-
Something wrong with this record ?
MAPK p38alpha Kinase Influences Haematopoiesis in Embryonic Stem Cells
K. Štefková, M. Hanáčková, J. Kučera, KA. Radaszkiewicz, B. Ambrůžová, L. Kubala, J. Pacherník,
Language English Country United States
Document type Journal Article
NLK
Directory of Open Access Journals
from 2010
Free Medical Journals
from 2010
PubMed Central
from 2010
Europe PubMed Central
from 2010
ProQuest Central
from 2014-01-01
Open Access Digital Library
from 2009-08-26
Open Access Digital Library
from 2010-01-01
Open Access Digital Library
from 2010-01-01
Health & Medicine (ProQuest)
from 2014-01-01
Wiley-Blackwell Open Access Titles
from 2010
ROAD: Directory of Open Access Scholarly Resources
from 2010
PubMed
31281375
DOI
10.1155/2019/5128135
Knihovny.cz E-resources
- Publication type
- Journal Article MeSH
The activation of p38alpha kinase mediates cell response to various extracellular factors including many interleukins and growth factors important for haematopoiesis. The role of p38alpha kinase was previously analysed in particular haematopoietic cells. In this study and for the first time, the role of p38alpha kinase in haematopoiesis was studied using a model of continuous haematopoietic development in pluripotent embryonic stem cells in vitro. The expression of transcripts associated with haematopoiesis and the potential for the formation of specific haematopoietic cell colonies were compared between wild-type and mutant p38alpha gene-depleted cells. The absence of p38alpha kinase led to the inhibition of hemangioblast formation during the first step of haematopoiesis. Later, during differentiation, due to the lack of p38alpha kinase, erythrocyte maturation was impaired. Mutant p38α-/- cells also exhibited decreased potential with respect to the expansion of granulocyte colony-forming units. This effect was reversed in the absence of erythropoietin as shown by colony-forming unit assay in media for colony-forming unit granulocytes/macrophages. p38alpha kinase thus plays an important role in the differentiation of common myeloid precursor cells into granulocyte lineages.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19035977
- 003
- CZ-PrNML
- 005
- 20240717093602.0
- 007
- ta
- 008
- 191007e20190602xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1155/2019/5128135 $2 doi
- 035 __
- $a (PubMed)31281375
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Štefková, Kateřina $u Institute of Experimental Biology, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic.
- 245 10
- $a MAPK p38alpha Kinase Influences Haematopoiesis in Embryonic Stem Cells / $c K. Štefková, M. Hanáčková, J. Kučera, KA. Radaszkiewicz, B. Ambrůžová, L. Kubala, J. Pacherník,
- 520 9_
- $a The activation of p38alpha kinase mediates cell response to various extracellular factors including many interleukins and growth factors important for haematopoiesis. The role of p38alpha kinase was previously analysed in particular haematopoietic cells. In this study and for the first time, the role of p38alpha kinase in haematopoiesis was studied using a model of continuous haematopoietic development in pluripotent embryonic stem cells in vitro. The expression of transcripts associated with haematopoiesis and the potential for the formation of specific haematopoietic cell colonies were compared between wild-type and mutant p38alpha gene-depleted cells. The absence of p38alpha kinase led to the inhibition of hemangioblast formation during the first step of haematopoiesis. Later, during differentiation, due to the lack of p38alpha kinase, erythrocyte maturation was impaired. Mutant p38α-/- cells also exhibited decreased potential with respect to the expansion of granulocyte colony-forming units. This effect was reversed in the absence of erythropoietin as shown by colony-forming unit assay in media for colony-forming unit granulocytes/macrophages. p38alpha kinase thus plays an important role in the differentiation of common myeloid precursor cells into granulocyte lineages.
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Hanáčková, Markéta $u Institute of Experimental Biology, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic.
- 700 1_
- $a Kučera, Jan $u Institute of Experimental Biology, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic.
- 700 1_
- $a Radaszkiewicz, Katarzyna $u Institute of Experimental Biology, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic. $7 xx0320047
- 700 1_
- $a Ambrůžová, Barbora $u Institute of Experimental Biology, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic. Institute of Biophysics, Academy of Sciences of the Czech Republic, Královopolská 2590/135, 61200 Brno, Czech Republic.
- 700 1_
- $a Kubala, Lukáš $u Institute of Experimental Biology, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic. Institute of Biophysics, Academy of Sciences of the Czech Republic, Královopolská 2590/135, 61200 Brno, Czech Republic.
- 700 1_
- $a Pacherník, Jiří $u Institute of Experimental Biology, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic.
- 773 0_
- $w MED00188142 $t Stem cells international $x 1687-966X $g Roč. 2019 (20190602), s. 5128135
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31281375 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20191007 $b ABA008
- 991 __
- $a 20240717093558 $b ABA008
- 999 __
- $a ind $b bmc $g 1452637 $s 1074527
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 2019 $c - $d 5128135 $e 20190602 $i 1687-966X $m Stem cells international $n Stem cells int $x MED00188142
- LZP __
- $a Pubmed-20191007