
<ns0:uwmetadata xmlns:ns0="http://phaidra.univie.ac.at/XML/metadata/V1.0" xmlns:ns1="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0" xmlns:ns10="http://phaidra.univie.ac.at/XML/metadata/provenience/V1.0" xmlns:ns11="http://phaidra.univie.ac.at/XML/metadata/provenience/V1.0/entity" xmlns:ns12="http://phaidra.univie.ac.at/XML/metadata/digitalbook/V1.0" xmlns:ns13="http://phaidra.univie.ac.at/XML/metadata/etheses/V1.0" xmlns:ns2="http://phaidra.univie.ac.at/XML/metadata/extended/V1.0" xmlns:ns3="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/entity" xmlns:ns4="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/requirement" xmlns:ns5="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/educational" xmlns:ns6="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/annotation" xmlns:ns7="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/classification" xmlns:ns8="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/organization" xmlns:ns9="http://phaidra.univie.ac.at/XML/metadata/histkult/V1.0">
  <ns1:general>
    <ns1:identifier>o:28468</ns1:identifier>
    <ns1:title language="en">Exogenous alpha-ketoglutarate impair differentiation and maturation of human dendritic cells</ns1:title>
    <ns2:alt_title language="sr">Egzogeni alfa-ketoglutarat sprečava diferencijaciju i sazrevanje humanih dendritskih ćelija</ns2:alt_title>
    <ns1:language>en</ns1:language>
    <ns1:description language="en">ABSTRACT
Alpha-ketoglutarate (AKG) is a crucial intermediate in cell metabolism. Exogenous AKG
has been shown to extend the lifespan by regulating the cellular response to calorie
restriction. However, how the exogenous AKG affects immune responses is unknown, particularly those mediated by critical immunoregulatory and dendritic cells (DC). Using a
model of human monocyte-derived DC, we found that exogenous AKG (10 mM or 50
mM) does not induce autophagy in DC (according to LC3II expression) but impairs the
differentiation of DC from monocytes (according to CD1a and CD14 co-expression).
Additionally, AKG inhibited LPS/IFN-γ-induced upregulation of NLRP-3, IL-1β, HLADR, CD83, CD86, CD40, CCR7, CD209, IL-33, IL-10, and IL-12p70 expression in DC, but potentiated the capacity of these cells to express TGF-β, CD73, and IL-23 in a dose-dependent manner. Although AKG-treated DC displayed a lower ability to stimulate proliferation of alloreactive T cells than control mature DC, the normalized number of CD4+RORγt+IL17+ (Th17) and CD4+GATA3+IL-4+ (Th2) cells was higher. The number of CD4+T-bet+IFN-γ+ (Th1) and CD8+IFN-γ+GranzA+
Perf+ (CTL) was lower in co-cultures with AKG-treated DC compared to corresponding control DC. Moreover, AKG increased the capacity of DC significantly to induce CD4+
CD25hiCD127-FoxP3+ Tregs in a dose-dependent manner. These results suggested that, while exogenous AKG could have
beneficial effects on lifespan, the quality of life might be compromised due to its
immunomodulatory effects related to the reduction of Th1 mediated immune responses.</ns1:description>
  </ns1:general>
  <ns1:lifecycle>
    <ns1:upload_date>2023-03-29T12:57:19.258Z</ns1:upload_date>
    <ns1:status>44</ns1:status>
    <ns2:peer_reviewed>yes</ns2:peer_reviewed>
    <ns1:contribute seq="0">
      <ns1:role>46</ns1:role>
      <ns1:entity seq="0">
        <ns3:firstname>Marijana</ns3:firstname>
        <ns3:lastname>Milanović</ns3:lastname>
        <ns3:institution>University of Defense, Medical Faculty of the Military Medical Academy, Belgrade, Serbia</ns3:institution>
      </ns1:entity>
      <ns1:entity seq="4">
        <ns3:firstname>Marina</ns3:firstname>
        <ns3:lastname>Bekić</ns3:lastname>
        <ns3:institution>University of Belgrade, Institute for the Application of Nuclear Energy INEP, Serbia</ns3:institution>
        <ns3:type>person</ns3:type>
        <ns3:orcid>0000-0002-6945-4241</ns3:orcid>
      </ns1:entity>
      <ns1:entity seq="3">
        <ns3:firstname>Dragana</ns3:firstname>
        <ns3:lastname>Vučević</ns3:lastname>
        <ns3:institution>University of Defense, Medical Faculty of the Military Medical Academy, Belgrade, Serbia</ns3:institution>
        <ns3:type>person</ns3:type>
      </ns1:entity>
      <ns1:entity seq="2">
        <ns3:firstname>Miodrag</ns3:firstname>
        <ns3:lastname>Čolić</ns3:lastname>
        <ns3:institution>University of Belgrade, Institute for the Application of Nuclear Energy INEP, Serbia</ns3:institution>
        <ns3:type>person</ns3:type>
      </ns1:entity>
      <ns1:entity seq="1">
        <ns3:firstname>Sergej</ns3:firstname>
        <ns3:lastname>Tomić</ns3:lastname>
        <ns3:institution>University of Belgrade, Institute for the Application of Nuclear Energy INEP, Serbia</ns3:institution>
        <ns3:title1>doktor bioloških nauka</ns3:title1>
        <ns3:type>person</ns3:type>
        <ns3:orcid>0000-0003-2570-1295</ns3:orcid>
      </ns1:entity>
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  <ns1:technical>
    <ns1:format>application/pdf</ns1:format>
    <ns1:size>1317639</ns1:size>
    <ns1:location>https://phaidrabg.bg.ac.rs/o:28468</ns1:location>
  </ns1:technical>
  <ns1:rights>
    <ns1:cost>no</ns1:cost>
    <ns1:copyright>yes</ns1:copyright>
    <ns1:license>18</ns1:license>
  </ns1:rights>
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    <ns1:purpose>70</ns1:purpose>
  </ns1:classification>
  <ns1:organization>
    <ns8:hoschtyp>92000004</ns8:hoschtyp>
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      <ns8:faculty>11A29</ns8:faculty>
      <ns8:department>11A2904</ns8:department>
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  <ns12:digitalbook>
    <ns12:name_magazine language="en">Proceedings of the Serbian Biochemical Society Tenth Conference </ns12:name_magazine>
    <ns12:reihentitel>Biochemical Insights into Molecular Mechanisms</ns12:reihentitel>
    <ns12:publisher>Faculty of Chemistry, Serbian Biochemical Society</ns12:publisher>
    <ns12:releaseyear>2021</ns12:releaseyear>
  </ns12:digitalbook>
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