Detailed Information on Publication Record
2021
TIME-LAPSE MONITORING OF CELL MECHANICAL PROPERTIES
PŘIBYL, Jan, Vladimír ROTREKL, Martin PEŠL, Šárka JELÍNKOVÁ, I. KRATOCHVILOVA et. al.Basic information
Original name
TIME-LAPSE MONITORING OF CELL MECHANICAL PROPERTIES
Authors
PŘIBYL, Jan (203 Czech Republic, belonging to the institution), Vladimír ROTREKL (203 Czech Republic, belonging to the institution), Martin PEŠL (203 Czech Republic, belonging to the institution), Šárka JELÍNKOVÁ (203 Czech Republic, belonging to the institution) and I. KRATOCHVILOVA
Edition
SLEZSKA, CONFERENCE PROCEEDINGS - NANOCON 2020, p. 416-421, 6 pp. 2021
Publisher
TANGER LTD
Other information
Language
English
Type of outcome
Stať ve sborníku
Field of Study
10601 Cell biology
Country of publisher
Czech Republic
Confidentiality degree
není předmětem státního či obchodního tajemství
Publication form
electronic version available online
References:
RIV identification code
RIV/00216224:14740/21:00120237
Organization unit
Central European Institute of Technology
ISBN
978-80-87294-98-7
ISSN
UT WoS
000664505500071
Keywords in English
Atomic Force Microscopy; Mechanical Mapping; Cell stiffness; Cryopreservation
Tags
International impact, Reviewed
Změněno: 23/3/2022 13:41, Mgr. Pavla Foltynová, Ph.D.
Abstract
V originále
Atomic force microscopy (AFM) is a highly sensitive non-invasive surface method able to provide insight into cells' mechanical parameters. Membrane and sub-membrane development, as well as internal cellular properties, can be monitored. The stiffness of cells is a fundamental phenomenon that reflects changes in cell physiology. More importantly, changes in cell mechanical properties are also often found to be closely associated with various disease conditions. Cell mechanics are mainly dependent on cytoskeletal architecture. The development of cryopreserved cells' mechanical properties (stiffness) after thawing was studied using AFM. Cell stiffness was mapped and thus monitored in time and space under nearly physiological conditions (i.e., in culture medium and at elevated temperature). In AFM force spectroscopy mode, cells are indented at many sites, and their complete elastic responses are recorded, enabling them to reconstruct a stiffness map. We measured the frozen cell surface stiffness immediately after thawing; they, when the dynamics of development of the cell stiffness were monitored in time up to 24 hours. Moreover, the AFM spectroscopy was combined with fluorescence-based staining of the cytoskeleton, thus enabling to directly correlate cytoskeleton development with stiffness mapping.
Links
LM2018127, research and development project |
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NU20-06-00156, research and development project |
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