Detailed Information on Publication Record
2019
The frequency and consequences of multipolar mitoses in undifferentiated embryonic stem cells
POSPÍŠILOVÁ, Veronika, Milan EŠNER, Iveta ČERVENKOVÁ, Radek FEDR, Jean-Yvez TINEVEZ et. al.Basic information
Original name
The frequency and consequences of multipolar mitoses in undifferentiated embryonic stem cells
Authors
POSPÍŠILOVÁ, Veronika (203 Czech Republic, belonging to the institution), Milan EŠNER (203 Czech Republic, belonging to the institution), Iveta ČERVENKOVÁ (703 Slovakia, belonging to the institution), Radek FEDR (203 Czech Republic), Jean-Yvez TINEVEZ (250 France), Aleš HAMPL (203 Czech Republic, belonging to the institution) and Martin ANGER (203 Czech Republic, guarantor, belonging to the institution)
Edition
Journal of applied biomedicine, České Budějovice, Faculty of Health and Social Care, University of South Bohemia, 2019, 1214-021X
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10601 Cell biology
Country of publisher
Czech Republic
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 1.700
RIV identification code
RIV/00216224:14110/19:00108159
Organization unit
Faculty of Medicine
UT WoS
000510179600002
Keywords in English
Embryonic stem (ES) cells; Mitosis length; Multipolar division; Single-cell tracking; Spindle assembly checkpoint (SAC); Time-lapse microscopy
Tags
International impact, Reviewed
Změněno: 24/10/2024 11:00, Mgr. Adéla Pešková
Abstract
V originále
Embryonic stem (ES) cells are pluripotent cells widely used in cell therapy and tissue engineering. However, the broader clinical applications of ES cells are limited by their genomic instability and karyotypic abnormalities. Thus, understanding the mechanisms underlying ES cell karyotypic abnormalities is critical to optimizing their dinical use. In this study, we focused on proliferating human and mouse ES cells undergoing multipolar divisions. Specifically, we analyzed the frequency and outcomes of such divisions using a combination of time-lapse microscopy and cell tracking. This revealed that cells resulting from multipolar divisions were not only viable, but they also frequently underwent subsequent cell divisions. Our novel data also showed that in human and mouse ES cells, multipolar spindles allowed more robust escape from chromosome segregation control mechanisms than bipolar spindles. Considering the frequency of multipolar divisions in proliferating ES cells, it is conceivable that cell division errors underlie ES cell karyotypic instability.
Links
EF16_013/0001775, research and development project |
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GA15-04844S, research and development project |
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GA15-11707S, research and development project |
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LM2015043, research and development project |
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LM2015062, research and development project |
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