Corneal epithelial cells function as surrogate Schwann cells for their sensory nerves
The eye is innervated by neurons derived from both the central nervous system and peripheral nervous system (PNS). While much is known about retinal neurobiology and phototransduction, less attention has been paid to the innervation of the eye by the PNS and the roles it plays in maintaining a funct...
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Veröffentlicht in: | Glia 2017-06, Vol.65 (6), p.851-863 |
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description | The eye is innervated by neurons derived from both the central nervous system and peripheral nervous system (PNS). While much is known about retinal neurobiology and phototransduction, less attention has been paid to the innervation of the eye by the PNS and the roles it plays in maintaining a functioning visual system. The ophthalmic branch of the trigeminal ganglion contains somas of neurons that innervate the cornea. These nerves provide sensory functions for the cornea and are referred to as intraepithelial corneal nerves (ICNs) consisting of subbasal nerves and their associated intraepithelial nerve terminals. ICNs project for several millimeters within the corneal epithelium without Schwann cell support. Here, we present evidence for the hypothesis that corneal epithelial cells function as glial cells to support the ICNs. Much of the data supporting this hypothesis is derived from studies of corneal development and the reinnervation of the ICNs in the rodent and rabbit cornea after superficial wounds. Corneal epithelial cells activate in response to injury via mechanisms similar to those induced in Schwann cells during Wallerian Degeneration. Corneal epithelial cells phagocytize distal axon fragments within hours of ICN crush wounds. During aging, the proteins, lipids, and mitochondria within the ICNs become damaged in a process exacerbated by UV light. We propose that ICNs shed their aged and damaged termini and continuously elongate to maintain their density. Available evidence points to new unexpected roles for corneal epithelial cells functioning as surrogate Schwann cells for the ICNs during homeostasis and in response to injury. GLIA 2017;65:851–863
Main points
Sensory subbasal nerves (SBN) of the cornea project for millimeters with no glial support.
Corneal epithelial cell (CEC) plasma membranes wrap around bundles of SBNs.
Axon fragments are phagocytized by CECs after crush injuries.
CECs function like Schwann cells in supporting SBNs. |
doi_str_mv | 10.1002/glia.23102 |
format | Article |
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Main points
Sensory subbasal nerves (SBN) of the cornea project for millimeters with no glial support.
Corneal epithelial cell (CEC) plasma membranes wrap around bundles of SBNs.
Axon fragments are phagocytized by CECs after crush injuries.
CECs function like Schwann cells in supporting SBNs.</description><identifier>ISSN: 0894-1491</identifier><identifier>EISSN: 1098-1136</identifier><identifier>DOI: 10.1002/glia.23102</identifier><identifier>PMID: 27878997</identifier><identifier>CODEN: GLIAEJ</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Animals ; Cornea ; corneal nerves ; epithelium ; Epithelium, Corneal - growth & development ; Epithelium, Corneal - injuries ; Epithelium, Corneal - physiology ; Epithelium, Corneal - physiopathology ; Humans ; Hypotheses ; Nervous system ; Neurosciences ; peripheral nervous system ; Peripheral Nervous System - growth & development ; Peripheral Nervous System - injuries ; Peripheral Nervous System - physiology ; Peripheral Nervous System - physiopathology ; Schwann cells ; Schwann Cells - physiology ; Sensory Receptor Cells - physiology ; wound response</subject><ispartof>Glia, 2017-06, Vol.65 (6), p.851-863</ispartof><rights>2016 Wiley Periodicals, Inc.</rights><rights>2017 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4462-cee3c1ef3133bcfa4cf1973842ab4b5e29036dc6fa406f3e3b8ec1a68fc16ab23</citedby><orcidid>0000-0001-5623-2538</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fglia.23102$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fglia.23102$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27878997$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stepp, Mary Ann</creatorcontrib><creatorcontrib>Tadvalkar, Gauri</creatorcontrib><creatorcontrib>Hakh, Raymond</creatorcontrib><creatorcontrib>Pal‐Ghosh, Sonali</creatorcontrib><title>Corneal epithelial cells function as surrogate Schwann cells for their sensory nerves</title><title>Glia</title><addtitle>Glia</addtitle><description>The eye is innervated by neurons derived from both the central nervous system and peripheral nervous system (PNS). While much is known about retinal neurobiology and phototransduction, less attention has been paid to the innervation of the eye by the PNS and the roles it plays in maintaining a functioning visual system. The ophthalmic branch of the trigeminal ganglion contains somas of neurons that innervate the cornea. These nerves provide sensory functions for the cornea and are referred to as intraepithelial corneal nerves (ICNs) consisting of subbasal nerves and their associated intraepithelial nerve terminals. ICNs project for several millimeters within the corneal epithelium without Schwann cell support. Here, we present evidence for the hypothesis that corneal epithelial cells function as glial cells to support the ICNs. Much of the data supporting this hypothesis is derived from studies of corneal development and the reinnervation of the ICNs in the rodent and rabbit cornea after superficial wounds. Corneal epithelial cells activate in response to injury via mechanisms similar to those induced in Schwann cells during Wallerian Degeneration. Corneal epithelial cells phagocytize distal axon fragments within hours of ICN crush wounds. During aging, the proteins, lipids, and mitochondria within the ICNs become damaged in a process exacerbated by UV light. We propose that ICNs shed their aged and damaged termini and continuously elongate to maintain their density. Available evidence points to new unexpected roles for corneal epithelial cells functioning as surrogate Schwann cells for the ICNs during homeostasis and in response to injury. GLIA 2017;65:851–863
Main points
Sensory subbasal nerves (SBN) of the cornea project for millimeters with no glial support.
Corneal epithelial cell (CEC) plasma membranes wrap around bundles of SBNs.
Axon fragments are phagocytized by CECs after crush injuries.
CECs function like Schwann cells in supporting SBNs.</description><subject>Animals</subject><subject>Cornea</subject><subject>corneal nerves</subject><subject>epithelium</subject><subject>Epithelium, Corneal - growth & development</subject><subject>Epithelium, Corneal - injuries</subject><subject>Epithelium, Corneal - physiology</subject><subject>Epithelium, Corneal - physiopathology</subject><subject>Humans</subject><subject>Hypotheses</subject><subject>Nervous system</subject><subject>Neurosciences</subject><subject>peripheral nervous system</subject><subject>Peripheral Nervous System - growth & development</subject><subject>Peripheral Nervous System - injuries</subject><subject>Peripheral Nervous System - physiology</subject><subject>Peripheral Nervous System - physiopathology</subject><subject>Schwann cells</subject><subject>Schwann Cells - physiology</subject><subject>Sensory Receptor Cells - physiology</subject><subject>wound response</subject><issn>0894-1491</issn><issn>1098-1136</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU9PGzEQxa2KqqS0l34AZIlLL0s99q7XviChqAWkSD20nC2vmU2MNnawd4Py7XH4J-ipJ4_1fvM0M4-Qb8BOgTH-Yzl4e8oFMP6BzIBpVQEIeUBmTOm6glrDIfmc8y1jUD7tJ3LIW9UqrdsZuZ7HFNAOFDd-XGFxGqjDYci0n4IbfQzUZpqnlOLSjkj_uNW9DeGFiYmWLp9oxpBj2tGAaYv5C_nY2yHj1-f3iFz_-vl3flktfl9czc8XlatrySuHKBxgL0CIzvW2dj3oVqia267uGuSaCXnjZFGY7AWKTqEDK1XvQNqOiyNy9uS7mbo13jgMY7KD2SS_tmlnovXmvRL8yizj1jRCN-VgxeD7s0GKdxPm0ax93u9mA8YpG1AalGq4lP-B1kJz1nIo6Mk_6G2cUiiXKJRSheKsKdTx2-Ffp34JpwDwBNz7AXevOjCzj93sYzePsZuLxdX5YyUeALGboXM</recordid><startdate>201706</startdate><enddate>201706</enddate><creator>Stepp, Mary Ann</creator><creator>Tadvalkar, Gauri</creator><creator>Hakh, Raymond</creator><creator>Pal‐Ghosh, Sonali</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QL</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5623-2538</orcidid></search><sort><creationdate>201706</creationdate><title>Corneal epithelial cells function as surrogate Schwann cells for their sensory nerves</title><author>Stepp, Mary Ann ; Tadvalkar, Gauri ; Hakh, Raymond ; Pal‐Ghosh, Sonali</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4462-cee3c1ef3133bcfa4cf1973842ab4b5e29036dc6fa406f3e3b8ec1a68fc16ab23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Cornea</topic><topic>corneal nerves</topic><topic>epithelium</topic><topic>Epithelium, Corneal - growth & development</topic><topic>Epithelium, Corneal - injuries</topic><topic>Epithelium, Corneal - physiology</topic><topic>Epithelium, Corneal - physiopathology</topic><topic>Humans</topic><topic>Hypotheses</topic><topic>Nervous system</topic><topic>Neurosciences</topic><topic>peripheral nervous system</topic><topic>Peripheral Nervous System - growth & development</topic><topic>Peripheral Nervous System - injuries</topic><topic>Peripheral Nervous System - physiology</topic><topic>Peripheral Nervous System - physiopathology</topic><topic>Schwann cells</topic><topic>Schwann Cells - physiology</topic><topic>Sensory Receptor Cells - physiology</topic><topic>wound response</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stepp, Mary Ann</creatorcontrib><creatorcontrib>Tadvalkar, Gauri</creatorcontrib><creatorcontrib>Hakh, Raymond</creatorcontrib><creatorcontrib>Pal‐Ghosh, Sonali</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Glia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stepp, Mary Ann</au><au>Tadvalkar, Gauri</au><au>Hakh, Raymond</au><au>Pal‐Ghosh, Sonali</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Corneal epithelial cells function as surrogate Schwann cells for their sensory nerves</atitle><jtitle>Glia</jtitle><addtitle>Glia</addtitle><date>2017-06</date><risdate>2017</risdate><volume>65</volume><issue>6</issue><spage>851</spage><epage>863</epage><pages>851-863</pages><issn>0894-1491</issn><eissn>1098-1136</eissn><coden>GLIAEJ</coden><abstract>The eye is innervated by neurons derived from both the central nervous system and peripheral nervous system (PNS). While much is known about retinal neurobiology and phototransduction, less attention has been paid to the innervation of the eye by the PNS and the roles it plays in maintaining a functioning visual system. The ophthalmic branch of the trigeminal ganglion contains somas of neurons that innervate the cornea. These nerves provide sensory functions for the cornea and are referred to as intraepithelial corneal nerves (ICNs) consisting of subbasal nerves and their associated intraepithelial nerve terminals. ICNs project for several millimeters within the corneal epithelium without Schwann cell support. Here, we present evidence for the hypothesis that corneal epithelial cells function as glial cells to support the ICNs. Much of the data supporting this hypothesis is derived from studies of corneal development and the reinnervation of the ICNs in the rodent and rabbit cornea after superficial wounds. Corneal epithelial cells activate in response to injury via mechanisms similar to those induced in Schwann cells during Wallerian Degeneration. Corneal epithelial cells phagocytize distal axon fragments within hours of ICN crush wounds. During aging, the proteins, lipids, and mitochondria within the ICNs become damaged in a process exacerbated by UV light. We propose that ICNs shed their aged and damaged termini and continuously elongate to maintain their density. Available evidence points to new unexpected roles for corneal epithelial cells functioning as surrogate Schwann cells for the ICNs during homeostasis and in response to injury. GLIA 2017;65:851–863
Main points
Sensory subbasal nerves (SBN) of the cornea project for millimeters with no glial support.
Corneal epithelial cell (CEC) plasma membranes wrap around bundles of SBNs.
Axon fragments are phagocytized by CECs after crush injuries.
CECs function like Schwann cells in supporting SBNs.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>27878997</pmid><doi>10.1002/glia.23102</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-5623-2538</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cornea corneal nerves epithelium Epithelium, Corneal - growth & development Epithelium, Corneal - injuries Epithelium, Corneal - physiology Epithelium, Corneal - physiopathology Humans Hypotheses Nervous system Neurosciences peripheral nervous system Peripheral Nervous System - growth & development Peripheral Nervous System - injuries Peripheral Nervous System - physiology Peripheral Nervous System - physiopathology Schwann cells Schwann Cells - physiology Sensory Receptor Cells - physiology wound response |
title | Corneal epithelial cells function as surrogate Schwann cells for their sensory nerves |
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