Lactate-dependent chaperone-mediated autophagy induces oscillatory HIF-1α activity promoting proliferation of hypoxic cells

Response to hypoxia is a highly regulated process, but little is known about single-cell responses to hypoxic conditions. Using fluorescent reporters of hypoxia response factor-1 alpha (HIF-1 alpha) activity in various cancer cell lines and patient-derived cancer cells, we show that hypoxic responses in individual cancer cells can be highly dynamic and variable. These responses fall into three classes, including oscillatory activity. We identify a molecular mechanism that can account for all three response classes, implicating reactive-oxygen-speciesdependent chaperone-mediated autophagy of HIF-1 alpha in a subset of cells. Furthermore, we show that oscillatory response is modulated by the abundance of extracellular lactate in a quorum-sensing-like mechanism. We show that oscillatory HIF-1 alpha activity rescues hypoxia-mediated inhibition of cell division and causes broad suppression of genes downregulated in cancers and activation of genes upregulated in many cancers, suggesting a mechanism for aggressive growth in a subset of hypoxic tumor cells.

Automated summary

The response of individual cancer cells to hypoxic conditions is dynamic and variable, with oscillatory activity being one of the response classes. Reactive-oxygen-species-dependent chaperone-mediated autophagy of HIF-1 alpha plays a role in regulating these responses in some cells. The abundance of extracellular lactate modulates the oscillatory response.