| Literature DB >> 33758062 |
Hannes G Roggenkamp1, Imrankhan Khansahib1, Lola C Hernandez C1, Yunpeng Zhang1, Dmitri Lodygin2, Aileen Krüger1, Feng Gu1, Franziska Möckl1, Anke Löhndorf1, Valerie Wolters1, Daniel Woike1, Anette Rosche1, Andreas Bauche1, Daniel Schetelig3, René Werner3, Hartmut Schlüter4, Antonio V Failla5, Chris Meier6, Ralf Fliegert1, Timothy F Walseth7, Alexander Flügel2, Björn-Philipp Diercks8, Andreas H Guse8.
Abstract
NAADP-evoked Ca2+ release through type 1 ryanodine receptors (RYR1) is a major mechanism underlying the earliest signals in T cell activation, which are the formation of Ca2+ 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 Hn1l/Jpt2 in human Jurkat and primary rat T cells resulted in decreased numbers of initial Ca2+ microdomains and delayed the onset and decreased the amplitude of global Ca2+ 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 Ca2+ release from the endoplasmic reticulum through RYR.Entities:
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Year: 2021 PMID: 33758062 DOI: 10.1126/scisignal.abd5647
Source DB: PubMed Journal: Sci Signal ISSN: 1945-0877 Impact factor: 8.192