Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2003-12-16
pubmed:abstractText
We describe a novel culture system for generating large numbers of murine skin-associated mast cells and distinguish their characteristics from bone marrow-derived cultured mast cells. Culture of day 16 fetal skin single cell suspensions in the presence of interleukin-3 and stem cell factor allowed expansion and maturation of mast cells in the presence of stromal cells. The average yield of mast cells after 2 wk was 7.3 million cells per fetus at a purity of 96%. These fetal skin-derived cultured mast cells increased their histamine content in a time-dependent manner to 3.6 pg per cell after 2 wk and 6.7 pg per cell after 4 wk. Phenotypic analyses revealed much greater expression of CD49b and CD81 and lesser expression of CD77 and CD102 on fetal skin-derived cultured mast cells as compared with bone marrow-derived cultured mast cells. These findings suggest a close similarity between fetal skin-derived cultured mast cells and freshly isolated cutaneous mast cells. Connective tissue mast cell characteristics of fetal skin-derived cultured mast cells were evidenced by: (1) their greater histamine content than bone marrow-derived cultured mast cells; (2) the presence of heparin; and (3) their degranulation in response to compound 48/80 and substance P. Importantly, fetal skin-derived cultured mast cells secreted greater amounts of interleukin-13 but much less MIP-1beta and interleukin-6 than bone marrow-derived cultured mast cells in response to ionomycin. Thus fetal skin-derived cultured mast cells have many characteristics distinct from bone marrow-derived cultured mast cells and can be used as a model of cutaneous mast cells to discern their functions.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0022-202X
pubmed:author
pubmed:issnType
Print
pubmed:volume
121
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1425-32
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:14675193-Age Factors, pubmed-meshheading:14675193-Animals, pubmed-meshheading:14675193-Cell Culture Techniques, pubmed-meshheading:14675193-Cell Degranulation, pubmed-meshheading:14675193-Cell Differentiation, pubmed-meshheading:14675193-Cell Division, pubmed-meshheading:14675193-Cells, Cultured, pubmed-meshheading:14675193-Chemokine CCL4, pubmed-meshheading:14675193-Fetus, pubmed-meshheading:14675193-Heparin, pubmed-meshheading:14675193-Histamine, pubmed-meshheading:14675193-Interleukin-13, pubmed-meshheading:14675193-Interleukin-6, pubmed-meshheading:14675193-Macrophage Inflammatory Proteins, pubmed-meshheading:14675193-Mast Cells, pubmed-meshheading:14675193-Mice, pubmed-meshheading:14675193-Mice, Inbred BALB C, pubmed-meshheading:14675193-Mice, Inbred C57BL, pubmed-meshheading:14675193-Monocyte Chemoattractant Proteins, pubmed-meshheading:14675193-Phenotype, pubmed-meshheading:14675193-RNA, Messenger, pubmed-meshheading:14675193-Receptors, IgE, pubmed-meshheading:14675193-Skin, pubmed-meshheading:14675193-Stromal Cells, pubmed-meshheading:14675193-p-Methoxy-N-methylphenethylamine
pubmed:year
2003
pubmed:articleTitle
Generation of a large number of connective tissue type mast cells by culture of murine fetal skin cells.
pubmed:affiliation
Dermatology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
pubmed:publicationType
Journal Article