RIO-kinase 2 is essential for hematopoiesis

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RIO-kinase 2 is essential for hematopoiesis. / Messling, Jan-Erik; Peña-Rømer, Isabel; Moroni, Ann Sophie; Bruestl, Sarah; Helin, Kristian.

I: PLoS ONE, Bind 19, Nr. 4 April, e0300623, 2024.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Messling, J-E, Peña-Rømer, I, Moroni, AS, Bruestl, S & Helin, K 2024, 'RIO-kinase 2 is essential for hematopoiesis', PLoS ONE, bind 19, nr. 4 April, e0300623. https://doi.org/10.1371/journal.pone.0300623

APA

Messling, J-E., Peña-Rømer, I., Moroni, A. S., Bruestl, S., & Helin, K. (2024). RIO-kinase 2 is essential for hematopoiesis. PLoS ONE, 19(4 April), [e0300623]. https://doi.org/10.1371/journal.pone.0300623

Vancouver

Messling J-E, Peña-Rømer I, Moroni AS, Bruestl S, Helin K. RIO-kinase 2 is essential for hematopoiesis. PLoS ONE. 2024;19(4 April). e0300623. https://doi.org/10.1371/journal.pone.0300623

Author

Messling, Jan-Erik ; Peña-Rømer, Isabel ; Moroni, Ann Sophie ; Bruestl, Sarah ; Helin, Kristian. / RIO-kinase 2 is essential for hematopoiesis. I: PLoS ONE. 2024 ; Bind 19, Nr. 4 April.

Bibtex

@article{b1dc2cfa31e348f29df8ee92b889bfb3,
title = "RIO-kinase 2 is essential for hematopoiesis",
abstract = "Regulation of protein synthesis is a key factor in hematopoietic stem cell maintenance and differentiation. Rio-kinase 2 (RIOK2) is a ribosome biogenesis factor that has recently been described an important regulator of human blood cell development. Additionally, we have previously identified RIOK2 as a regulator of protein synthesis and a potential target for the treatment of acute myeloid leukemia (AML). However, its functional relevance in several organ systems, including normal hematopoiesis, is not well understood. Here, we investigate the consequences of RIOK2 loss on normal hematopoiesis using two different conditional knockout mouse models. Using competitive and non-competitive bone marrow transplantations, we demonstrate that RIOK2 is essential for the differentiation of hematopoietic stem and progenitor cells (HSPCs) as well as for the maintenance of fully differentiated blood cells in vivo as well as in vitro. Loss of RIOK2 leads to rapid death in full-body knockout mice as well as mice with RIOK2 loss specific to the hematopoietic system. Taken together, our results indicate that regulation of protein synthesis and ribosome biogenesis by RIOK2 is essential for the function of the hematopoietic system.",
author = "Jan-Erik Messling and Isabel Pe{\~n}a-R{\o}mer and Moroni, {Ann Sophie} and Sarah Bruestl and Kristian Helin",
note = "Publisher Copyright: Copyright: {\textcopyright} 2024 Messling et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.",
year = "2024",
doi = "10.1371/journal.pone.0300623",
language = "English",
volume = "19",
journal = "PLoS ONE",
issn = "1932-6203",
publisher = "Public Library of Science",
number = "4 April",

}

RIS

TY - JOUR

T1 - RIO-kinase 2 is essential for hematopoiesis

AU - Messling, Jan-Erik

AU - Peña-Rømer, Isabel

AU - Moroni, Ann Sophie

AU - Bruestl, Sarah

AU - Helin, Kristian

N1 - Publisher Copyright: Copyright: © 2024 Messling et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

PY - 2024

Y1 - 2024

N2 - Regulation of protein synthesis is a key factor in hematopoietic stem cell maintenance and differentiation. Rio-kinase 2 (RIOK2) is a ribosome biogenesis factor that has recently been described an important regulator of human blood cell development. Additionally, we have previously identified RIOK2 as a regulator of protein synthesis and a potential target for the treatment of acute myeloid leukemia (AML). However, its functional relevance in several organ systems, including normal hematopoiesis, is not well understood. Here, we investigate the consequences of RIOK2 loss on normal hematopoiesis using two different conditional knockout mouse models. Using competitive and non-competitive bone marrow transplantations, we demonstrate that RIOK2 is essential for the differentiation of hematopoietic stem and progenitor cells (HSPCs) as well as for the maintenance of fully differentiated blood cells in vivo as well as in vitro. Loss of RIOK2 leads to rapid death in full-body knockout mice as well as mice with RIOK2 loss specific to the hematopoietic system. Taken together, our results indicate that regulation of protein synthesis and ribosome biogenesis by RIOK2 is essential for the function of the hematopoietic system.

AB - Regulation of protein synthesis is a key factor in hematopoietic stem cell maintenance and differentiation. Rio-kinase 2 (RIOK2) is a ribosome biogenesis factor that has recently been described an important regulator of human blood cell development. Additionally, we have previously identified RIOK2 as a regulator of protein synthesis and a potential target for the treatment of acute myeloid leukemia (AML). However, its functional relevance in several organ systems, including normal hematopoiesis, is not well understood. Here, we investigate the consequences of RIOK2 loss on normal hematopoiesis using two different conditional knockout mouse models. Using competitive and non-competitive bone marrow transplantations, we demonstrate that RIOK2 is essential for the differentiation of hematopoietic stem and progenitor cells (HSPCs) as well as for the maintenance of fully differentiated blood cells in vivo as well as in vitro. Loss of RIOK2 leads to rapid death in full-body knockout mice as well as mice with RIOK2 loss specific to the hematopoietic system. Taken together, our results indicate that regulation of protein synthesis and ribosome biogenesis by RIOK2 is essential for the function of the hematopoietic system.

U2 - 10.1371/journal.pone.0300623

DO - 10.1371/journal.pone.0300623

M3 - Journal article

C2 - 38564577

AN - SCOPUS:85189690987

VL - 19

JO - PLoS ONE

JF - PLoS ONE

SN - 1932-6203

IS - 4 April

M1 - e0300623

ER -

ID: 389001158