological sciences. Psychology Image Processing, Computer-Assisted Mice Mice, Inbred C57BL Microscopy Microscopy, Electron Models, Biological Neural networks Neuropil - physiology Retina - cytology Retina - physiology Retinal Ganglion Cells - cytology Retinal Ganglion Cells - physiology Studies Vertebrates: nervous system and sense organs |
Title | Connectomic reconstruction of the inner plexiform layer in the mouse retina |
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