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Early Hematopoietic Zinc Finger Protein Prevents Tumor Cell Recognition by Natural Killer Cells
Author(s) -
Rosanna La Rocca,
Mariateresa Fulciniti,
Tadepally Lakshmikanth,
Maria Mesuraca,
Talib Hassan Ali,
Valerio Mazzei,
Nicola Amodio,
Lucio Catalano,
Bruno Rotoli,
Ouathek Ouerfelli,
Michèle Grieco,
Elio Gulletta,
Heather M. Bond,
Giovanni Morrone,
Soldano Ferrone,
Ennio Carbone
Publication year - 2009
Publication title -
the journal of immunology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.0802109
Subject(s) - biology , mhc class i , zinc finger , cell culture , haematopoiesis , human leukocyte antigen , progenitor cell , transfection , cell , hela , microbiology and biotechnology , major histocompatibility complex , cancer research , stem cell , antigen , immunology , gene , biochemistry , genetics , transcription factor
Early hematopoietic zinc finger/zinc finger protein 521 (EHZF/ZNF521) is a novel zinc finger protein expressed in hematopoietic stem and progenitor cells and is down-regulated during their differentiation. Its transcript is also abundant in some hematopoietic malignancies. Analysis of the changes in the antigenic profile of cells transfected with EHZF cDNA revealed up-regulation of HLA class I cell surface expression. This phenotypic change was associated with an increased level of HLA class I H chain, in absence of detectable changes in the expression of other Ag-processing machinery components. Enhanced resistance of target cells to NK cell-mediated cytotoxicity was induced by enforced expression of EHZF in the cervical carcinoma cell line HeLa and in the B lymphoblastoid cell line IM9. Preincubation of transfected cells with HLA class I Ag-specific mAb restored target cell susceptibility to NK cell-mediated lysis, indicating a specific role for HLA class I Ag up-regulation in the NK resistance induced by EHZF. A potential clinical significance of these findings is further suggested by the inverse correlation between EHZF and MHC class I expression levels, and autologous NK susceptibility of freshly explanted multiple myeloma cells.

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