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Efficient isolation of interstitial fibroblasts directly from mouse kidneys or indirectly after ex vivo expansion

Renal interstitial fibroblasts are responsible for producing the erythroid growth factor Epo and the vasopressor renin in addition to kidney fibrosis, in which they are transformed into myofibroblasts. Therefore, analyses of fibroblasts may elucidate the complex mechanisms of kidney diseases. Howeve...

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Detalles Bibliográficos
Autores principales: Nakai, Taku, Iwamura, Yuma, Suzuki, Norio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8452886/
https://www.ncbi.nlm.nih.gov/pubmed/34585160
http://dx.doi.org/10.1016/j.xpro.2021.100826
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author Nakai, Taku
Iwamura, Yuma
Suzuki, Norio
author_facet Nakai, Taku
Iwamura, Yuma
Suzuki, Norio
author_sort Nakai, Taku
collection PubMed
description Renal interstitial fibroblasts are responsible for producing the erythroid growth factor Epo and the vasopressor renin in addition to kidney fibrosis, in which they are transformed into myofibroblasts. Therefore, analyses of fibroblasts may elucidate the complex mechanisms of kidney diseases. However, the fragility of these cells makes their isolation for in vitro analyses and ex vivo cultivation difficult. We have overcome these difficulties by mildly dissociating mouse kidneys and coculturing fibroblasts with other kidney cells in semisolid medium. For complete details on the use and execution of this protocol, please refer to Sato et al. (2019a) and Miyauchi et al. (2021).
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spelling pubmed-84528862021-09-27 Efficient isolation of interstitial fibroblasts directly from mouse kidneys or indirectly after ex vivo expansion Nakai, Taku Iwamura, Yuma Suzuki, Norio STAR Protoc Protocol Renal interstitial fibroblasts are responsible for producing the erythroid growth factor Epo and the vasopressor renin in addition to kidney fibrosis, in which they are transformed into myofibroblasts. Therefore, analyses of fibroblasts may elucidate the complex mechanisms of kidney diseases. However, the fragility of these cells makes their isolation for in vitro analyses and ex vivo cultivation difficult. We have overcome these difficulties by mildly dissociating mouse kidneys and coculturing fibroblasts with other kidney cells in semisolid medium. For complete details on the use and execution of this protocol, please refer to Sato et al. (2019a) and Miyauchi et al. (2021). Elsevier 2021-09-15 /pmc/articles/PMC8452886/ /pubmed/34585160 http://dx.doi.org/10.1016/j.xpro.2021.100826 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Nakai, Taku
Iwamura, Yuma
Suzuki, Norio
Efficient isolation of interstitial fibroblasts directly from mouse kidneys or indirectly after ex vivo expansion
title Efficient isolation of interstitial fibroblasts directly from mouse kidneys or indirectly after ex vivo expansion
title_full Efficient isolation of interstitial fibroblasts directly from mouse kidneys or indirectly after ex vivo expansion
title_fullStr Efficient isolation of interstitial fibroblasts directly from mouse kidneys or indirectly after ex vivo expansion
title_full_unstemmed Efficient isolation of interstitial fibroblasts directly from mouse kidneys or indirectly after ex vivo expansion
title_short Efficient isolation of interstitial fibroblasts directly from mouse kidneys or indirectly after ex vivo expansion
title_sort efficient isolation of interstitial fibroblasts directly from mouse kidneys or indirectly after ex vivo expansion
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8452886/
https://www.ncbi.nlm.nih.gov/pubmed/34585160
http://dx.doi.org/10.1016/j.xpro.2021.100826
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