Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2010 Jan;3(1):12-7.
doi: 10.4161/cib.3.1.9793.

Two-pore channels for integrative Ca signaling

Two-pore channels for integrative Ca signaling

Michael X Zhu et al. Commun Integr Biol. 2010 Jan.

Abstract

Two-pore channels (TPCs) are related to voltage-gated Ca(2+) and Na(+) channels. They most likely work as dimers with each of the two TPC protein subunits containing two pore-forming domains. Recent studies suggest that TPCs are expressed on the membranes of endosomes and lysosomes where they form receptors for nicotinic acid adenine dinucleotide phosphate (NAADP), the most potent Ca(2+) mobilizing messenger inside cells. Upon activation by NAADP, Ca(2+) release from endolysosomal stores through TPCs triggers cytoplasmic Ca(2+) signals. Because of discrete localizations of these acidic vesicles and their small, albeit variable, sizes, the Ca(2+) signals from endolysosomes are local and, perhaps, represent unique elementary Ca(2+) events. These localized signals can be converted into regenerative global Ca(2+) waves by triggering Ca(2+)-induced Ca(2+) release from endoplasmic reticulum. We will discuss the implications of these findings and the significance of TPCs in integrative Ca(2+) signaling in animal cells.

Keywords: Ca2+ channels; Ca2+ mobilization; NAADP; endoplasmic reticulum; endosomes; lysosomes.

PubMed Disclaimer

Figures

Figure 1
Figure 1
The proposed role for two-pore channels in integrative Ca2+ signaling. Flow chart shows pathways for NAADP, cADPR and IP3 production and their effects on intracellular Ca2+. The drawings at the bottom depict elementary Ca2+ signals generated by TPCs (left, lighter color and higher position for higher Ca2+ concentrations) and global Ca2+ signals generated by activating IP3Rs and/or RyRs (right). Red dashed lines indicate alternative pathways. The green pathway on the left shows an alternative consequence of TPC-mediated Ca2+ release. ARC, ADP-ribose cyclase, including CD38, PLC, phospholipase C, Ψ, membrane potential. ICa, Ca2+ current through plasma membrane.

Similar articles

Cited by

References

    1. Galione A, Petersen OH. The NAADP receptor: new receptors or new regulation? Mol Interv. 2005;5:73–79. - PubMed
    1. Calcraft PJ, Ruas M, Pan Z, Cheng X, Arredouani A, Hao X, et al. NAADP mobilizes calcium from acidic organelles through two-pore channels. Nature. 2009;459:596–600. - PMC - PubMed
    1. Yu FH, Yarov-Yarovoy V, Gutman GA, Catterall WA. Overview of molecular relationships in the voltagegated ion channel superfamily. Pharmacol Rev. 2005;57:387–395. - PubMed
    1. Zong X, Schieder M, Cuny H, Fenske S, Gruner C, Rötzer K, et al. The two-pore channel TPCN2 mediates NAADP-dependent Ca2+-release from lysosomal stores. Pflugers Arch. 2009;458:891–899. - PMC - PubMed
    1. Lee HC, Aarhus R. A derivative of NADP mobilizes calcium stores insensitive to inositol trisphosphate and cyclic ADP-ribose. J Biol Chem. 1995;270:2152–2157. - PubMed

LinkOut - more resources