Literature DB >> 8592066

Functional CD86 (B7-2/B70) on cultured human Langerhans cells.

H Yokozeki1, I Katayama, O Ohki, T Matsunaga, K Watanabe, T Satoh, M Azuma, K Okumura, K Nishioka.   

Abstract

CD86 (B70/B7-2) has recently been identified as an alternative CD28/CTLA-4 ligand on activated B cells. CD86 has also been demonstrated as possibly serving as a primary costimulatory molecule in the initial immune response. Since the human Langerhans cell is one of the most potent antigen-presenting cells, we examined whether CD86 expression and function are found on organ-cultured skin, freshly isolated Langerhans cells, and cultured Langerhans cells in normal human epidermis. Immunohistochemical study in situ revealed that CD86 was expressed on dendritic cells with CD1a antigen in organ-cultured but not fresh skin. Fluorescence-activated cell sorter analysis revealed that no staining for either CD80 or CD86 was observed in freshly isolated Langerhans cells but that both CD80 and CD86 were expressed on cultured Langerhans cells. The actual expression of CD86 on cultured Langerhans cells was further confirmed by the detection of 70-kDa glycoprotein on Western blot analysis. Analysis of polymerase chain reaction demonstrated that both CD80 and CD86 were specifically amplified from purified cultured and freshly isolated Langerhans cells but not from Langerhans cell-depleted epidermal cells, indicating that both CD80 and CD86 genes were expressed by Langerhans cells. The functional importance of CD86 on Langerhans cells was confirmed by the allogeneic CD4 T cell proliferative responses with enriched Langerhans cells. A monoclonal antibody against CD86 caused 81% inhibition in contrast with 29% inhibition produced by anti-CD80 monoclonal antibody. This inhibitory effect was enhanced to 85.3% inhibition when a combination of anti-CD86 and anti-CD80 was administered. These results indicate that CD86 is predominantly expressed on the surface of cultured Langerhans cells and may transduce a primordial costimulatory signal in the interaction of Langerhans cells and T cells.

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Year:  1996        PMID: 8592066     DOI: 10.1111/1523-1747.ep12329735

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  4 in total

1.  In vitro treatment of human transforming growth factor-beta1-treated monocyte-derived dendritic cells with haptens can induce the phenotypic and functional changes similar to epidermal Langerhans cells in the initiation phase of allergic contact sensitivity reaction.

Authors:  S Aiba; H Manome; Y Yoshino; H Tagami
Journal:  Immunology       Date:  2000-09       Impact factor: 7.397

2.  Altered cutaneous immune parameters in transgenic mice overexpressing viral IL-10 in the epidermis.

Authors:  Wanhong Ding; Stefan Beissert; Liang Deng; Edward Miranda; Christopher Cassetty; Kristina Seiffert; Kristina L Campton; Zhengmin Yan; George F Murphy; Jeffrey A Bluestone; Richard D Granstein
Journal:  J Clin Invest       Date:  2003-06       Impact factor: 14.808

3.  Blockade of T lymphocyte costimulation with cytotoxic T lymphocyte-associated antigen 4-immunoglobulin (CTLA4Ig) reverses the cellular pathology of psoriatic plaques, including the activation of keratinocytes, dendritic cells, and endothelial cells.

Authors:  J R Abrams; S L Kelley; E Hayes; T Kikuchi; M J Brown; S Kang; M G Lebwohl; C A Guzzo; B V Jegasothy; P S Linsley; J G Krueger
Journal:  J Exp Med       Date:  2000-09-04       Impact factor: 14.307

4.  Signal transducer and activator of transcription 6 is essential in the induction of contact hypersensitivity.

Authors:  H Yokozeki; M Ghoreishi; S Takagawa; K Takayama; T Satoh; I Katayama; K Takeda; S Akira; K Nishioka
Journal:  J Exp Med       Date:  2000-03-20       Impact factor: 14.307

  4 in total

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