ERLIN2通过Ca2+-CREB信号通路协调CRY1/CRY2反馈调控昼夜节律的机制

Abstract

Circadian regulation in peripheral cells depends on calcium dynamics, but the upstream mechanisms remain unclear. We identify endoplasmic reticulum lipid raft-associated protein 2 (ERLIN2) as a regulator of the peripheral clock. Knockdown and overexpression of ERLIN2 in C2C12 skeletal muscle cells show that ERLIN2 positively regulates cryptochrome circadian regulator 1/2 (CRY1/2) transcription and maintains rhythmicity. ERLIN2 regulates inositol 1,4,5-trisphosphate receptor (IP 3 R)-mediated Ca 2+ release and activates the calcium/calmodulin-dependent protein kinase II (CaMKII) – mitogen-activated protein kinase (MAPK) – cAMP response element-binding protein (CREB) pathway. ATP induced IP 3 R-dependent Ca 2+ transients, CREB phosphorylation, and Per1 expression, reshaping circadian rhythm, effects blocked by IP 3 R, Ca 2+ , or CaMKII inhibition. CRY1 enhances and CRY2 suppresses CREB signaling, establishing a feedback loop with ERLIN2. This ERLIN2–Ca 2+ –CREB–CRY1/2 axis couples membrane contact sites to circadian regulation. Impact statement This study reveals ERLIN2 as a key regulator linking calcium signaling to circadian rhythms, establishing an ERLIN2–Ca 2+ –CREB–CRY1/2 axis that advances understanding of cellular clock control.