Identification of a prostaglandin D2 metabolite as a neuritogenesis enhancer targeting the TRPV1 ion channel

Shibata, Takahiro; Takahashi, Katsuhiro; Matsubara, Yui; Inuzuka, Emi; Nakashima, Fumie; Takahashi, Nobuaki; Kozai, Daisuke; Mori, Yasuo; Uchida, Koji

doi:10.1038/srep21261

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Published: 16 February 2016

Identification of a prostaglandin D₂ metabolite as a neuritogenesis enhancer targeting the TRPV1 ion channel

Takahiro Shibata^1,2,
Katsuhiro Takahashi¹,
Yui Matsubara¹,
Emi Inuzuka¹,
Fumie Nakashima¹,
Nobuaki Takahashi³,
Daisuke Kozai³,
Yasuo Mori³ &
…
Koji Uchida¹

Scientific Reports volume 6, Article number: 21261 (2016) Cite this article

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Abstract

Mast cells play important roles in allergic inflammation by secreting various mediators. In the present study, based on the finding that the medium conditioned by activated RBL-2H3 mast cells enhanced the nerve growth factor (NGF)-induced neuritogenesis of PC12 cells, we attempted to isolate an active compound from the mast cell conditioned culture medium. Our experiment identified 15-deoxy-Δ^12,14-PGJ₂ (15d-PGJ₂), one of the PGD₂ metabolites, as a potential enhancer of neuritogenesis. 15d-PGJ₂ strongly enhanced the neuritogenesis elicited by a low-concentration of NGF that alone was insufficient to induce the neuronal differentiation. This 15d-PGJ₂ effect was exerted in a Ca²⁺-dependent manner, but independently of the NGF receptor TrkA. Importantly, 15d-PGJ₂ activated the transient receptor potential vanilloid-type 1 (TRPV1), a non-selective cation channel, leading to the Ca²⁺ influx. In addition, we observed that (i) NGF promoted the insertion of TRPV1 into the cell surface membrane and (ii) 15d-PGJ₂ covalently bound to TRPV1. These findings suggest that the NGF/15d-PGJ₂-induced neuritogenesis may be regulated by two sets of mechanisms, one for the translocation of TRPV1 into the cell surface by NGF and one for the activation of TRPV1 by 15d-PGJ₂. Thus, there is most likely a link between allergic inflammation and activation of the neuronal differentiation.

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Introduction

Mast cells are some of the principal effector cells involved in the pathogenesis of allergic diseases and in certain host responses against infection. The roles of mast cells in mediating an allergic reaction are well understood. The aggregation of the high affinity IgE receptor (FcεRI) on mast cells by allergen/antigen results in the rapid release of pro-inflammatory mediators. This is followed by a delayed phase of mast cell activation resulting in the production and secretion of cytokines and chemokines that recruit other immune cells, such as lymphocytes and eosinophils, leading to chronic inflammation¹. Although the view that mast cells are primarily involved in the immune responses has been prevalent², there is increasing evidence that mast cells participate in other physiological processes such as nervous system functions³.

The activation of mast cells leads to the rapid production of a large variety of mediators, such as prostaglandins (PGs)^4,5. PGD₂ is known to be one of the major PGs produced from mast cells, which has significant effects on a number of biological processes, such as platelet aggregation, relaxation of smooth muscles and nerve cell functions. PGD₂ also exerts its allergic inflammatory effects, including blood flow changes, influx of Th2 lymphocytes and eosinophils and induction of Th2 cytokine production, through high affinity interactions with the G-protein coupled receptors DP1 and chemoattractant-homologous receptor expressed on T-helper type 2 cells (CRTH2). Both receptors act in concert to facilitate a variety of biological functions involved in the development and maintenance of the allergic response^6,7. Meanwhile, PGD₂ is a relatively unstable molecule. PGD₂ readily undergoes spontaneous dehydration in aqueous media to yield biologically active cyclopentenone PGs of the J₂ series, such as PGJ₂, Δ^12,14-PGJ₂ and 15d-PGJ₂^8,9,10. Unlike other classes of prostanoids, the J-series PGs have their own unique spectrum of biological effects, including anti-inflammatory effects^11,12 and an agonistic effect on the peroxisome proliferator-activated receptor γ (PPARγ)^13,14.

Neurotrophins, such as the nerve growth factor (NGF), act as important regulators of the neuronal survival, growth, development and functional maintenance in the central and peripheral nervous systems. They also prevent neuronal cell damage under various pathophysiological conditions, including ischemia and neuronal diseases. NGF, the first and best characterized member of the neurotrophin family, induces neuronal differentiation and neuritogenesis by binding to TrkA, a receptor tyrosine kinase for NGF. The ligand-bound NGF receptor undergoes autophosphorylation and associates with multiple signaling proteins through the phosphorylated tyrosine moiety. TrkA activates several small G proteins, such as Rap1, Ras and the Cdc42-Rac1-RhoA family, as well as pathways mediated by the extracellular signal-regulated kinase (ERK), PI3-kinase/Akt and phospholipase C-γ¹⁵.

In the current study, based on the finding that the conditioned medium from the activated mast cell with IgE/antigen potently promoted the NGF-induced neurite outgrowth, we attempted to isolate an active compound from the medium and identified a PGD₂ metabolite as a potential neuritogenesis enhancer. In addition, we characterized the cellular events and established a possible mechanism, in which the PGD₂ metabolite accelerates the NGF-mediated neuritogenesis via activation of a calcium ion channel.

Results

Effect of conditioned medium from activated mast cells on NGF-induced neuritogenesis

Upon activation, mast cells release numerous vasoactive and pro-inflammatory mediators and play an important role in allergic inflammation. To find an active molecule providing a link between inflammation and the neuronal response, we examined the effect of the conditioned medium from the activated mast cells on the NGF-induced neuritogenesis. The RBL-2H3 mast cells were stimulated with anti-DNP IgE/DNP-BSA and the medium of the activated mast cells was examined for the NGF-induced neuritogenesis of rat pheochromocytoma PC12 cells. As shown in Fig. 1A, the medium significantly enhanced the NGF-induced neurite outgrowth in a time-dependent manner. The pretreatment of the cyclooxygenase (COX) inhibitor NS398 decreased the activity of the medium, whereas the lipoxygenase (LOX) inhibitor, nordihydroguaiaretic acid (NDGA) had little effect (Fig. 1B). These data suggest the involvement of the COX-derived product(s) in the promotion of neuritogenesis.

Identification of a neuritogenic enhancer in conditioned medium from activated mast cells

To identify the COX products responsible for the synergistic effect on the NGF-dependent neuritogenesis, we conducted an activity-guided separation of a principal enhancer in the conditioned medium from the activated RBL-2H3 cells. The ethyl acetate extract was fractionated into 15 fractions by HPLC using a reverse-phase column and the resulting fractions were assayed for synergistic activity in the PC12 cells. As shown in Fig. 2A, fraction No. 12 exhibited the most potent enhancing activity. The LC-ESI-MS analysis of fraction No. 12 showed a single peak with a pseudomolecular ion peak at m/z 315.3 (M-H)⁻ (Fig. 2B,C). Among the COX products, a PGD₂ metabolite, 15-deoxy-Δ^12,14-PGJ₂ (15d-PGJ₂; molecular weight 316.4), has a similar molecular mass. Indeed, the main product in fraction No. 12 showed the same retention time as the peak for the authentic 15d-PGJ₂ (Fig. 2D,E). In addition, when the formation of 15d-PGJ₂ was examined in the conditioned medium from the activated RBL-2H3 mast cells using the LC-ESI-MS/MS technique (Fig. S1), the stimulation of the cells with the antigen for 8 h gave about 180 nM of 15d-PGJ₂ in the medium (Fig. 2F). In addition to 15d-PGJ₂, other PGs, such as PGE₂, PGD₂, 15-deoxy-PGD₂, PGJ₂ and Δ¹²-PGJ₂, were also detected in the conditioned medium from the activated mast cells by LC-ESI-MS/MS (Fig. S2). Hence, to further confirm that 15d-PGJ₂ is the major active component, we examined the effect of the PGs on the NGF-induced neurite outgrowth and found that the neuritogenesis was very potently enhanced by 15d-PGJ₂ (Fig. 2G and S3). Beside 15d-PGJ₂, PGJ₂ and Δ¹²-PGJ₂ moderately enhanced the neurite outgrowth, suggesting that the J₂-type PGs could typically act as a neuritogenic enhancer. Indeed, J₂-type PGs including 15d-PGJ₂ were previously reported to promote the NGF-induced neurite outgrowth in PC12h cells by Satoh et al.¹⁶.

15d-PGJ₂ accelerates neuritogenesis in cooperation with NGF

As shown in Fig. 3A,B, 15d-PGJ₂ had no significant effect on the neurite outgrowth in the absence of NGF, whereas it strongly enhanced the neuritogenesis elicited by a low-concentration of NGF that alone was insufficient to induce neuronal outgrowth. Consistent with these results, 15d-PGJ₂ alone had little effect on the expression of a neurofilament light (NF-L) protein, a neuronal differentiation marker, whereas the combined stimulus of 15d-PGJ₂ and NGF enhanced the expression of NF-L (Fig. 3C). The 15d-PGJ₂-enhanced neurite outgrowth was also observed in the rat primary dorsal root ganglia (DRG) cells and the level of outgrowth in the DRG cells exposed to 15d-PGJ₂/NGF was ∼4-fold higher than that in the cells exposed to NGF alone (Fig. 3D,E). Thus, 15d-PGJ₂ accelerates the neuritogenesis in cooperation with NGF.

15d-PGJ₂ accelerates NGF-induced neuritogenesis in a Ca²⁺-dependent manner

It has been established that NGF induces cell differentiation and neurite outgrowth via the TrkA receptor^17,18. However, 15d-PGJ₂ did not have any effect on the NGF-induced autophosphorylation of TrkA (Fig. S4A), suggesting that 15d-PGJ₂ might act downstream of the NGF-TrkA signaling pathway. Indeed, downstream signaling pathways, including ERK, JNK and PKC, were enhanced by the co-treatment of 15d-PGJ₂ and NGF (Fig. S4B–D). To gain insight into the molecular mechanism underlying the acceleration of the NGF-induced neurite outgrowth by 15d-PGJ₂, we tested several small molecule inhibitors directed against the downstream signaling molecules of the NGF-TrkA pathway and found that the neuritogenesis was most effectively inhibited by the Ca²⁺ chelators. The pretreatment of the 1,2-bis-(2-amino-phenoxy)ethane-N,N,N’,N’-tetraacetic acid acetoxymethyl ester (BAPTA-AM), a cell-permeable Ca²⁺ chelator, significantly inhibited the 15d-PGJ₂-enhanced neurite outgrowth (Fig. 4A,B). Similar results were also observed when the cells were treated with EGTA, an extracellular calcium chelator (Fig. 4C,D). In addition, the Ca²⁺ ionophore ionomycin dramatically enhanced the neuritogenesis in PC12 cells treated with NGF (Fig. S5). In addition, we measured the changes in the intracellular Ca²⁺ levels in PC12 cells using the Ca²⁺-specific fluorescence probe, Fluo-8 and found that the co-treatment of 15d-PGJ₂ and NGF significantly increased the Ca²⁺ levels in the PC12 (Fig. 4E) and DRG cells (Fig. 4F). Thus, it appeared that 15d-PGJ₂ acts on a Ca²⁺-dependent signaling pathway.

Involvement of TRPV1 in the 15d-PGJ₂/NGF-induced neuritogenesis

Based on the previous findings that 15d-PGJ₂ could target the Ca²⁺ channels, such as TRP ankyrin-1 (TRPA1)^19,20,21,22, we tested the effect of the Ca²⁺ channel inhibitors on the 15d-PGJ₂/NGF-induced neuritogenesis. Capsazepine, a TRP vanilloid receptor 1 (TRPV1) inhibitor, showed the most significant inhibitory effect (Fig. 5A–C). However, the inhibitors directed against TRPA1 (AP-18) and TRPC (Pyr2) were only slightly inhibitory (Fig. 5A). Other inhibitors, including the L-type Ca²⁺ channel and Na⁺ channel inhibitors, did not show any effect (Fig. S6). In addition, the TRPV1 channel inhibitor inhibited the 15d-PGJ₂-induced increase in intracellular Ca²⁺ level in the PC12 cells (Fig. 5D). We also observed that (i) 15d-PGJ₂ increased the intracellular Ca²⁺ level in the HEK293 cells transfected with TRPV1 cDNA (Fig. 5E), (ii) the effect of 15d-PGJ₂ on the NGF-induced neuritogenesis was fully reproduced by treatment of the cells with capsaicin, a TRPV1 agonist (Fig. 5F), (iii) capsaicin-enhanced neuritogenesis was inhibited by the treatment of BAPTA-AM (Fig. S7A,B) and (iv) the TRPV1 channel inhibitor significantly reduced the neuritogenesis in the DRG cells (Fig. S7C). These data strongly suggest the involvement of TRPV1 in the 15d-PGJ₂-enhanced neuritogenesis.

To further confirm the involvement of TRPV1 in the 15d-PGJ₂/NGF-induced neuritogenesis, we examined the effect of the TRPV1 overexpression on the neuritogenesis. PC12 cells were transfected with the expression plasmids for the TRPV1 or empty vector and were stimulated with 15d-PGJ₂ together with NGF. The expression level of TRPV1 was assessed by immunoblotting with the anti-TRPV1 antibody (Fig. 6A). As shown in Fig. 6B, neurite outgrowth was significantly enhanced by the transfection of TRPV1 (Fig. 6B). In addition, we also examined the effect of the TRPV1 down-regulation on the 15d-PGJ₂-enhanced neuritogenesis using RNAi and observed that the siRNA of the TRPV1 resulted in the corresponding changes in the expression of TRPV1 (Fig. 6C). The knock down of TRPV1 reduced the neurite outgrowth enhanced by 15d-PGJ₂ (Fig. 6D). These data also support our hypothesis and confirmed that 15d-PGJ₂ acts as an enhancer of neuritogenesis via activation of TRPV1.

15d-PGJ₂ as a covalent ligand of TRPV1

It has been established that the electrophilic α,β-unsaturated carbonyl group in the cyclopentenone ring of 15d-PGJ₂ is essential for a variety of biological functions²³. Hence, we tested the effect of 9,10-dihydro-15d-PGJ₂, lacking the electrophilic α,β-unsaturated functionality (Fig. 7A), on the NGF-induced neuritogenesis. As shown in Fig. 7B, the NGF-induced neurite outgrowth was enhanced by 15d-PGJ₂ in a dose-dependent manner. In contrast, 9,10-dihydro-15d-PGJ₂ had no significant effects on the neuritogenesis. In a manner similar to the induction of the neuritogenesis, 15d-PGJ₂ resulted in a rapid increase in the intracellular Ca²⁺ level, whereas the Ca²⁺ levels were maintained at about the basal level in the cells exposed to 9,10-dihydro-15d-PGJ₂ (Fig. 7C). Thus, the reduction of the double bond in the cyclopentenone ring virtually abolished the neuritogenic activity and induction of the Ca²⁺ influx of 15d-PGJ₂, indicating that the neuritogenesis-enhancer activity can be attributed to the electrophilic center of 15d-PGJ₂.

Finally, to examine whether 15d-PGJ₂ could covalently bind TRPV1 in the intact cells, we incubated the GFP-tagged TRPV1-introduced HEK293 cells with a biotinylated 15d-PGJ₂ (Bt-15d-PGJ₂), which retains the α,β-unsaturated ketone substituent and the neuritogenesis-enhancing activity (Fig. S8), followed by Avidin pull-down and immunoprecipitation experiments. The cell lysates were incubated with NeutrAvidin beads and the biotinylated proteins bound to the beads were then eluted and analyzed by immunoblot using the anti-GFP antibody. As shown in Fig. 7D, the GFP-tagged TRPV1 was detected in the precipitate from the Bt-15d-PGJ₂-treated cells. Alternatively, the cell lysates were subjected to immunoprecipitation with an anti-GFP antibody and the presence of the Bt-15d-PGJ₂-modified proteins was detected using HRP-conjugated NeutrAvidin (Fig. 7D). In addition, we investigated the covalent modification of endogenous TRPV1 in intact PC12 cells in the presence or absence of NGF. Intriguingly, pull-down and immunoprecipitation studies showed that 15d-PGJ₂ could react with TRPV1 only in the presence of NGF in the PC12 cells (Fig. 7E). More strikingly, consistent with the observations that NGF induced the translocation of TRPV1 into the cell membrane (Fig. S9A), immunocytochemical studies showed colocalization of Bt-15d-PGJ₂ and TRPV1 in the cell surface membrane of the NGF-treated PC12 cells (Fig. S10).These and the findings that (i) specific inhibitor for PI3K, which regulates the translocation and sensitization of TRPV1^24,25, inhibited the 15d-PGJ₂-enhanced neuritogenesis without showing cytotoxicity (Fig. S9B,C), (ii) 15d-PGJ₂-enhanced PKC activation was reduced by the treatment of PI3K inhibitor and TRPV1 antagonist (Fig. S11), suggest the involvement of NGF-induced translocation of TRPV1 through PI3K signaling in the 15d-PGJ₂-enhanced neuritogenesis.

Discussion

In the present study, based on the finding that the conditioned medium from the activated RBL-2H3 mast cells accelerated the NGF-induced neuritogenesis of the PC12 cells, we attempted to separate and purify the active compound from the conditioned medium and identified 15d-PGJ₂, one of the PGD₂ metabolites, as an enhancer of the NGF-induced neuritogenesis. Moreover, using LC-ESI-MS/MS in the MRM mode, we extensively analyzed PGD₂ and its metabolites in the medium of stimulated mast cells and detected 15d-PGJ₂ as a major product. Strikingly, the maximum yield of 15d-PGJ₂ was about 180 nM. The amounts of 15d-PGJ₂ generated, at least in vitro, may be sufficient for it to play a role in modulating most of the responses. These data suggested that 15d-PGJ₂ might represent a bona fide active component essential for the induction of neuritogenesis by NGF and that the neuronal response during mast cell degranulation might be ascribed, at least in part, to the production of PGD₂ followed by the conversion to 15d-PGJ₂.

It has been previously established^8,9,10 that PGD₂ can be spontaneously converted to 15d-PGJ₂ as follows: (i) PGD₂ is initially converted to the dehydration products, PGJ₂; (ii) PGJ₂ is isomerized to an α,β-unsaturated enone intermediate followed by dehydration to form 15d-PGJ₂. Although it remains unknown if this PGD₂ metabolism is utilized in an organism, 15d-PGJ₂ has been detected in many types of human and animal samples. The presence of 15d-PGJ₂ in vivo was first demonstrated in the inflammatory exudates of the carrageenin-induced pleurisy²⁶. Later, using a murine monoclonal antibody against 15d-PGJ₂, the accumulation of 15d-PGJ₂ was demonstrated in the cytoplasm of most of the foamy or spindle macrophages in human atherosclerotic plaques¹⁰ and in the spinal cord of sporadic amyotrophic lateral sclerosis (ALS) patients²⁷. These findings suggested that, because PGD₂ is the major prostanoid in most tissues, 15d-PGJ₂ could be produced at a number of sites and ubiquitously involved in inflammation and its related disorders.

Our current study showed that 15d-PGJ₂ enhanced the neuritogenesis in an NGF-dependent manner. However, the NGF-induced autophosphorylation of the NGF receptor (TrkA) was not affected by 15d-PGJ₂ (Fig. S4). This is in striking contrast to the previous finding that an enhanced autophosphorylation of the receptor is involved in the enhancement of the NGF-induced neuritogenesis by an electrophilic isothiocyanate compound²⁸. On the other hand, based on the fact that the effect of 15d-PGJ₂ on the neuritogenesis is NGF-dependent, we speculated that 15d-PGJ₂ might act somewhere downstream on the NGF-TrkA signaling pathway. A crucial hint for the molecular mechanism was obtained when we tested several inhibitors directed against the downstream signaling molecules of the NGF-TrkA pathway. Among the tested inhibitors, Ca²⁺ chelators significantly inhibited the 15d-PGJ₂/NGF-induced neuritogenesis (Figs 4 and 5). 15d-PGJ₂ indeed enhanced the Ca²⁺ influx and, in addition, the Ca²⁺ ionophore dramatically enhanced the NGF-induced neuritogenesis (Fig. S5). Thus, it was anticipated that the Ca²⁺ influx might play a key role in the 15d-PGJ₂-enhanced neuritogenesis. Indeed, the increase in the intracellular Ca²⁺ concentration via activation of the intracellular sigma-1 and IP3 receptors has been shown to facilitate the NGF-induced neuritogenesis of the PC12 cells²⁹.

The involvement of the Ca²⁺ influx in the enhancement of the NGF-induced neuritogenesis by 15d-PGJ₂ led us to assume that a Ca²⁺ channel might be involved in the mechanisms. Hence, we tested several agonists and antagonists of the Ca²⁺ channels and putatively identified TRPV1 as a key regulator of the NGF/15d-PGJ₂-induced neuritogenesis. This result was further confirmed by the transfection experiments (Fig. 6). These findings suggest the existence of a mechanism whereby 15d-PGJ₂ induces the Ca²⁺ influx via activation of a Ca²⁺ channel protein (TRPV1), leading to acceleration of the NGF-TrkA signaling pathway. On the other hand, it was previously reported that CRTH2, a PGD₂ receptor, is involved in the 15d-PGJ₂-enhanced neuritogenesis of the PC12 cells³⁰. However, PGD₂, a CRTH2 ligand, was found to be a weak enhancer of the neuritogenesis (Fig. 2G). In addition, the selective CRTH2 agonist, 13,14-dihydro-15-keto-PGD₂, failed to influence the neuritogenesis regardless of the presence of NGF³⁰. Thus, the involvement of CRTH2 as the target of 15d-PGJ₂ in the NGF-induced neuritogenesis is still questionable.

The TRP superfamily is composed of six subfamilies. TRPV1, among them, is a thermosensitive, nonselective cation channel and can be activated by noxious heat and acidic conditions. It can also recognize a variety of small molecules, such as acrolein and capsaicin, as ligands³¹. We have confirmed that 15d-PGJ₂ directly interacted with the TRPV1 protein when the GFP-tagged TRPV1-introduced HEK293 cells were incubated with a biotinylated 15d-PGJ₂ (Bt-15d-PGJ₂) (Fig. 7). Modification of the cysteine residues in the TRPV1 could be associated with the activation of its channel activity^32,33,34,35. It has also been reported that 15d-PG₂ covalently modifies another TRP cannel, TRPA1, to activate the channel protein^19,20,21,22. Thus, it is not unlikely that the binding of 15d-PG₂ to TRPV1 might lead to the activation of the TRPV1 channel protein. Although regulation of the 15d-PGJ₂-mediated TRPV1 activation and its significance need to be further confirmed in vivo in future studies, our in vitro studies demonstrated that the allergic inflammation, generating PGD₂ and its metabolites, may result in the neuronal response via activation of the TRPV1.

Zhang et al.²⁴ have previously shown that NGF activates the PI3K-Src signaling pathway, followed by the phosphorylation and translocation of TRPV1 into the cell membrane. Indeed, we characterized the cellular events triggered by the combined stimulus of NGF and 15d-PGJ₂ and observed that NGF promoted the insertion of TRPV1 into the cell surface membrane and the PI3K specific inhibitor LY294002 significantly inhibited the neuritogenesis (Fig. S9). Thus, it is likely that the NGF-induced translocation of TRPV1 into the cell surface may play an essential role in the 15d-PGJ₂-accelerated neuritogenesis. On the other hand, Ca²⁺ influx through the TRP channels leads to mitogen-activated protein kinase (MAPK) activation in the neuronal cells³⁶. In addition, studies using selective pharmacological inhibitors and constitutive-active/dominant-negative mutants have demonstrated the essential role for the MAPKs in the NGF-induced PC12 differentiation^37,38,39,40. We indeed observed that 15d-PGJ₂ enhanced the phosphorylation of the MAPKs, such as ERK and JNK, as well as the neuritogenesis (Fig. S4B,C). Thus, the Ca²⁺ influx through the TRPV1 followed by activation of the MAPKs may represent a key mechanism for the 15d-PGJ₂-enhanced neuritogenesis. Taken together, the NGF/15d-PGJ₂-induced neuritogenesis may be regulated by two sets of mechanisms, one for the translocation of TRPV1 into the cell surface by NGF and one for the activation of TRPV1 followed by the Ca²⁺ influx by 15d-PGJ₂ (Fig. 7F).

In summary, we screened PGs based on the neurite outgrowth-inducing effect and identified 15d-PGJ₂ as a neuritogenic enhancer derived from activated mast cells. Furthermore, we identified the TRPV1 as a molecular target for the neuritogenesis by 15d-PGJ₂, presenting a molecular basis for the neuronal differentiation by endogenous lipid mediators. Although the endogenous production of 15d-PGJ₂ needs to be confirmed in future studies, our observation suggest that 15d-PGJ₂ may act as a mediator that enhances the neuritogenesis. Our current findings may provide clues to the physiological and/or pathophysiological mechanisms of neuritogenesis.

Methods

Materials

The antibodies against neurofilament-L and GAPDH were purchased from Chemicon. The anti-GFP-tag and anti-TRPV1 antibodies were from MBL and Santa Cruz Biotechnology, respectively. The anti-PKCβ antibody was obtained from BD Transduction Laboratories. The antibodies against phospho-ERK, phospho-p38 and phospho-JNK were from Cell Signaling Technology. The recombinant β-NGF was obtained from R&D systems, Inc. PGs and NS398 were purchased from Cayman Chemical. Anti-flotillin antibody, Nordihydroguaiaretic acid (NDGA), Capsaicin and Capsazepine, were obtained from Sigma. Preparation of biotinylated 15d-PGJ₂ was described previously⁴¹.

Cell Culture and Neurite Outgrowth Assay

The culture of PC12 cells and neurite outgrowth assay were performed as previously described²⁸.

Preparation of conditioned medium from rat mast cell RBL-2H3

The rat RBL-2H3 mast cell line was obtained from the Human Science Research Resource Bank (Japan). RBL-2H3 cells were grown in DMEM supplemented with 10% FBS, penicillin (100 units/ml), streptomycin (100 μg/ml) and 0.2% NaHCO₃ at 37 °C in an atmosphere of 95% air and 5% CO₂. For preparation of the conditioned medium, the RBL-2H3 cells were sensitized overnight with 100 ng/ml anti-DNP IgE (Sigma), then washed and stimulated with 20 ng/ml DNP-BSA (Calbiochem) for the indicated times (0-24h). The resulting medium was used for the neuritogenesis assay and the quantification of 15d-PGJ₂.

Isolation of active component from the conditioned medium from activated mast cells

The conditioned medium from the activated RBL-2H3 cells was extracted with ethyl acetate. The resulting ethyl acetate extract was separated by reverse-phase HPLC on a C18 column (Sunniest C18, 4.6 × 250 mM; ChromaNik) at the flow rate of 0.8 ml/min. A gradient was used by solvent A (H₂O containing 0.1% trifluoroacetic acid) and solvent B (acetonitrile) as follows: time = 0–5 min, 40% B; 35 min, 100% B; 40 min, 100% B. The extract was fractionated in two-minute intervals from 5 to 35 min. The resulting fractions (15 fractions) were evaporated to dryness and redissolved in ethanol.

LC-ESI-MS/MS analysis for quantification of 15d-PGJ₂

The conditioned medium was partially separated using Sep-Pak C18 cartridges (Waters). The internal standard, 15d-PGJ₂-d₄, was added to the samples prior to the column separation. After the sample loading, the Sep-Pak cartridges were washed with 5 ml of H₂O containing 0.1% TFA and the PGs were eluted with 5 ml of ethyl acetate. The samples were then dried, dissolved in ethanol and subjected to UPLC-ESI-MS analysis. The UPLC-EIS-MS/MS analyses were performed using a Xevo TQD triple quadrupole mass spectrometer system (Waters). The UPLC used a reverse-phase C30 column (Develosil HB C30-UG-3, 100 mM × 2.0 mM, Nomura Chemical, Japan) operated in a column oven set at 40 °C. A discontinuous gradient used solvent A (H₂O containing 2% isopropanol and 0.05% formic acid) with solvent B (acetonitrile containing 2% isopropanol and 0.05% formic acid) as follows: 40% B at 0 min, 40% B at 1 min, 48% B at 2 min, 48% B at 5 min, 94% B at 6.5 min, 94% B at 12 min, at the flow rate of 0.3ml/min. The negative ion mode MRM transitions were monitored as follows: 15d-PGJ₂, m/z 315.2 > 271.2 (cone potential 25 eV/collision energy 12 eV); 15d-PGJ₂-d₄, m/z 319.2 > 275.2(cone potential 25 eV/collision energy 12 eV); Δ¹²-PGJ₂, PGJ₂ and PGJ₂, m/z 333.2 > 271.2 (cone potential 20 eV/collision energy 14 eV); PGD₂ and PGE₂, m/z 351.2 > 271.2 (cone potential 20 eV/collision energy 15 eV). The amount of 15d-PGJ₂ was quantified by the ratio of the peak area of the target 15d-PGJ₂ and of the 15d-PGJ₂-d₄. QuanLynx software (Waters) was used to create the standard curve and to calculate the 15d-PGJ₂ concentrations.

SDS-PAGE and immunoblot analysis

The SDS-PAGE and immunoblot analysis were performed as previously described²⁸. Total plasma membrane proteins were extracted using plasma membrane protein extraction kit (101Bio, Palo Alto, CA).

Isolation of rat DRG neuron

Isolation of the DRG neuron was performed as previously described¹⁸ with a few modifications. The DRG from the thoracic and lumbar spinal cord of 1–3 day-old rats were cut in small pieces and incubated for 1h at 37 °C in a solution containing 124 mM NaCl, 5 mM KCl, 1.2 mM KH₂PO₄, 1.3 mM MgSO₄, 2.4 mM CaCl₂, 24 mM NaHCO₃, 10 mM Glucose, 1.6 mg/ml collagenase type II (Sigma) and 1.6 mg/ml trypsin (Difco Laboratories). They were gently triturated with a fire-polished glass pipette and the resulting solution was centrifuged at 800 rpm for 2 min. The obtained pellet was resuspended in DMEM-F12 HAM medium (Sigma) containing 10% FBS, penicillin and streptomycin. Cells were plated onto dishes coated with poly-L-lysine (Sigma). The cells were cultured in the DMEM-F12 HAM medium containing 10% FBS at 37 °C under 5% CO₂. All animal protocols were approved by the Animal Experiment Committee in the Graduate School of Bioagricultural Sciences of Nagoya University.

Ca²⁺ imaging

The cells were seeded in a poly-L-lysine-coated glass bottom dish and cultured for overnight. Assay buffer (140 mM NaCl, 5 mM KCl, 1 mg MgCl₂, 1 mM Na₂HPO₄, 10 mM glucose, 10 mM HEPES, 2 mM CaCl_2, and 1.5 mM Probenecid; pH = 7.3) and loading buffer (assay buffer containing 5 μM Fluo-8 AM (ABD Bioquest, Inc.)) were freshly prepared. After washing twice with the assay buffer, the cells were incubated with loading buffer for 30 min, then incubated with the assay buffer for 15 min. Fluorescence measurements were performed using a confocal microscope (FV1000D IX81; Olympus Optical Co., Ltd.).

Transfection in PC12 Cells

Transfections using Lipofectamine 2000TM (Life technologies) was performed as previously described²⁸.

Pull-down Assay in HEK293 cells

The HEK293 cells transfected with empty or GFP-tagged TRPV1 were treated with 1 μM Bt-15d-PGJ₂ for 10 min. After treatment, the cells were washed twice with cold PBS and lysed with RIPA buffer containing the protease inhibitor cocktail and the resulting lysate was treated with NaBH₄ (20 mM) for 1 h on ice. After removing NaBH₄ by ultrafiltration, the cell lysate was incubated with immobilized NeutrAvidin or with anti-GFP-Protein G beads, as indicated, at 4 ^oC overnight. After incubation, the beads were washed three times with lysis buffer, then boiled with the SDS sample buffer. The presence of the GFP-tagged TRPV1 was detected by immunoblotting with the anti-GFP antibody and the incorporation of Bt-15d-PGJ₂ into the TRPV1 immunoprecipitates was detected with HRP-NeutrAvidin.

Pull-down Assay in PC12 cells

The PC12 cells were treated with 1 μM Bt-15d-PGJ₂ with or without 1.5 ng/ml NGF for 10 min. After treatment, the cells were washed twice with cold PBS and lysed with RIPA buffer containing the protease inhibitor cocktail. The cell lysate was incubated with immobilized NeutrAvidin or with anti-TRPV1-Protein G beads, as indicated, at 4 ^oC overnight. After incubation, the beads were washed three times with RIPA buffer, then boiled with the SDS sample buffer. The presence of TRPV1 was detected by immunoblotting with the anti-TRPV1 antibody and the incorporation of Bt-15d-PGJ₂ into the TRPV1 immunoprecipitates was detected with HRP-NeutrAvidin.

Immunocytochemical staining

Cells were fixed with 4% paraformaldehyde in PBS for 15 min at room temperature, then permeabilized by treatment with PBS containing 0.5% Triton X-100. The cells were sequentially incubated in 1% bovine serum albumin in PBS for 1h, then incubated with the primary anti-TRPV1 at 4 ^oC overnight. The cells were then washed with PBS and incubated for 1 h in the presence of Alexa488-labeled donkey anti-goat IgG (Molecular Probes) and Cy5-labeled Avidin (GE Healthcare), rinsed with PBS and covered with anti-fade solution. The immunofluorescent images were analyzed using a confocal microscope (FV1000; Olympus Optical Co., Ltd., Tokyo, Japan).

Additional Information

How to cite this article: Shibata, T. et al. Identification of a prostaglandin D₂ metabolite as a neuritogenesis enhancer targeting the TRPV1 ion channel. Sci. Rep. 6, 21261; doi: 10.1038/srep21261 (2016).

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Acknowledgements

This work was supported in part by a Grant-in-Aid for ScientificResearch (A) (No. 26252018) (K.U.) and Grant-in-Aid for Scientific Research on Innovative Areas “Oxygen Biology: a new criterion for integrated understanding of life” (No. 26111011) (K.U.) of the ministry of Education, Sciences, Sports, Technology (MEXT), Japan; a grant from the JST PRESTO program (T.S.). We thank Ms Yuki Hondoh for her excellent editorial support.

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Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, 464-8601, Japan
Takahiro Shibata, Katsuhiro Takahashi, Yui Matsubara, Emi Inuzuka, Fumie Nakashima & Koji Uchida
PRESTO, Japan Science and Technology Agency (JST), Kawaguchi, Saitama, 332-0012, Japan
Takahiro Shibata
Department of Synthetic Chemistry and Biological Chemistry, Laboratory of Molecular Biology, Graduate School of Engineering, Kyoto University, 615-8510, Kyoto, Japan
Nobuaki Takahashi, Daisuke Kozai & Yasuo Mori

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Takahiro Shibata
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Katsuhiro Takahashi
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Contributions

T.S. and K.U. designed research; T.S., K.T., Y.M., E.I., F.N., N.T. and D.K. performed research; N.T., D.K. and Y.M. contributed new reagents/analytic tools; T.S., Y.M. and K.U. analyzed data; and T.S. and K.U. wrote the paper.

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Shibata, T., Takahashi, K., Matsubara, Y. et al. Identification of a prostaglandin D₂ metabolite as a neuritogenesis enhancer targeting the TRPV1 ion channel. Sci Rep 6, 21261 (2016). https://doi.org/10.1038/srep21261

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Received: 11 October 2015
Accepted: 20 January 2016
Published: 16 February 2016
DOI: https://doi.org/10.1038/srep21261

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