RT Journal Article
T1 Palmitoylation of MICA, a ligand for NKG2D, mediates its recruitment to membrane microdomains and promotes its shedding
A1 Agüera‐González, Sonia
A1 Gross, Catharina
A1 Fernández Messina, Lola María
A1 Ashiru, Omodele
A1 Esteso, Gloria
A1 Hang, Howard
A1 Reyburn, Hugh
A1 Long, Eric
A1 Valés‐Gómez, Mar
AB MICA and MICB (MHC‐class‐I‐related chain A/B) are transmembrane proteins expressed in pathological conditions that are ligands for NKG2D, an activating receptor found on cytotoxic lymphocytes. The recognition on target cells of NKG2D ligands leads to the activation of lysis and cytokine secretion by NK cells and T cells. Besides being expressed at the cell surface, MICA/B can be released as soluble proteins. Soluble NKG2D ligands downmodulate expression of the NKG2D receptor on lymphocytes, leading to a diminished cytotoxic response. Prior studies suggested that recruitment of MICA/B molecules to cholesterol‐enriched microdomains was an important factor regulating the proteolytic release of these molecules. We now show that recruitment of MICA to these microdomains depends on palmitoylation of two cysteine residues that allow MICA molecules to reside in the membrane in the same domains as caveolin‐1. Compared with WT molecules, nonpalmitoylated mutant MICA molecules were shed to the supernatant with low efficiency; however, both WT and mutant MICA were able to trigger NK cell cytotoxicity. These data suggest that the presence of NKG2D ligands at the plasma membrane is sufficient to activate cytotoxicity and reflect the need of different ligands to exploit different cellular pathways to reach the cell surface upon different stress situations.
PB Wiley
SN 0014-2980
YR 2011
FD 2011
LK https://hdl.handle.net/20.500.14352/97191
UL https://hdl.handle.net/20.500.14352/97191
LA eng
NO Agüera‐González, Sonia, et al. «Palmitoylation of MICA, a Ligand for NKG2D, Mediates Its Recruitment to Membrane Microdomains and Promotes Its Shedding». European Journal of Immunology, vol. 41, n.o 12, diciembre de 2011, pp. 3667-76. https://doi.org/10.1002/eji.201141645.
NO AcknowledgementsThe authors thank Nigel Miller for assistance with cell sorting. This work was supported by grants from the Medical Research Council (New Investigator Grant to M. V. G.) and Fondo de Investigación Sanitaria (PS09/00181 and PI08/1701) and, in part, by the Intramural Research Program of the National Institutes of Health, National Institute of Allergy and Infectious Diseases. O. A. was supported by the Leukaemia Research Fund and The Newton Trust. H. C. H. was supported by grants from Ellison Medical Foundation and NIH/NIGMS GM087544. S. A. was a recipient of a short-term fellowship from the European Molecular Biology Organization and supported in part by fellowships from Caja Madrid and Ibercaja.
NO Medical Research Council (UK)
NO National Institutes of Health
NO The Isaac Newton Trust
NO Leukaemia Research Fund
NO Ellison Medical Foundation
NO European Molecular Biology Organization
NO Caja Madrid
NO Ibercaja
DS Docta Complutense
RD 5 abr 2025