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PMID: 16698441 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Release of MICB molecules by tumor cells: mechanism and soluble MICB in sera of cancer patients.

Human immunology ·Vol. 67 ·No. 3 ·2006-03-00 ·Pages 188-95

Salih HR, Goehlsdorf D, Steinle A

Abstract

MICA, a ligand of the activating immunoreceptor NKG2D, is released by tumor cells in a soluble form and can be detected in sera of tumor patients at significant levels. Soluble MICA has been proposed to counteract NKG2D-mediated immunosurveillance of tumors. Here, we report that MICB, the second member of the human MIC protein family, is likewise shed by metalloproteases from tumor cells and is present in sera of patients with gastrointestinal tumors. While cell-bound MICB causes downregulation of surface NKG2D, soluble MICB did not alter NKG2D expression on NK cells in vitro. Thus, proteolytic shedding of MICB by tumor cells may impair immunogenicity of tumors primarily by reducing NKG2D-ligand densities on malignant cells.

MeSH Terms
Cell Line, Tumor Cell Membrane/metabolism Down-Regulation Gastrointestinal Neoplasms/blood Hematologic Neoplasms/blood Histocompatibility Antigens Class I/blood,metabolism Humans Killer Cells, Natural/metabolism Matrix Metalloproteinase 1/metabolism NK Cell Lectin-Like Receptor Subfamily K Receptors, Immunologic/biosynthesis Receptors, Natural Killer Cell
Chemicals
Histocompatibility Antigens Class I KLRK1 protein, human MHC class I-related chain A MICB antigen NK Cell Lectin-Like Receptor Subfamily K Receptors, Immunologic Receptors, Natural Killer Cell Matrix Metalloproteinase 1
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Salih Helmut Rainer
Department of Internal Medicine II, Eberhard-Karls-University Tübingen, 72076 Tübingen, Germany.
Goehlsdorf Dennis
Steinle Alexander
Article Info
Journal
Human immunology
Abbr.
Hum Immunol
ISSN
0198-8859
Published
2006-03-00
Epub
2006-00-29
Pages
188-95
Language
English
Region
United States
NLM ID
8010936
Subset
IM
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