1. Academic Validation
  2. NAADP and the two-pore channel protein 1 participate in the acrosome reaction in mammalian spermatozoa

NAADP and the two-pore channel protein 1 participate in the acrosome reaction in mammalian spermatozoa

  • Mol Biol Cell. 2014 Mar;25(6):948-64. doi: 10.1091/mbc.E13-09-0523.
Lilli Arndt 1 Jan Castonguay Elisabeth Arlt Dorke Meyer Sami Hassan Heike Borth Susanna Zierler Gunther Wennemuth Andreas Breit Martin Biel Christian Wahl-Schott Thomas Gudermann Norbert Klugbauer Ingrid Boekhoff
Affiliations

Affiliation

  • 1 Walther Straub Institute of Pharmacology and Toxicology, Ludwig-Maximilians University, 81377 München, Germany Department of Pharmacy, Ludwig-Maximilians University, 81377 München, Germany Institute for Experimental and Clinical Pharmacology and Toxicology, Albert-Ludwigs-University, 79104 Freiburg, Germany Institute for Anatomy, University of Duisburg-Essen, 45141 Essen, Germany.
Abstract

The functional relationship between the formation of hundreds of fusion pores during the acrosome reaction in spermatozoa and the mobilization of calcium from the acrosome has been determined only partially. Hence, the second messenger NAADP, promoting efflux of calcium from lysosome-like compartments and one of its potential molecular targets, the two-pore channel 1 (TPC1), were analyzed for its involvement in triggering the acrosome reaction using a TPCN1 gene-deficient mouse strain. The present study documents that TPC1 and NAADP-binding sites showed a colocalization at the acrosomal region and that treatment of spermatozoa with NAADP resulted in a loss of the acrosomal vesicle that showed typical properties described for TPCs: Registered responses were not detectable for its chemical analogue NADP and were blocked by the NAADP antagonist trans-Ned-19. In addition, two narrow bell-shaped dose-response curves were identified with maxima in either the nanomolar or low micromolar NAADP concentration range, where TPC1 was found to be responsible for activating the low affinity pathway. Our finding that two convergent NAADP-dependent pathways are operative in driving acrosomal exocytosis supports the concept that both NAADP-gated cascades match local NAADP concentrations with the efflux of acrosomal calcium, thereby ensuring complete fusion of the large acrosomal vesicle.

Figures
Products