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Functional kupffer cells migrate to the liver from the intraperitoneal cavity

We established a method of KC transplantation by intraperitoneal (i.p.) injection using EGFP-expressing cells (EGFP-KCs) and normal KCs. The novel method is easier and less invasive than conventional methods so that it is not only technically advantageous but also ethically preferable for experiment...

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Detalles Bibliográficos
Autores principales: Lin, Wen-Ling, Mizobuchi, Mizuki, Kawahigashi, Mina, Nakahashi, Otoki, Maekawa, Yuuki, Sakai, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379421/
https://www.ncbi.nlm.nih.gov/pubmed/34458593
http://dx.doi.org/10.1016/j.bbrep.2021.101103
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author Lin, Wen-Ling
Mizobuchi, Mizuki
Kawahigashi, Mina
Nakahashi, Otoki
Maekawa, Yuuki
Sakai, Takashi
author_facet Lin, Wen-Ling
Mizobuchi, Mizuki
Kawahigashi, Mina
Nakahashi, Otoki
Maekawa, Yuuki
Sakai, Takashi
author_sort Lin, Wen-Ling
collection PubMed
description We established a method of KC transplantation by intraperitoneal (i.p.) injection using EGFP-expressing cells (EGFP-KCs) and normal KCs. The novel method is easier and less invasive than conventional methods so that it is not only technically advantageous but also ethically preferable for experiments using animals. We demonstrated that KCs migrated to the liver following i.p. Injection. Engraftment in the liver was not observed for peritoneal macrophages (pMPs). This suggests that KCs migrate to the liver via a sorting mechanism. KC injection decreased the KC number at 24 h and then recovered the KCs at 10 days to a normal level. Additionally, recovery to the normal level by KC injection was observed in mice with KC depletion induced by GdCl(3). These results suggest that a regulatory mechanism exists for controlling the number of KCs.
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spelling pubmed-83794212021-08-26 Functional kupffer cells migrate to the liver from the intraperitoneal cavity Lin, Wen-Ling Mizobuchi, Mizuki Kawahigashi, Mina Nakahashi, Otoki Maekawa, Yuuki Sakai, Takashi Biochem Biophys Rep Research Article We established a method of KC transplantation by intraperitoneal (i.p.) injection using EGFP-expressing cells (EGFP-KCs) and normal KCs. The novel method is easier and less invasive than conventional methods so that it is not only technically advantageous but also ethically preferable for experiments using animals. We demonstrated that KCs migrated to the liver following i.p. Injection. Engraftment in the liver was not observed for peritoneal macrophages (pMPs). This suggests that KCs migrate to the liver via a sorting mechanism. KC injection decreased the KC number at 24 h and then recovered the KCs at 10 days to a normal level. Additionally, recovery to the normal level by KC injection was observed in mice with KC depletion induced by GdCl(3). These results suggest that a regulatory mechanism exists for controlling the number of KCs. Elsevier 2021-08-17 /pmc/articles/PMC8379421/ /pubmed/34458593 http://dx.doi.org/10.1016/j.bbrep.2021.101103 Text en © 2021 The Authors 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 Research Article
Lin, Wen-Ling
Mizobuchi, Mizuki
Kawahigashi, Mina
Nakahashi, Otoki
Maekawa, Yuuki
Sakai, Takashi
Functional kupffer cells migrate to the liver from the intraperitoneal cavity
title Functional kupffer cells migrate to the liver from the intraperitoneal cavity
title_full Functional kupffer cells migrate to the liver from the intraperitoneal cavity
title_fullStr Functional kupffer cells migrate to the liver from the intraperitoneal cavity
title_full_unstemmed Functional kupffer cells migrate to the liver from the intraperitoneal cavity
title_short Functional kupffer cells migrate to the liver from the intraperitoneal cavity
title_sort functional kupffer cells migrate to the liver from the intraperitoneal cavity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379421/
https://www.ncbi.nlm.nih.gov/pubmed/34458593
http://dx.doi.org/10.1016/j.bbrep.2021.101103
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