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Resolution: standard / high Figure 4.
Calcium signaling pathways in stem cells and neural progenitor cells. Left panel represents a embryonic or adult stem cells and right panel the neuronal
progenitor cells. Ca2+ signaling depends on the increase of the intracellular Ca2+ levels [Ca2+]i, derived from extracellular calcium (Ca2+)o sources or intracellular stores of the endoplasmic reticulum (ER Ca2+). It can enter through calcium channels operated by voltage (voltage-operated Ca2+ channels, VOCCs) in excitable cells such as neurons and muscular cells, or through
calcium channels operated by receptors (receptor-operated Ca2+ channels, ROCs) in response to neurotransmitters. SOC's (store-operated Ca2+ channels, SOCs), open when internal Ca2+ stores are empty, and are generally present in non-excitable cells. Calcium from the
ER is released by two types of channels, Inositol 1,4,5-trisphosphate (IP3) channels
and ryanodine channels. The first is present in both neural progenitor and stem cells,
while the latter is expressed only in nural progenitor cells. IP3 is generated by
the action of the enzyme PLC in phosphatidylinositol 4,5-bisphosphate (PIP2). IP3
acts on receptors in the endoplasmic reticulum, promoting the release of Ca2+ from ER stores. IP3PIP2.
Resende and Adhikari Cell Communication and Signaling 2009 7:20 doi:10.1186/1478-811X-7-20 |