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Acidocalcisomes are acidic calcium-storage compartments described from bacteria to humans and characterized by their high content in poly P (polyphosphate), a linear polymer of many tens to hundreds of Pi residues linked by high-energy phosphoanhydride bonds. In the present paper we report that millimolar levels of short-chain poly P (in terms of Pi residues) and inorganic PPi are present in sea urchin extracts as detected using 31P-NMR, enzymatic determinations and agarose gel electrophoresis. Poly P was localized to granules randomly distributed in the sea urchin eggs, as shown by labelling with the poly-P-binding domain of Escherichia coli exopolyphosphatase. These granules were enriched using iodixanol centrifugation and shown to be acidic and to contain poly P, as determined by Acridine Orange and DAPI (4′,6′-diamidino-2-phenylindole) staining respectively. These granules also contained large amounts of calcium, sodium, magnesium, potassium and zinc, as detected by X-ray microanalysis, and bafilomycin A1-sensitive ATPase, pyrophosphatase and exopolyphosphatase activities, as well as Ca2+/H+ and Na+/H+ exchange activities, being therefore similar to acidocalcisomes described in other organisms. Calcium release from these granules induced by nigericin was associated with poly P hydrolysis. Although NAADP (nicotinic acid–adenine dinucleotide phosphate) released calcium from the granule fraction, this activity was not significantly enriched as compared with the NAADP-stimulated calcium release from homogenates and was not accompanied by poly P hydrolysis. GPN (glycyl-L-phenylalanine-naphthylamide) released calcium when added to sea urchin homogenates, but was unable to release calcium from acidocalcisome-enriched fractions, suggesting that these acidic stores are not the targets for NAADP.
The sea urchin egg has been an invaluable model for studying Ca2+ homoeostasis and signalling. Intracellular Ca2+ increases upon fertilization and is important for the generation of the fertilization envelope and for initiation of the biochemical events that serve to wake the egg from a state of dormancy .
A number of second messengers able to release Ca2+ from different intracellular stores were described for the first time in sea urchin eggs, such as cADPR (cyclic adenosine diphosphate ribose)  and NAADP (nicotinic acid–adenine dinucleotide phosphate) . Whereas cADPR and IP3 (inositol 1,4,5-trisphosphate) release Ca2+ from the ER (endoplasmic reticulum) of sea urchin eggs, NAADP does it from acidic vesicles that were proposed to be lysosome-like organelles , possibly the so-called yolk platelets . NAADP was also shown to increase the pH of these acidic vesicles by a mechanism coupled to Ca2+ release via the NAADP receptor . It was proposed that the fall in the luminal [Ca2+] allows H+ to bind to vacated sites on a luminal polyanionic matrix, thus resulting in alkalinization of the store .
The findings that NAADP released Ca2+ from acidic organelles of sea urchin eggs  led to investigations as to whether NAADP was also able to mobilize Ca2+ from lysosomes of mammalian cells. NAADP was shown initially to release Ca2+ from acidic organelles of pancreatic acinar and β-cells [7,8], coronary artery myocytes  and the phaeochromocytoma cell line PC12 , but apparently not from T-lymphocyte cell lines [11,12]. It was found that NAADP-induced Ca2+ release was associated with endolysosomal function because the Ca2+-release response was dependent on a proton gradient maintained by an ATP-dependent vacuolar-type proton pump that is primarily present in the endocytic pathway . Accumulating evidence showed that this NAADP-sensitive Ca2+ store was unique and distinct from IP3- and cADPR-sensitive Ca2+ stores [14,15], and results suggested that, at least in rat liver, it is the lysosome . Two-pore channels have recently emerged as potential receptors for NAADP in the lysosomes of mammalian cells [16–18], and they have now been identified as NAADP targets for Ca2+ release in the sea urchin .
Sea urchin eggs have a number of intracellular vesicles and several types of granules in their cytoplasm, as identified by electron microscopy. Among them are the cortical granules, which are located close to the surface and are exocytosed upon fertilization and formation of the fertilization envelope, the yolk platelets, which are an abundant group of organelles of high and uniform electron-density and that can occupy approximately half the volume of the egg , and the clear granules [21,22] characterized by their clear appearance, that are distributed at random in the unfertilized eggs . Both the cortical granules  and the clear granules  are acidic, whereas the yolk platelets increase their acidity from pH 6.8 to pH 6.1 upon fertilization . These changes in pH in yolk platelets (alkalinization on NAADP stimulation and acidification upon fertilization) reveals the multiphasic nature of this phenomenon, with the NAADP-induced response being a ‘rapid’ response and acidification upon fertilization being a ‘slow’ response.
Yolk platelets have been proposed to be the acidic organelles responsible for Ca2+ release upon NAADP stimulation [4,5]. This is in agreement with experiments using eggs stratified by centrifugation. Under these conditions, yolk platelets localize to the centrifugal pole, which is the site where the higher Ca2+ release occurs upon local photolysis of caged NAADP  and is opposite to the nucleus and lipid droplets. However, photolysis of NAADP at the centripetal pole, which is the region where clear granules localize, also results in a transient Ca2+ release . Interestingly this region of clear granules is the one more intensely labelled with Acridine Orange , suggesting that clear granules are more acidic than yolk platelets. In contrast LysoTracker Red appears to preferentially label the yolk platelets  and this labelling disappears after treatment with GPN (glycyl-L-phenylalanine-naphthylamide), a substrate of the lysosomal cathepsin C that selectively disrupts these organelles via osmotic lysis . Interestingly, although yolk platelets are distributed at random in the sea urchin egg, NAADP induces a peripheral vesicular alkalinization, even when injected into the middle of the egg, suggesting the presence of a subpopulation of NAADP-sensitive stores .
The clear granules of sea urchin eggs are morphologically very similar to acidocalcisomes, which are lysosome-related organelles characterized by their abundant content of the polyanion poly P (polyphosphate) bound to cations such as calcium, magnesium and zinc . Acidocalcisomes are present in trypanosomatid and apicomplexan parasites , as well as in the green alga Chlamydomonas reinhardtii  and the slime mould Dictyostelium discoideum , and were also identified in bacteria [29,30], human platelets , and insect  and chicken  eggs. As acidocalcisomes are acidic, rich in Ca2+ and in the polyanion poly P, and it has been shown that Ca2+ can be released from them after their alkalinization with NH4Cl or by the K+/H+ ionophore nigericin , we investigated whether some of the acidic granules of sea urchin eggs are equivalent to acidocalcisomes, and whether they are also targets for NAADP-stimulated Ca2+ release.
ATP, nigericin, valinomycin, DAPI (4′,6-diamidino-2-phenylindole), IP3, NAADP, PPi, tripolyphosphate (poly P3), poly P75+ and protease inhibitors (P8340) were purchased from Sigma Chemical. Coomassie Blue protein assay reagent was from Bio-Rad Laboratories. The anti-Xpress epitope monoclonal antibody and Fluo-3 were from Invitrogen. Bafilomycin A1 was from Kamiya Biomedical. Escherichia coli strain CA38 pTrcPPX1 was kindly provided by Professor Arthur Kornberg (Stanford University School of Medicine, Stanford, CA, U.S.A.). E. coli DH5a harbouring pTrc-PPBD was provided by Dr Katsuharu Saito (Shinshu University, Nagano-Ken, Japan). LysoTracker Red DND-99 was from Invitrogen. All other reagents were of analytical grade.
Sea urchins were obtained from Gulf Specimen Marine Laboratories or from the Guanabara Bay (Rio de Janeiro, Brazil). Eggs from Lytechinus variegatus or Arbacia punctulata were harvested by intracoelomic injection of 0.5 M KCl and collected in ASW (artificial sea water; 435 mM NaCl, 40 mM MgCl2, 15 mM MgSO4, 11 mM CaCl2, 10 mM KCl, 2.5 mM NaHCO3 and 20 mM Tris base, pH 8.0). Egg homogenates were prepared as described previously . Briefly, eggs were washed four times in Ca2+-free ASW (the first two washes containing 1 mM EGTA) and then washed in GluIM (gluconate intracellular-like medium; 250 mM potassium gluconate, 250 mM N-methylglucamine, 20 mM Hepes and 1 mM MgCl2, pH 7.2) without an ATP-generating system. Eggs were then homogenized in the same medium in the presence of protease inhibitors (P8340, Sigma). The homogenate (50%, v/v) was centrifuged at 13000 g for 10 s at 4 °C, and the supernatant was sequentially diluted in equal volumes of GluIM over a period of 3 h, as described previously . Microscopy experiments were performed with both species of sea urchin eggs with similar results. All other experiments were performed using L. variegatus eggs.
The egg homogenate (8 ml, ~4×105 eggs/ml) was centrifuged at 5000 g for 10 min at 4 °C. The supernatant (4 ml) was then loaded on to the top of a 20% iodixanol fractionation medium (OptiPrep™, Greiner Bio-One) diluted in GluIM buffer (20 ml). The preparation was centrifuged at 60000 g for 60 min at 4 °C. The pellet was resuspended in 100 μl of GluIM buffer, washed at least three times in GluIM, and used as the dense granule fraction.
For imaging, whole cells and dense granule fractions were washed first in 100 mM Hepes buffer (pH 7.4) and directly applied to Formvar-coated 200-mesh copper grids, allowed to adhere for 10 min at room temperature (22 °C), blotted dry and observed directly in an energy-filtering Zeiss 902 transmission electron microscope. This treatment avoided salt precipitation. Electron energy-filtered images were taken at an energy loss of 70 eV using a spectrometer slit width of 10 eV. For X-ray microanalysis, samples were examined in a JEOL 1200 EX transmission electron microscope. X-rays were collected for 150 s using a Si (Li) detector with a Norvar window on a 0–10 KeV energy range with a resolution of 10 eV/channel. Analysis was performed using a Noran Voyager III analyser with a standard analysis identification program. No changes in the size of the organelles were detected when the fractions were suspended in 100 mM Hepes (pH 7.4), plus 300 mM or 400 mM sucrose, instead of 100 mM Hepes alone.
For conventional electron microscopy, eggs and dense granule fractions were fixed in 4% formaldehyde and 2.5% glutaraldehyde diluted in 0.1 M sodium cacodylate buffer (pH 7.3) at 4 °C for 24 h, and then embedded in epoxy resin, sectioned and stained using standard methods. To verify that osmotic conditions did not change the size of organelles, the fixative was also diluted in ASW, but no changes in the morphology of different organelles were observed.
Egg homogenates were centrifuged at 16000 g for 30 min at 4 °C and the pellet was treated with methods to extract either LC (long-chain) or SC (short-chain) poly P and PPi. Different samples were used for each method. Aliquots of known volumes from different steps of the dense granule fraction separation were also obtained and centrifuged at 14000 g for 30 min at 4 °C. The pellets were extracted and used for poly P and PPi determinations. LC poly P extraction was performed as described by Ault-Riché et al. . SC poly P and PPi extraction was performed as described by Ruiz et al. . Protein measurements were performed using the Bradford protein assay kit (Bio-Rad Laboratories).
Poly P levels were determined from the amount of Pi released upon treatment with an excess of rPPX1 [recombinant Saccharomyces cerevisiae PPX (exopolyphosphatase) 1]. The recombinant enzyme was prepared as described previously . Aliquots of LC and SC poly P extracts (always less than 1.5 nmol) were incubated for 15 min at 37 °C with 60 mM Tris/HCl (pH 7.5), 6.0 mM MgCl2 and 3000–5000 units of purified rPPX1 in a final volume of 100 μl. One unit corresponds to the release of 1 pmol of Pi/min at 35 °C. Release of Pi was monitored using the method of Lanzetta et al. . For PPi quantification, the procedure was essentially the same, but using an excess of soluble TiPPase [thermostable inorganic PPase (pyrophosphatase); New England Biolabs], 0.04 unit per reaction, in 50 mM Tris/HCl (pH 7.5) and 5 mM MgCl2, for 30 min at 35 °C. To detect poly P degradation by dense granule fractions in the presence of 10 μM nigericin, aliquots were collected after 5, 10 and 15 min and centrifuged at 14000 g for 10 s, and the pellets were used for poly P extraction and determinations, as described above. The intracellular concentration of phosphate compounds was calculated taking into account a volume of 904 pl/egg.
For NMR analyses, EDTA was added to poly P extracts to a final concentration of 25 mM prior to adjusting to pH 7.0. All of the extracts contained 10% (v/v) 2H2O to provide a field-frequency lock. Phosphorus NMR spectra were acquired at 242.8 MHz using a Varian INOVA NMR spectrometer equipped with a 14.1 T Oxford Instruments magnet. For perchloric acid extracts, 10784 transients were collected at room temperature using 25 μs (90 °) pulse excitation, a 20-kHz spectral width, 32768 data points and a 5 s recycle time. Inverse gated proton decoupling was used to remove NOE (nuclear Overhauser effect) and J-coupling effects. The chemical shifts of all the 31P spectra were referenced to 0 p.p.m. using an 85% phosphoric acid external standard. The specific assignments of individual resonances were based on published chemical shifts and 31P–31P scalar couplings and, in some cases, co-addition of authentic compounds. NMR spectra were processed using the MacNuts 0.9.4 program (Acorn NMR) and included base-line correction, zero-filling and a 2-Hz exponential line broadening prior to Fourier transformation.
For poly P localization in whole eggs, the recombinant PPBD (poly-P-binding domain) of E. coli PPX linked to an Xpress epitope tag was used, as described previously . Briefly, eggs suspended in ASW were permeabilized with 0.1% Triton X-100 for 2 min. After washing in TBS [Tris-buffered saline; 100 mM Tris/HCl (pH 7.2) and 150 mM NaCl], eggs were incubated in blocking buffer (3% BSA in TBS, pH 7.2) for 30 min. PPBD (8 μg/ml) and 10 μg/ml anti-Xpress epitope monoclonal antibody were added, and the samples were incubated for 1 h under gentle agitation. The samples were washed with blocking buffer and TBS, and fixed in 4% paraformaldehyde diluted in TBS for 30 min. After fixation the eggs were blocked for 15 min in 100 mM NH4Cl in TBS, and for an additional 30 min in blocking buffer plus 0.1% Tween 20. Secondary antibodies (Alexa Fluor® 488-conjugated goat anti-mouse IgG; Invitrogen) were diluted in the same buffer (1:1000) and incubated with the eggs for 1 h under gentle agitation. After washing in blocking buffer plus Tween 20, the samples were observed using an Olympus IX-71 fluorescence microscope with a Photometrix CoolSnapHQ CCD (charge-coupled device) camera driven by Delta Vision software (Applied Precision) using filters with excitation at 480–500 nm and emission at 510–550 nm. For the egg three-dimensional projection (Supplementary Movie S1 at http://www.BiochemJ.org/bj/429/bj4290485add.htm), z-stacks were acquired and reconstructed using the same software as described above.
For localization of Acridine Orange and DAPI, the dense granule fraction was incubated with 3 μM Acridine Orange or 10 μg/ml DAPI for 10 min at room temperature in the presence of protease inhibitor cocktail (Sigma, P8340), 2 μg/ml oligomycin and 2 μg/ml antimycin, and observed in the microscope described above with excitation at 340–380 nm for DAPI and at 450–490 nm for Acridine Orange, and emission >500 nm for both dyes.
Egg stratification was performed as reported previously [4,24]. PPBD and DAPI staining were performed as described above. For LysoTracker staining, eggs were incubated with 0.5 nM LysoTracker Red DND-99 for 30 min at room temperature before stratification , and then stained with PPBD as described above.
H+ movements, and Ca2+ release were monitored using a fluorimeter (F4500, Hitachi Instruments). H+ movements were monitored by following changes in Acridine Orange (6 μM) fluorescence (excitation at 495 nm, emission at 530 nm) after incubating dense granule fractions (50–80 μg of protein for bafilomycin experiments; 600–800 μg of protein for Na+/H+ and Ca2+/H+ experiments) in 2 ml of GluIM containing 2 μg/ml oligomycin and 2 μg/ml antimycin A. Acridine Orange was allowed to equilibrate for 2–5 min, whereas the dye partitioned into dense granules, and then valinomycin (10 μM), bafilomycin A1 (1 μM) and/or nigericin (5 μM) were added as indicated. Ca2+ release was measured following changes in the fluorescence (excitation 506 nm, emission 526 nm) of Fluo-3 (3 μM). Total homogenates and dense granule fractions (310 μg of protein for NAADP experiments; 600–800 μg of protein for GPN experiments) were diluted in 2 ml of GluIM buffer. IP3 (300 nM), NAADP (200 nM) and nigericin (5 μM) were added where indicated in the Figures.
Perchloric acid extracts were dried in a SpeedVac and resuspended in 60 mM Tris/HCl (pH 7.5) and 6.0 mM MgCl2. For PPX-treated samples, rPPX1  was added (3000–5000 units) in a final volume of 50 μl and incubated for 30 min at 35 °C. Poly P samples were then mixed with DNA-loading buffer [10 mM Tris/HCl (pH 7.5), 10 mM EDTA, 0.25% Orange-G and 0.65% sucrose] and loaded into 1–2% agarose gels. The gels were run at 200 V in TAE buffer [40 mM Tris/acetate (pH 8.2) and 1 mM EDTA] until the dye (Orange-G) reached the middle of the gel. The gels were then stained with 0.1% Toluidine Blue for 1 h, and then de-stained with several changes of deionized water for 4 h.
Dense granule fractions were homogenized using a Teflon pestle tissue homogenizer in ice-cold reaction buffer for PPX [20 mM Tris/HCl, 5 mM magnesium acetate and 100 mM ammonium acetate (pH 7.5)], or PPase [50 mM Tris/HCl and 5 mM MgCl2 (pH 7.5)] activities, and supplemented with protease inhibitor cocktail (P8340, Sigma). To these samples, 0.1 mM poly P75+ or 0.1 μM PPi was added and aliquots were collected at 5, 10 and 15 min after substrate addition. The aliquots were centrifuged at 14000 g for 10 s, and the pellets were processed for poly P and PPi determinations as described before. Controls were performed with no sample, incubating the substrates in plain buffer under the same conditions.
All results are expressed as means±S.D. or, when appropriate, S.E.M. for n different experiments. Statistical significance was determined using a Student's t test or by one-way ANOVA at P<0.05.
Ultrastructural analysis of sea urchin eggs allowed the identification of several granules. The cortical granules (whose size varies from 0.39±0.02 to 0.92±0.05 μm diameter in different sea urchin species ) are located close to the surface and are identified by the presence of star-like dense material in their interior (Figure 1A, cg, thin arrow). An abundant group of organelles of approx. 1–2 μm diameter, oval form and high and uniform electron-density are known as yolk platelets (Figures 1B and and1C;1C; YP) . In addition, clear granules [21,22], characterized by their clear appearance and the presence in most of them of an electron-dense material in various states of condensation (Figures 1A and and1B,1B, thick arrows), are distributed at random in the unfertilized eggs . These clear granules, of an average diameter of 0.83±0.29 μm, are very similar in their appearance to the acidocalcisomes described in different organisms . A large number of other clear granules that are smaller (average diameter 0.19±0.04 μm) than the granules described above, but which also have a similar appearance to acidocalcisomes (empty appearance with a thin-layer of dense material that sticks to the inner face of the membrane; Figures 1B and and1E,1E, white arrowheads) and mitochondria (Figures 1B and and1D,1D, black arrowheads) are also visible.
To investigate whether the clear granules correspond to acidocalcisomes, whole-cell mounts of sea urchin eggs or homogenates were analysed by energy-filtering transmission electron microscopy. Using this technique, the contrast of a given structure in the image solely arises from its mass density since these preparations are not stained. Many electron-dense vesicles of various diameter (average 0.73±0.09 μm) were seen in intact eggs (Figure 2A, black arrows) or homogenates (Figure 2B, black arrow). Other larger and less electron-dense vesicles (probably yolk platelets) were also observed (Figure 2B, white arrow). X-ray microanalysis of these vesicles was performed (Figures 2C and and2D).2D). All ten spectra of the very-electron-dense vesicles taken from different homogenates were qualitatively similar showing considerable amounts of oxygen, sodium, magnesium, phosphorus, sulfur, calcium and zinc concentrated in their matrix (Figure 2C). X-ray microanalysis of the less electron-dense granules, probably corresponding to yolk platelets (Figure 2B, white arrow), revealed only the presence of sulfur (Figure 2D), suggesting that they are rich in proteins. Copper arose from the Formvar-coated grids in both cases and was also detected in spectra taken from the background (results not shown).
One of the characteristics of acidocalcisomes is that they contain large amounts of SC and LC poly P, and also PPi . As shown in Figure 3(A) egg homogenates contain ~220-fold more SC than LC poly P, whereas PPi content was approximately half the amount of SC poly P (all expressed in terms of Pi residues for comparative purposes). Poly P was also detected by electrophoresis of extracts in 1% agarose gels stained with Toluidine Blue (Figure 3B, lane 1), and pre-treatment of these samples with rPPX1 resulted in considerable decrease in staining (Figure 3B, lane 2).
Figure 3(C) shows a representative 242.8 MHz (1H-decoupled) 31P-NMR spectrum of perchloric acid extracts of sea urchin eggs. Resonance assignments for this spectrum are given in Table 1. The predominant peak in the spectrum is Pi (peak B). The inset region at ~−6 p.p.m. (left-hand inset) contains the PPi resonance, peak F. The region between −19 and −22 p.p.m. is shown in the right-hand inset and contains peaks for the β-phosphate of nucleoside triphosphates (M), in addition to the central phosphate of poly P (L). The spectrum shows considerable amounts of phosphorylcholine (A) and phosphoarginine (C).
Poly P, as detected using the PPBD of S. cerevisiae PPX , was localized in small vesicles randomly distributed in the egg (Figures 3D and and3E,3E, and Supplementary Movie S1). There was no poly P signal in the negative controls (i.e. in the absence of PPBD).
To isolate the dense granules (Figure 2) and investigate their chemical and enzymatic content, we used iodixanol centrifugation as described in the Materials and methods section. The pellet fraction was applied to Formvar-coated grids, and direct observation showed the presence of multiple electron- dense granules of variable size (Supplementary Figure S1A at http://www.BiochemJ.org/bj/429/bj4290485add.htm). X-ray microanalysis (Supplementary Figures S1B and S1C) showed that most of these granules (15 out of 25) contained a similar elemental composition to that of dense granules in whole eggs or homogenates (Figure 2C). Standard transmission electron microscopy of this fraction revealed the presence of clear granules (corresponding to dense granules), which most of the time appeared empty or containing a residual electron-dense material, as previously observed in whole eggs (Figure 1), and some mitochondrial contamination (results not shown).
The presence of granules in the dense fraction was confirmed by incubation of the preparation in the presence of Acridine Orange. The Acridine Orange-stained granules appeared in groups (Figure 4A) or as isolated vesicles (Figure 4C). We also investigated the location of poly P using DAPI (Figures 4B and and4D).4D). DAPI is known to shift its emission fluorescence to a maximum wavelength of 525 nm (yellow) in the presence of poly P, this change being specific for poly P and not produced by PPi or other anions . We detected the staining of numerous vesicles, either in groups (Figure 4B) or isolated (Figure 4D). No staining was detected when DAPI was omitted (results not shown).
Work by Morgan and Galione  has shown that acidification of granules in sea urchin eggs is maintained by a V-H+-ATPase (vacuolar type H+-ATPase), as happens with other acidic organelles, including the acidocalcisomes of Trypanosoma cruzi , Trypanosoma brucei , D. discoideum , C. reinhardtii  and human platelets . Interestingly, the function of this proton pump could be demonstrated only by inhibition of acidification by bafilomycin A1 after pre-incubation of the preparation with either valinomycin or FCCP (carbonyl cyanide p-trifluoromethoxyphenylhydrazone) . In agreement with those results, bafilomycin A1 released Acridine Orange after pre-incubation of the dense granule fractions with valinomycin (Figure 4E, black trace), but not in its absence (Figure 4E, grey trace), although this could be accomplished by nigericin (Figure 4E, grey trace). Addition of nigericin after bafilomycin A1 completed the release of Acridine Orange from the vesicles (Figure 4E, black trace).
Acidocalcisomes of T. brucei [40,41] and Leishmania donovani [42,43] have been reported to contain Na+/H+ and Ca2+/H+ exchangers and the coupled interaction of these exchangers was postulated to result in a mechanism of Ca2+ release upon alkalinization or Na+ entry into acidocalcisomes . Experiments on enriched dense granule fractions showed the presence of these ion-exchange mechanisms. For example, addition of 100 mM NaCl (Figure 4F, black trace), but not of 100 mM KCl (Figure 4F, light grey trace) resulted in Acridine Orange efflux, suggesting the activity of a Na+/H+ exchanger in the dense granule fraction. Addition of 10 and 50 μM CaCl2 under similar conditions also resulted in Acridine Orange efflux (Figure 4G, black and dark grey traces respectively), suggesting the operation of a Ca2+/H+ exchanger, and the potential function of these exchangers as a mechanism of Ca2+ release upon alkalinization of dense granules . Under physiological conditions, these exchangers could contribute to Na+ and Ca2+ uptake into these acidic compartments, as occurs with the plant vacuole .
It has been shown that Ca2+ release from acidocalcisomes of T. cruzi occurs in parallel with poly P hydrolysis . We therefore investigated whether there was a correlation between Ca2+ release from the acidic compartment containing poly P in the sea urchin egg dense granule fraction and poly P hydrolysis. Addition of nigericin resulted in Ca2+ release from the dense granule fraction, as detected by changes in the fluorescence of Fluo-3 (Figure 5A) and this resulted in a significant decrease in the levels of SC poly P, but not in the levels of LC poly P (Figure 5C). Addition of nigericin also resulted in alkalinization of the vesicles (Figure 5B) confirming the link between alkalinization of acidocalcisomes and Ca2+ release.
Acidocalcisomes are known to possess enzymes linked to PPi and poly P metabolism . The rapid hydrolysis of poly P that occurs when Ca2+ release is stimulated by nigericin (Figure 5) suggested the presence of an PPX activity in the dense granule fraction. To know whether this was the case, we investigated PPi and poly P hydrolysis by dense granule fractions. Hydrolysis of poly P3 (Figure 6A) or PPi (Figure 6B) was approximately linear with time, whereas hydrolysis of poly P75+ stopped after 5 min. This probably indicates the hydrolysis of contaminating SC poly Ps in the poly P75+ sample (which is a mixture of poly P molecules with a mean length of 84), and the inability of the polyphosphatase to cleave LC poly Ps.
NAADP has been shown to release Ca2+ from acidic granules of sea urchin eggs , whereas IP3 releases Ca2+ from the ER . Figures 7(A) and and7(D)7(D) show that both NAADP and IP3 were able to release comparable amounts of Ca2+ from vesicular compartments in egg homogenates. A second addition of NAADP showed no response revealing desensitization (results not shown). NAADP (Figure 7B) or IP3 (Figure 7E) were, however, less efficacious in the dense granule fraction. We next tested whether poly P hydrolysis occurred as a consequence of Ca2+ release by NAADP in dense granule fractions, but no significant changes were detected (Figure 7G). The lack of enrichment in NAADP-sensitive calcium stores, together with the lack of poly P hydrolysis accompanying calcium release by NAADP suggests that the acidocalcisome-related organelles of sea urchin eggs are not the calcium stores sensitive to NAADP.
The presence of releasable Ca2+ in lysosomes has been demonstrated based on experiments using GPN and it has been reported that NAADP-targeted stores are sensitive to GPN . GPN is a lysosome-disrupting cathepsin-C substrate that was originally used to distinguish lysosomes, which contain cathepsin C, from pre-lysosomal endocytic vacuoles, which do not . Hydrolysis of GPN by cathepsin C induces osmotic swelling of the lysosome and release of its content, including Ca2+, into the cytoplasm. Treatment of sea urchin homogenates with GPN caused Ca2+ release, which was completed by nigericin (Figure 7H, trace TH). In contrast, addition of GPN to dense granule fractions did not cause Ca2+ release (Figure 7H, trace DF) suggesting that this fraction is not contaminated with lysosomes.
As discussed above, when eggs are stratified by centrifugation, yolk platelets localize to the centrifugal pole which is the site where higher Ca2+ release occurs upon local photolysis of caged NAADP and which is opposite to the nucleus and lipid droplets, where clear granules localize . When eggs were stratified and stained with either PPBD (Supplementary Figures S2B and S2C at http://www.BiochemJ.org/bj/429/bj4290485add.htm) or DAPI (Supplementary Figures S2E and S2F), staining was detected in the centripetal pole in agreement with the reported localization of the clear granules  and with the results showing negligible NAADP-stimulated Ca2+ release by dense granule fractions. In contrast, staining with LysoTracker Red was in the centrifugal pole, where the yolk platelets localize and where higher NAADP-stimulated Ca2+ release has been detected  (Supplementary Figures S2G–S2J).
We report in the present paper that sea urchin eggs are rich in poly P. Poly P was detected by a biochemical method based on its specific hydrolysis by a PPX, by Toluidine Blue staining in agarose gels, by 31P-NMR and by a recently developed method based on staining with the specific poly-P-binding region of S. cerevisiae PPX . This was confirmed by visualization of poly P in the dense granule fraction using DAPI and by its hydrolysis when nigericin released Ca2+ from these fractions. We also found considerable amounts of phosphoarginine, a phosphagen present in many invertebrates although not previously reported in sea urchin eggs .
Our results also suggest that the dense granules of sea urchin eggs, which could correspond to the clear granules detected by transmission electron microscopy (both large and small; Figure 1) have many characteristics in common with acidocalcisomes : (i) they are acidic due to the operation of a bafilomycin A1-sensitive vacuolar ATPase and are able to accumulate acidophilic dyes such as Acridine Orange; (ii) they can store extremely large amounts of calcium and other cations such as magnesium, sodium and zinc, and can release Ca2+ in the presence of nigericin; (iii) they contain very large amounts of phosphorus in the form of phosphate, PPi, and poly P; (iv) they have very high electron density, when examined by energy-filtering transmission electron microscopy, and have an empty appearance with condensed material in their interior, when examined by standard transmission electron microscopy; and (v) they possess activities commonly found in acidocalcisomes, such as PPase , PPX , and Ca2+/H+ and Na+/H+ exchangers [40–43].
Clear granules are distributed at random in unfertilized sea urchin eggs , in agreement with the distribution of poly P-labelled granules (Figure 3E, and Supplementary Movie S1). The function of these clear granules is unknown, but their composition, investigated in the present study, implies an important role in storage of phosphorus and cations needed for embryo development. Our results suggest that, although these granules are acidic and contain large amounts of calcium, they are not the targets for NAADP-stimulated Ca2+ release.
It has been reported that fertilization induces pH changes in acidic stores of sea urchin eggs , and we have demonstrated that alkalinization of dense granules leads to Ca2+ release and poly P hydrolysis. Alkalinization of acidic stores of the sea urchin egg could be either upon vesicle fusion with the plasma membrane, when the alkaline extracellular medium exchanges with the acidic lumen of cortical granules that are the primary egg exocytic vesicles, or upon Ca2+ release from yolk platelets stimulated by NAADP . It has been reported that cortical alkalinization coincides with NAADP-induced Ca2+ release from intracellular stores , and that this alkalinization appears to occur at the individual vesicle level . Alkalinization of yolk platelets is increased by NAADP by a mechanism coupled to Ca2+ release via the NAADP receptor . It has been proposed that the fall in the luminal [Ca2+] allows H+ to bind to vacated sites on a luminal polyanionic matrix, thus resulting in alkalinization of the store .
In addition to acidic store alkalinization, it has been shown that fertilization of sea urchin eggs led to a change in cytosolic pH from 6.9 to 7.3 with a concomitant acidification of the sea water, and that the egg remains alkaline for approx. 60 min [48,49]. This change in cytosolic pH is driven by a plasma membrane Na+/H+ exchanger . An increase in cytosolic sodium has been shown previously to increase the release of calcium from acidocalcisomes of T. brucei [40,41] and L. donovani [42,43], and this could potentially occur with the sea urchin egg dense granules. It has also been shown that suspension of sea urchin eggs in NH4Cl (5 mM, pH 8.0), which could lead to alkalinization of all acidic granules, stimulates their metabolism and ability to undergo chromosome replication and condensation without triggering the cortical granule reaction . Therefore we cannot rule out that alkalinization of dense granules could lead to an additional Ca2+ release.
Previous studies have indicated that the acidic compartments responsible for Ca2+ release induced by NAADP are lysosome-like organelles , possibly the yolk platelets . This was based on experiments showing that GPN-mediated disruption of the organelles reduced the response to photoreleased or microinjected free NAADP, and on the response of yolk-platelet-enriched fractions to NAADP . The lack of calcium detection in yolk platelets in our X-ray microanalyses (Figure 2D) does not indicate its absence, but simply that the amount of calcium present is below the limit of detection of this technique, which cannot discriminate between bound and free calcium. Yolk platelets would then be equivalent to the lysosomes of mammalian cells that are emerging as important calcium stores , whereas the clear (dense) granules would be, as acidocalcisomes, equivalent to lysosome-related organelles .
NAADP-induced Ca2+ signals are small and possibly localized, but can trigger ER Ca2+ mobilization through Ca2+-induced Ca2+ release via IP3 and ryanodine receptors , thus explaining the extensive Ca2+ waves detected after fertilization. Alkalinization of the cytosol and Ca2+ release from dense granules (acidocalcisomes) could also contribute to these Ca2+ waves. Supplementary Figure S3 (at http://www.BiochemJ.org/bj/429/bj4290485add.htm) shows a model of the Ca2+ mobilization pathways that could be involved in sea urchin eggs. NAADP would trigger Ca2+ release from yolk platelets that could then trigger ER Ca2+ mobilization through Ca2+-induced Ca2+ release via IP3 and ryanodine receptors. Alkalinization of the egg cytoplasm by Na+ entry would release additional Ca2+ from dense granules (acidocalcisomes). Therefore acidocalcisomes, which are randomly distributed, could contribute to the NAADP-mediated two-phase Ca2+ release response. Alkalinization of these acidocalcisomes would lead to the hydrolysis of poly P, which would provide an important source of Pi for the anabolic reactions necessary for embryogenesis.
Isabela Ramos performed most of the experiments and participated in planning and writing of the paper; Douglas Pace assisted in sea urchin egg preparation and writing of the paper; Katherine Verbist prepared the recombinant PPBD of E. coli PPX; Fu-Yang Lin, Yonghui Zhang and Eric Oldfield carried out the NMR experiments and interpreted the results; Kildare Miranda, Ednildo Machado and Wanderley de Souza assisted in the design of the study, planning and manuscript preparation; and Roberto Docampo designed the study, and participated in planning and writing of the paper.
We thank the late Professor Arthur Kornberg for E. coli CA38 pTrcPPX1, and Dr Katsuharu Saito for E. coli DH5a pTrc-PPBD.
This work was supported by the Georgia Research Alliance/Barbara and Sanford Orkin Chair in Tropical and Emerging Global Diseases and Cellular Biology (to R.D.); I.B.R. was supported, in part, by a training grant from the Ellison Medical Foundation to the Center for Tropical and Emerging Global Diseases. D.A.P. was partially supported by the National Institutes of Health [NIH T32 training grant number AI-060546]. E.O., F.-Y.L and Y.Z. were supported, in part, by the National Institutes of Health [grant number GM-065307]. I.B.R., K.M., E.A.M. and W.S. were supported, in part, by the Fundação de Amparo a Pesquisa do Estado de Rio de Janeiro (FAPERJ) and the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq, Brazil).