TY - JOUR
T1 - Ribosome Incorporation into Somatic Cells Promotes Lineage Transdifferentiation towards Multipotency
AU - Ito, Naofumi
AU - Katoh, Kaoru
AU - Kushige, Hiroko
AU - Saito, Yutaka
AU - Umemoto, Terumasa
AU - Matsuzaki, Yu
AU - Kiyonari, Hiroshi
AU - Kobayashi, Daiki
AU - Soga, Minami
AU - Era, Takumi
AU - Araki, Norie
AU - Furuta, Yasuhide
AU - Suda, Toshio
AU - Kida, Yasuyuki
AU - Ohta, Kunimasa
N1 - Funding Information:
We thank Drs Goro Eguchi, Hajime Fujisawa and Harukazu Nakamura for critical reading of the manuscript; Mihoko Iimori, Kazumi Yamada, Ai Hamashima, Mitsue Kumamaru, Shah Adil Ishtiyaq Ahmad, Mohammad Badrul Anam, Sayoko Fujimura, Mariko Yamane and Hitoshi Niwa for technical assistance; and Atsushi Tsurumune and Junya Ohkawa in the Bioscience Development Department of NIKON for technical suggestions regarding the latest version of enhanced image-processing systems. We are grateful to the Institute of Molecular Embryology, Genetics, Gene Technology Center, and Instrumental Analysis Center of Pharmacy at Kumamoto University, for providing experimental support. This work was supported by grants from KAKENHI (25650082), Kumamoto University Advanced Research Project “Stem Cell-Based Tissue Regeneration Research and Education Unit, Japan Agency for Medical Research and Development,” Astellas Foundation for Research on Metabolic Disorders, the Mitsubishi Foundation, the Yamada Science Foundation, and Institute for Fermentation Osaka.
Publisher Copyright:
© 2018 The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - 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.
AB - 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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U2 - 10.1038/s41598-018-20057-1
DO - 10.1038/s41598-018-20057-1
M3 - Article
C2 - 29374279
AN - SCOPUS:85041130850
SN - 2045-2322
VL - 8
JO - Scientific reports
JF - Scientific reports
IS - 1
M1 - 1634
ER -