Detailed Information on Publication Record
2017
Properties of Human Embryonic Stem Cells and Their Differentiated Derivatives Depend on Nonhistone DNA-Binding HMGB1 and HMGB2 Proteins
BAGHERPOOR, Alireza Jian, Dáša DOLEŽALOVÁ, Tomáš BÁRTA, Martin KUČÍREK, Soodabeh Abbasi SANI et. al.Basic information
Original name
Properties of Human Embryonic Stem Cells and Their Differentiated Derivatives Depend on Nonhistone DNA-Binding HMGB1 and HMGB2 Proteins
Authors
BAGHERPOOR, Alireza Jian (203 Czech Republic), Dáša DOLEŽALOVÁ (703 Slovakia, guarantor, belonging to the institution), Tomáš BÁRTA (203 Czech Republic, belonging to the institution), Martin KUČÍREK (203 Czech Republic), Soodabeh Abbasi SANI (203 Czech Republic), Milan EŠNER (203 Czech Republic, belonging to the institution), Michaela BOSÁKOVÁ (203 Czech Republic, belonging to the institution), Vladimír VINARSKÝ (203 Czech Republic), Lucie PEŠKOVÁ (203 Czech Republic, belonging to the institution), Aleš HAMPL (203 Czech Republic, belonging to the institution) and Michal ŠTROS (203 Czech Republic)
Edition
Stem Cells and Development, New Rochelle, Mary Ann Liebert, 2017, 1547-3287
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
Impact factor
Impact factor: 3.315
RIV identification code
RIV/00216224:14110/17:00094624
Organization unit
Faculty of Medicine
UT WoS
000394588800003
Keywords in English
human embryonic stem cells; HMGB1; HMGB2; neuroectodermal cells; differentiation
Tags
Tags
International impact, Reviewed
Změněno: 20/3/2018 18:19, Soňa Böhmová
Abstract
V originále
HMGB1 and HMGB2 proteins have been implicated in numerous cellular processes, including proliferation, differentiation, apoptosis, and tumor growth. It is unknown whether they are involved in regulating the typical functions of pluripotent human embryonic stem cells (hESCs) and/or those of the differentiated derivatives of hESCs. Using inducible, stably transfected hESCs capable of shRNA-mediated knockdown of HMGB1 and HMGB2, we provide evidence that downregulation of HMGB1 and/or HMGB2 in undifferentiated hESCs does not affect the stemness of cells and induces only minor changes to the proliferation rate, cell-cycle profile, and apoptosis. After differentiation is induced, however, the downregulation of those proteins has important effects on proliferation, apoptosis, telomerase activity, and the efficiency of differentiation toward the neuroectodermal lineage. Furthermore, those processes are affected only when one, but not both, of the two proteins is downregulated; the knockdown of both HMGB1 and HMGB2 results in a normal phenotype. Those results advance our knowledge of regulation of hESC and human neuroectodermal cell differentiation and illustrate the distinct roles of HMGB1 and HMGB2 during early human development.
Links
GAP305/12/2475, research and development project |
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GA15-23033S, research and development project |
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GJ15-18316Y, research and development project |
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GJ16-24004Y, research and development project |
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MUNI/A/1352/2015, interní kód MU |
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