Cryopreserved human precision-cut lung slices provide an immune competent pulmonary test system for "on-demand" use and long-term cultures
Human precision-cut lung slices (hPCLS), considered a highly relevant ex vivo model of the lung, offer native architecture and cells of the lung tissue including respiratory parenchyma, small airways, and immune competent cells. However, the irregular availability of donor lungs has limited the acce...
Gespeichert in:
Veröffentlicht in: | Toxicological sciences 2023-02, Vol.191 (2), p.253-265 |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 265 |
---|---|
container_issue | 2 |
container_start_page | 253 |
container_title | Toxicological sciences |
container_volume | 191 |
creator | Patel, Vivek S Amin, Khalid Wahab, Adam Marimoutou, Méry Ukishima, Lindsey Alvarez, Jose Battle, Kelley Stucki, Andreas O Clippinger, Amy J Behrsing, Holger P |
description | Human precision-cut lung slices (hPCLS), considered a highly relevant ex vivo model of the lung, offer native architecture and cells of the lung tissue including respiratory parenchyma, small airways, and immune competent cells. However, the irregular availability of donor lungs has limited the accessibility of this system. As described here, thousands of hPCLS can be created from 1 lung, cryopreserved, and used "on demand" by applying slicing and cryopreservation methodology improvements. Fresh and cryopreserved (∼7 and ∼34 weeks; F&C) hPCLS from 1 donor lung were cultured for up to 29 days and evaluated for biomass, viability, tissue integrity, and inflammatory markers in response to lipopolysaccharide (LPS; 5 µg/ml) and Triton X-100 (TX100; 0.1%) challenge (24 h) at days 1, 8, 15, 22, and 29 following culture initiation. The F&C hPCLS retained biomass, viability, and tissue integrity throughout the 29 days and demonstrated immune responsiveness with up to ∼30-fold LPS-induced cytokine increases. Histologically, more than 70% of normal cytomorphological features were preserved in all groups through day 29. Similar retention of tissue viability and immune responsiveness post cryopreservation (4-6 weeks) and culture (up to 14 days) was observed in hPCLS from additional 3 donor lungs. Banking cryopreserved hPCLS from various donors (and disease states) provides a critical element in researching human-derived pulmonary tissue. The retention of viability and functional responsiveness (≥4 weeks) allows evaluation of long-term, complex endpoints reflecting key events in Adverse Outcome Pathways and positions hPCLS as a valuable human-relevant model for use in regulatory applications. |
doi_str_mv | 10.1093/toxsci/kfac136 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9936202</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2761982243</sourcerecordid><originalsourceid>FETCH-LOGICAL-c390t-96f852009d1a54f6f47cee3c953185c9c208a2471c5dfef26600f25107b87fcf3</originalsourceid><addsrcrecordid>eNpVkUlvFDEQhS0EIiFw5YisnLh04mXa3b4goRGbFIkLnC3HXZ4YvDReRpm_wK_G0QwRnLzUq69e6SH0mpIrSiS_rum-GHf902pDuXiCzvuvGIhk8unpLshMztCLUn4QQqkg8jk640LQic7jOfq9zYe0ZiiQ97DguxZ0xP1tXHEpDqZV7Fvc4eKdgdIrae8WwF3kQmgRsElhhQqx4rX5kKLOB1yhVFwOpULANmV82UkLdPJyiVt56F6wT3E3VMgBm-Zr6w5eomdW-wKvTucF-v7xw7ft5-Hm66cv2_c3g-GS1EEKO4-MELlQPW6ssJvJAHAjR943MtIwMmu2magZFwuWCUGIZSMl0-08WWP5BXp35K7tNsBiuvesvVqzC928Stqp_yvR3ald2ispuWCEdcDbEyCnX63vqoIrBrzXEVIrik2CypmxDe_Sq6PU5FRKBvs4hhL1EKA6BqhOAfaGN_-ae5T_TYz_AZJMnfc</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2761982243</pqid></control><display><type>article</type><title>Cryopreserved human precision-cut lung slices provide an immune competent pulmonary test system for "on-demand" use and long-term cultures</title><source>MEDLINE</source><source>Full-Text Journals in Chemistry (Open access)</source><source>Oxford Academic Journals (OUP)</source><source>Alma/SFX Local Collection</source><creator>Patel, Vivek S ; Amin, Khalid ; Wahab, Adam ; Marimoutou, Méry ; Ukishima, Lindsey ; Alvarez, Jose ; Battle, Kelley ; Stucki, Andreas O ; Clippinger, Amy J ; Behrsing, Holger P</creator><creatorcontrib>Patel, Vivek S ; Amin, Khalid ; Wahab, Adam ; Marimoutou, Méry ; Ukishima, Lindsey ; Alvarez, Jose ; Battle, Kelley ; Stucki, Andreas O ; Clippinger, Amy J ; Behrsing, Holger P</creatorcontrib><description>Human precision-cut lung slices (hPCLS), considered a highly relevant ex vivo model of the lung, offer native architecture and cells of the lung tissue including respiratory parenchyma, small airways, and immune competent cells. However, the irregular availability of donor lungs has limited the accessibility of this system. As described here, thousands of hPCLS can be created from 1 lung, cryopreserved, and used "on demand" by applying slicing and cryopreservation methodology improvements. Fresh and cryopreserved (∼7 and ∼34 weeks; F&C) hPCLS from 1 donor lung were cultured for up to 29 days and evaluated for biomass, viability, tissue integrity, and inflammatory markers in response to lipopolysaccharide (LPS; 5 µg/ml) and Triton X-100 (TX100; 0.1%) challenge (24 h) at days 1, 8, 15, 22, and 29 following culture initiation. The F&C hPCLS retained biomass, viability, and tissue integrity throughout the 29 days and demonstrated immune responsiveness with up to ∼30-fold LPS-induced cytokine increases. Histologically, more than 70% of normal cytomorphological features were preserved in all groups through day 29. Similar retention of tissue viability and immune responsiveness post cryopreservation (4-6 weeks) and culture (up to 14 days) was observed in hPCLS from additional 3 donor lungs. Banking cryopreserved hPCLS from various donors (and disease states) provides a critical element in researching human-derived pulmonary tissue. The retention of viability and functional responsiveness (≥4 weeks) allows evaluation of long-term, complex endpoints reflecting key events in Adverse Outcome Pathways and positions hPCLS as a valuable human-relevant model for use in regulatory applications.</description><identifier>ISSN: 1096-6080</identifier><identifier>EISSN: 1096-0929</identifier><identifier>DOI: 10.1093/toxsci/kfac136</identifier><identifier>PMID: 36617185</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Cryopreservation - methods ; Emerging Technologies, Methods, and Models ; Humans ; Immune System ; Lipopolysaccharides - toxicity ; Lung - pathology</subject><ispartof>Toxicological sciences, 2023-02, Vol.191 (2), p.253-265</ispartof><rights>The Author(s) 2023. Published by Oxford University Press on behalf of the Society of Toxicology.</rights><rights>The Author(s) 2023. Published by Oxford University Press on behalf of the Society of Toxicology. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-96f852009d1a54f6f47cee3c953185c9c208a2471c5dfef26600f25107b87fcf3</citedby><cites>FETCH-LOGICAL-c390t-96f852009d1a54f6f47cee3c953185c9c208a2471c5dfef26600f25107b87fcf3</cites><orcidid>0000-0001-7284-9837 ; 0000-0003-3623-1196 ; 0000-0001-8583-1548 ; 0000-0002-0997-8502</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36617185$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Patel, Vivek S</creatorcontrib><creatorcontrib>Amin, Khalid</creatorcontrib><creatorcontrib>Wahab, Adam</creatorcontrib><creatorcontrib>Marimoutou, Méry</creatorcontrib><creatorcontrib>Ukishima, Lindsey</creatorcontrib><creatorcontrib>Alvarez, Jose</creatorcontrib><creatorcontrib>Battle, Kelley</creatorcontrib><creatorcontrib>Stucki, Andreas O</creatorcontrib><creatorcontrib>Clippinger, Amy J</creatorcontrib><creatorcontrib>Behrsing, Holger P</creatorcontrib><title>Cryopreserved human precision-cut lung slices provide an immune competent pulmonary test system for "on-demand" use and long-term cultures</title><title>Toxicological sciences</title><addtitle>Toxicol Sci</addtitle><description>Human precision-cut lung slices (hPCLS), considered a highly relevant ex vivo model of the lung, offer native architecture and cells of the lung tissue including respiratory parenchyma, small airways, and immune competent cells. However, the irregular availability of donor lungs has limited the accessibility of this system. As described here, thousands of hPCLS can be created from 1 lung, cryopreserved, and used "on demand" by applying slicing and cryopreservation methodology improvements. Fresh and cryopreserved (∼7 and ∼34 weeks; F&C) hPCLS from 1 donor lung were cultured for up to 29 days and evaluated for biomass, viability, tissue integrity, and inflammatory markers in response to lipopolysaccharide (LPS; 5 µg/ml) and Triton X-100 (TX100; 0.1%) challenge (24 h) at days 1, 8, 15, 22, and 29 following culture initiation. The F&C hPCLS retained biomass, viability, and tissue integrity throughout the 29 days and demonstrated immune responsiveness with up to ∼30-fold LPS-induced cytokine increases. Histologically, more than 70% of normal cytomorphological features were preserved in all groups through day 29. Similar retention of tissue viability and immune responsiveness post cryopreservation (4-6 weeks) and culture (up to 14 days) was observed in hPCLS from additional 3 donor lungs. Banking cryopreserved hPCLS from various donors (and disease states) provides a critical element in researching human-derived pulmonary tissue. The retention of viability and functional responsiveness (≥4 weeks) allows evaluation of long-term, complex endpoints reflecting key events in Adverse Outcome Pathways and positions hPCLS as a valuable human-relevant model for use in regulatory applications.</description><subject>Cryopreservation - methods</subject><subject>Emerging Technologies, Methods, and Models</subject><subject>Humans</subject><subject>Immune System</subject><subject>Lipopolysaccharides - toxicity</subject><subject>Lung - pathology</subject><issn>1096-6080</issn><issn>1096-0929</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkUlvFDEQhS0EIiFw5YisnLh04mXa3b4goRGbFIkLnC3HXZ4YvDReRpm_wK_G0QwRnLzUq69e6SH0mpIrSiS_rum-GHf902pDuXiCzvuvGIhk8unpLshMztCLUn4QQqkg8jk640LQic7jOfq9zYe0ZiiQ97DguxZ0xP1tXHEpDqZV7Fvc4eKdgdIrae8WwF3kQmgRsElhhQqx4rX5kKLOB1yhVFwOpULANmV82UkLdPJyiVt56F6wT3E3VMgBm-Zr6w5eomdW-wKvTucF-v7xw7ft5-Hm66cv2_c3g-GS1EEKO4-MELlQPW6ssJvJAHAjR943MtIwMmu2magZFwuWCUGIZSMl0-08WWP5BXp35K7tNsBiuvesvVqzC928Stqp_yvR3ald2ispuWCEdcDbEyCnX63vqoIrBrzXEVIrik2CypmxDe_Sq6PU5FRKBvs4hhL1EKA6BqhOAfaGN_-ae5T_TYz_AZJMnfc</recordid><startdate>20230217</startdate><enddate>20230217</enddate><creator>Patel, Vivek S</creator><creator>Amin, Khalid</creator><creator>Wahab, Adam</creator><creator>Marimoutou, Méry</creator><creator>Ukishima, Lindsey</creator><creator>Alvarez, Jose</creator><creator>Battle, Kelley</creator><creator>Stucki, Andreas O</creator><creator>Clippinger, Amy J</creator><creator>Behrsing, Holger P</creator><general>Oxford University Press</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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7284-9837</orcidid><orcidid>https://orcid.org/0000-0003-3623-1196</orcidid><orcidid>https://orcid.org/0000-0001-8583-1548</orcidid><orcidid>https://orcid.org/0000-0002-0997-8502</orcidid></search><sort><creationdate>20230217</creationdate><title>Cryopreserved human precision-cut lung slices provide an immune competent pulmonary test system for "on-demand" use and long-term cultures</title><author>Patel, Vivek S ; Amin, Khalid ; Wahab, Adam ; Marimoutou, Méry ; Ukishima, Lindsey ; Alvarez, Jose ; Battle, Kelley ; Stucki, Andreas O ; Clippinger, Amy J ; Behrsing, Holger P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-96f852009d1a54f6f47cee3c953185c9c208a2471c5dfef26600f25107b87fcf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Cryopreservation - methods</topic><topic>Emerging Technologies, Methods, and Models</topic><topic>Humans</topic><topic>Immune System</topic><topic>Lipopolysaccharides - toxicity</topic><topic>Lung - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Patel, Vivek S</creatorcontrib><creatorcontrib>Amin, Khalid</creatorcontrib><creatorcontrib>Wahab, Adam</creatorcontrib><creatorcontrib>Marimoutou, Méry</creatorcontrib><creatorcontrib>Ukishima, Lindsey</creatorcontrib><creatorcontrib>Alvarez, Jose</creatorcontrib><creatorcontrib>Battle, Kelley</creatorcontrib><creatorcontrib>Stucki, Andreas O</creatorcontrib><creatorcontrib>Clippinger, Amy J</creatorcontrib><creatorcontrib>Behrsing, Holger P</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Toxicological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Patel, Vivek S</au><au>Amin, Khalid</au><au>Wahab, Adam</au><au>Marimoutou, Méry</au><au>Ukishima, Lindsey</au><au>Alvarez, Jose</au><au>Battle, Kelley</au><au>Stucki, Andreas O</au><au>Clippinger, Amy J</au><au>Behrsing, Holger P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cryopreserved human precision-cut lung slices provide an immune competent pulmonary test system for "on-demand" use and long-term cultures</atitle><jtitle>Toxicological sciences</jtitle><addtitle>Toxicol Sci</addtitle><date>2023-02-17</date><risdate>2023</risdate><volume>191</volume><issue>2</issue><spage>253</spage><epage>265</epage><pages>253-265</pages><issn>1096-6080</issn><eissn>1096-0929</eissn><abstract>Human precision-cut lung slices (hPCLS), considered a highly relevant ex vivo model of the lung, offer native architecture and cells of the lung tissue including respiratory parenchyma, small airways, and immune competent cells. However, the irregular availability of donor lungs has limited the accessibility of this system. As described here, thousands of hPCLS can be created from 1 lung, cryopreserved, and used "on demand" by applying slicing and cryopreservation methodology improvements. Fresh and cryopreserved (∼7 and ∼34 weeks; F&C) hPCLS from 1 donor lung were cultured for up to 29 days and evaluated for biomass, viability, tissue integrity, and inflammatory markers in response to lipopolysaccharide (LPS; 5 µg/ml) and Triton X-100 (TX100; 0.1%) challenge (24 h) at days 1, 8, 15, 22, and 29 following culture initiation. The F&C hPCLS retained biomass, viability, and tissue integrity throughout the 29 days and demonstrated immune responsiveness with up to ∼30-fold LPS-induced cytokine increases. Histologically, more than 70% of normal cytomorphological features were preserved in all groups through day 29. Similar retention of tissue viability and immune responsiveness post cryopreservation (4-6 weeks) and culture (up to 14 days) was observed in hPCLS from additional 3 donor lungs. Banking cryopreserved hPCLS from various donors (and disease states) provides a critical element in researching human-derived pulmonary tissue. The retention of viability and functional responsiveness (≥4 weeks) allows evaluation of long-term, complex endpoints reflecting key events in Adverse Outcome Pathways and positions hPCLS as a valuable human-relevant model for use in regulatory applications.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>36617185</pmid><doi>10.1093/toxsci/kfac136</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-7284-9837</orcidid><orcidid>https://orcid.org/0000-0003-3623-1196</orcidid><orcidid>https://orcid.org/0000-0001-8583-1548</orcidid><orcidid>https://orcid.org/0000-0002-0997-8502</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1096-6080 |
ispartof | Toxicological sciences, 2023-02, Vol.191 (2), p.253-265 |
issn | 1096-6080 1096-0929 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9936202 |
source | MEDLINE; Full-Text Journals in Chemistry (Open access); Oxford Academic Journals (OUP); Alma/SFX Local Collection |
subjects | Cryopreservation - methods Emerging Technologies, Methods, and Models Humans Immune System Lipopolysaccharides - toxicity Lung - pathology |
title | Cryopreserved human precision-cut lung slices provide an immune competent pulmonary test system for "on-demand" use and long-term cultures |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T18%3A05%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cryopreserved%20human%20precision-cut%20lung%20slices%20provide%20an%20immune%20competent%20pulmonary%20test%20system%20for%20%22on-demand%22%20use%20and%20long-term%20cultures&rft.jtitle=Toxicological%20sciences&rft.au=Patel,%20Vivek%20S&rft.date=2023-02-17&rft.volume=191&rft.issue=2&rft.spage=253&rft.epage=265&rft.pages=253-265&rft.issn=1096-6080&rft.eissn=1096-0929&rft_id=info:doi/10.1093/toxsci/kfac136&rft_dat=%3Cproquest_pubme%3E2761982243%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2761982243&rft_id=info:pmid/36617185&rfr_iscdi=true |