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Ex vivo functional responses to HLA-G differ between blood and decidual NK cells

  1. Author:
    Apps, R.
    Sharkey, A.
    Gardner, L.
    Male, V.
    Kennedy, P.
    Masters, L.
    Farrell, L.
    Jones, D.
    Thomas, R.
    Moffett, A.
  2. Author Address

    [Apps, R; Sharkey, A; Gardner, L; Male, V; Kennedy, P; Masters, L; Farrell, L; Jones, D; Moffett, A] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England. [Apps, R; Sharkey, A; Gardner, L; Male, V; Kennedy, P; Masters, L; Farrell, L; Jones, D; Moffett, A] Univ Cambridge, Ctr Trophoblast Res, Cambridge CB2 1QP, England. [Apps, R; Thomas, R] SAIC Frederick Inc, Canc & Inflammat Program, Expt Immunol Lab, NCI Frederick, Frederick, MD USA.;Moffett, A (reprint author), Univ Cambridge, Dept Pathol, Tennis Court Rd, Cambridge CB2 1QP, England;am485@cam.ac.uk
    1. Year: 2011
    2. Date: Sep
  1. Journal: Molecular Human Reproduction
    1. 17
    2. 9
    3. Pages: 577-586
  2. Type of Article: Article
  3. ISSN: 1360-9947
  1. Abstract:

    Restricted expression of human leucocyte antigen-G (HLA-G) to fetal extravillous trophoblast cells, which invade the decidua during implantation, suggests a role for HLA-G in placentation. In this study, we have investigated several aspects of HLA-G expression and function. Surface levels of HLA-G expression were measured in 70 normal pregnancies. We show the dimeric conformation that is unique to HLA-G forms after passage through the Golgi apparatus. Differences were found in the receptor repertoire of decidual natural killer (dNK) cells that express the leucocyte immunoglobulin-like receptor B1 (LILRB1), which binds dimeric HLA-G strongly. We then measured functional responses of dNK cells with LILRB1, when stimulated by HLA-G in both monomeric and dimeric conformations. Degranulation, interferon-gamma and interleukin-8 production by dNK cells freshly isolated from the first trimester implantation site were either undetected or not affected by HLA-G. These findings should be considered when inferring the activity of tissue NK cells from results obtained with cell lines, peripheral NK or cultured dNK cells.

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External Sources

  1. DOI: 10.1093/molehr/gar022
  2. WOS: 000294553900005

Library Notes

  1. Fiscal Year: FY2011-2012
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