Gelatin-Based Hybrid Hydrogels as Matrices for Organoid Culture
The application of liver organoids is very promising in the field of liver tissue engineering; however, it is still facing some limitations. One of the current major limitations is the matrix in which they are cultured. The mainly undefined and murine-originated tumor matrices derived from Engelbret...
Gespeichert in:
Veröffentlicht in: | Biomacromolecules 2024-02, Vol.25 (2), p.590-604 |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 604 |
---|---|
container_issue | 2 |
container_start_page | 590 |
container_title | Biomacromolecules |
container_volume | 25 |
creator | Carpentier, Nathan Ye, Shicheng Delemarre, Maarten D. Van der Meeren, Louis Skirtach, André G. van der Laan, Luc J. W. Schneeberger, Kerstin Spee, Bart Dubruel, Peter Van Vlierberghe, Sandra |
description | The application of liver organoids is very promising in the field of liver tissue engineering; however, it is still facing some limitations. One of the current major limitations is the matrix in which they are cultured. The mainly undefined and murine-originated tumor matrices derived from Engelbreth–Holm–Swarm (EHS) sarcoma, such as Matrigel, are still the standard culturing matrices for expansion and differentiation of organoids toward hepatocyte-like cells, which will obstruct its future clinical application potential. In this study, we exploited the use of newly developed highly defined hydrogels as potential matrices for the culture of liver organoids and compared them to Matrigel and two hydrogels that were already researched in the field of organoid research [i.e., polyisocyanopeptides, enriched with laminin–entactin complex (PIC-LEC) and gelatin methacryloyl (GelMA)]. The newly developed hydrogels are materials that have a physicochemical resemblance with native liver tissue. Norbornene-modified dextran cross-linked with thiolated gelatin (DexNB-GelSH) has a swelling ratio and macro- and microscale properties that highly mimic liver tissue. Norbornene-modified chondroitin sulfate cross-linked with thiolated gelatin (CSNB-GelSH) contains chondroitin sulfate, which is a glycosaminoglycan (GAG) that is present in the liver ECM. Furthermore, CSNB-GelSH hydrogels with different mechanical properties were evaluated. Bipotent intrahepatic cholangiocyte organoids (ICOs) were applied in this work and encapsulated in these materials. This research revealed that the newly developed materials outperformed Matrigel, PIC-LEC, and GelMA in the differentiation of ICOs toward hepatocyte-like cells. Furthermore, some trends indicate that an interplay of both the chemical composition and the mechanical properties has an influence on the relative expression of certain hepatocyte markers. Both DexNB-GelSH and CSNB-GelSH showed promising results for the expansion and differentiation of intrahepatic cholangiocyte organoids. The stiffest CSNB-GelSH hydrogel even significantly outperformed Matrigel based on ALB, BSEP, and CYP3A4 gene expression, being three important hepatocyte markers. |
doi_str_mv | 10.1021/acs.biomac.2c01496 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2910197196</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2910197196</sourcerecordid><originalsourceid>FETCH-LOGICAL-a337t-e7d3ca81f9be99da921a9518e320a113e51d1f52de356ed0902c2a4263b99d893</originalsourceid><addsrcrecordid>eNp9kD1PwzAURS0EoqXwBxhQRpYEPztfnhBU0CIVdYHZcuyXKlUaFzsZ-u9xSWFkum8490rvEHILNAHK4EFpn1SN3SmdME0hFfkZmULG8jjNKTv_ubO4KEQxIVfebymlgqfZJZnwEoqAsyl5XGCr-qaLn5VHEy0PlWuOYZzdYOsj5aN31btGo49q66K126jOBmQ-tP3g8Jpc1Kr1eHPKGfl8ffmYL-PVevE2f1rFivOij7EwXKsSalGhEEYJBkpkUCJnVAFwzMBAnTGDPMvRUEGZZiplOa8CXgo-I_fj7t7ZrwF9L3eN19i2qkM7eMkEUBAFiDygbES1s947rOXeNTvlDhKoPIqTQZwcxcmTuFC6O-0P1Q7NX-XXVACSETiWt3ZwXXj3v8VvoiV6Rg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2910197196</pqid></control><display><type>article</type><title>Gelatin-Based Hybrid Hydrogels as Matrices for Organoid Culture</title><source>MEDLINE</source><source>ACS Publications</source><creator>Carpentier, Nathan ; Ye, Shicheng ; Delemarre, Maarten D. ; Van der Meeren, Louis ; Skirtach, André G. ; van der Laan, Luc J. W. ; Schneeberger, Kerstin ; Spee, Bart ; Dubruel, Peter ; Van Vlierberghe, Sandra</creator><creatorcontrib>Carpentier, Nathan ; Ye, Shicheng ; Delemarre, Maarten D. ; Van der Meeren, Louis ; Skirtach, André G. ; van der Laan, Luc J. W. ; Schneeberger, Kerstin ; Spee, Bart ; Dubruel, Peter ; Van Vlierberghe, Sandra</creatorcontrib><description>The application of liver organoids is very promising in the field of liver tissue engineering; however, it is still facing some limitations. One of the current major limitations is the matrix in which they are cultured. The mainly undefined and murine-originated tumor matrices derived from Engelbreth–Holm–Swarm (EHS) sarcoma, such as Matrigel, are still the standard culturing matrices for expansion and differentiation of organoids toward hepatocyte-like cells, which will obstruct its future clinical application potential. In this study, we exploited the use of newly developed highly defined hydrogels as potential matrices for the culture of liver organoids and compared them to Matrigel and two hydrogels that were already researched in the field of organoid research [i.e., polyisocyanopeptides, enriched with laminin–entactin complex (PIC-LEC) and gelatin methacryloyl (GelMA)]. The newly developed hydrogels are materials that have a physicochemical resemblance with native liver tissue. Norbornene-modified dextran cross-linked with thiolated gelatin (DexNB-GelSH) has a swelling ratio and macro- and microscale properties that highly mimic liver tissue. Norbornene-modified chondroitin sulfate cross-linked with thiolated gelatin (CSNB-GelSH) contains chondroitin sulfate, which is a glycosaminoglycan (GAG) that is present in the liver ECM. Furthermore, CSNB-GelSH hydrogels with different mechanical properties were evaluated. Bipotent intrahepatic cholangiocyte organoids (ICOs) were applied in this work and encapsulated in these materials. This research revealed that the newly developed materials outperformed Matrigel, PIC-LEC, and GelMA in the differentiation of ICOs toward hepatocyte-like cells. Furthermore, some trends indicate that an interplay of both the chemical composition and the mechanical properties has an influence on the relative expression of certain hepatocyte markers. Both DexNB-GelSH and CSNB-GelSH showed promising results for the expansion and differentiation of intrahepatic cholangiocyte organoids. The stiffest CSNB-GelSH hydrogel even significantly outperformed Matrigel based on ALB, BSEP, and CYP3A4 gene expression, being three important hepatocyte markers.</description><identifier>ISSN: 1525-7797</identifier><identifier>ISSN: 1526-4602</identifier><identifier>EISSN: 1526-4602</identifier><identifier>DOI: 10.1021/acs.biomac.2c01496</identifier><identifier>PMID: 38174962</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Animals ; Chondroitin Sulfates ; Gelatin - chemistry ; Hydrogels - chemistry ; Hydrogels - pharmacology ; Mice ; Norbornanes ; Organoids ; Tissue Engineering - methods</subject><ispartof>Biomacromolecules, 2024-02, Vol.25 (2), p.590-604</ispartof><rights>2024 American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-a337t-e7d3ca81f9be99da921a9518e320a113e51d1f52de356ed0902c2a4263b99d893</cites><orcidid>0000-0002-7985-4310 ; 0000-0002-4468-7620 ; 0000-0002-6671-5055 ; 0000-0001-7688-1682</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.biomac.2c01496$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.biomac.2c01496$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2764,27075,27923,27924,56737,56787</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38174962$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Carpentier, Nathan</creatorcontrib><creatorcontrib>Ye, Shicheng</creatorcontrib><creatorcontrib>Delemarre, Maarten D.</creatorcontrib><creatorcontrib>Van der Meeren, Louis</creatorcontrib><creatorcontrib>Skirtach, André G.</creatorcontrib><creatorcontrib>van der Laan, Luc J. W.</creatorcontrib><creatorcontrib>Schneeberger, Kerstin</creatorcontrib><creatorcontrib>Spee, Bart</creatorcontrib><creatorcontrib>Dubruel, Peter</creatorcontrib><creatorcontrib>Van Vlierberghe, Sandra</creatorcontrib><title>Gelatin-Based Hybrid Hydrogels as Matrices for Organoid Culture</title><title>Biomacromolecules</title><addtitle>Biomacromolecules</addtitle><description>The application of liver organoids is very promising in the field of liver tissue engineering; however, it is still facing some limitations. One of the current major limitations is the matrix in which they are cultured. The mainly undefined and murine-originated tumor matrices derived from Engelbreth–Holm–Swarm (EHS) sarcoma, such as Matrigel, are still the standard culturing matrices for expansion and differentiation of organoids toward hepatocyte-like cells, which will obstruct its future clinical application potential. In this study, we exploited the use of newly developed highly defined hydrogels as potential matrices for the culture of liver organoids and compared them to Matrigel and two hydrogels that were already researched in the field of organoid research [i.e., polyisocyanopeptides, enriched with laminin–entactin complex (PIC-LEC) and gelatin methacryloyl (GelMA)]. The newly developed hydrogels are materials that have a physicochemical resemblance with native liver tissue. Norbornene-modified dextran cross-linked with thiolated gelatin (DexNB-GelSH) has a swelling ratio and macro- and microscale properties that highly mimic liver tissue. Norbornene-modified chondroitin sulfate cross-linked with thiolated gelatin (CSNB-GelSH) contains chondroitin sulfate, which is a glycosaminoglycan (GAG) that is present in the liver ECM. Furthermore, CSNB-GelSH hydrogels with different mechanical properties were evaluated. Bipotent intrahepatic cholangiocyte organoids (ICOs) were applied in this work and encapsulated in these materials. This research revealed that the newly developed materials outperformed Matrigel, PIC-LEC, and GelMA in the differentiation of ICOs toward hepatocyte-like cells. Furthermore, some trends indicate that an interplay of both the chemical composition and the mechanical properties has an influence on the relative expression of certain hepatocyte markers. Both DexNB-GelSH and CSNB-GelSH showed promising results for the expansion and differentiation of intrahepatic cholangiocyte organoids. The stiffest CSNB-GelSH hydrogel even significantly outperformed Matrigel based on ALB, BSEP, and CYP3A4 gene expression, being three important hepatocyte markers.</description><subject>Animals</subject><subject>Chondroitin Sulfates</subject><subject>Gelatin - chemistry</subject><subject>Hydrogels - chemistry</subject><subject>Hydrogels - pharmacology</subject><subject>Mice</subject><subject>Norbornanes</subject><subject>Organoids</subject><subject>Tissue Engineering - methods</subject><issn>1525-7797</issn><issn>1526-4602</issn><issn>1526-4602</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kD1PwzAURS0EoqXwBxhQRpYEPztfnhBU0CIVdYHZcuyXKlUaFzsZ-u9xSWFkum8490rvEHILNAHK4EFpn1SN3SmdME0hFfkZmULG8jjNKTv_ubO4KEQxIVfebymlgqfZJZnwEoqAsyl5XGCr-qaLn5VHEy0PlWuOYZzdYOsj5aN31btGo49q66K126jOBmQ-tP3g8Jpc1Kr1eHPKGfl8ffmYL-PVevE2f1rFivOij7EwXKsSalGhEEYJBkpkUCJnVAFwzMBAnTGDPMvRUEGZZiplOa8CXgo-I_fj7t7ZrwF9L3eN19i2qkM7eMkEUBAFiDygbES1s947rOXeNTvlDhKoPIqTQZwcxcmTuFC6O-0P1Q7NX-XXVACSETiWt3ZwXXj3v8VvoiV6Rg</recordid><startdate>20240212</startdate><enddate>20240212</enddate><creator>Carpentier, Nathan</creator><creator>Ye, Shicheng</creator><creator>Delemarre, Maarten D.</creator><creator>Van der Meeren, Louis</creator><creator>Skirtach, André G.</creator><creator>van der Laan, Luc J. W.</creator><creator>Schneeberger, Kerstin</creator><creator>Spee, Bart</creator><creator>Dubruel, Peter</creator><creator>Van Vlierberghe, Sandra</creator><general>American Chemical Society</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><orcidid>https://orcid.org/0000-0002-7985-4310</orcidid><orcidid>https://orcid.org/0000-0002-4468-7620</orcidid><orcidid>https://orcid.org/0000-0002-6671-5055</orcidid><orcidid>https://orcid.org/0000-0001-7688-1682</orcidid></search><sort><creationdate>20240212</creationdate><title>Gelatin-Based Hybrid Hydrogels as Matrices for Organoid Culture</title><author>Carpentier, Nathan ; Ye, Shicheng ; Delemarre, Maarten D. ; Van der Meeren, Louis ; Skirtach, André G. ; van der Laan, Luc J. W. ; Schneeberger, Kerstin ; Spee, Bart ; Dubruel, Peter ; Van Vlierberghe, Sandra</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a337t-e7d3ca81f9be99da921a9518e320a113e51d1f52de356ed0902c2a4263b99d893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Chondroitin Sulfates</topic><topic>Gelatin - chemistry</topic><topic>Hydrogels - chemistry</topic><topic>Hydrogels - pharmacology</topic><topic>Mice</topic><topic>Norbornanes</topic><topic>Organoids</topic><topic>Tissue Engineering - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carpentier, Nathan</creatorcontrib><creatorcontrib>Ye, Shicheng</creatorcontrib><creatorcontrib>Delemarre, Maarten D.</creatorcontrib><creatorcontrib>Van der Meeren, Louis</creatorcontrib><creatorcontrib>Skirtach, André G.</creatorcontrib><creatorcontrib>van der Laan, Luc J. W.</creatorcontrib><creatorcontrib>Schneeberger, Kerstin</creatorcontrib><creatorcontrib>Spee, Bart</creatorcontrib><creatorcontrib>Dubruel, Peter</creatorcontrib><creatorcontrib>Van Vlierberghe, Sandra</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><jtitle>Biomacromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carpentier, Nathan</au><au>Ye, Shicheng</au><au>Delemarre, Maarten D.</au><au>Van der Meeren, Louis</au><au>Skirtach, André G.</au><au>van der Laan, Luc J. W.</au><au>Schneeberger, Kerstin</au><au>Spee, Bart</au><au>Dubruel, Peter</au><au>Van Vlierberghe, Sandra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gelatin-Based Hybrid Hydrogels as Matrices for Organoid Culture</atitle><jtitle>Biomacromolecules</jtitle><addtitle>Biomacromolecules</addtitle><date>2024-02-12</date><risdate>2024</risdate><volume>25</volume><issue>2</issue><spage>590</spage><epage>604</epage><pages>590-604</pages><issn>1525-7797</issn><issn>1526-4602</issn><eissn>1526-4602</eissn><abstract>The application of liver organoids is very promising in the field of liver tissue engineering; however, it is still facing some limitations. One of the current major limitations is the matrix in which they are cultured. The mainly undefined and murine-originated tumor matrices derived from Engelbreth–Holm–Swarm (EHS) sarcoma, such as Matrigel, are still the standard culturing matrices for expansion and differentiation of organoids toward hepatocyte-like cells, which will obstruct its future clinical application potential. In this study, we exploited the use of newly developed highly defined hydrogels as potential matrices for the culture of liver organoids and compared them to Matrigel and two hydrogels that were already researched in the field of organoid research [i.e., polyisocyanopeptides, enriched with laminin–entactin complex (PIC-LEC) and gelatin methacryloyl (GelMA)]. The newly developed hydrogels are materials that have a physicochemical resemblance with native liver tissue. Norbornene-modified dextran cross-linked with thiolated gelatin (DexNB-GelSH) has a swelling ratio and macro- and microscale properties that highly mimic liver tissue. Norbornene-modified chondroitin sulfate cross-linked with thiolated gelatin (CSNB-GelSH) contains chondroitin sulfate, which is a glycosaminoglycan (GAG) that is present in the liver ECM. Furthermore, CSNB-GelSH hydrogels with different mechanical properties were evaluated. Bipotent intrahepatic cholangiocyte organoids (ICOs) were applied in this work and encapsulated in these materials. This research revealed that the newly developed materials outperformed Matrigel, PIC-LEC, and GelMA in the differentiation of ICOs toward hepatocyte-like cells. Furthermore, some trends indicate that an interplay of both the chemical composition and the mechanical properties has an influence on the relative expression of certain hepatocyte markers. Both DexNB-GelSH and CSNB-GelSH showed promising results for the expansion and differentiation of intrahepatic cholangiocyte organoids. The stiffest CSNB-GelSH hydrogel even significantly outperformed Matrigel based on ALB, BSEP, and CYP3A4 gene expression, being three important hepatocyte markers.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>38174962</pmid><doi>10.1021/acs.biomac.2c01496</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-7985-4310</orcidid><orcidid>https://orcid.org/0000-0002-4468-7620</orcidid><orcidid>https://orcid.org/0000-0002-6671-5055</orcidid><orcidid>https://orcid.org/0000-0001-7688-1682</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1525-7797 |
ispartof | Biomacromolecules, 2024-02, Vol.25 (2), p.590-604 |
issn | 1525-7797 1526-4602 1526-4602 |
language | eng |
recordid | cdi_proquest_miscellaneous_2910197196 |
source | MEDLINE; ACS Publications |
subjects | Animals Chondroitin Sulfates Gelatin - chemistry Hydrogels - chemistry Hydrogels - pharmacology Mice Norbornanes Organoids Tissue Engineering - methods |
title | Gelatin-Based Hybrid Hydrogels as Matrices for Organoid Culture |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T11%3A03%3A59IST&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=Gelatin-Based%20Hybrid%20Hydrogels%20as%20Matrices%20for%20Organoid%20Culture&rft.jtitle=Biomacromolecules&rft.au=Carpentier,%20Nathan&rft.date=2024-02-12&rft.volume=25&rft.issue=2&rft.spage=590&rft.epage=604&rft.pages=590-604&rft.issn=1525-7797&rft.eissn=1526-4602&rft_id=info:doi/10.1021/acs.biomac.2c01496&rft_dat=%3Cproquest_cross%3E2910197196%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=2910197196&rft_id=info:pmid/38174962&rfr_iscdi=true |