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Hematopoietic stem cells undergo a lymphoid to myeloid switch in early stages of emergency granulopoiesis

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    SYSNO ASEP0579429
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleHematopoietic stem cells undergo a lymphoid to myeloid switch in early stages of emergency granulopoiesis
    Author(s) Vaníčková, Karolína (UMG-J)
    Miloševič, Mirko (BTO-N)
    Ribeiro Bas, Irina (UMG-J) ORCID
    Burocziová, Monika (UMG-J)
    Yokota, A. (JP)
    Daněk, Petr (UMG-J)
    Grušanovič, Srdjan (UMG-J)
    Chilinski, M. (PL)
    Plewczynski, D. (PL)
    Rohlena, Jakub (BTO-N) RID, ORCID
    Hirai, H. (JP)
    Rohlenová, Kateřina (BTO-N) ORCID, RID
    Alberich-Jorda, Meritxell (UMG-J) RID
    Number of authors13
    Article numbere113527
    Source TitleEMBO Journal. - : Wiley - ISSN 0261-4189
    Roč. 42, č. 23 (2023)
    Number of pages18 s.
    Languageeng - English
    CountryUS - United States
    Keywordsprotein-c receptor ; c/ebp-beta ; progenitor cells ; self-renewal ; steady-state ; gene ; differentiation ; signals ; driven ; cd201 ; cd201 ; emergency granulopoiesis ; lymphoid-biased HSC ; myeloid-biased HSC
    OECD categoryCell biology
    R&D ProjectsLX22NPO5102 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    GA22-18300S GA ČR - Czech Science Foundation (CSF)
    Method of publishingOpen access
    Institutional supportUMG-J - RVO:68378050 ; BTO-N - RVO:86652036
    UT WOS001083429900001
    EID SCOPUS85174320525
    DOI10.15252/embj.2023113527
    AnnotationEmergency granulopoiesis is the enhanced and accelerated production of granulocytes that occurs during acute infection. The contribution of hematopoietic stem cells (HSCs) to this process was reported, however, how HSCs participate in emergency granulopoiesis remains elusive. Here, using a mouse model of emergency granulopoiesis we observe transcriptional changes in HSCs as early as 4 h after lipopolysaccharide (LPS) administration. We observe that the HSC identity is changed towards a myeloid-biased HSC and show that CD201 is enriched in lymphoid-biased HSCs. While CD201 expression under steady-state conditions reveals a lymphoid bias, under emergency granulopoiesis loss of CD201 marks the lymphoid-to-myeloid transcriptional switch. Mechanistically, we determine that lymphoid-biased CD201+ HSCs act as a first response during emergency granulopoiesis due to direct sensing of LPS by TLR4 and downstream activation of NF-kappa Beta signaling. The myeloid-biased CD201- HSC population responds indirectly during an acute infection by sensing G-CSF, increasing STAT3 phosphorylation, and upregulating LAP/LAP* C/EBP beta isoforms. In conclusion, HSC subpopulations support early phases of emergency granulopoiesis due to their transcriptional rewiring from a lymphoid-biased to myeloid-biased population and thus establishing alternative paths to supply elevated numbers of granulocytes.
    WorkplaceInstitute of Molecular Genetics
    ContactNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Year of Publishing2024
    Electronic addresshttps://www.embopress.org/doi/epdf/10.15252/embj.2023113527?src=getftr
Number of the records: 1  

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