Evidence that phosphatidylinositol 3-kinase is involved in sperm-induced tyrosine kinase signaling in Xenopus egg fertilization
© Mammadova et al; licensee BioMed Central Ltd. 2009
Received: 31 March 2009
Accepted: 17 December 2009
Published: 17 December 2009
Studies have examined the function of PI 3-kinase in the early developmental processes that operate in oocytes or early embryos of various species. However, the roles of egg-associated PI 3-kinase and Akt, especially in signal transduction at fertilization, are not well understood.
Here we show that in Xenopus eggs, a potent inhibitor of phosphatidylinositol 3-kinase (PI 3-kinase), LY294002 inhibits sperm-induced activation of the tyrosine kinase Src and a transient increase in the intracellular concentration of Ca2+ at fertilization. LY294002 also inhibits sperm-induced dephosphorylation of mitogen-activated protein kinase, breakdown of cyclin B2 and Mos, and first embryonic cleavage, all of which are events of Ca2+-dependent egg activation. In fertilized eggs, an 85-kDa subunit of PI 3-kinase (p85) undergoes a transient translocation to the low-density, detergent-insoluble membranes (membrane microdomains) where Src tyrosine kinase signaling is operating. However, the tyrosine phosphorylation of p85 in fertilized eggs is not as evident as that in H2O2-activated eggs, arguing against the possibility that PI 3-kinase is activated by Src phosphorylation. Nevertheless, sperm-induced activation of PI 3-kinase has been demonstrated by the finding that Akt, a serine/threonine-specific protein kinase, is phosphorylated at threonine-308. The threonine-phosphorylated Akt also localizes to the membrane microdomains of fertilized eggs. Application of bp(V), an inhibitor of PTEN that dephosphorylates PIP3, the enzymatic product of PI 3-kinase, promotes parthenogenetic activation of Xenopus eggs. In vitro kinase assays demonstrate that PIP3 activates Src in a dose-dependent manner.
These results suggest that PI 3-kinase is involved in sperm-induced egg activation via production of PIP3 that would act as a positive regulator of the Src signaling pathway in Xenopus fertilization.
At fertilization, the union of egg and sperm promotes a series of biochemical and cell biological changes within the fertilized egg. This phenomenon is termed 'egg activation' [1–3]. A trigger of egg activation, which acts inside the fertilized egg after the egg-sperm union, is a transient increase in intracellular Ca2+ (Ca2+ transient) [4–6]. One important consequence of egg activation is that the egg acquires the ability to exclude additional fertilizing sperm (block to polyspermy). In many, but not all species, the block to polyspermy is achieved by an altered membrane potential and/or by the formation of a fertilization envelope. Another important consequence is that the activated egg resumes meiotic cell division. In the case of amphibian and most mammalian species, the meiotic cell cycle of unfertilized eggs pauses at metaphase II, and successful fertilization promotes meiotic resumption and extrusion of the second polar body. These egg activation events are followed by the fusion of maternal and paternal nuclei and the initiation of embryonic cell division that produce an offspring.
The sperm-induced Ca2+ transient, a key event in the initiation of egg activation, is commonly mediated by inositol 1,4,5-trisphosphate (IP3), a second messenger that is produced by the phospholipase C (PLC)-catalyzed hydrolysis of phosphatidylinositol 4,5-bisphosphate. The molecular mechanism operating between egg-sperm membrane interaction/fusion and the activation of PLC, however, varies among species: in mammals and the newt Cynops pyrrohogaster, introduction of the sperm-derived proteins PLCζ  and citrate synthase , respectively, may account for this task. In these cases, egg-sperm membrane fusion, rather than egg-sperm membrane interaction, is crucial for initiating the Ca2+ transient. On the other hand, for some sea invertebrates, fish and frogs, there is still a debate over the mechanism by which the egg undergoes a Ca2+ transient. That sequential activation of the egg-associated Src tyrosine kinase and PLCγ is required for the Ca2+ transient in the sea urchin, starfish, fish, and frog [9–14] suggests that these species employ the membrane interaction machinery. Also, some membrane-associated molecules have been postulated as sperm-interacting and signal-transducing elements in Xenopus eggs [15–18].
Several studies have evaluated the function of PI 3-kinase in the early developmental processes that operate in oocytes or early embryos of various species. In Xenopus, PI 3-kinase and Akt are required for insulin-induced, but not progesterone-induced, oocyte maturation [19, 20], although one report has shown a requirement of PI 3-kinase for progesterone-induced oocyte maturation . There are also reports that the activation of γ-subspecies of PI 3-kinase  or application of wortmannin  induces oocyte maturation. On the other hand, oocyte maturation in the ascidian , mouse [25, 26] and starfish  has been shown to require activity of PI 3-kinase. Oocyte-specific deletion of PTEN is shown to cause premature activation of the primordial follicle cells , suggesting that a precise level of PIP3 is important for this process.
Moreover, the importance of PI 3-kinase and/or Akt has been demonstrated in FGF-dependent signal transduction [29, 30] and glucose transport in Xenopus oocytes , the first mitotic cell division in the sea urchin  and starfish , autocrine-mediated survival signaling of mouse two-cell embryos , mesoderm induction , gastrulation [36, 37] and neurogenesis  in Xenopus. Collectively, these studies demonstrate the general importance of PI 3-kinase and its enzymatic products in several aspects of development. However, a study on egg-associated PI 3-kinase and Akt with a focus on fertilization signaling has yet to be done, though Mehlmann et al.  found that LY294002 does not inhibit Ca2+ transients in fertilized mouse eggs.
Here, we provide evidence that the sperm-induced Ca2+ transient requires the activity of the egg-associated PI 3-kinase in Xenopus. Many somatic cell systems utilize PI 3-kinase as a downstream effector of tyrosine kinase signaling [40, 41]. In fertilized Xenopus eggs, however, tyrosine phosphorylation of the p85 subunit of PI 3-kinase is not evident. On the other hand, PI 3-kinase seems to act as an upstream, positive regulator for the Src-PLCγ pathway, because the PI 3-kinase inhibitor LY294002 inhibits the sperm-induced activation of Src, Ca2+ transient, and subsequent egg activation events. Subcellular fractionation studies demonstrate that the 85-kDa subunit of PI 3-kinase undergoes a transient translocation to low-density, detergent-insoluble membranes (membrane microdomains), where Src is present even before fertilization, awaiting a fertilization signal from sperm . Activation of PI 3-kinase in fertilized Xenopus eggs is suggested by the finding that Akt becomes phosphorylated at threonine-308 in fertilized eggs. These results highlight for the first time that activity of the egg PI 3-kinase may play an important role in signal transduction for fertilization.
We have previously shown that activation of Src and PLCγ is necessary for sperm-induced activation of Xenopus eggs. Therefore, we examined the effect of LY294002 on the downstream events of the Src-PLCγ pathway; namely the transient Ca2+ release (Figure 1B), inactivation of components of the cytostatic factor (Figure 1C), and first cell cleavage (Figure 1D). All of the LY294002-injected eggs exhibited features of an impaired transient Ca2+ release, as monitored using the fluorescent signal of fura-2 that was introduced into the eggs (Figure 1B). Seven of nine eggs tested showed no transient Ca2+ release, and two of nine showed a transient Ca2+ release of decreased amplitude (Figure 1B). LY294002 also had an inhibitory effect on the Ca2+-dependent breakdown of the Mos protein kinase and cyclin B2 as well as dephosphorylation of mitogen-activated protein kinase (MAPK) (Figure 1C). These Ca2+-dependent events are required for cancelling the arrest of the second meiotic cell cycle and for starting embryonic cell division. Actually, eggs injected with 10 μM LY294002 failed to undergo normal first cell cleavage (Figure 1D).
We also examined the effect of LY294002 on egg activation, as evaluated by the occurrence of cortical contraction, induced by several artificial egg activators. LY294002 effectively inhibited the egg activation induced by cathepsin B at 5 U/ml (23 of 90 eggs showed cortical contraction). On the other hand, the egg activation induced by A23187 at 2 μM and that by H2O2 at 10 mM were not inhibited; 85 of 90 eggs and 76 of 90 eggs were activated, respectively. These data suggest that egg activation by cathepsin B, which mimics the action of sperm protease and requires the egg Src activity, also requires the activity of PI 3-kinase. It should be noted that we did not employ LY294002 higher than 10 μM, because it required more volume of DMSO solution to be injected that would show a toxic effect on eggs.
Subcellular fractionation experiments demonstrated that Akt protein undergoes translocation to membrane microdomains in fertilized eggs (Figure 3D). The translocation of Akt occurred as early as 2 min after insemination (Figure 3E), a time course that is similar to translocation of p85 (Figure 2B). Quantitative analysis demonstrated that only a small fraction of Akt localized to membrane microdomains in fertilized eggs (Figure 3F, IB: Akt). However, the threonine-308-phosphorylated forms of Akt were predominantly present in the membrane microdomains (Figure 3F, IB: pThr308-Akt). These results suggest that the sperm-induced functional interaction, and activation, of PI 3-kinase and Akt take place specifically in the egg membrane microdomains. We also examined whether the sperm-induced re-localization of Akt requires the activity of PI 3-kinase. LY294002 was shown to inhibit the sperm-induced appearance of both p85 and Akt in the membrane microdomains (Figure 3G). Like in the case of the threonine-308-phosphorylation described above, PP2 did not affect the re-localization of p85 or Akt (Figure 3G).
In Xenopus eggs, the sperm-induced activation of Src tyrosine kinase plays an essential role in Ca2+ transient and egg activation [11, 43, 44]. The present study has indicated the activity of PI 3-kinase to connect egg-sperm interaction/fusion with the activation of Src, because 1) LY294002 inhibits the sperm-induced activation of Src, suggesting that PI 3-kinase acts as an upstream activator for Src, and 2) tyrosine phosphorylation of the p85 subunit of PI 3-kinase, a well-known phenomenon in several cellular systems, in which one or more tyrosine kinase is activated, is not stimulated in fertilized eggs. If so, what is the mechanism for Src activation by PI 3-kinase activity? One possibility is, as demonstrated in the present study, the kinase-activating interaction of PIP3 with Src. The Src homology 2 (SH2) domain of the Src protein is capable of binding PIP3 , supporting the possibility that interaction with PIP3 would displace the negative-regulatory intramolecular interaction involving the SH2 domain, leading to the Src kinase's activation.
In our experimental system, Wortmannin, another potent inhibitor for PI 3-kinase, is not inhibitory to the sperm-induced egg activation in Xenopus: in eggs injected with Wortmannin at up to 20 μM, sperm could promote Src activation, p85 translocation, cortical contraction, and most importantly Akt phosphorylation, all of which are events of egg activation (data not shown). There is a possibility that, in Xenopus eggs, Wortmannin binds preferentially to molecules other than PI 3-kinase. This idea is supported by the finding of Carnero and Lacal  that wortmannin is able to induce meiotic maturation in Xenopus oocytes at doses slightly higher that those required for complete inhibition of PI 3-kinase. The authors have also suggested that this effect is independent of the ability of Wortmannin to inhibit PI 3-kinase since LY294002 was unable to induce oocyte maturation at concentrations inhibitory to PI 3-kinase, and that the mechanism for wortmannin-induced maturation involves the activation of a maturation-promoting factor and MAPK .
A positive regulatory role for PIP3 in egg activation signaling has been suggested by the finding that bp(V), a potent inhibitor for PTEN phosphoinositide phosphatase, promotes tyrosine phosphorylation of Src and cortical contraction of Xenopus eggs. (Figure 4A-C) The results indicate that the elevation of PIP3 levels in eggs is sufficient for promoting Src-dependent signal transduction for egg activation.
We demonstrated that, in fertilized eggs, Akt was phosphorylated at Thr308. However, we did not detect the phosphorylation of another well-known site, Ser473. This could be because the phosphoSer473-specific antibody employed in this study was not suitable for analysis of the Xenopus Akt protein. However, immunoblotting has demonstrated that the phosphoSer473-specific antibody well recognizes Akt protein in immature Xenopus oocytes and that the phosphoSer473 signals become decreased in progesterone-treated, fully matured oocytes (unpublished results). Therefore, we suggest that fertilization promotes the phosphorylation of Akt selectively at threonine-308. In mammals, phosphorylation of Akt Thr308 and Ser473 is catalyzed by phosphoinositide-dependent protein kinase PDK1  and mammalian target of rapamycin mTOR , respectively. So, we assume that the signaling pathway involving PDK1, not mTOR, operates to promote the phosphorylation and activation of Akt in fertilized eggs.
Several cellular functions involve the activation of Akt [46, 48]. Of particular interest is the anti-apoptotic function of Akt. Our preliminary experiments have shown that a caspase-like protease is activated in eggs left unfertilized for several hours (unpublished results). The results suggest that fertilization is responsible for suppression of the caspase's activation. Therefore, our future efforts will be directed at examining whether an anti-apoptotic mechanism is really operating in fertilized eggs and, if so, to clarify how and where Akt is involved in this cellular function.
Several studies have focused on the roles of sperm-associated PI 3-kinase in mammalian species. In human sperm, LY294002 blocks the acrosome reaction  and enhances motility , but does not affect egg-sperm interaction . More recently, Jungnickel et al.  demonstrated that in the mouse, the zona pellucida glycoprotein 3-induced acrosome reaction involves the PIP3-dependent activation of Akt. These results suggest that PI 3-kinase is required for Ca2+ signaling in fertilizing sperm. In Xenopus, however, no information has yet been available for the role of PI 3-kinase and/or Akt in the acrosome reaction or other fertilization-related functions of sperm.
Another important question is how PI 3-kinase could be activated after egg-sperm interaction/fusion (without the involvement of tyrosine phosphorylation)? In this connection, the fact that fertilization is accompanied by a transient accumulation of the p85 subunit of PI 3-kinase and Thr308-phosphorylated form of Akt in the egg membrane microdomains may be important. As we reported earlier, egg membrane microdomains are abundant in cholesterol, the ganglioside GM1, and several signaling molecules, and serve as a platform for egg-sperm interaction and subsequent Src-dependent signal transduction [42, 53]. More recently, we have identified and characterized a membrane microdomain-associated protein, uroplakin III, which might act as a target of sperm-derived protease and as a substrate of the activated Src at fertilization [16, 54, 55]. Although the signal transduction pathway connecting uroplakin III and Src is not yet known, the involvement of GTP-binding proteins has been inferred because the application of GTP to the isolated egg membrane microdomains could reconstitute the Src activity in vitro (Iwasaki et al. manuscript in preparation; 53). So, it is tempting to speculate that PI 3-kinase acts as a downstream target of GTP-binding proteins, as demonstrated in the case of γ-subspecies of PI 3-kinase , so that GTP- and PIP3-dependent activation of Src is possible.
The specific activation of PI 3-kinase, however, is not necessarily required for egg activation signaling. Rather, the rapid and transient accumulations of PI 3-kinase at membrane microdomains by itself maybe important. Such a local concentration of PI 3-kinase may contribute to the effective propagation of PIP3-dependent and LY294002-sensitive signals for egg activation. In support of this, PIP2 is known to predominantly localize to membrane microdomains of mammalian cells [57, 58]. Further study should be directed toward analyzing the mechanism by which membrane microdomains allow the precise localization of these signaling molecules before and after fertilization.
In this study, we show that LY294002 effectively inhibited several early steps of sperm-induced egg activation, including the activation of Src. Although we should keep in mind that the effect of LY294002 could be mediated through other targets than PI 3-kinase, we think that the inhibitory effect of LY294002 is most likely due to the inhibition of PI 3-kinase: because not only several steps of Src-dependent egg activation but also sperm-induced phosphorylation of Akt are inhibited by this inhibitor. PI 3-kinase and Akt become activated and temporarily localize to the egg membrane microdomains where sperm-induced tyrosine kinase machinery operates for successful fertilization. These results highlight for the first time the important role the egg-associated PI 3-kinase plays in signal transduction for Xenopus fertilization.
Animals, antibodies, cultured cells and chemicals
Frogs were purchased from local dealers and maintained as described [11, 42]. Rabbit antibody to human Src phosphorylated at Tyr418 was obtained from Oncogene Research Products (CA, USA). Mouse anti-mouse PLCγ antibody was from Upstate Biotechnology (NY, USA). Rabbit antibodies against the recombinant Xenopus UPIII extracellular domain (xUPIII-ED) or a part of the Xenopus Src amino-terminal region were prepared as described previously [54, 59]. The mouse anti-phosphotyrosine antibody PY99 was purchased from Santa Cruz (CA, USA). Rabbit antibodies against phosphorylated human MAPK, human cyclin B2, and Xenopus Mos were from BioLabs (MA, USA) or Santa Cruz Biotechnology. Rabbit antibody against the 85-kDa subunit of human PI 3-kinase was obtained from Upstate Cell Signaling Solution (VA, USA). Rabbit antibodies against human Akt, and the phosphorylated Thr308 or phosphorylated Ser473 form of human Akt were obtained from Cell Signaling Technology (MA, USA). Human embryonic kidney 293 cells were grown in Dulbecco's Modified Eagle's Medium supplemented with 10% fetal calf serum at 37°C/5% CO2 in a humidified incubator. A Src-specific inhibitor, PP2, its inactive analog, PP3, a PLC-specific inhibitor, U73122, and a PI 3-kinase-specific inhibitor, LY294002, were purchased from Calbiochem. A23187 and bovine spleen cathepsin B were from Sigma (MO, USA). Leupeptin was from Peptide Institute (Osaka, Japan). H2O2 was from Santoku Chemical Industries (Tokyo, Japan). (p-amidinophenyl)methanesulfonyl fluoride hydrochloride (APMSF) was from Calbiochem (CA, USA). A synthetic tyrosine kinase substrate peptide (Cdk1 peptide) was synthesized and purified as described previously . The fluorescent Ca2+ indicator fura-2 was obtained from Calbiochem. Xenopus Src was partially (one column chromatography-processed) or fully (four column chromatography-processed) purified from immature oocytes as described previously , and used for kinase assays in vitro (see below). [γ-32P]ATP was obtained from ICN (OH, USA). A potent PTEN (phosphatase and tensin homolog deleted from chromosome 10) inhibitor bp(V) [dipotassium bisperoxo (picolinato) oxovanadate (V)] was purchased from Calbiochem. Phosphatidylinositol (PI) was obtained from Serdary Research Laboratories (Ontario, Canada). PI 4-phosphate and PI 4,5-bisphosphate were prepared from bovine brain as described previously . PI 3,4,5-trisphosphate (fatty acid moieties are palmitate, C16:0) was prepared as described . All the phospholipids were lyophilized from the chloroform solution and suspended in distilled water or 20 mM Tris-HCl (pH 7.5) by sonication. Protein A-Sepharose was obtained from GE Healthcare Biosciences (Uppsala, Sweden). Unless otherwise indicated, other chemicals were purchased from Sigma, Wakenyaku (Kyoto, Japan), Wako (Osaka, Japan), or Nacalai Tesque (Kyoto, Japan).
Eggs, sperm, and embryos
The collection of unfertilized eggs and sperm, removal of the jelly layer from eggs, and jelly water treatment of sperm were carried out as described previously [11, 42]. The activation of jelly layer-free eggs was done by insemination with jelly water-treated sperm (106 sperm/ml) or by parthenogenetic activation with the calcium ionophore A23187 (0.5 μM), H2O2 (10 mM), cathepsin B (5 U/ml), or bp(V) (200 μM) for the periods specified in the text. After the activation treatments, egg samples were washed with ice-cold DeBoer's solution containing 110 mM NaCl, 1.3 mM KCl, and 0.44 mM CaCl2, pH 7.2, immediately frozen in liquid nitrogen, and kept at -80°C. Activation was monitored by the occurrence of cortical contraction and first cell cleavage in a group of control eggs.
To determine the requirement of egg PI 3-kinase activity for Xenopus egg activation, the unfertilized eggs were microinjected with LY294002 as described previously . The microinjection of PP2, PP3, U73122, or DMSO alone was also performed. Briefly, stock solutions (5 mM in DMSO) for each compound were diluted with buffer containing 20 mM sodium phosphate, pH 7.4, and 100 mM NaCl. The inhibitor solutions were then loaded into an oil-filled glass capillary (Drummond), with a tip diameter of 10-30 μm, which was connected to a pulse-directed injector system (Nanoject; Drummond). Before being microinjected, dejellied eggs were washed and incubated with injection buffer containing 110 mM NaCl, 1.3 mM KCl, 20 mM MgSO4, 0.1 mM EGTA, and 10 mM chlorobutanol. A quantitative injection of the inhibitor solution (25-50 nl per egg) was conducted under microscopic observation, healed, and the eggs subjected to activation treatment (see above).
To analyze the presence and/or the phosphorylation status of proteins of interest, egg samples were homogenized or vortex-crushed with 10 μl per egg of ice-cold extraction buffer containing 1% (w/v) Triton X-100, 20 mM Tris-HCl, pH 7.5, 150 mM NaCl, 1 mM EDTA, 1 mM EGTA, 10 mM β-mercaptoethanol, 1 mM Na3VO4, 10 μg/ml leupeptin, and 20 μM APMSF. The extract was centrifuged at 12,000 g and the supernatant was used as the Triton X-100-solubilized egg extract (note that the extract contained Triton X-100-resistant membranes). In some experiments, egg samples were subjected to the preparation of crude membrane fractions as described . The membrane fractions were solubilized with the extraction buffer containing 0.1% SDS, and subjected to further experiments. Alternatively, eggs were subjected to the preparation of membrane microdomains as described previously . Briefly, eggs were homogenized with a 5-fold volume of ice-cold extraction buffer without Triton X-100. The homogenates devoid of debris were centrifuged at 150,000 g for 1 h. After the centrifugation, the fluffy layer of the pellets, rich in plasma membranes, were collected and adjusted to 1% Triton X-100 (w/v) and 42.5% (w/v) sucrose. The mixtures were then layered with 30% (first) and 5% (second) sucrose in the extraction buffer and centrifuged at 200,000 g for 24 h in an SW55 rotor (Beckman). After the centrifugation, aliquots of 12 fractions were collected from the top to bottom of the tubes. Fractions 3-6 were pooled as low density, detergent-insoluble membrane fractions (membrane microdomains) whereas fractions 9-12 were pooled as detergent-soluble, non-microdomain fractions. Protein concentrations were determined by the dye-binding assay (Bio-Rad, CA, USA).
Immunoprecipitation, immunoblotting, and SDS-PAGE
Protein samples (50-500 μg, 1 mg/ml) were immunoprecipitated with antibodies as specified in the text for 2 h at 4°C. The immune complexes were adsorbed onto 10 μl of protein A-Sepharose beads by gentle mixing for 30 min at 4°C. The beads were washed three times with 500 μl of buffer containing 0.1% SDS, 1% Triton X-100, 1% sodium deoxycholate, 150 mM NaCl, 50 mM Tris-HCl, pH 7.5, 1 mM Na3VO4, 10 μg/ml leupeptin, and 20 μM APMSF. The washed beads were treated with Laemmli's SDS sample buffer  at 98°C for 5 min. SDS-denatured proteins were separated by SDS-polyacrylamide gel electrophoresis using 10% gels and analyzed by immunoblotting as described previously .
In vitro kinase assay
The protein kinase assay was carried out in a standard reaction mixture (25 μl) containing an immunoprecipitated or purified Xenopus Src, 50 mM Tris-HCl (pH 7.5), 5 mM MgCl2, 2 μM [γ-32P]ATP (3.7 kBq/pmol), 1 mM dithiothreitol, and 1 mM Cdk1 peptide. Anti-pepY antibody, which recognized the autophosphorylation site of Src, and SDS-solubilized egg membrane fractions were used for immunoprecipitation as described previously [43, 60]. When the effect of several phospholipids was evaluated, purified Xenopus Src and non-radioactive ATP (at 1 mM) were employed, and Cdk1 peptide was omitted. The reaction was initiated by the addition of [γ-32P]ATP or non-radioactive ATP at 30°C for 10 min and terminated by the addition of SDS-sample buffer  followed by boiling for 3 min. Phosphorylation of Cdk1 peptide (radioactive assay) was analyzed by separating the reaction mixtures on 18% SDS-polyacrylamide slab gels, followed by visualization and quantification by a BAS2000 Bioimaging Analyzer (Fuji Film, Tokyo, Japan). Autophosphorylation of Xenopus Src (non-radioactive assay) was analyzed by separating the reaction mixtures by using 10% SDS-polyacrylamide slab gels, followed by immunoblotting with the anti-phosphorylated Tyr418 antibody.
Intracellular Ca2+ measurement
For Ca2+ measurements, dejellied eggs prepared from albino Xenopus females were co-microinjected with 50 nl of 160 μM fura-2 plus 200 μM LY294002 (see "Microinjection"). The injected eggs were then fertilized and fluorescent signals were recorded by ratio-imaging microscopy using a high-frame digital CCD imaging ARGUS/HISCA system (Hamamatsu Photonics, Japan) with a 10× planneofluar objective, NA 0.3 (Zeiss, Germany). Excitation wavelengths of 340 and 380 nm (each irradiation constant was set to about 800 ms) were used while monitoring the emission at 510 nm. All data collections were made at 10-s intervals at 18-21°C.
This work is supported in part by a Grant-in-Aid for Scientific Research (B), Japan Society for the Promotion of Science (19370094) and a grant from Hyogo Science and Technology Association (19I020) to KS.
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