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Ribosome Incorporation into Somatic Cells Promotes Lineage Transdifferentiation towards Multipotency

Recently, we reported that bacterial incorporation induces cellular transdifferentiation of human fibroblasts. However, the bacterium-intrinsic cellular- transdifferentiation factor remained unknown. Here, we found that cellular transdifferentiation is caused by ribosomes. Ribosomes, isolated from b...

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Autores principales: Ito, Naofumi, Katoh, Kaoru, Kushige, Hiroko, Saito, Yutaka, Umemoto, Terumasa, Matsuzaki, Yu, Kiyonari, Hiroshi, Kobayashi, Daiki, Soga, Minami, Era, Takumi, Araki, Norie, Furuta, Yasuhide, Suda, Toshio, Kida, Yasuyuki, Ohta, Kunimasa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786109/
https://www.ncbi.nlm.nih.gov/pubmed/29374279
http://dx.doi.org/10.1038/s41598-018-20057-1
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author Ito, Naofumi
Katoh, Kaoru
Kushige, Hiroko
Saito, Yutaka
Umemoto, Terumasa
Matsuzaki, Yu
Kiyonari, Hiroshi
Kobayashi, Daiki
Soga, Minami
Era, Takumi
Araki, Norie
Furuta, Yasuhide
Suda, Toshio
Kida, Yasuyuki
Ohta, Kunimasa
author_facet Ito, Naofumi
Katoh, Kaoru
Kushige, Hiroko
Saito, Yutaka
Umemoto, Terumasa
Matsuzaki, Yu
Kiyonari, Hiroshi
Kobayashi, Daiki
Soga, Minami
Era, Takumi
Araki, Norie
Furuta, Yasuhide
Suda, Toshio
Kida, Yasuyuki
Ohta, Kunimasa
author_sort Ito, Naofumi
collection PubMed
description Recently, we reported that bacterial incorporation induces cellular transdifferentiation of human fibroblasts. However, the bacterium-intrinsic cellular- transdifferentiation factor remained unknown. Here, we found that cellular transdifferentiation is caused by ribosomes. Ribosomes, isolated from both prokaryotic and eukaryotic cells, induce the formation of embryoid body-like cell clusters. Numerous ribosomes are incorporated into both the cytoplasm and nucleus through trypsin-activated endocytosis, which leads to cell-cluster formation. Although ribosome-induced cell clusters (RICs) express several stemness markers and differentiate into derivatives of all three germ layers in heterogeneous cell populations, RICs fail to proliferate, alter the methylation states of pluripotent genes, or contribute to teratoma or chimera formation. However, RICs express markers of epithelial–mesenchymal transition without altering the cell cycle, despite their proliferation obstruction. These findings demonstrate that incorporation of ribosomes into host cells induces cell transdifferentiation and alters cellular plasticity.
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spelling pubmed-57861092018-02-07 Ribosome Incorporation into Somatic Cells Promotes Lineage Transdifferentiation towards Multipotency Ito, Naofumi Katoh, Kaoru Kushige, Hiroko Saito, Yutaka Umemoto, Terumasa Matsuzaki, Yu Kiyonari, Hiroshi Kobayashi, Daiki Soga, Minami Era, Takumi Araki, Norie Furuta, Yasuhide Suda, Toshio Kida, Yasuyuki Ohta, Kunimasa Sci Rep Article Recently, we reported that bacterial incorporation induces cellular transdifferentiation of human fibroblasts. However, the bacterium-intrinsic cellular- transdifferentiation factor remained unknown. Here, we found that cellular transdifferentiation is caused by ribosomes. Ribosomes, isolated from both prokaryotic and eukaryotic cells, induce the formation of embryoid body-like cell clusters. Numerous ribosomes are incorporated into both the cytoplasm and nucleus through trypsin-activated endocytosis, which leads to cell-cluster formation. Although ribosome-induced cell clusters (RICs) express several stemness markers and differentiate into derivatives of all three germ layers in heterogeneous cell populations, RICs fail to proliferate, alter the methylation states of pluripotent genes, or contribute to teratoma or chimera formation. However, RICs express markers of epithelial–mesenchymal transition without altering the cell cycle, despite their proliferation obstruction. These findings demonstrate that incorporation of ribosomes into host cells induces cell transdifferentiation and alters cellular plasticity. Nature Publishing Group UK 2018-01-26 /pmc/articles/PMC5786109/ /pubmed/29374279 http://dx.doi.org/10.1038/s41598-018-20057-1 Text en © The Author(s) 2018 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/.
spellingShingle Article
Ito, Naofumi
Katoh, Kaoru
Kushige, Hiroko
Saito, Yutaka
Umemoto, Terumasa
Matsuzaki, Yu
Kiyonari, Hiroshi
Kobayashi, Daiki
Soga, Minami
Era, Takumi
Araki, Norie
Furuta, Yasuhide
Suda, Toshio
Kida, Yasuyuki
Ohta, Kunimasa
Ribosome Incorporation into Somatic Cells Promotes Lineage Transdifferentiation towards Multipotency
title Ribosome Incorporation into Somatic Cells Promotes Lineage Transdifferentiation towards Multipotency
title_full Ribosome Incorporation into Somatic Cells Promotes Lineage Transdifferentiation towards Multipotency
title_fullStr Ribosome Incorporation into Somatic Cells Promotes Lineage Transdifferentiation towards Multipotency
title_full_unstemmed Ribosome Incorporation into Somatic Cells Promotes Lineage Transdifferentiation towards Multipotency
title_short Ribosome Incorporation into Somatic Cells Promotes Lineage Transdifferentiation towards Multipotency
title_sort ribosome incorporation into somatic cells promotes lineage transdifferentiation towards multipotency
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786109/
https://www.ncbi.nlm.nih.gov/pubmed/29374279
http://dx.doi.org/10.1038/s41598-018-20057-1
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