Upon stimulation of membrane receptors, nicotinic acid adenine dinucleotide phosphate (NAADP) is formed as second messenger within seconds and evokes Ca signaling in many different cell types. Here, to directly stimulate NAADP signaling, MASTER-NAADP, a Membrane permeAble, STabilized, bio-rEversibly pRotected precursor of NAADP is synthesized and release of its active NAADP mimetic, benzoic acid C-nucleoside, 2'-phospho-3'F-adenosine-diphosphate, by esterase digestion is confirmed. In the presence of NAADP receptor HN1L/JPT2 (hematological and neurological expressed 1-like protein, HN1L, also known as Jupiter microtubule-associated homolog 2, JPT2), this active NAADP mimetic releases Ca and increases the open probability of type 1 ryanodine receptor. When added to intact cells, MASTER-NAADP initially evokes single local Ca signals of low amplitude. Subsequently, also global Ca signaling is observed in T cells, natural killer cells, and Neuro2A cells. In contrast, control compound MASTER-NADP does not stimulate Ca signaling. Likewise, in cells devoid of HN1L/JPT2, MASTER-NAADP does not affect Ca signaling, confirming that the product released from MASTER-NAADP is a bona fide NAADP mimetic.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11399135 | PMC |
http://dx.doi.org/10.1038/s41467-024-52024-y | DOI Listing |
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