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Decellularized scaffold of cryopreserved rat kidney retains its recellularization potential

The multi-cellular nature of renal tissue makes it the most challenging organ for regeneration. Therefore, till date whole organ transplantations remain the definitive treatment for the end stage renal disease (ESRD). The shortage of available organs for the transplantation has, thus, remained a maj...

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Autores principales: Chani, Baldeep, Puri, Veena, Sobti, Ranbir C., Jha, Vivekanand, Puri, Sanjeev
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340383/
https://www.ncbi.nlm.nih.gov/pubmed/28267813
http://dx.doi.org/10.1371/journal.pone.0173040
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author Chani, Baldeep
Puri, Veena
Sobti, Ranbir C.
Jha, Vivekanand
Puri, Sanjeev
author_facet Chani, Baldeep
Puri, Veena
Sobti, Ranbir C.
Jha, Vivekanand
Puri, Sanjeev
author_sort Chani, Baldeep
collection PubMed
description The multi-cellular nature of renal tissue makes it the most challenging organ for regeneration. Therefore, till date whole organ transplantations remain the definitive treatment for the end stage renal disease (ESRD). The shortage of available organs for the transplantation has, thus, remained a major concern as well as an unsolved problem. In this regard generation of whole organ scaffold through decellularization followed by regeneration of the whole organ by recellularization is being viewed as a potential alternative for generating functional tissues. Despite its growing interest, the optimal processing to achieve functional organ still remains unsolved. The biggest challenge remains is the time line for obtaining kidney. Keeping these facts in mind, we have assessed the effects of cryostorage (3 months) on renal tissue architecture and its potential for decellularization and recellularization in comparison to the freshly isolated kidneys. The light microscopy exploiting different microscopic stains as well as immuno-histochemistry and Scanning electron microscopy (SEM) demonstrated that ECM framework is well retained following kidney cryopreservation. The strength of these structures was reinforced by calculating mechanical stress which confirmed the similarity between the freshly isolated and cryopreserved tissue. The recellularization of these bio-scaffolds, with mesenchymal stem cells quickly repopulated the decellularized structures irrespective of the kidneys status, i.e. freshly isolated or the cryopreserved. The growth pattern employing mesenchymal stem cells demonstrated their equivalent recellularization potential. Based on these observations, it may be concluded that cryopreserved kidneys can be exploited as scaffolds for future development of functional organ.
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spelling pubmed-53403832017-03-29 Decellularized scaffold of cryopreserved rat kidney retains its recellularization potential Chani, Baldeep Puri, Veena Sobti, Ranbir C. Jha, Vivekanand Puri, Sanjeev PLoS One Research Article The multi-cellular nature of renal tissue makes it the most challenging organ for regeneration. Therefore, till date whole organ transplantations remain the definitive treatment for the end stage renal disease (ESRD). The shortage of available organs for the transplantation has, thus, remained a major concern as well as an unsolved problem. In this regard generation of whole organ scaffold through decellularization followed by regeneration of the whole organ by recellularization is being viewed as a potential alternative for generating functional tissues. Despite its growing interest, the optimal processing to achieve functional organ still remains unsolved. The biggest challenge remains is the time line for obtaining kidney. Keeping these facts in mind, we have assessed the effects of cryostorage (3 months) on renal tissue architecture and its potential for decellularization and recellularization in comparison to the freshly isolated kidneys. The light microscopy exploiting different microscopic stains as well as immuno-histochemistry and Scanning electron microscopy (SEM) demonstrated that ECM framework is well retained following kidney cryopreservation. The strength of these structures was reinforced by calculating mechanical stress which confirmed the similarity between the freshly isolated and cryopreserved tissue. The recellularization of these bio-scaffolds, with mesenchymal stem cells quickly repopulated the decellularized structures irrespective of the kidneys status, i.e. freshly isolated or the cryopreserved. The growth pattern employing mesenchymal stem cells demonstrated their equivalent recellularization potential. Based on these observations, it may be concluded that cryopreserved kidneys can be exploited as scaffolds for future development of functional organ. Public Library of Science 2017-03-07 /pmc/articles/PMC5340383/ /pubmed/28267813 http://dx.doi.org/10.1371/journal.pone.0173040 Text en © 2017 Chani et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Chani, Baldeep
Puri, Veena
Sobti, Ranbir C.
Jha, Vivekanand
Puri, Sanjeev
Decellularized scaffold of cryopreserved rat kidney retains its recellularization potential
title Decellularized scaffold of cryopreserved rat kidney retains its recellularization potential
title_full Decellularized scaffold of cryopreserved rat kidney retains its recellularization potential
title_fullStr Decellularized scaffold of cryopreserved rat kidney retains its recellularization potential
title_full_unstemmed Decellularized scaffold of cryopreserved rat kidney retains its recellularization potential
title_short Decellularized scaffold of cryopreserved rat kidney retains its recellularization potential
title_sort decellularized scaffold of cryopreserved rat kidney retains its recellularization potential
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340383/
https://www.ncbi.nlm.nih.gov/pubmed/28267813
http://dx.doi.org/10.1371/journal.pone.0173040
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