Atomic force microscopy imaging and mechanical properties measurement of red blood cells and aggressive cancer cells

Mi Li, LianQing Liu, Ning Xi, YueChao Wang, ZaiLi Dong, XiuBin Xiao, WeiJing Zhang

    Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

    92 Citations (Scopus)
    61 Downloads (CityUHK Scholars)

    Abstract

    Mechanical properties play an important role in regulating cellular activities and are critical for unlocking the mysteries of life. Atomic force microscopy (AFM) enables researchers to measure mechanical properties of single living cells under physiological conditions. Here, AFM was used to investigate the topography and mechanical properties of red blood cells (RBCs) and three types of aggressive cancer cells (Burkitt's lymphoma Raji, cutaneous lymphoma Hut, and chronic myeloid leukemia K562). The surface topography of the RBCs and the three cancer cells was mapped with a conventional AFM probe, while mechanical properties were investigated with a micro-sphere glued onto a tip-less cantilever. The diameters of RBCs are significantly smaller than those of the cancer cells, and mechanical measurements indicated that Young's modulus of RBCs is smaller than those of the cancer cells. Aggressive cancer cells have a lower Young's modulus than that of indolent cancer cells, which may improve our understanding of metastasis. © 2012 The Author(s).
    Original languageEnglish
    Pages (from-to)968-973
    JournalScience China Life Sciences
    Volume55
    Issue number11
    DOIs
    Publication statusPublished - Nov 2012

    Research Keywords

    • atomic force microscopy
    • cancer cell
    • mechanical properties
    • red blood cell
    • Young's modulus

    Publisher's Copyright Statement

    • This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

    Fingerprint

    Dive into the research topics of 'Atomic force microscopy imaging and mechanical properties measurement of red blood cells and aggressive cancer cells'. Together they form a unique fingerprint.

    Cite this