
<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:14164</ns1:identifier>
    <ns1:title language="sr">Uticaj mezenhimskih ćelija belog masnog tkiva miša, indukovanih in vitro ka endotelskim i osteogenim ćelijama, na vaskularizovanost ektopičnih osteogenih implanata</ns1:title>
    <ns2:subtitle language="sr">doktorska disertacija</ns2:subtitle>
    <ns2:alt_title language="en">Influence of adipose-derived mesenchymal stem cells in vitro induced into endothelial and osteogenic cells on vascularization of ectopic osteogenic implants  : doctoral dissertation</ns2:alt_title>
    <ns1:language>sr</ns1:language>
    <ns1:description language="sr">Koštano tkivo je dobro vaskularizovano, visokog kapaciteta regeneracije, ali su
hirurške intervencije neophodne kod defekata kritične veličine. U tkivnom inženjerstvu
kosti, problem nedovoljne vaskularizacije nema adekvatno rešenje, pa je s tim ciljem u
ovoj disertaciji ispitivan uticaj mezenhimskih matičnih ćelija belog masnog tkiva
(ADSC – Adipose-derived mesenchymal stem cells, engl.), indukovanih in vitro ka
endotelskim (EĆ) i osteogenim ćelijama (OĆ), na vaskularizovanost ektopičnih
osteogenih implanata. U ADSC dobijenim in vitro ekspanzijom ćelija stromalne
vaskularne frakcije masnog tkiva BALB/c miševa muškog pola, pre i nakon ekspanzije
je praćena imunoekspresija pozitivnih i negativnih ADSC-markera. ADSC iz trećeg
pasaža su in vitro indukovane u EĆ ili OĆ ili ekspandirane bez induktivnih faktora.
Tokom diferencijacije, praćena je ekspresija markerskih gena i proteina. Ekspandirane
ADSC i plazma obogaćena trombocitima (PRP – Platelet-rich plasma, engl.) nanete na
mineralni matriks kosti (MMK) su subkutano implantirane. Vaskularizacija i osteogeni
proces u implantima (MMK, MMK/PRP, MMK/PRP/neindukovane ADSC,
MMK/PRP/EĆ, MMK/PRP/OĆ, MMK/PRP/EĆ/OĆ) su procenjivani na osnovu
ekspresije gena i proteina, histološke slike i histomorfometrijskih parametara. Ćelije iz
trećeg pasaža su mezenhimske matične, a ADSC su diferentovane u EĆ ili OĆ. Implanti
sa ili EĆ ili OĆ indukuju vaskularizaciju najpovoljniju za ektopični osteogeni proces.
Dobijeni rezultati daju nove podatke o ćelijskim i molekularnim mehanizmima
vaskulogenog i angiogenog procesa u osteogenezi i otvaraju nove mogućnosti u
tkivnom inženjerstvu kosti i kliničkom tretmanu defekata koštano-zglobnog sistema.
</ns1:description>
    <ns1:description language="en">Bone tissue is well vascularized, with high regenerative capacity, but surgical
interventions are necessary in critical-sized defects. Since in bone tissue engineering
(BTE), insufficient vascularization problem has no adequate solution, the influence of
mesenchymal stem cells isolated from white adipose tissue (ADSCs – Adipose-derived
mesenchymal stem cells) and in vitro induced into endothelial (ECs) and osteogenic
(OCs) cells, on vascularization of ectopic osteogenic implants was examined in this
dissertation. In ADSCs, obtained by in vitro expansion of stromal vascular fraction cells
isolated from adipose tissue of male BALB/c mice, immunoexpression of positive and
negative ADSCs-markers was examined before and after expansion. ADSC from the
third passage were in vitro induced into ECs and OCs, or expanded without inductive
factors. During differentiation, the expression of gene and protein markers was also
examined. Expanded ADSCs and platelet-rich plasma (PRP) seeded onto bone mineral
matrix (BMM) were subcutaneously implanted. Vascularization and osteogenic process
in implants (BMM, BMM/PRP, BMM/PRP/uninduced ADSCs, BMM/PRP/ECs,
BMM/PRP/OCs, MMK/PRP/ECs/OCs) were assessed on the basis of the gene and
protein expression, histological picture and histomorphometrical parameters. The cells
from the third passage were mesenchymal stem cells, and ADSCs were differentiated
into ECs and OCs. Implants with ECs or OCs induced the most favorable
vascularization for ectopic osteogenic process. The obtained results give some new data
about cellular and molecular mechanisms of vasculogenic and angiogenic process
during osteogenesis and open some new possibilities in BTE and in clinical treatments
of skeletal and articular system defects.
</ns1:description>
    <ns1:description language="sr">Biologija - Biologija ćelija i tkiva / Biology - Cell and tissue biology  
Datum odbrane: 24.09.2016.</ns1:description>
    <ns1:keyword language="sr">vaskularizacija, ektopična osteogeneza, mezenhimske matične ćelijemasnog tkiva, miš, in vitro diferencijacija, endotelske ćelije, osteogene ćelije, mineralnimatriks kosti, plazma obogaćena trombocitima, tkivno inženjerstvo kosti.</ns1:keyword>
    <ns1:keyword language="en">vascularization, ectopic osteogenesis, adipose-derived mesenchymal stemcells, mice, in vitro differentiation, endothelial cells, osteogenic cells, bone mineralmatrix, platelet-rich plasma, bone tissue engineering</ns1:keyword>
    <ns1:keyword language="sr">[591.476 : [611.018 : 591.413]] : 611.018.4(043.3)</ns1:keyword>
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      <ns2:identifier>1025140658</ns2:identifier>
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    <ns1:upload_date>2016-12-15T13:00:35.053Z</ns1:upload_date>
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    <ns2:peer_reviewed>no</ns2:peer_reviewed>
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      <ns1:role>46</ns1:role>
      <ns1:ext_role>mentor</ns1:ext_role>
      <ns1:entity seq="0">
        <ns3:firstname> Jelena G., 1982- </ns3:firstname>
        <ns3:lastname>Najdanović</ns3:lastname>
      </ns1:entity>
      <ns1:date>2016</ns1:date>
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      <ns1:role>63</ns1:role>
      <ns1:ext_role>mentor</ns1:ext_role>
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        <ns3:firstname> Stevo </ns3:firstname>
        <ns3:lastname>Najman</ns3:lastname>
      </ns1:entity>
      <ns1:date>2016</ns1:date>
    </ns1:contribute>
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      <ns1:role>63</ns1:role>
      <ns1:ext_role>član komisije</ns1:ext_role>
      <ns1:entity seq="0">
        <ns3:firstname> Maja, 1964- </ns3:firstname>
        <ns3:lastname>Čakić-Milošević</ns3:lastname>
      </ns1:entity>
      <ns1:date>2016</ns1:date>
    </ns1:contribute>
    <ns1:contribute seq="3">
      <ns1:role>63</ns1:role>
      <ns1:ext_role>član komisije</ns1:ext_role>
      <ns1:entity seq="0">
        <ns3:firstname> Jelena. </ns3:firstname>
        <ns3:lastname>Živanov-Čurlis</ns3:lastname>
      </ns1:entity>
      <ns1:date>2016</ns1:date>
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    <ns1:copyright>yes</ns1:copyright>
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    <ns7:keyword language="sr" seq="0">vaskularizacija, ektopična osteogeneza, mezenhimske matične ćelijemasnog tkiva, miš, in vitro diferencijacija, endotelske ćelije, osteogene ćelije, mineralnimatriks kosti, plazma obogaćena trombocitima, tkivno inženjerstvo kosti.</ns7:keyword>
    <ns7:keyword language="en" seq="1">vascularization, ectopic osteogenesis, adipose-derived mesenchymal stemcells, mice, in vitro differentiation, endothelial cells, osteogenic cells, bone mineralmatrix, platelet-rich plasma, bone tissue engineering</ns7:keyword>
    <ns7:keyword language="sr" seq="2">[591.476 : [611.018 : 591.413]] : 611.018.4(043.3)</ns7:keyword>
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    <ns8:orgassignment>
      <ns8:faculty>11A02</ns8:faculty>
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  <ns12:digitalbook>
    <ns12:releaseyear>2016</ns12:releaseyear>
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