Number of the records: 1  

3D visualization of collagen in artificial scaffolds using two-photon excitation and second-harmonic generation imaging

  1. 1.
    SYSNO ASEP0373200
    Document TypeO - Others
    R&D Document TypeOthers
    Title3D visualization of collagen in artificial scaffolds using two-photon excitation and second-harmonic generation imaging
    Author(s) Čapek, M. (CZ)
    Burdíková, Zuzana (FGU-C) RID
    Filová, Eva (UEM-P) RID, ORCID
    Košťáková, E. (CZ)
    Janáček, Jiří (FGU-C) RID, ORCID
    Source TitleProceedings 10th Multinational Congress on Microscopy 2011. - Urbino : Societa Italiana Scienze Micriscopiche, 2011
    S. 261-262
    Number of pages2 s.
    ActionMultinational Congress on Microscopy 2011 /10./ - MCM 2011
    Event date04.09.2011-09.09.2011
    VEvent locationUrbino
    CountryIT - Italy
    Event typeWRD
    Languageeng - English
    CountryIT - Italy
    Keywordsmulti-photon microscopy ; artificial scaffolds ; collagen
    Subject RIVEA - Cell Biology
    R&D ProjectsLC06063 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    MEB0810092 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    GAP501/10/0340 GA ČR - Czech Science Foundation (CSF)
    GA304/09/0733 GA ČR - Czech Science Foundation (CSF)
    IAA500390702 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    7E09088 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z50110509 - FGU-C (2005-2011)
    AV0Z50390512 - UEM-P (2005-2011)
    AnnotationNonlinear microscopy can employ two different types of signals, fluorescence and second-harmonic generation (SHG), to image biological structures with subcellular resolution. SHG imaging was used for the identification of type II collagen in an extracellular matrix. Chondrocyte proliferation was linked to production of the extracellular matrix proteins. Collagen as a typical extracellular cartilage protein was visualized, first, by CLSM using fluorescently labeled monoclonal antibodies against type II collagen. Conventional confocal microscopy images were compared with the SHG imaging in both forward and backward nondescanned modes. Well detectable signals were observed in PCL and gelatine scaffolds. Detection of collagen by SHG imaging corresponded well with collagen detection by immunohistochemical staining
    WorkplaceInstitute of Physiology
    ContactLucie Trajhanová, lucie.trajhanova@fgu.cas.cz, Tel.: 241 062 400
    Year of Publishing2012
Number of the records: 1  

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