henhaobio
Sign in

Cell Death and DiseaseCancer BiologyPeer-reviewed journal article

UPR-induced intracellular C5aR1 promotes adaptation to the hypoxic tumour microenvironment by regulating tumour cell fate

Tatsuya SuwaiD, Kelly SW. LeeiD, Ian J. ChaiiD, Heather O. L. Clark, David MacLeaniD, Nicole MachadoiD, Gonzalo Rodríguez‐BerrigueteiD, Lolita Singh, Geoff Stuart HigginsiD, Ester M. HammondiD, Monica M. OlcinaiD

PDFDOIPreprint

Abstract

Dysregulation of the C5a-C5a receptor 1 (C5aR1) signalling axis underlies inflammation and immune-driven pathology. C5aR1 was traditionally thought to be primarily expressed on the cell membrane, although recent reports indicate the importance of intracellular C5aR1 expression for the inflammatory effector functions of various cell types. However, the mechanisms regulating C5aR1 expression and localisation remain unclear. In tumours with an immunosuppressive microenvironment, we recently found robust C5aR1 expression on malignant epithelial cells, highlighting potential tumour cell-specific functions. Here, we show that hypoxia, a hallmark of immunosuppressive microenvironments, induces C5aR1 expression in an unfolded protein response (UPR)-dependent manner via enhanced endoplasmic reticulum stress. Furthermore, hypoxia drives endocytosis, relocating C5aR1 from the cell membrane to the intracellular compartment. By genetically and pharmacologically targeting the C5a/C5aR1 axis, we show that C5aR1 mediates cellular adaptation to hypoxia by regulating processes associated with cell fate, including autophagy and apoptosis. In line with hypoxia-induced intracellular C5aR1 pools, pharmacological inhibition of C5aR1, particularly with cell-permeable small molecule inhibitors, significantly reduces tumour cell survival. These results suggest that the dysregulated C5a/C5aR1 axis and the hypoxia-induced shift in C5aR1 localisation, support tumour cell survival and provide new insights into therapeutic strategies for targeting the C5a/C5aR1 axis.

Citations
6
FWCI
2.02
Field percentile
top 13%

Reproducibility ledger

Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.

Sign in to file a reproducibility report.