Detailed Information on Publication Record
2018
Inactivation of PLK4-STIL Module Prevents Self-Renewal and Triggers p53-Dependent Differentiation in Human Pluripotent Stem Cells
RENZOVÁ, Tereza, Dáša BOHAČIAKOVÁ, Milan EŠNER, Veronika POSPÍŠILOVÁ, Tomáš BÁRTA et. al.Basic information
Original name
Inactivation of PLK4-STIL Module Prevents Self-Renewal and Triggers p53-Dependent Differentiation in Human Pluripotent Stem Cells
Authors
RENZOVÁ, Tereza (203 Czech Republic, belonging to the institution), Dáša BOHAČIAKOVÁ (703 Slovakia, belonging to the institution), Milan EŠNER (203 Czech Republic, belonging to the institution), Veronika POSPÍŠILOVÁ (203 Czech Republic, belonging to the institution), Tomáš BÁRTA (203 Czech Republic, belonging to the institution), Aleš HAMPL (203 Czech Republic, belonging to the institution) and Lukáš ČAJÁNEK (203 Czech Republic, guarantor, belonging to the institution)
Edition
STEM CELL REPORTS, CAMBRIDGE, CELL PRESS, 2018, 2213-6711
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10601 Cell biology
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 5.499
RIV identification code
RIV/00216224:14110/18:00101379
Organization unit
Faculty of Medicine
UT WoS
000446691800011
Keywords in English
PLK4-STIL module
Změněno: 8/10/2024 08:42, Mgr. Eva Dubská
Abstract
V originále
Centrioles account for centrosomes and cilia formation. Recently, a link between centrosomal components and human developmental disorders has been established. However, the exact mechanisms how centrosome abnormalities influence embryogenesis and cell fate are not understood. PLK4-STIL module represents a key element of centrosome duplication cycle. We analyzed consequences of inactivation of the module for early events of embryogenesis in human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs). We demonstrate that blocking of PLK4 or STIL functions leads to centrosome loss followed by both p53-dependent and -independent defects, including prolonged cell divisions, upregulation of p53, chromosome instability, and, importantly, reduction of pluripotency markers and induction of differentiation. We show that the observed loss of key stem cells properties is connected to alterations in mitotic timing and protein turnover. In sum, our data define a link between centrosome, its regulators, and the control of pluripotency and differentiation in PSCs.
Links
GJ15-18316Y, research and development project |
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GJ16-03269Y, research and development project |
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GJ16-24004Y, research and development project |
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GJ18-25429Y, research and development project |
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LM2015062, research and development project |
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MUNI/E/1310/2017, interní kód MU |
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MUNI/G/1131/2017, interní kód MU |
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ROZV/24/LF/2016, interní kód MU |
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ROZV/24/LF/2018, interní kód MU |
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ROZV/25/LF/2017, interní kód MU |
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90062, large research infrastructures |
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