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Sulfated Alginate Reduces Pericapsular Fibrotic Overgrowth on Encapsulated cGMP-Compliant hPSC-Hepatocytes in Mice
Intra-peritoneal placement of alginate encapsulated human induced pluripotent stem cell-derived hepatocytes (hPSC-Heps) represents a potential new bridging therapy for acute liver failure. One of the rate-limiting steps that needs to be overcome to make such a procedure more efficacious and safer is...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8928731/ https://www.ncbi.nlm.nih.gov/pubmed/35308825 http://dx.doi.org/10.3389/fbioe.2021.816542 |
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author | Syanda, Adam M. Kringstad, Vera I. Blackford, Samuel J. I. Kjesbu, Joachim S. Ng, Soon Seng Ma, Liang Xiao, Fang Coron, Abba E. Rokstad, Anne Mari A. Modi, Sunil Rashid, S. Tamir Strand, Berit Løkensgard |
author_facet | Syanda, Adam M. Kringstad, Vera I. Blackford, Samuel J. I. Kjesbu, Joachim S. Ng, Soon Seng Ma, Liang Xiao, Fang Coron, Abba E. Rokstad, Anne Mari A. Modi, Sunil Rashid, S. Tamir Strand, Berit Løkensgard |
author_sort | Syanda, Adam M. |
collection | PubMed |
description | Intra-peritoneal placement of alginate encapsulated human induced pluripotent stem cell-derived hepatocytes (hPSC-Heps) represents a potential new bridging therapy for acute liver failure. One of the rate-limiting steps that needs to be overcome to make such a procedure more efficacious and safer is to reduce the accumulation of fibrotic tissue around the encapsulated cells to allow the free passage of relevant molecules in and out for metabolism. Novel chemical compositions of alginate afford the possibility of achieving this aim. We accordingly used sulfated alginate and demonstrated that this material reduced fibrotic overgrowth whilst not impeding the process of encapsulation nor cell function. Cumulatively, this suggests sulfated alginate could be a more suitable material to encapsulate hPSC-hepatocyte prior to human use. |
format | Online Article Text |
id | pubmed-8928731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89287312022-03-18 Sulfated Alginate Reduces Pericapsular Fibrotic Overgrowth on Encapsulated cGMP-Compliant hPSC-Hepatocytes in Mice Syanda, Adam M. Kringstad, Vera I. Blackford, Samuel J. I. Kjesbu, Joachim S. Ng, Soon Seng Ma, Liang Xiao, Fang Coron, Abba E. Rokstad, Anne Mari A. Modi, Sunil Rashid, S. Tamir Strand, Berit Løkensgard Front Bioeng Biotechnol Bioengineering and Biotechnology Intra-peritoneal placement of alginate encapsulated human induced pluripotent stem cell-derived hepatocytes (hPSC-Heps) represents a potential new bridging therapy for acute liver failure. One of the rate-limiting steps that needs to be overcome to make such a procedure more efficacious and safer is to reduce the accumulation of fibrotic tissue around the encapsulated cells to allow the free passage of relevant molecules in and out for metabolism. Novel chemical compositions of alginate afford the possibility of achieving this aim. We accordingly used sulfated alginate and demonstrated that this material reduced fibrotic overgrowth whilst not impeding the process of encapsulation nor cell function. Cumulatively, this suggests sulfated alginate could be a more suitable material to encapsulate hPSC-hepatocyte prior to human use. Frontiers Media S.A. 2022-03-03 /pmc/articles/PMC8928731/ /pubmed/35308825 http://dx.doi.org/10.3389/fbioe.2021.816542 Text en Copyright © 2022 Syanda, Kringstad, Blackford, Kjesbu, Ng, Ma, Xiao, Coron, Rokstad, Modi, Rashid and Strand. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Syanda, Adam M. Kringstad, Vera I. Blackford, Samuel J. I. Kjesbu, Joachim S. Ng, Soon Seng Ma, Liang Xiao, Fang Coron, Abba E. Rokstad, Anne Mari A. Modi, Sunil Rashid, S. Tamir Strand, Berit Løkensgard Sulfated Alginate Reduces Pericapsular Fibrotic Overgrowth on Encapsulated cGMP-Compliant hPSC-Hepatocytes in Mice |
title | Sulfated Alginate Reduces Pericapsular Fibrotic Overgrowth on Encapsulated cGMP-Compliant hPSC-Hepatocytes in Mice |
title_full | Sulfated Alginate Reduces Pericapsular Fibrotic Overgrowth on Encapsulated cGMP-Compliant hPSC-Hepatocytes in Mice |
title_fullStr | Sulfated Alginate Reduces Pericapsular Fibrotic Overgrowth on Encapsulated cGMP-Compliant hPSC-Hepatocytes in Mice |
title_full_unstemmed | Sulfated Alginate Reduces Pericapsular Fibrotic Overgrowth on Encapsulated cGMP-Compliant hPSC-Hepatocytes in Mice |
title_short | Sulfated Alginate Reduces Pericapsular Fibrotic Overgrowth on Encapsulated cGMP-Compliant hPSC-Hepatocytes in Mice |
title_sort | sulfated alginate reduces pericapsular fibrotic overgrowth on encapsulated cgmp-compliant hpsc-hepatocytes in mice |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8928731/ https://www.ncbi.nlm.nih.gov/pubmed/35308825 http://dx.doi.org/10.3389/fbioe.2021.816542 |
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