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HN1L/JPT2: A signaling protein that connects NAADP generation to Ca 2+ microdomain formation.

Authors :
Roggenkamp HG
Khansahib I
Hernandez C LC
Zhang Y
Lodygin D
Krüger A
Gu F
Möckl F
Löhndorf A
Wolters V
Woike D
Rosche A
Bauche A
Schetelig D
Werner R
Schlüter H
Failla AV
Meier C
Fliegert R
Walseth TF
Flügel A
Diercks BP
Guse AH
Source :
Science signaling [Sci Signal] 2021 Mar 23; Vol. 14 (675). Date of Electronic Publication: 2021 Mar 23.
Publication Year :
2021

Abstract

NAADP-evoked Ca <superscript>2+</superscript> 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 <superscript>2+</superscript> 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 Ca <superscript>2+</superscript> microdomains and delayed the onset and decreased the amplitude of global Ca <superscript>2+</superscript> 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 <superscript>2+</superscript> release from the endoplasmic reticulum through RYR.<br /> (Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.)

Details

Language :
English
ISSN :
1937-9145
Volume :
14
Issue :
675
Database :
MEDLINE
Journal :
Science signaling
Publication Type :
Academic Journal
Accession number :
33758062
Full Text :
https://doi.org/10.1126/scisignal.abd5647