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Published on: September 2, 2019
JPT2/HN1L functions as an NAADP-binding protein in a cell-type-specific manner
Roger Ottenheijm1, Kai J Winterberg2, Vivien Throm1
1Institute of Pharmacology, Heidelberg University, INF-366, D-69120 Heidelberg, Heidelberg, 69120, Germany; DZHK (German Centre for Cardiovascular Research), partner site Heidelberg/Mannheim, Heidelberg, Germany.
Abstract:
Nicotinic acid adenine dinucleotide phosphate (NAADP) is a second messenger evoking Ca²⁺ release from intracellular Ca²⁺ stores by targeting several Ca2+ channels, including two-pore channels (TPC1/2), transient receptor potential mucolipin-1 (TRPML1), or ryanodine receptor type 1 (RYR1). For activation of Ca2+ channels, NAADP requires binding proteins, such as JPT2/HN1L and LSM12. So far, their function has been analyzed in several cell lines and only a very limited number of primary cells; however, their physiological relevance in cell types known to utilize NAADP signaling remains unclear. Here, we generated Jpt2/Hn1L-/- mice to evaluate the contribution of JPT2/HN1L proteins to platelet aggregation and Ca2+ signaling in cardiomyocytes, mast cells, and T cells. NAADP is known to contribute to collagen-related peptide (CRP-XL)-evoked platelet aggregation, but this was not altered by JPT2/HN1L deletion. Functional Ca²⁺ imaging revealed that JPT2/HN1L plays a strikingly cell-type specific role in NAADP-mediated Ca2+ release. In electrically paced ventricular cardiomyocytes, β-adrenergic stimulation is known to evoke arrhythmogenic spontaneous diastolic Ca2+ transients, which were not altered in their frequency in Jpt2/Hn1L-/- myocytes. Further, antigen-evoked Ca2+ transients in peritoneal mast cells (PMCs) are not changed in Jpt2/Hn1L-/- PMCs. However, CD4⁺ T cells displayed a pronounced requirement for JPT2/HN1L. Following T cell receptor/CD3 stimulation, global Ca²⁺ elevations and early NAADP-driven Ca²⁺ microdomains, which occur within tens of milliseconds of TCR/CD3 engagement and serve as initiating signals for downstream immune activation, were significantly decreased in Jpt2/Hn1L-/- CD4+ cells. We conclude that JPT2/HN1L is indispensable for NAADP-mediated Ca²⁺ release in T cells, but dispensable in cardiomyocytes, platelets, and mast cells, at least for the agonists employed. Accordingly, LSM12 might compensate for the loss of JPT2/HN1L. Together, JPT2/HN1L is not universally required as an NAADP-binding protein but exhibits cell-type specificity, with an essential function in T cell Ca²⁺ signaling.
Insights
JPT2/HN1L proteins are essential for nicotinic acid adenine dinucleotide phosphate (NAADP)-mediated calcium release in T cells, but not in cardiomyocytes, platelets, or mast cells, highlighting cell-type specific roles.
Area of Science:
- Cellular Signaling
- Immunology
- Physiology
Background:
- Nicotinic acid adenine dinucleotide phosphate (NAADP) is a crucial second messenger regulating intracellular calcium (Ca²⁺) release.
- NAADP activates various Ca²⁺ channels, requiring binding proteins like JPT2/HN1L for its function.
- The physiological relevance of JPT2/HN1L in primary cells utilizing NAADP signaling remains largely uncharacterized.
Purpose of the Study:
- To investigate the in vivo role of JPT2/HN1L in NAADP-mediated Ca²⁺ signaling and physiological responses.
- To determine the cell-type specificity of JPT2/HN1L function in platelets, cardiomyocytes, mast cells, and T cells.
Main Methods:
- Generation of Jpt2/Hn1L knockout mice (Jpt2/Hn1L-/-).
- Assessment of platelet aggregation evoked by collagen-related peptide (CRP-XL).
- Functional Ca²⁺ imaging in isolated cardiomyocytes, peritoneal mast cells (PMCs), and CD4⁺ T cells following specific stimulations (e.g., TCR/CD3).
Main Results:
- JPT2/HN1L deletion did not affect CRP-XL-induced platelet aggregation.
- JPT2/HN1L deficiency did not alter Ca²⁺ transients in cardiomyocytes or antigen-evoked Ca²⁺ signaling in mast cells.
- Jpt2/Hn1L-/- CD4⁺ T cells showed significantly reduced global Ca²⁺ elevations and early NAADP-driven Ca²⁺ microdomains upon TCR/CD3 stimulation.
Conclusions:
- JPT2/HN1L is indispensable for NAADP-mediated Ca²⁺ release in CD4⁺ T cells, playing a critical role in initiating immune responses.
- JPT2/HN1L function is dispensable in cardiomyocytes, platelets, and mast cells for the tested agonists.
- The findings underscore the cell-type specificity of JPT2/HN1L and suggest potential compensatory roles for other proteins like LSM12.
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