STIM Proteins: The Gas and Brake of Calcium Entry in Neurons
- PMID: 39266936
- PMCID: PMC11794855
- DOI: 10.1007/s12264-024-01272-5
STIM Proteins: The Gas and Brake of Calcium Entry in Neurons
Abstract
Stromal interaction molecules (STIM)s are Ca2+ sensors in internal Ca2+ stores of the endoplasmic reticulum. They activate the store-operated Ca2+ channels, which are the main source of Ca2+ entry in non-excitable cells. Moreover, STIM proteins interact with other Ca2+ channel subunits and active transporters, making STIMs an important intermediate molecule in orchestrating a wide variety of Ca2+ influxes into excitable cells. Nevertheless, little is known about the role of STIM proteins in brain functioning. Being involved in many signaling pathways, STIMs replenish internal Ca2+ stores in neurons and mediate synaptic transmission and neuronal excitability. Ca2+ dyshomeostasis is a signature of many pathological conditions of the brain, including neurodegenerative diseases, injuries, stroke, and epilepsy. STIMs play a role in these disturbances not only by supporting abnormal store-operated Ca2+ entry but also by regulating Ca2+ influx through other channels. Here, we review the present knowledge of STIMs in neurons and their involvement in brain pathology.
Keywords: Brain; Calcium; Calcium channels; Calcium entry; Neurons; STIM1; STIM2.
© 2024. Center for Excellence in Brain Science and Intelligence Technology, Chinese Academy of Sciences.
References
-
- Berna-Erro A, Braun A, Kraft R, Kleinschnitz C, Schuhmann MK, Stegner D, et al. STIM2 regulates capacitive Ca2+ entry in neurons and plays a key role in hypoxic neuronal cell death. Sci Signal 2009, 2: ra67. - PubMed
-
- Hartmann J, Karl RM, Alexander RP, Adelsberger H, Brill MS, Rühlmann C. STIM1 controls neuronal Ca2⁺ signaling, mGluR1-dependent synaptic transmission, and cerebellar motor behavior. Neuron 2014, 82: 635–644. - PubMed
-
- Park CY, Shcheglovitov A, Dolmetsch R. The CRAC channel activator STIM1 binds and inhibits L-type voltage-gated calcium channels. Science 2010, 330: 101–105. - PubMed
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