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NAADP-evoked Ca release through type 1 ryanodine receptors (RYR1) is a major mechanism underlying the earliest signals in T cell activation, which are the formation of Ca microdomains. In our characterization of the molecular machinery underlying NAADP action, we identified an NAADP-binding protein, called hematological and neurological expressed 1-like protein (HN1L) [also known as Jupiter microtubule-associated homolog 2 (JPT2)]. Gene deletion of in human Jurkat and primary rat T cells resulted in decreased numbers of initial Ca microdomains and delayed the onset and decreased the amplitude of global Ca signaling. Photoaffinity labeling demonstrated direct binding of NAADP to recombinant HN1L/JPT2. T cell receptor/CD3-dependent coprecipitation of HN1L/JPT2 with RYRs and colocalization of these proteins suggest that HN1L/JPT2 connects NAADP formation with the activation of RYR channels within the first seconds of T cell activation. Thus, HN1L/JPT2 enables NAADP to activate Ca release from the endoplasmic reticulum through RYR.
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http://dx.doi.org/10.1126/scisignal.abd5647 | DOI Listing |
Biochim Biophys Acta Mol Cell Res
October 2023
The Calcium Signaling Group, Dept. of Biochemistry and Molecular Cell Biology, University Medical Center Hamburg-Eppendorf (UKE), Hamburg, Germany.
NAADP is one of the most potent calcium mobilizing second messengers. Only recently, two NAADP-binding proteins have been identified: HN1L/JPT2 and LSM12. Further, ASPDH was suggested as a less selective binding partner.
View Article and Find Full Text PDFBiomedicines
November 2021
Department of Experimental Biology, Faculty of Science, Masaryk University, 62500 Brno, Czech Republic.
In tumor cells with defects in apoptosis, autophagy allows prolonged survival. Autophagy leads to an accumulation of damaged mitochondria by autophagosomes. An acidic environment is maintained in compartments of cells, such as autophagosomes, late endosomes, and lysosomes; these organelles belong to the "acid store" of the cells.
View Article and Find Full Text PDFSci Signal
March 2021
The Ca Signalling Group, Department of Biochemistry and Molecular Cell Biology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Front Plant Sci
June 2019
State Key Laboratory of Crop Stress Biology in Arid Area/College of Life Sciences, Northwest A&F University, Yangling, China.
Calcium (Ca) signaling and nicotinamide adenine dinucleotide (NAD) signaling are two basic signal regulation pathways in organisms, playing crucial roles in signal transduction, energy metabolism, stress tolerance, and various developmental processes. Notably, calmodulins (CaMs) and NAD kinases (NADKs) are important hubs for connecting these two types of signaling networks, where CaMs are the unique activators of NADKs. NADK is a key enzyme for NADP (including NADP and NADPH) biosynthesis by phosphorylating NAD (including NAD and NADH) and therefore, maintains the balance between NAD pool and NADP pool through an allosteric regulation mode.
View Article and Find Full Text PDFJ Cell Physiol
April 2019
Laboratory of General Physiology, Department of Biology and Biotechnology "Lazzaro Spallanzani, " University of Pavia, Pavia, Italy.
The neurotransmitter glutamate increases cerebral blood flow by activating postsynaptic neurons and presynaptic glial cells within the neurovascular unit. Glutamate does so by causing an increase in intracellular Ca concentration ([Ca ] ) in the target cells, which activates the Ca /Calmodulin-dependent nitric oxide (NO) synthase to release NO. It is unclear whether brain endothelial cells also sense glutamate through an elevation in [Ca ] and NO production.
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