Abstract
Increase in intracellular levels of calcium ions (Ca2+) is one of the key triggering signals for the development of B cell response to the antigen. The diverse Ca2+ signals finely controlled by multiple factors participate in the regulation of gene expression, B cell development, and effector functions. B cell receptor (BCR)-initiated Ca2+ mobilization is sourced from two pathways: one is the release of Ca2+ from the intracellular stores, endoplasmic reticulum (ER), and other is the prolonged influx of extracellular Ca2+ induced by depleting the stores via store-operated calcium entry (SOCE) and calcium release-activated calcium (CRAC) channels. The identification of stromal interaction molecule 1(STIM1), the ER Ca2+ sensor, and Orai1, a key subunit of the CRAC channel pore, has now provided the tools to understand the mode of Ca2+ influx regulation and physiological relevance. Herein, we discuss our current understanding of the molecular mechanisms underlying BCR-triggered Ca2+ signaling as well as its contribution to the B cell biological processes and diseases.
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Abbreviations
- EAE:
-
Experimental autoimmune encephalomyelitis
- CRAC:
-
Ca2+ release-activated Ca2+
- DAG:
-
Diacylglycerol
- ER:
-
Endoplasmic reticulum
- IP3:
-
Inositol-1,4,5,-triphosphate
- ITIM:
-
Immunoreceptor tyrosine-based inhibition motifs
- Phospholipase C-γ2:
-
PLC-γ2
- PI3K:
-
Phosphoinositide 3-kinase
- PIP5K:
-
Phosphatidylinositol-4-phosphate 5-kinases
- PM:
-
Plasma membrane
- PtdIns(3,4)P2:
-
Phosphatidylinositol-3,4-bisphosphate
- PtdIns(4,5)P2:
-
Phosphatidylinositol-4,5-bisphosphate
- PtdIns(3,4,5)P3:
-
Phosphatidylinositol-3,4,5-trisphosphate
- SHP1:
-
SH2-domain-containing protein tyrosine phosphatase 1
- SHIP:
-
SH2-domain-containing inositol polyphosphate 5′ phosphatase
- SOCE:
-
Store-operated Ca2+ entry
- STIM1:
-
Stromal interaction molecule 1
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Baba, Y., Kurosaki, T. (2015). Role of Calcium Signaling in B Cell Activation and Biology. In: Kurosaki, T., Wienands, J. (eds) B Cell Receptor Signaling. Current Topics in Microbiology and Immunology, vol 393. Springer, Cham. https://doi.org/10.1007/82_2015_477
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