Optical clearing improves the imaging depth and signal‐to‐noise ratio for digital analysis and three‐dimensional projection of the human enteric nervous system

Background  Due to the dispersed nature of neurites and fibers, the microtome‐based 2‐dimensional histology provides only a limited perspective of the enteric nervous system. To visualize the enteric plexus, we applied optical clearing to avoid scattering in the human ileum to facilitate photon pene...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Neurogastroenterology and motility 2011-10, Vol.23 (10), p.e446-e457
Hauptverfasser: Liu, Y.‐A., Chen, Y., Chiang, A.‐S., Peng, S.‐J., Pasricha, P. J., Tang, S.‐C.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page e457
container_issue 10
container_start_page e446
container_title Neurogastroenterology and motility
container_volume 23
creator Liu, Y.‐A.
Chen, Y.
Chiang, A.‐S.
Peng, S.‐J.
Pasricha, P. J.
Tang, S.‐C.
description Background  Due to the dispersed nature of neurites and fibers, the microtome‐based 2‐dimensional histology provides only a limited perspective of the enteric nervous system. To visualize the enteric plexus, we applied optical clearing to avoid scattering in the human ileum to facilitate photon penetration for 3‐dimensional (3‐D) microscopy of the neural tissue. Methods  Human ileal specimens were derived by trimming the donor bowel due to its excess length during the clinical trial of small intestinal transplantation. The pan‐neuronal marker PGP9.5 was used as the immunostaining target to reveal the enteric plexuses. The labeled tissues were immersed in the optical‐clearing solution prior to deep‐tissue confocal microscopy. The serial sections were digitally analyzed and processed by reconstruction algorithms for 3‐D visualization. Key Results  Optical clearing of the ileal specimen led to less fluorescence signal decay along the focal path in the tissue and a higher signal‐to‐noise ratio of the confocal micrographs in comparison with the untreated saline control. Taking advantage of the high signal‐to‐noise ratio images, we applied software‐based signal analysis to identify the presence of the nerve fibers and quantify the signal peaks. The image stacks derived from the serial anatomic micrographs created panoramic views of the gut wall innervations with their associated microstructures. Conclusions & Inferences  We provide an optical approach to improve the imaging depth in 3‐D neurohistology of the human ileum. This methodology has significant promise in facilitating our understanding of the enteric nervous system in health and disease.
doi_str_mv 10.1111/j.1365-2982.2011.01773.x
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_890032628</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1328508828</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4013-fc1cf81592b0e219c70f80245c22a3ba39147e83bc6ec765cee40c5e3c7af9ba3</originalsourceid><addsrcrecordid>eNqNkUtu2zAQhomiQfNor1Bw126k8iFK1KKLIkiTAmm8adcETY1sGhLpkrQT73qEXCIXy0lK2UmWRbggh5zvnxnwRwhTUtK8vqxKymtRsFaykhFKS0Kbhpd3b9DJS-LtFAtS0JaJY3Qa44oQUrOqfoeOGZWtkE19gh5m62SNHrAZQAfrFtiO6-C3EHFaQr7oxfTYwTotsXYdjnbh9PD49z75vDlvI-Cgk_W49wF3dmFTrqYzs4s27iVpGQAy3NkRXLQ-53DusQKTZQ77ft9quRm1w-ASBGuwg7D1m4jjLiYY36OjXg8RPjydZ-j394tf51fF9ezyx_m368JUhPKiN9T0koqWzQkw2pqG9JKwShjGNJ9r3tKqAcnnpgbT1MIAVMQI4KbRfZvzZ-jToW4e788GYlKjjQaGQTvI0yjZEsJZzWQmP_-XpJxJQaTco_KAmuBjDNCrdcj_GnaKEjXZqVZqck1NrqnJTrW3U91l6cenLpv5CN2L8Nm_DHw9ALd2gN2rC6ubn7Mp4v8ATJi1fQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1328508828</pqid></control><display><type>article</type><title>Optical clearing improves the imaging depth and signal‐to‐noise ratio for digital analysis and three‐dimensional projection of the human enteric nervous system</title><source>Wiley Free Content</source><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Liu, Y.‐A. ; Chen, Y. ; Chiang, A.‐S. ; Peng, S.‐J. ; Pasricha, P. J. ; Tang, S.‐C.</creator><creatorcontrib>Liu, Y.‐A. ; Chen, Y. ; Chiang, A.‐S. ; Peng, S.‐J. ; Pasricha, P. J. ; Tang, S.‐C.</creatorcontrib><description>Background  Due to the dispersed nature of neurites and fibers, the microtome‐based 2‐dimensional histology provides only a limited perspective of the enteric nervous system. To visualize the enteric plexus, we applied optical clearing to avoid scattering in the human ileum to facilitate photon penetration for 3‐dimensional (3‐D) microscopy of the neural tissue. Methods  Human ileal specimens were derived by trimming the donor bowel due to its excess length during the clinical trial of small intestinal transplantation. The pan‐neuronal marker PGP9.5 was used as the immunostaining target to reveal the enteric plexuses. The labeled tissues were immersed in the optical‐clearing solution prior to deep‐tissue confocal microscopy. The serial sections were digitally analyzed and processed by reconstruction algorithms for 3‐D visualization. Key Results  Optical clearing of the ileal specimen led to less fluorescence signal decay along the focal path in the tissue and a higher signal‐to‐noise ratio of the confocal micrographs in comparison with the untreated saline control. Taking advantage of the high signal‐to‐noise ratio images, we applied software‐based signal analysis to identify the presence of the nerve fibers and quantify the signal peaks. The image stacks derived from the serial anatomic micrographs created panoramic views of the gut wall innervations with their associated microstructures. Conclusions &amp; Inferences  We provide an optical approach to improve the imaging depth in 3‐D neurohistology of the human ileum. This methodology has significant promise in facilitating our understanding of the enteric nervous system in health and disease.</description><identifier>ISSN: 1350-1925</identifier><identifier>EISSN: 1365-2982</identifier><identifier>DOI: 10.1111/j.1365-2982.2011.01773.x</identifier><identifier>PMID: 21895876</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>3‐D histology ; Algorithms ; Axons ; Buffers ; Clinical trials ; Confocal microscopy ; Data processing ; Digestive tract ; Donors ; Enteric nervous system ; Enteric Nervous System - anatomy &amp; histology ; Fluorescence ; human intestine ; Humans ; Ileum ; Ileum - innervation ; Image Processing, Computer-Assisted ; Imaging, Three-Dimensional - methods ; Innervation ; Intestine ; Microscopy, Confocal - methods ; optical clearing ; Photons ; Transplantation</subject><ispartof>Neurogastroenterology and motility, 2011-10, Vol.23 (10), p.e446-e457</ispartof><rights>2011 Blackwell Publishing Ltd</rights><rights>2011 Blackwell Publishing Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4013-fc1cf81592b0e219c70f80245c22a3ba39147e83bc6ec765cee40c5e3c7af9ba3</citedby><cites>FETCH-LOGICAL-c4013-fc1cf81592b0e219c70f80245c22a3ba39147e83bc6ec765cee40c5e3c7af9ba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2982.2011.01773.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2982.2011.01773.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21895876$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Y.‐A.</creatorcontrib><creatorcontrib>Chen, Y.</creatorcontrib><creatorcontrib>Chiang, A.‐S.</creatorcontrib><creatorcontrib>Peng, S.‐J.</creatorcontrib><creatorcontrib>Pasricha, P. J.</creatorcontrib><creatorcontrib>Tang, S.‐C.</creatorcontrib><title>Optical clearing improves the imaging depth and signal‐to‐noise ratio for digital analysis and three‐dimensional projection of the human enteric nervous system</title><title>Neurogastroenterology and motility</title><addtitle>Neurogastroenterol Motil</addtitle><description>Background  Due to the dispersed nature of neurites and fibers, the microtome‐based 2‐dimensional histology provides only a limited perspective of the enteric nervous system. To visualize the enteric plexus, we applied optical clearing to avoid scattering in the human ileum to facilitate photon penetration for 3‐dimensional (3‐D) microscopy of the neural tissue. Methods  Human ileal specimens were derived by trimming the donor bowel due to its excess length during the clinical trial of small intestinal transplantation. The pan‐neuronal marker PGP9.5 was used as the immunostaining target to reveal the enteric plexuses. The labeled tissues were immersed in the optical‐clearing solution prior to deep‐tissue confocal microscopy. The serial sections were digitally analyzed and processed by reconstruction algorithms for 3‐D visualization. Key Results  Optical clearing of the ileal specimen led to less fluorescence signal decay along the focal path in the tissue and a higher signal‐to‐noise ratio of the confocal micrographs in comparison with the untreated saline control. Taking advantage of the high signal‐to‐noise ratio images, we applied software‐based signal analysis to identify the presence of the nerve fibers and quantify the signal peaks. The image stacks derived from the serial anatomic micrographs created panoramic views of the gut wall innervations with their associated microstructures. Conclusions &amp; Inferences  We provide an optical approach to improve the imaging depth in 3‐D neurohistology of the human ileum. This methodology has significant promise in facilitating our understanding of the enteric nervous system in health and disease.</description><subject>3‐D histology</subject><subject>Algorithms</subject><subject>Axons</subject><subject>Buffers</subject><subject>Clinical trials</subject><subject>Confocal microscopy</subject><subject>Data processing</subject><subject>Digestive tract</subject><subject>Donors</subject><subject>Enteric nervous system</subject><subject>Enteric Nervous System - anatomy &amp; histology</subject><subject>Fluorescence</subject><subject>human intestine</subject><subject>Humans</subject><subject>Ileum</subject><subject>Ileum - innervation</subject><subject>Image Processing, Computer-Assisted</subject><subject>Imaging, Three-Dimensional - methods</subject><subject>Innervation</subject><subject>Intestine</subject><subject>Microscopy, Confocal - methods</subject><subject>optical clearing</subject><subject>Photons</subject><subject>Transplantation</subject><issn>1350-1925</issn><issn>1365-2982</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtu2zAQhomiQfNor1Bw126k8iFK1KKLIkiTAmm8adcETY1sGhLpkrQT73qEXCIXy0lK2UmWRbggh5zvnxnwRwhTUtK8vqxKymtRsFaykhFKS0Kbhpd3b9DJS-LtFAtS0JaJY3Qa44oQUrOqfoeOGZWtkE19gh5m62SNHrAZQAfrFtiO6-C3EHFaQr7oxfTYwTotsXYdjnbh9PD49z75vDlvI-Cgk_W49wF3dmFTrqYzs4s27iVpGQAy3NkRXLQ-53DusQKTZQ77ft9quRm1w-ASBGuwg7D1m4jjLiYY36OjXg8RPjydZ-j394tf51fF9ezyx_m368JUhPKiN9T0koqWzQkw2pqG9JKwShjGNJ9r3tKqAcnnpgbT1MIAVMQI4KbRfZvzZ-jToW4e788GYlKjjQaGQTvI0yjZEsJZzWQmP_-XpJxJQaTco_KAmuBjDNCrdcj_GnaKEjXZqVZqck1NrqnJTrW3U91l6cenLpv5CN2L8Nm_DHw9ALd2gN2rC6ubn7Mp4v8ATJi1fQ</recordid><startdate>201110</startdate><enddate>201110</enddate><creator>Liu, Y.‐A.</creator><creator>Chen, Y.</creator><creator>Chiang, A.‐S.</creator><creator>Peng, S.‐J.</creator><creator>Pasricha, P. J.</creator><creator>Tang, S.‐C.</creator><general>Blackwell Publishing Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>201110</creationdate><title>Optical clearing improves the imaging depth and signal‐to‐noise ratio for digital analysis and three‐dimensional projection of the human enteric nervous system</title><author>Liu, Y.‐A. ; Chen, Y. ; Chiang, A.‐S. ; Peng, S.‐J. ; Pasricha, P. J. ; Tang, S.‐C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4013-fc1cf81592b0e219c70f80245c22a3ba39147e83bc6ec765cee40c5e3c7af9ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>3‐D histology</topic><topic>Algorithms</topic><topic>Axons</topic><topic>Buffers</topic><topic>Clinical trials</topic><topic>Confocal microscopy</topic><topic>Data processing</topic><topic>Digestive tract</topic><topic>Donors</topic><topic>Enteric nervous system</topic><topic>Enteric Nervous System - anatomy &amp; histology</topic><topic>Fluorescence</topic><topic>human intestine</topic><topic>Humans</topic><topic>Ileum</topic><topic>Ileum - innervation</topic><topic>Image Processing, Computer-Assisted</topic><topic>Imaging, Three-Dimensional - methods</topic><topic>Innervation</topic><topic>Intestine</topic><topic>Microscopy, Confocal - methods</topic><topic>optical clearing</topic><topic>Photons</topic><topic>Transplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Y.‐A.</creatorcontrib><creatorcontrib>Chen, Y.</creatorcontrib><creatorcontrib>Chiang, A.‐S.</creatorcontrib><creatorcontrib>Peng, S.‐J.</creatorcontrib><creatorcontrib>Pasricha, P. J.</creatorcontrib><creatorcontrib>Tang, S.‐C.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neurogastroenterology and motility</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Y.‐A.</au><au>Chen, Y.</au><au>Chiang, A.‐S.</au><au>Peng, S.‐J.</au><au>Pasricha, P. J.</au><au>Tang, S.‐C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optical clearing improves the imaging depth and signal‐to‐noise ratio for digital analysis and three‐dimensional projection of the human enteric nervous system</atitle><jtitle>Neurogastroenterology and motility</jtitle><addtitle>Neurogastroenterol Motil</addtitle><date>2011-10</date><risdate>2011</risdate><volume>23</volume><issue>10</issue><spage>e446</spage><epage>e457</epage><pages>e446-e457</pages><issn>1350-1925</issn><eissn>1365-2982</eissn><abstract>Background  Due to the dispersed nature of neurites and fibers, the microtome‐based 2‐dimensional histology provides only a limited perspective of the enteric nervous system. To visualize the enteric plexus, we applied optical clearing to avoid scattering in the human ileum to facilitate photon penetration for 3‐dimensional (3‐D) microscopy of the neural tissue. Methods  Human ileal specimens were derived by trimming the donor bowel due to its excess length during the clinical trial of small intestinal transplantation. The pan‐neuronal marker PGP9.5 was used as the immunostaining target to reveal the enteric plexuses. The labeled tissues were immersed in the optical‐clearing solution prior to deep‐tissue confocal microscopy. The serial sections were digitally analyzed and processed by reconstruction algorithms for 3‐D visualization. Key Results  Optical clearing of the ileal specimen led to less fluorescence signal decay along the focal path in the tissue and a higher signal‐to‐noise ratio of the confocal micrographs in comparison with the untreated saline control. Taking advantage of the high signal‐to‐noise ratio images, we applied software‐based signal analysis to identify the presence of the nerve fibers and quantify the signal peaks. The image stacks derived from the serial anatomic micrographs created panoramic views of the gut wall innervations with their associated microstructures. Conclusions &amp; Inferences  We provide an optical approach to improve the imaging depth in 3‐D neurohistology of the human ileum. This methodology has significant promise in facilitating our understanding of the enteric nervous system in health and disease.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21895876</pmid><doi>10.1111/j.1365-2982.2011.01773.x</doi><tpages>12</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1350-1925
ispartof Neurogastroenterology and motility, 2011-10, Vol.23 (10), p.e446-e457
issn 1350-1925
1365-2982
language eng
recordid cdi_proquest_miscellaneous_890032628
source Wiley Free Content; MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects 3‐D histology
Algorithms
Axons
Buffers
Clinical trials
Confocal microscopy
Data processing
Digestive tract
Donors
Enteric nervous system
Enteric Nervous System - anatomy & histology
Fluorescence
human intestine
Humans
Ileum
Ileum - innervation
Image Processing, Computer-Assisted
Imaging, Three-Dimensional - methods
Innervation
Intestine
Microscopy, Confocal - methods
optical clearing
Photons
Transplantation
title Optical clearing improves the imaging depth and signal‐to‐noise ratio for digital analysis and three‐dimensional projection of the human enteric nervous system
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T12%3A16%3A02IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Optical%20clearing%20improves%20the%20imaging%20depth%20and%20signal%E2%80%90to%E2%80%90noise%20ratio%20for%20digital%20analysis%20and%20three%E2%80%90dimensional%20projection%20of%20the%20human%20enteric%20nervous%20system&rft.jtitle=Neurogastroenterology%20and%20motility&rft.au=Liu,%20Y.%E2%80%90A.&rft.date=2011-10&rft.volume=23&rft.issue=10&rft.spage=e446&rft.epage=e457&rft.pages=e446-e457&rft.issn=1350-1925&rft.eissn=1365-2982&rft_id=info:doi/10.1111/j.1365-2982.2011.01773.x&rft_dat=%3Cproquest_cross%3E1328508828%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1328508828&rft_id=info:pmid/21895876&rfr_iscdi=true