Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1997-11-19
pubmed:abstractText
Investigation of primitive human haemopoietic cell behaviour requires methodologies for monitoring asynchronously activated cells over several generations. We describe a high-resolution procedure for tracking 5- (and 6-) carboxyfluorescein diacetate succinimidyl ester (CFSE)- labelled human haemopoietic cells through six cell cycles based on the precise halving of their CFSE-fluorescence at each mitosis. Using this approach in combination with DNA or surface antigen staining, we show that the addition of Flt3-ligand (FL) to a cytokine cocktail consisting of Steel factor, IL-3, IL-6 and G-CSF increased the proportion of CD34+ (CD45RA/CD71)-, but not CD34+(CD45RA/CD71)+, human marrow cells initially recruited into division in vitro, shortened the overall cycle time of their progeny, and enhanced the production of a derivative CD34+CD38- population through several (up to four) cell generations. These studies also showed that during the first 4d there was no detectable apoptosis among the progeny of the CD34+(CD45RA/CD71)- cells generated in the presence of this four-cytokine cocktail, regardless of the presence of FL. The availability of a technique for monitoring changes in the properties of individual cells as a function of their mitotic history and under conditions where they are asynchronously recruited to divide provides a new and powerful approach for studies of the regulation of primitive human haemopoietic cell proliferation and differentiation.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/5-(6)-carboxyfluorescein diacetate..., http://linkedlifedata.com/resource/pubmed/chemical/ADP-ribosyl Cyclase, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD34, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD38, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Differentiation, http://linkedlifedata.com/resource/pubmed/chemical/CD38 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Fluoresceins, http://linkedlifedata.com/resource/pubmed/chemical/Fluorescent Dyes, http://linkedlifedata.com/resource/pubmed/chemical/Growth Substances, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/NAD Nucleosidase, http://linkedlifedata.com/resource/pubmed/chemical/Succinimides, http://linkedlifedata.com/resource/pubmed/chemical/flt3 ligand protein
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0007-1048
pubmed:author
pubmed:issnType
Print
pubmed:volume
98
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
528-39
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:9332305-ADP-ribosyl Cyclase, pubmed-meshheading:9332305-Antigens, CD, pubmed-meshheading:9332305-Antigens, CD34, pubmed-meshheading:9332305-Antigens, CD38, pubmed-meshheading:9332305-Antigens, Differentiation, pubmed-meshheading:9332305-Cell Division, pubmed-meshheading:9332305-Cell Line, pubmed-meshheading:9332305-Cell Lineage, pubmed-meshheading:9332305-Fluoresceins, pubmed-meshheading:9332305-Fluorescence, pubmed-meshheading:9332305-Fluorescent Dyes, pubmed-meshheading:9332305-Growth Substances, pubmed-meshheading:9332305-Hematopoietic Stem Cells, pubmed-meshheading:9332305-Humans, pubmed-meshheading:9332305-Membrane Glycoproteins, pubmed-meshheading:9332305-Membrane Proteins, pubmed-meshheading:9332305-NAD+ Nucleosidase, pubmed-meshheading:9332305-Phenotype, pubmed-meshheading:9332305-Succinimides
pubmed:year
1997
pubmed:articleTitle
High-resolution cell division tracking demonstrates the FLt3-ligand-dependence of human marrow CD34+CD38- cell production in vitro.
pubmed:affiliation
Terry Fox Laboratory, British Columbia Cancer Agency, Vancouver, Canada.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't