TPC: the NAADP discovery channel?

Author:

Morgan Anthony J.1,Davis Lianne C.1,Ruas Margarida1,Galione Antony1

Affiliation:

1. Department of Pharmacology, University of Oxford, Mansfield Road, Oxford, OX1 3QT, U.K.

Abstract

The Ca2+-mobilizing second messenger, NAADP (nicotinic acid adenine dinucleotide phosphate), has been with us for nearly 20 years and yet we still cannot fully agree on the identity of its target Ca2+-release channel. In spite of some recent robust challenges to the idea that two-pore channels (TPCs) represent the elusive “NAADP receptor”, evidence continues to accumulate that TPCs are important for NAADP-mediated responses. This article will briefly outline the background and review more recent work pertaining to the TPC story.

Publisher

Portland Press Ltd.

Subject

Biochemistry

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1. Convergent activation of two-pore channels mediated by the NAADP-binding proteins JPT2 and LSM12;Science Signaling;2023-08-22

2. ENZYMATIC AND ENDOGENOUS SYNTHESIS OF NAD(P)‐DERIVED CALCIUM‐MOBILIZING MESSENGERS;Nucleic Acids in Medicinal Chemistry and Chemical Biology;2022-12-16

3. Two-pore channels: going with the flows;Biochemical Society Transactions;2022-08-12

4. Relevance of lysosomal Ca2+ signalling machinery in cancer;Cell Calcium;2022-03

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