Capture at the ER-mitochondrial contacts licenses IP₃ receptors to stimulate local Ca²⁺ transfer and oxidative metabolism.

ABSTRACT: Endoplasmic reticulum-mitochondria contacts (ERMCs) are restructured in response to changes in cell state. While this restructuring has been implicated as a cause or consequence of pathology in numerous systems, the underlying molecular dynamics are poorly understood. Here, we show means to visualize the capture of motile IP₃ receptors (IP3Rs) at ERMCs and document the immediate consequences for calcium signaling and metabolism. IP3Rs are of particular interest because their presence provides a scaffold for ERMCs that mediate local calcium signaling, and their function outside of ERMCs depends on their motility. Unexpectedly, in a cell model with little ERMC Ca²⁺ coupling, IP3Rs captured at mitochondria promptly mediate Ca²⁺ transfer, stimulating mitochondr

SUBMITTER: Katona M 

PROVIDER: S-EPMC9646835 | biostudies-literature | 2022 Nov

REPOSITORIES: biostudies-literature