The essential role of ORAI1 channels in receptor-evoked Ca signaling is well understood, yet little is known about the physiological activation of the ORAI channel trio natively expressed in all cells. The roles of ORAI2 and ORAI3 have remained obscure. We show that ORAI2 and ORAI3 channels play a critical role in mediating the regenerative Ca oscillations induced by physiological receptor activation, yet ORAI1 is dispensable in generation of oscillations. We reveal that ORAI2 and ORAI3 channels multimerize with ORAI1 to expand the range of sensitivity of receptor-activated Ca signals, reflecting their enhanced basal STIM1-binding and heightened Ca-dependent inactivation. This broadened bandwidth of Ca influx is translated by cells into differential activation of NFAT1 and NFAT4 isoforms. Our results uncover a long-sought role for ORAI2 and ORAI3, revealing an intricate control mechanism whereby heteromerization of ORAI channels mediates graded Ca signals that extend the agonist-sensitivity to fine-tune transcriptional control.
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http://dx.doi.org/10.1038/s41467-020-16232-6 | DOI Listing |
Proc Natl Acad Sci U S A
December 2024
Institute of Biomedical Research, School of Biomedical Sciences, Catholic University of Argentina, Buenos Aires C1107AFF, Argentina.
J Agric Food Chem
December 2024
College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China.
Ca is an important regulator of endoplasmic reticulum (ER) and mitochondrial function. Store-operated calcium entry (SOCE) serves as the predominant pathway for the influx of extracellular Ca into the cell. ORAI1, ORAI2, and ORAI3 are the main proteins of SOCE.
View Article and Find Full Text PDFKorean J Physiol Pharmacol
January 2025
Department of Physiology, Yonsei University Wonju College of Medicine, Wonju 26426, Korea.
Renal cell carcinoma (RCC) presents significant clinical challenges, highlighting the importance of understanding its molecular mechanisms. While store-operated Ca entry (SOCE) is known to play an essential role in tumorigenesis and metastasis, its specific implications across various RCC subtypes remain underexplored. This study analyzed SOCE-related mRNA profiles from the KIRC and KIRP projects in The Cancer Genome Atlas (TCGA) database, focusing on differential gene expression and overall survival outcomes.
View Article and Find Full Text PDFCell Calcium
November 2024
Division of Genetic, Environmental and Inhalational Disease, Department of Internal Medicine, Kansas University Medical Center, Kansas City, KS 66103, USA. Electronic address:
Orai1 is a plasma membrane Ca channel involved in store operated calcium entry (SOCE). SOCE can regulate cell growth, exocytosis, gene expression and inflammation. We previously found that short palate lung and nasal epithelial clone 1's (SPLUNC1) sixth α-helix (α6) bound Orai1 to inhibit SOCE.
View Article and Find Full Text PDFBiochemistry (Mosc)
September 2023
School of Basic Medical Sciences, Hubei University of Medicine, Shiyan, 442000, China.
Store-operated calcium entry (SOCE) is the main mechanism for the Ca2+ influx in non-excitable cells. The two major components of SOCE are stromal interaction molecule 1 (STIM1) in the endoplasmic reticulum and Ca2+ release-activated Ca2+ channel (CRAC) Orai on the plasma membrane. SOCE requires interaction between STIM1 and Orai.
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