New fluorogenic dyes for analysis of cellular processes by flow cytometry and confocal microscopy

被引:10
|
作者
Nikolova, Kalina [1 ]
Kaloyanova, Stefka [2 ]
Mihaylova, Nikolina [1 ]
Stoitsova, Stoyanka [1 ]
Chausheva, Stela [1 ]
Vasilev, Aleksey [2 ]
Lesev, Nedyalko [2 ]
Dimitrova, Petya [1 ]
Deligeorgiev, Todor [2 ]
Tchorbanov, Andrey [1 ]
机构
[1] Bulgarian Acad Sci, Stephan Angeloff Inst Microbiol, BU-1113 Sofia, Bulgaria
[2] Univ Sofia, Fac Chem & Pharm, Dept Appl Organ Chem, Sofia 1164, Bulgaria
关键词
Cyanine dyes; DNA-binding dyes; Apoptosis; Flow cytometry; Fluorescence; PROPIDIUM IODIDE; DNA QUANTIFICATION; CYCLE ANALYSIS; APOPTOSIS; CELLS; DEATH; HOECHST-33342; PROBES; ASSAY;
D O I
10.1016/j.jphotobiol.2013.10.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fluorescent microscopy and fluorescent imaging by flow cytometry are two of the fastest growing areas in the medical and biological research. Innovations in fluorescent chemistry and synthesis of new dye probes are closely related to the development of service equipment such as light sources, and detection techniques. Among compounds known as fluorescent labels, the cyanine-based dyes have become widely used since they have high excitation coefficients, narrow emission bands and high fluorescence upon binding to nucleic acids. The key methods for evaluation of apoptosis and cell cycle allow measuring DNA content by several flow cytometric techniques. We have synthesized new monomethine cyanine dyes and have characterized their applicability for staining of live and/or apoptotic cells. Imaging experiments by flow cytometry and confocal laser scanning microscopy (CLSM) have been also performed. Two of the dyes have shown high-affinity binding to the nuclei at high dilutions, up to 10(-9) M. Flow cytometry and CLSM have confirmed that these dyes labeled selectively non-living, e.g. ethanol-fixed cells that makes them appropriate for estimations of cell viability and apoptosis. The novel structures proved to be appropriate also for analysis of the cell cycle. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:125 / 134
页数:10
相关论文
共 50 条
  • [31] Simultaneous detection of apoptosis and mitochondrial superoxide production in live cells by flow cytometry and confocal microscopy
    Partha Mukhopadhyay
    Mohanraj Rajesh
    György Haskó
    Brian J Hawkins
    Muniswamy Madesh
    Pál Pacher
    Nature Protocols, 2007, 2 : 2295 - 2301
  • [32] Evaluation of isolated caprine pancreatic islets cytoarchitecture by laser scanning confocal microscopy and flow cytometry
    Hani, Homayoun
    Allaudin, Zeenathul Nazariah
    Mohd-Lila, Mohd-Azmi
    Sarsaifi, Kazhal
    Tengku-Ibrahim, Tengku-Azmi
    Othman, Abas Mazni
    XENOTRANSPLANTATION, 2016, 23 (02) : 128 - 136
  • [33] Encystation of Acanthamoeba castellanii:: Dye uptake for assessment by flow cytometry and confocal laser scanning microscopy
    Connell, C
    Rutter, A
    Hill, B
    Suller, M
    Lloyd, D
    JOURNAL OF APPLIED MICROBIOLOGY, 2001, 90 (05) : 706 - 712
  • [34] Assessment of sperm nuclear decondensation ability using confocal microscopy and flow cytometry in human infertility
    Soffer, Y
    Golan, R
    Shochat, L
    Oschry, Y
    Mittelman, L
    Strassburger, D
    Kaufman, S
    Raziel, A
    Lewin, LM
    ANDROLOGY IN THE 21ST CENTURY, SHORT COMMUNICATIONS, 2001, : 403 - 408
  • [35] Computational detection and quantification of human and mouse neutrophil extracellular traps in flow cytometry and confocal microscopy
    Ginley, Brandon G.
    Emmons, Tiffany
    Lutnick, Brendon
    Urban, Constantin F.
    Segal, Brahm H.
    Sarder, Pinaki
    SCIENTIFIC REPORTS, 2017, 7
  • [36] Computational detection and quantification of human and mouse neutrophil extracellular traps in flow cytometry and confocal microscopy
    Brandon G. Ginley
    Tiffany Emmons
    Brendon Lutnick
    Constantin F. Urban
    Brahm H. Segal
    Pinaki Sarder
    Scientific Reports, 7
  • [37] INTERNALIZATION OF SURFACE HLA-DR MOLECULES BY HUMAN EPIDERMAL LANGERHANS CELLS - ANALYSIS BY FLOW-CYTOMETRY AND CONFOCAL MICROSCOPY
    RIZOVA, H
    CARAYON, P
    MICHEL, L
    BARBIER, A
    LACHERETZ, F
    DUBERTRET, L
    CELL BIOLOGY AND TOXICOLOGY, 1994, 10 (5-6) : 367 - 373
  • [38] Meiosis in the golden hamster: a confocal microscopy and flow cytometric analysis
    Vigodner, M
    Lewin, LM
    Shochat, L
    Mittelman, L
    Golan, R
    MOLECULAR REPRODUCTION AND DEVELOPMENT, 2003, 64 (01) : 86 - 95
  • [39] Evaluation of murine renal phagocyte-fungal interactions using intravital confocal microscopy and flow cytometry
    Desai, Jigar, V
    Lionakis, Michail S.
    STAR PROTOCOLS, 2024, 5 (01): : 102781
  • [40] Stabilized cellular immunofluorescent analysis (SCIFA): A new concept for quantitative flow cytometry in routine immunohaematology
    Janossy, G
    Bikoue, A
    Tilling, RE
    Reilly, JT
    Granger, V
    Barnett, D
    BRITISH JOURNAL OF HAEMATOLOGY, 1998, 101 : 107 - 107