-
Something wrong with this record ?
Tracing colonic embryonic transcriptional profiles and their reactivation upon intestinal damage
H. Fazilaty, MD. Brügger, T. Valenta, BM. Szczerba, L. Berkova, N. Doumpas, G. Hausmann, M. Scharl, K. Basler
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Cell Press Free Archives
from 2012
Directory of Open Access Journals
from 2012
Free Medical Journals
from 2012
Freely Accessible Science Journals
from 2012-01-26
Open Access Digital Library
from 2012-01-26
Open Access Digital Library
from 2012-01-01
- MeSH
- Single-Cell Analysis MeSH
- Cell Differentiation MeSH
- Embryo, Mammalian metabolism MeSH
- Inflammatory Bowel Diseases genetics pathology MeSH
- Colitis genetics MeSH
- Colon embryology pathology MeSH
- Humans MeSH
- Mesoderm embryology MeSH
- Disease Models, Animal MeSH
- Mice, Inbred C57BL MeSH
- Gene Expression Profiling * MeSH
- Intestinal Mucosa embryology metabolism pathology MeSH
- Gene Expression Regulation, Developmental MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
We lack a holistic understanding of the genetic programs orchestrating embryonic colon morphogenesis and governing damage response in the adult. A window into these programs is the transcriptomes of the epithelial and mesenchymal cell populations in the colon. Performing unbiased single-cell transcriptomic analyses of the developing mouse colon at different embryonic stages (embryonic day 14.5 [E14.5], E15.5, and E18.5), we capture cellular and molecular profiles of the stages before, during, and after the appearance of crypt structures, as well as in a model of adult colitis. The data suggest most adult lineages are established by E18.5. We find embryonic-specific gene expression profiles and cell populations that reappear in response to tissue damage. Comparison of the datasets from mice and human colitis suggests the processes are conserved. In this study, we provide a comprehensive single-cell atlas of the developing mouse colon and evidence for the reactivation of embryonic genes in disease.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc22012301
- 003
- CZ-PrNML
- 005
- 20220506131311.0
- 007
- ta
- 008
- 220425s2021 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.celrep.2021.109484 $2 doi
- 035 __
- $a (PubMed)34348153
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Fazilaty, Hassan $u Department of Molecular Life Sciences, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland
- 245 10
- $a Tracing colonic embryonic transcriptional profiles and their reactivation upon intestinal damage / $c H. Fazilaty, MD. Brügger, T. Valenta, BM. Szczerba, L. Berkova, N. Doumpas, G. Hausmann, M. Scharl, K. Basler
- 520 9_
- $a We lack a holistic understanding of the genetic programs orchestrating embryonic colon morphogenesis and governing damage response in the adult. A window into these programs is the transcriptomes of the epithelial and mesenchymal cell populations in the colon. Performing unbiased single-cell transcriptomic analyses of the developing mouse colon at different embryonic stages (embryonic day 14.5 [E14.5], E15.5, and E18.5), we capture cellular and molecular profiles of the stages before, during, and after the appearance of crypt structures, as well as in a model of adult colitis. The data suggest most adult lineages are established by E18.5. We find embryonic-specific gene expression profiles and cell populations that reappear in response to tissue damage. Comparison of the datasets from mice and human colitis suggests the processes are conserved. In this study, we provide a comprehensive single-cell atlas of the developing mouse colon and evidence for the reactivation of embryonic genes in disease.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a buněčná diferenciace $7 D002454
- 650 _2
- $a kolitida $x genetika $7 D003092
- 650 _2
- $a kolon $x embryologie $x patologie $7 D003106
- 650 _2
- $a modely nemocí na zvířatech $7 D004195
- 650 _2
- $a embryo savčí $x metabolismus $7 D004622
- 650 12
- $a stanovení celkové genové exprese $7 D020869
- 650 _2
- $a vývojová regulace genové exprese $7 D018507
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a idiopatické střevní záněty $x genetika $x patologie $7 D015212
- 650 _2
- $a střevní sliznice $x embryologie $x metabolismus $x patologie $7 D007413
- 650 _2
- $a mezoderm $x embryologie $7 D008648
- 650 _2
- $a myši inbrední C57BL $7 D008810
- 650 _2
- $a analýza jednotlivých buněk $7 D059010
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Brügger, Michael David $u Department of Molecular Life Sciences, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland
- 700 1_
- $a Valenta, Tomas $u Department of Molecular Life Sciences, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland; Institute of Molecular Genetics of the ASCR, v. v. i., Vídeňská 1083, 142 20 Prague 4, Czech Republic. Electronic address: tomas.valenta@imls.uzh.ch
- 700 1_
- $a Szczerba, Barbara M $u Department of Gastroenterology and Hepatology, University Hospital Zurich, Rämistrasse 100, 8091 Zurich, Switzerland
- 700 1_
- $a Berkova, Linda $u Institute of Molecular Genetics of the ASCR, v. v. i., Vídeňská 1083, 142 20 Prague 4, Czech Republic
- 700 1_
- $a Doumpas, Nikolaos $u Department of Molecular Life Sciences, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland
- 700 1_
- $a Hausmann, George $u Department of Molecular Life Sciences, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland
- 700 1_
- $a Scharl, Michael $u Department of Gastroenterology and Hepatology, University Hospital Zurich, Rämistrasse 100, 8091 Zurich, Switzerland
- 700 1_
- $a Basler, Konrad $u Department of Molecular Life Sciences, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland. Electronic address: konrad.basler@imls.uzh.ch
- 773 0_
- $w MED00188029 $t Cell reports $x 2211-1247 $g Roč. 36, č. 5 (2021), s. 109484
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/34348153 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20220425 $b ABA008
- 991 __
- $a 20220506131303 $b ABA008
- 999 __
- $a ok $b bmc $g 1789754 $s 1163502
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 36 $c 5 $d 109484 $e 20210803 $i 2211-1247 $m Cell reports $n Cell Rep $x MED00188029
- LZP __
- $a Pubmed-20220425