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An organ-derived extracellular matrix triggers in situ kidney regeneration in a preclinical model

It has not been considered that nephrons regenerate in adult mammals. We present that an organ-derived extracellular matrix in situ induces nephron regeneration in a preclinical model. A porcine kidney-derived extracellular matrix was sutured onto the surface of partial nephrectomy (PN)-treated kidn...

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Autores principales: Tajima, Kazuki, Yagi, Hiroshi, Morisaku, Toshinori, Nishi, Kotaro, Kushige, Hiroko, Kojima, Hideaki, Higashi, Hisanobu, Kuroda, Kohei, Kitago, Minoru, Adachi, Shungo, Natsume, Tohru, Nishimura, Kumiko, Oya, Mototsugu, Kitagawa, Yuko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885654/
https://www.ncbi.nlm.nih.gov/pubmed/35228532
http://dx.doi.org/10.1038/s41536-022-00213-y
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author Tajima, Kazuki
Yagi, Hiroshi
Morisaku, Toshinori
Nishi, Kotaro
Kushige, Hiroko
Kojima, Hideaki
Higashi, Hisanobu
Kuroda, Kohei
Kitago, Minoru
Adachi, Shungo
Natsume, Tohru
Nishimura, Kumiko
Oya, Mototsugu
Kitagawa, Yuko
author_facet Tajima, Kazuki
Yagi, Hiroshi
Morisaku, Toshinori
Nishi, Kotaro
Kushige, Hiroko
Kojima, Hideaki
Higashi, Hisanobu
Kuroda, Kohei
Kitago, Minoru
Adachi, Shungo
Natsume, Tohru
Nishimura, Kumiko
Oya, Mototsugu
Kitagawa, Yuko
author_sort Tajima, Kazuki
collection PubMed
description It has not been considered that nephrons regenerate in adult mammals. We present that an organ-derived extracellular matrix in situ induces nephron regeneration in a preclinical model. A porcine kidney-derived extracellular matrix was sutured onto the surface of partial nephrectomy (PN)-treated kidney. Twenty-eight days after implantation, glomeruli, vessels, and renal tubules, characteristic of nephrons, were histologically observed within the matrix. No fibrillogenesis was observed in the matrix nor the matrix-sutured kidney, although this occurred in a PN kidney without the matrix, indicating the structures were newly induced by the matrix. The expression of renal progenitor markers, including Sall1, Six2, and WT-1, within the matrix supported the induction of nephron regeneration by the matrix. Furthermore, active blood flow was observed inside the matrix using computed tomography. The matrix provides structural and functional foundations for the development of cell-free scaffolds with a remarkably low risk of immune rejection and cancerization.
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spelling pubmed-88856542022-03-17 An organ-derived extracellular matrix triggers in situ kidney regeneration in a preclinical model Tajima, Kazuki Yagi, Hiroshi Morisaku, Toshinori Nishi, Kotaro Kushige, Hiroko Kojima, Hideaki Higashi, Hisanobu Kuroda, Kohei Kitago, Minoru Adachi, Shungo Natsume, Tohru Nishimura, Kumiko Oya, Mototsugu Kitagawa, Yuko NPJ Regen Med Article It has not been considered that nephrons regenerate in adult mammals. We present that an organ-derived extracellular matrix in situ induces nephron regeneration in a preclinical model. A porcine kidney-derived extracellular matrix was sutured onto the surface of partial nephrectomy (PN)-treated kidney. Twenty-eight days after implantation, glomeruli, vessels, and renal tubules, characteristic of nephrons, were histologically observed within the matrix. No fibrillogenesis was observed in the matrix nor the matrix-sutured kidney, although this occurred in a PN kidney without the matrix, indicating the structures were newly induced by the matrix. The expression of renal progenitor markers, including Sall1, Six2, and WT-1, within the matrix supported the induction of nephron regeneration by the matrix. Furthermore, active blood flow was observed inside the matrix using computed tomography. The matrix provides structural and functional foundations for the development of cell-free scaffolds with a remarkably low risk of immune rejection and cancerization. Nature Publishing Group UK 2022-02-28 /pmc/articles/PMC8885654/ /pubmed/35228532 http://dx.doi.org/10.1038/s41536-022-00213-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Tajima, Kazuki
Yagi, Hiroshi
Morisaku, Toshinori
Nishi, Kotaro
Kushige, Hiroko
Kojima, Hideaki
Higashi, Hisanobu
Kuroda, Kohei
Kitago, Minoru
Adachi, Shungo
Natsume, Tohru
Nishimura, Kumiko
Oya, Mototsugu
Kitagawa, Yuko
An organ-derived extracellular matrix triggers in situ kidney regeneration in a preclinical model
title An organ-derived extracellular matrix triggers in situ kidney regeneration in a preclinical model
title_full An organ-derived extracellular matrix triggers in situ kidney regeneration in a preclinical model
title_fullStr An organ-derived extracellular matrix triggers in situ kidney regeneration in a preclinical model
title_full_unstemmed An organ-derived extracellular matrix triggers in situ kidney regeneration in a preclinical model
title_short An organ-derived extracellular matrix triggers in situ kidney regeneration in a preclinical model
title_sort organ-derived extracellular matrix triggers in situ kidney regeneration in a preclinical model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885654/
https://www.ncbi.nlm.nih.gov/pubmed/35228532
http://dx.doi.org/10.1038/s41536-022-00213-y
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