-
Something wrong with this record ?
Stochastic NANOG fluctuations allow mouse embryonic stem cells to explore pluripotency
E. Abranches, AM. Guedes, M. Moravec, H. Maamar, P. Svoboda, A. Raj, D. Henrique,
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 1953 to 6 months ago
Open Access Digital Library
from 1953-03-01 to 6 months ago
PubMed
25005472
DOI
10.1242/dev.108910
Knihovny.cz E-resources
- MeSH
- Principal Component Analysis MeSH
- Clone Cells MeSH
- Cell Line MeSH
- Cell Lineage genetics MeSH
- Time-Lapse Imaging MeSH
- Embryonic Stem Cells cytology metabolism MeSH
- Transcription, Genetic MeSH
- Homeodomain Proteins genetics metabolism MeSH
- Kinetics MeSH
- RNA, Messenger genetics metabolism MeSH
- Mice MeSH
- Pluripotent Stem Cells cytology metabolism MeSH
- Cell Proliferation MeSH
- Flow Cytometry MeSH
- Gene Expression Profiling MeSH
- Stochastic Processes MeSH
- Gene Expression Regulation, Developmental MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Heterogeneous expression of the transcription factor NANOG has been linked to the existence of various functional states in pluripotent stem cells. This heterogeneity seems to arise from fluctuations of Nanog expression in individual cells, but a thorough characterization of these fluctuations and their impact on the pluripotent state is still lacking. Here, we have used a novel fluorescent reporter to investigate the temporal dynamics of NANOG expression in mouse embryonic stem cells (mESCs), and to dissect the lineage potential of mESCs at different NANOG states. Our results show that stochastic NANOG fluctuations are widespread in mESCs, with essentially all expressing cells showing fluctuations in NANOG levels, even when cultured in ground-state conditions (2i media). We further show that fluctuations have similar kinetics when mESCs are cultured in standard conditions (serum plus leukemia inhibitory factor) or ground-state conditions, implying that NANOG fluctuations are inherent to the pluripotent state. We have then compared the developmental potential of low-NANOG and high-NANOG mESCs, grown in different conditions, and confirm that mESCs are more susceptible to enter differentiation at the low-NANOG state. Further analysis by gene expression profiling reveals that low-NANOG cells have marked expression of lineage-affiliated genes, with variable profiles according to the signalling environment. By contrast, high-NANOG cells show a more stable expression profile in different environments, with minimal expression of lineage markers. Altogether, our data support a model in which stochastic NANOG fluctuations provide opportunities for mESCs to explore multiple lineage options, modulating their probability to change functional state.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc14074129
- 003
- CZ-PrNML
- 005
- 20141007121415.0
- 007
- ta
- 008
- 141006s2014 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1242/dev.108910 $2 doi
- 035 __
- $a (PubMed)25005472
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Abranches, Elsa $u Instituto de Medicina Molecular and Instituto de Histologia e Biologia do Desenvolvimento, Faculdade de Medicina da Universidade de Lisboa, Avenida Prof. Egas Moniz, Lisboa 1649-028, Portugal Champalimaud Neuroscience Programme, Champalimaud Centre for the Unknown, Avenida Brasilia - Doca de Pedrouços, Lisboa 1400-038, Portugal elsa.abranches@gmail.com henrique@fm.ul.pt. $7 gn_A_00000799
- 245 10
- $a Stochastic NANOG fluctuations allow mouse embryonic stem cells to explore pluripotency / $c E. Abranches, AM. Guedes, M. Moravec, H. Maamar, P. Svoboda, A. Raj, D. Henrique,
- 520 9_
- $a Heterogeneous expression of the transcription factor NANOG has been linked to the existence of various functional states in pluripotent stem cells. This heterogeneity seems to arise from fluctuations of Nanog expression in individual cells, but a thorough characterization of these fluctuations and their impact on the pluripotent state is still lacking. Here, we have used a novel fluorescent reporter to investigate the temporal dynamics of NANOG expression in mouse embryonic stem cells (mESCs), and to dissect the lineage potential of mESCs at different NANOG states. Our results show that stochastic NANOG fluctuations are widespread in mESCs, with essentially all expressing cells showing fluctuations in NANOG levels, even when cultured in ground-state conditions (2i media). We further show that fluctuations have similar kinetics when mESCs are cultured in standard conditions (serum plus leukemia inhibitory factor) or ground-state conditions, implying that NANOG fluctuations are inherent to the pluripotent state. We have then compared the developmental potential of low-NANOG and high-NANOG mESCs, grown in different conditions, and confirm that mESCs are more susceptible to enter differentiation at the low-NANOG state. Further analysis by gene expression profiling reveals that low-NANOG cells have marked expression of lineage-affiliated genes, with variable profiles according to the signalling environment. By contrast, high-NANOG cells show a more stable expression profile in different environments, with minimal expression of lineage markers. Altogether, our data support a model in which stochastic NANOG fluctuations provide opportunities for mESCs to explore multiple lineage options, modulating their probability to change functional state.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a buněčné linie $7 D002460
- 650 _2
- $a buněčný rodokmen $x genetika $7 D019070
- 650 _2
- $a proliferace buněk $7 D049109
- 650 _2
- $a buněčné klony $7 D002999
- 650 _2
- $a embryonální kmenové buňky $x cytologie $x metabolismus $7 D053595
- 650 _2
- $a průtoková cytometrie $7 D005434
- 650 _2
- $a stanovení celkové genové exprese $7 D020869
- 650 _2
- $a vývojová regulace genové exprese $7 D018507
- 650 _2
- $a homeodoménové proteiny $x genetika $x metabolismus $7 D018398
- 650 _2
- $a kinetika $7 D007700
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a pluripotentní kmenové buňky $x cytologie $x metabolismus $7 D039904
- 650 _2
- $a analýza hlavních komponent $7 D025341
- 650 _2
- $a messenger RNA $x genetika $x metabolismus $7 D012333
- 650 _2
- $a stochastické procesy $7 D013269
- 650 _2
- $a časosběrné zobrazování $7 D059008
- 650 _2
- $a genetická transkripce $7 D014158
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Guedes, Ana M V $u Instituto de Medicina Molecular and Instituto de Histologia e Biologia do Desenvolvimento, Faculdade de Medicina da Universidade de Lisboa, Avenida Prof. Egas Moniz, Lisboa 1649-028, Portugal Champalimaud Neuroscience Programme, Champalimaud Centre for the Unknown, Avenida Brasilia - Doca de Pedrouços, Lisboa 1400-038, Portugal.
- 700 1_
- $a Moravec, Martin $u Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, Videnska 1083, 142 20 Prague 4, Czech Republic.
- 700 1_
- $a Maamar, Hedia $u Department of Bioengineering, University of Pennsylvania, 210 South 33rd Street, Philadelphia, PA 19104, USA.
- 700 1_
- $a Svoboda, Petr $u Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, Videnska 1083, 142 20 Prague 4, Czech Republic.
- 700 1_
- $a Raj, Arjun $u Department of Bioengineering, University of Pennsylvania, 210 South 33rd Street, Philadelphia, PA 19104, USA.
- 700 1_
- $a Henrique, Domingos $u Instituto de Medicina Molecular and Instituto de Histologia e Biologia do Desenvolvimento, Faculdade de Medicina da Universidade de Lisboa, Avenida Prof. Egas Moniz, Lisboa 1649-028, Portugal Champalimaud Neuroscience Programme, Champalimaud Centre for the Unknown, Avenida Brasilia - Doca de Pedrouços, Lisboa 1400-038, Portugal elsa.abranches@gmail.com henrique@fm.ul.pt.
- 773 0_
- $w MED00001363 $t Development (Cambridge, England) $x 1477-9129 $g Roč. 141, č. 14 (2014), s. 2770-9
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/25005472 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20141006 $b ABA008
- 991 __
- $a 20141007121853 $b ABA008
- 999 __
- $a ok $b bmc $g 1042012 $s 873041
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2014 $b 141 $c 14 $d 2770-9 $i 1477-9129 $m Development $n Development $x MED00001363
- LZP __
- $a Pubmed-20141006