Hypoxia and glucose deprivation are often observed in the microenvironment surrounding solid tumors in vivo. However, how they interfere with MHC class I antigen processing and CD8 + T-cell responses remains unclear. In this study, we analyzed the production of antigenic peptides presented by classical MHC class I in mice, and showed that it is quantitatively decreased in the cells exposed to either hypoxia or glucose deprivation. In addition, we unexpectedly found increased surface expression of HLA-E in human and Qa-1 in mouse tumor cells exposed to combined oxygen and glucose deprivation. The induced Qa-1 on the stressed tumor model interacted with an inhibitory NKG2/CD94 receptor on activated CD8 + T cells and attenuated their specific response to the antigen. Our results thus suggest that microenvironmental stresses modulate not only classical but also nonclassical MHC class I presentation, and confer the stressed cells the capability to escape from the CD8 + T-cell recognition.Keywords: Antigen presentation r Glucose deprivation hypoxia r HLA-E r MHC class I r Microenvironmental stress r Qa-1 Additional supporting information may be found in the online version of this article at the publisher's web-site
IntroductionSolid tumors provide a special microenvironment that alters the biological aspects of the cells within [1]. Because of aberrant Correspondence: Dr. Takayuki Kanaseki e-mail: kanaseki@sapmed.ac.jp and disorganized vasculature, tumor cells inside a mass are often exposed to chronic hypoxia, which induces stress-related gene expression as well as resistance to apoptosis, radiation, and chemotherapy [2,3]. Moreover, tumor cells predominantly use the tricarboxylic acid cycle rather than oxidative phosphorylation for energy production (Warburg effect) and they are exposed to severe glucose deprivation [4,5]. The biological adaptation models of tumor cells to survive under such combined-stress condition C 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim www.eji-journal.eu
930Takanori Sasaki et al. Eur. J. Immunol. 2016. 46: 929-940 have been established [6][7][8][9], however the understanding of how the microenvironmental stresses interfere MHC class I antigen processing and CD8 + T-cell responses is incomplete. MHC class I molecules are expressed on most nucleated cells and determine the outcome of CD8 + T-cell mediated immune surveillance. They are classified into highly polymorphic classical MHC class I molecules and nonpolymorphic nonclassical MHC class I molecules. The classical MHC I molecules on the surface present short peptides originating from endogenous self or foreign proteins and form complexes with a diverse set of peptide (pMHC I) [10,11]. Such short peptides are generally 8-10-mer in length and conserve anchor residues that locate at discrete positions, allowing the peptide to be bound to MHC I molecules [12]. The peptides are produced by MHC I antigen processing that begins in the cytosol and continues in the ER where the precursor peptides are optimized for binding and finally load...