Functional Expression of ICAM-3 on Human Epidermal Langerhans Cells View Full Text


Ontology type: schema:Chapter     


Chapter Info

DATE

1995

AUTHORS

Giovanna Zambruno , Andrea Cossarizza , Valentina Zacchi , Daniela Ottani , Anna Maria Luppi , Alberto Giannetti , Giampiero Girolomoni

ABSTRACT

Optimal activation of T lymphocytes by APC requires two different sets of signals: MHC-peptide complexes that interact with the TCR and costimulatory signals. These are especially important for activation of resting and naive T cells, which in the absence of costimulation, may undergo to long lasting functional impairment1. Dendritic cells, including epidermal Langerhans cells (LC), are the most efficient activators of naive T cells and the most potent inducers of primary T cell mediated immune responses2, a property that has been attributed, at least in part, to the constitutive expression of high levels of MHC and various accessory molecules. Human freshly isolated LC (fLC) do not display significant numbers of membrane costimulatory molecules. Following short-term culture, LC (cLC) upregulate the intercellular adhesion molecule (ICAM)-l (CD54), the leucocyte function-associated antigen (LFA)-3 (CD58) and B7-1 (CD80) and markedly increase their antigen presenting capacity3,4. The LFA-1 (CD 11a/CD18) adhesion molecule plays a pivotal role in cellular interactions between APC and T lymphocytes. At least three counter-receptors able to bind to LFA-1 have been described, namely ICAM-1, ICAM-2 (CD102) and ICAM-3 (CD50), all belonging to the Ig gene superfamily5. Recently, ICAM-3, but not ICAM-2, has been detected in LC in sections of human epidermis6,7. In this study, we examined the expression and function of ICAM-2 and ICAM-3 in human LC, and their possible regulation during culture. More... »

PAGES

263-265

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/978-1-4615-1971-3_58

DOI

http://dx.doi.org/10.1007/978-1-4615-1971-3_58

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1010852887

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/8526069


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