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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0003315,
umls-concept:C0007634,
umls-concept:C0017349,
umls-concept:C0019409,
umls-concept:C0020792,
umls-concept:C0023005,
umls-concept:C0032659,
umls-concept:C0038960,
umls-concept:C0086418,
umls-concept:C0221928,
umls-concept:C0441655,
umls-concept:C1273518,
umls-concept:C1515021,
umls-concept:C2348519
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pubmed:issue |
8
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pubmed:dateCreated |
1993-11-9
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pubmed:abstractText |
Little is known regarding the identification, classification, and function of class II MHC+ dendritic cells in the perivasculature of human connective tissues, such as the dermis. We developed a method for preparing papillary dermal cell suspensions from human keratome strips. Among the class II MHC+ populations of the dermis identified using triple color flow cytometry, cells of monocyte/macrophage lineage (CD45+ CD1- CD11b+ CD11clo-mid CD32+ CD36+ or - CD11a-) and mesenchymal cells of non-bone marrow origin (CD45-) were identified and characterized. Another distinct class II MHC+ subset was identified, which expressed a number of features analogous to epidermal Langerhans cells (LC) and other dendritic APC. These were a numerically minor population comprising only 2.7% +/- 1% (n = 7) of dermal cells. Like LC, they express HLA-DR, CD45, CD1a (albeit at a lower level of expression), CD1c, and CD32 and lack constitutive CD11a or ICAM-1. In contrast to LC, this dermal CD1a+CD1c+ subset expresses CD1b, CD11b, a higher level of CD11c, and intracytoplasmic factor XIIIa. Alloantigen presentation by unfractionated dermal cells was reduced by prior removal of this CD1b+ subset to the same degree achieved by removal of the entire DR+ population (20% of dermal cells), indicating that this was the critical DR+ subset. Cocultures of CD4+ T lymphocytes with cells sorted by flow cytometry into CD1c+DR+, CD1c-DR+ and DR- dermal cell subsets positively identified the CD1c+DR+ population as the most potent of potential APC subsets in human dermis. Thus, in distinction to other dermal macrophage and mesenchymal subsets with elongate morphology, the CD1aloCD1b,c+CD11c(hi)CD11b+CD32+DR+ population in human dermis is highly analogous to cells of LC/dendritic APC lineage in its phenotype and in its exclusive ability to potently present Ag to T lymphocytes. These studies identify and characterize the APC subset most potent in inducing activation of T cells initially entering the perivasculature of human dermis to be of LC/dendritic APC, and not tissue macrophage, lineage.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
151
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4067-80
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8409386-Adult,
pubmed-meshheading:8409386-Antigen-Presenting Cells,
pubmed-meshheading:8409386-Antigens, CD,
pubmed-meshheading:8409386-Flow Cytometry,
pubmed-meshheading:8409386-HLA-DR Antigens,
pubmed-meshheading:8409386-Humans,
pubmed-meshheading:8409386-Langerhans Cells,
pubmed-meshheading:8409386-Macrophages,
pubmed-meshheading:8409386-Microscopy, Fluorescence,
pubmed-meshheading:8409386-Skin,
pubmed-meshheading:8409386-Suspensions
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pubmed:year |
1993
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pubmed:articleTitle |
Heterogeneous populations of class II MHC+ cells in human dermal cell suspensions. Identification of a small subset responsible for potent dermal antigen-presenting cell activity with features analogous to Langerhans cells.
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pubmed:affiliation |
Department of Dermatology, University of Michigan, Ann Arbor 48109.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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