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Tytuł pozycji:

The transcription factor repertoire of Flt3+ hematopoietic stem cells.

Tytuł:
The transcription factor repertoire of Flt3+ hematopoietic stem cells.
Autorzy:
Hieronymus T; Institute for Biomedical Engineering, Department of Cell Biology, RWTH Aachen University Medical School, Aachen, Germany.
Ruau D
Ober-Blöbaum J
Baek JH
Rolletschek A
Rose-John S
Wobus AM
Müller AM
Zenke M
Źródło:
Cells, tissues, organs [Cells Tissues Organs] 2008; Vol. 188 (1-2), pp. 103-15. Date of Electronic Publication: 2008 Jan 04.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Original Publication: Basel ; New York : Karger, c1999-
MeSH Terms:
Hematopoietic Stem Cells/*metabolism
Transcription Factors/*genetics
fms-Like Tyrosine Kinase 3/*metabolism
Animals ; Bone Marrow Cells/drug effects ; Bone Marrow Cells/metabolism ; CD11b Antigen/metabolism ; Cell Line ; Cluster Analysis ; Embryonic Stem Cells/drug effects ; Embryonic Stem Cells/metabolism ; Gene Expression Profiling ; Gene Expression Regulation, Developmental/drug effects ; Hematopoietic Stem Cells/drug effects ; Humans ; Intercellular Signaling Peptides and Proteins/pharmacology ; Mice ; Mice, Inbred C57BL ; Oligonucleotide Array Sequence Analysis ; Phenotype ; Transcription Factors/metabolism
Substance Nomenclature:
0 (CD11b Antigen)
0 (Intercellular Signaling Peptides and Proteins)
0 (Transcription Factors)
EC 2.7.10.1 (Flt3 protein, mouse)
EC 2.7.10.1 (fms-Like Tyrosine Kinase 3)
Entry Date(s):
Date Created: 20080705 Date Completed: 20080919 Latest Revision: 20171116
Update Code:
20240104
DOI:
10.1159/000112836
PMID:
18600024
Czasopismo naukowe
Hematopoietic stem cells maintain the development of all mature blood cells throughout life due to their sustained self-renewal capacity and multilineage differentiation potential. During development into specific cell lineages, the options of stem cells and multipotent progenitor cells become increasingly restricted concomitant with a successive decline in self-renewal potential. Here we describe an Flt3+CD11b+ multipotent progenitor that can be amplified in vitro with a specific combination of cytokines to yield homogeneous populations in high cell numbers. By employing gene expression profiling with DNA microarrays, we studied the transcription factor repertoire of Flt3+CD11b+ progenitors and related it to the transcription factor repertoire of hematopoietic stem cells and embryonic stem cells. We report here on overlapping and nonoverlapping expression patterns of transcription factors in these cells and thus provide novel insights into the dynamic networks of transcriptional regulators in embryonic and adult stem cells. Additionally, the results obtained open the perspective for elucidating lineage and 'stemness' determinants in hematopoiesis.
((c) 2008 S. Karger AG, Basel.)

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