Acidic NAADP-releasable Ca(2+) compartments in the megakaryoblastic cell line MEG01

Biochim Biophys Acta. 2011 Aug;1813(8):1483-94. doi: 10.1016/j.bbamcr.2011.05.005. Epub 2011 May 13.

Abstract

Background: A novel family of intracellular Ca(2+)-release channels termed two-pore channels (TPCs) has been presented as the receptors of NAADP (nicotinic acid adenine dinucleotide phosphate), the most potent Ca(2+) mobilizing intracellular messenger. TPCs have been shown to be exclusively localized to the endolysosomal system mediating NAADP-evoked Ca(2+) release from the acidic compartments.

Objectives: The present study is aimed to investigate NAADP-mediated Ca(2+) release from intracellular stores in the megakaryoblastic cell line MEG01.

Methods: Changes in cytosolic and intraluminal free Ca(2+) concentrations were registered by fluorimetry using fura-2 and fura-ff, respectively; TPC expression was detected by PCR.

Results: Treatment of MEG01 cells with the H(+)/K(+) ionophore nigericin or the V-type H(+)-ATPase selective inhibitor bafilomycin A1 revealed the presence of acidic Ca(2+) stores in these cells, sensitive to the SERCA inhibitor 2,5-di-(tert-butyl)-1,4-hydroquinone (TBHQ). NAADP releases Ca(2+) from acidic lysosomal-like Ca(2+) stores in MEG01 cells probably mediated by the activation of TPC1 and TPC2 as demonstrated by TPC1 and TPC2 expression silencing and overexpression. Ca(2+) efflux from the acidic lysosomal-like Ca(2+) stores or the endoplasmic reticulum (ER) results in ryanodine-sensitive activation of Ca(2+)-induced Ca(2+) release (CICR) from the complementary Ca(2+) compartment.

Conclusion: Our results show for the first time NAADP-evoked Ca(2+) release from acidic compartments through the activation of TPC1 and TPC2, and CICR, in a megakaryoblastic cell line.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Calcium Channels / genetics
  • Calcium Channels / metabolism
  • Calcium Signaling / drug effects
  • Calcium Signaling / physiology*
  • Cell Compartmentation
  • Cell Line
  • Endoplasmic Reticulum / drug effects
  • Endoplasmic Reticulum / metabolism
  • Enzyme Inhibitors / pharmacology
  • Humans
  • Hydrogen-Ion Concentration
  • Hydroquinones / pharmacology
  • Ionophores / pharmacology
  • Lysosomes / drug effects
  • Lysosomes / metabolism
  • Macrolides / pharmacology
  • Megakaryocyte Progenitor Cells / drug effects
  • Megakaryocyte Progenitor Cells / metabolism*
  • NADP / analogs & derivatives*
  • NADP / metabolism
  • Nigericin / pharmacology
  • RNA, Small Interfering / genetics
  • Vacuolar Proton-Translocating ATPases / antagonists & inhibitors

Substances

  • Calcium Channels
  • Enzyme Inhibitors
  • Hydroquinones
  • Ionophores
  • Macrolides
  • RNA, Small Interfering
  • TPCN1 protein, human
  • TPCN2 protein, human
  • NADP
  • NAADP
  • bafilomycin A1
  • 2-tert-butylhydroquinone
  • Vacuolar Proton-Translocating ATPases
  • Nigericin