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Ca 2+ tunnelling through the ER lumen as a mechanism for delivering Ca 2+ entering via store‐operated Ca 2+ channels to specific target sites
Author(s) -
Petersen Ole H,
Courjaret Raphael,
Machaca Khaled
Publication year - 2017
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jp272772
Subject(s) - endoplasmic reticulum , cytosol , biophysics , extracellular , microbiology and biotechnology , calcium signaling , calcium , plasma membrane ca2+ atpase , chemistry , stim1 , lumen (anatomy) , intracellular , biochemistry , biology , enzyme , atpase , organic chemistry
Ca 2+ signalling is perhaps the most universal and versatile mechanism regulating a wide range of cellular processes. Because of the many different calcium‐binding proteins distributed throughout cells, signalling precision requires localized rises in the cytosolic Ca 2+ concentration. In electrically non‐excitable cells, for example epithelial cells, this is achieved by primary release of Ca 2+ from the endoplasmic reticulum via Ca 2+ release channels placed close to the physiological target. Because any rise in the cytosolic Ca 2+ concentration activates Ca 2+ extrusion, and in order for cells not to run out of Ca 2+ , there is a need for compensatory Ca 2+ uptake from the extracellular fluid. This Ca 2+ uptake occurs through a process known as store‐operated Ca 2+ entry. Ideally Ca 2+ entering the cell should not diffuse to the target site through the cytosol, as this would potentially activate undesirable processes. Ca 2+ tunnelling through the lumen of the endoplasmic reticulum is a mechanism for delivering Ca 2+ entering via store‐operated Ca 2+ channels to specific target sites, and this process has been described in considerable detail in pancreatic acinar cells and oocytes. Here we review the most important evidence and present a generalized concept.