Preferential Localization of STIM1 to Dendritic Subsurface ER Structures in Mouse Purkinje Cells

Abstract

The endoplasmic reticulum (ER) is the largest intracellular Ca 2+ store, serving as the source and sink of intracellular Ca 2+ . The ER Ca 2+ store is continuous yet organized into distinct subcompartments with spatial and functional heterogeneity. In cerebellar Purkinje cells (PCs), glutamatergic inputs trigger Ca 2+ release from specific ER domains via inositol 1,4,5-trisphosphate receptors (IP 3 Rs) or ryanodine receptors (RyRs). Upon ER store depletion, refilling occurs through store-operated Ca 2+ entry mediated by stromal interaction molecule-1 (STIM1). Although the significance of STIM1-mediated Ca 2+ regulation within PCs is established, STIM1 localization in ER subcompartments in PCs for Ca 2+ release and refilling remains elusive. Using validated antibodies, we demonstrated that STIM1 was predominantly localized as intense puncta along dendritic shafts in male and female mice, colocalizing with IP 3 R1 but not with RyR1. Immunoelectron microscopy revealed that STIM1 was accumulated in the subsurface ER in the dendritic shaft but excluded from those in the dendritic spine, the primary site of metabotropic glutamate receptor 1 (mGluR1)–IP 3 R-mediated Ca 2+ signaling. Ca 2+ imaging from control and STIM1-knockdown (STIM1-KD) PCs demonstrated that mGluR1-mediated Ca 2+ release is more critically dependent on STIM1 than RyR-mediated Ca 2+ release. These findings reveal a spatially organized ER network in PCs, where specialized ER subcompartments differentially regulate Ca 2+ release and refilling. These findings suggest that STIM1 preferentially regulates Ca 2+ dynamics associated with mGluR1–IP 3 R signaling, supporting specialized ER subcompartments for Ca 2+ release and refilling. These findings highlight the intricate molecular–anatomical organization of dendritic ER Ca 2+ signaling in PCs, crucial for synaptic plasticity and motor learning.