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HN1L/JPT2: A signaling protein that connects NAADP generation to Ca2+ microdomain formation.

Hannes G RoggenkampImrankhan KhansahibLola C Hernandez CYunpeng ZhangDmitri LodyginAileen KrügerFeng GuFranziska MöcklAnke LöhndorfValerie WoltersDaniel WoikeAnette RoscheAndreas BaucheDaniel ScheteligRene WernerHartmut SchlüterAntonio V FaillaChris MeierRalf FliegertTimothy F WalsethAlexander FlügelBjörn-Philipp DiercksAndreas H Guse
Published in: Science signaling (2021)
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.
Keyphrases
  • binding protein
  • protein kinase
  • endoplasmic reticulum
  • endothelial cells
  • oxidative stress
  • copy number
  • dna methylation
  • induced pluripotent stem cells
  • amino acid