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Article

Pituitary Adenylate Cyclase-Activating Polypeptide Protects Corneal Epithelial Cells against UV-B-Induced Apoptosis via ROS/JNK Pathway Inhibition

by
Grazia Maugeri
1,†,
Agata Grazia D’Amico
2,†,
Benedetta Magrì
1,
Elisabetta Pricoco
3,
Cesarina Giallongo
3,
Giuseppe Musumeci
1,
Claudio Bucolo
4,5,
Salvatore Giunta
1 and
Velia D’Agata
1,*
1
Section of Anatomy, Histology and Movement Sciences, Department of Biomedical and Biotechnological Sciences, University of Catania, 95123 Catania, Italy
2
Department of Drug Sciences, University of Catania, 95123 Catania, Italy
3
Department of Medical, Surgical Sciences and Advanced Technologies G.F. Ingrassia, University of Catania, 95123 Catania, Italy
4
Pharmacology Section, Department of Biomedical and Biotechnological Sciences, University of Catania, 95123 Catania, Italy
5
Center for Research in Ocular Pharmacology (CERFO), University of Catania, 95123 Catania, Italy
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Appl. Sci. 2022, 12(7), 3435; https://doi.org/10.3390/app12073435
Submission received: 2 March 2022 / Revised: 25 March 2022 / Accepted: 26 March 2022 / Published: 28 March 2022
(This article belongs to the Special Issue Advances in Neuropeptide Biology)
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Abstract

:
PACAP is widely expressed throughout the body. It exerts a beneficial role in the eye, including the cornea. The corneal epithelium is regularly exposed to diverse types of insults, including ultraviolet B (UV-B) radiation. Previously, we showed the protective role played by PACAP in counteracting UV-B ray insults in human corneal endothelial cells; however, its involvement in corneal epithelium protection against ROS induced by UV-B radiation, and the underlying mechanisms, remain to be determined. Here, we demonstrated that the peptide treatment reduced UV-B-induced ROS generation by playing an anti-apoptotic role via JNK-signaling pathway inhibition. Overall, our results can provide guidance in the therapeutic use of PACAP for the treatment of epithelial corneal damage.
Keywords:
cornea; UV-B; PACAP; ROS; apoptosis; JNK

1. Introduction

Sunlight covers a wide range of the electromagnetic spectrum. Visible light, ultraviolet (UV) rays, and infrared rays reach the Earth’s surface to form terrestrial sunlight. There are three types of UV radiation: UV-A, UV-B, and UV-C. Since UV-C is completely absorbed by the ozone layer, the UV radiation component of terrestrial light consists of ~4% UV-B and ~96% UV-A. The depletion of the ozone layer causes increased human exposure to UV rays. The overexposure of eyes to UV radiation causes harmful effects in the cornea, lens, and retina [1,2,3]. In particular, the cornea, a natural UV-B filter, represents the most exposed structure of the eye to oxidative stress since it absorbs the major part of UV-B at 300 nm [4,5]. The corneal epithelial layer is the most anterior region of the eye, characterized by about six cell layers. It exhibits a smooth, regular surface and consists of nonkeratinized stratified squamous cells. Beneath the epithelium is a fibrous meshwork called Bowman’s layer, which is a condensation of collagen and proteoglycans. The stroma, representing 90% of the corneal thickness, is formed by a collagen-rich central layer in contact with the underlying Descemet’s membrane, which sustains the endothelial cells’ monolayer of posterior cornea [6].
UV-B rays’ dangerous mechanism of action is composed of the aberrant increase in reactive oxygen species (ROS) [7]. The UV-B-induced apoptotic process is regulated by some intracellular signaling, including the JNK pathway mediation of UV-B/ROS-induced apoptosis [8,9,10].
The healthy cornea contains antioxidant molecules involved in the scavenging of ROS [11]. However, when UV-B-induced ROS overwhelmed the corneal antioxidant mechanisms, a reduction in its epithelium thickness was observed [12].
Corneal epithelial damage affects millions of people around the world. Therefore, there is increased interest in discovering new strategies to repair corneal damage and promote proper corneal re-epithelialization.
Pituitary adenylate cyclase-activating polypeptide (PACAP) is a neuropeptide belonging to the secretin and histidine-isoleucine (PHI) superfamily peptides. It exerts multiple activities in a tissue-specific manner by binding to G protein-coupled receptors comprising PAC1, VPAC-1, and VPAC-2 receptors [13,14,15]. Moreover, PACAP promotes the activity-dependent neuroprotective protein (ADNP) [16,17]. Accordingly, NAP, the smallest active element of ADNP, plays a beneficial role, acting in a synergic way with PACAP [18,19,20]. PACAP is widely expressed in the nervous system and shows a neuroprotective role in several neurodegenerative diseases [21,22,23,24,25,26,27,28]. The peptide and its receptors are distributed in different regions of the eye [29,30,31,32]. The effects of the peptide in the visual system were repeatedly described, especially in the retina, where PACAP showed a neuroprotective role against different types of insult [33,34,35,36,37]. In the cornea, PACAP displayed different pleiotropic effects. It decreased corneal endothelial cell loss after transplantation, protected the corneal surface by stimulating tear secretion, and defended the endothelium against UV damage [38,39,40,41,42]. The involvement of PACAP in corneal epithelium protection against UV-B-radiation-induced ROS formation, and the underlying mechanisms therein, remains to be determined. Here, we assessed the expression of PACAP and its receptors in rabbit corneal epithelium. Then, we investigated its role in UV-B-irradiation-induced damage in rabbit corneal epithelial cells. Our results demonstrated that the peptide was strongly expressed in the corneal epithelial layer. Moreover, it affected UV-B-induced ROS generation and JNK pathway activation, counteracting apoptotic cell death induced by UV-B irradiation.

2. Materials and Methods

2.1. Animals

The experiments were performed on male New Zealand White rabbits (n = 12), in accordance with the Association for Research in Vision and Ophthalmology (ARVO) Statement for the Use of Animals in Ophthalmic and Vision Research.

2.2. Immunohistochemistry (IHC) Analysis

PACAP, PAC1R, VPAC1R, and VPAC2R expression in rabbit cornea was analyzed through immunohistochemical analysis [43] using the following primary antibodies: rabbit anti-PACAP (H-76, sc-25439, 1:200), rabbit anti-PAC1 receptor (H-55, sc-30018, 1:300), rabbit anti-VPAC1 (H-130, sc-30019, 1:200), and rabbit anti-VPAC2 (H-50, sc-30020, 1:200) diluted in PBS and 1%BSA. The immunoreaction was observed using 3,3′-diaminobenzidine solution. The samples were lightly counterstained with hematoxylin.

2.3. Cell Cultures

Experiments were performed on rabbit corneal cell lines (Statens Seruminstitut Rabbit Cornea (SIRC) treated with vehicle (CTRL), or in the presence of PACAP (100 nM)) and subjected to 30 s UV-B rays at a dose of 20 mJ/cm2 through UVllink (UVItec, Cambridge, UK).

2.4. Cell Viability Assay

Cell viability was investigated through an MTT assay (11465007001, Roche Diagnostics, Indianapolis, IN, USA) as previously demonstrated [43]. The absorbance was measured with the a Varioskan reader (Thermo Fisher Scientific, Waltham, MA, USA).

2.5. Assessment of Cell Death Using Fluorescence Microscope

The SIRC cells were cultured at a density of 4 × 103 cells/well in 500 μL of the culture medium. The day after, cells were incubated in the control medium (CTRL) in the presence of 100 nM PACAP, or exposed to 30s UV-B-irradiation (20 mJ/cm2) in the presence or absence of 100 nM PACAP. After 24 h, cells were incubated with 0.4 μg/mL Hoechst 33342 dye as previously described [43]. Two investigators carried out the counting of apoptotic nuclei independently.

2.6. Western Blot Analysis

Western blot analysis was performed as described by D’Amico et al. [18]. Membranes were incubated with the following primary antibodies: rabbit anti-PACAP (1:500); rabbit anti-PAC1 receptor (1:1000); rabbit anti-VPAC1 (1:500); rabbit anti-VPAC2 (1:500); mouse anti-Bcl2 (sc-509, 1:200); mouse anti-Bax (sc-20067, 1:200); rabbit anti-JNK (sc-571; 1:200); mouse anti-p-JNK (sc-6254, 1:200), and rabbit anti-β-tubulin, which was used as a loading control (sc-9104, 1:500). Densitometric analyses were performed using ImageJ software (last access 22 March 2022).

2.7. Detection of ROS

To quantitatively assess the ROS production, the DCFDA/H2DCFDA assay (ab113851, Abcam, Cambridge, UK) was performed on SIRC cells cultured at a density of 1 × 104 cells/well for 24 h. ROS concentration was measured with the Varioskan reader.
Mitochondrial-derived ROS (mtROS) detection was assessed using the MitoSOX™ Red Mitochondrial Superoxide Indicator. The MACSQuant Analyzer 10 was used to measure mtROS.

2.8. Statistical Analysis

Data reported mean ± SEM. One-way analysis of variance was performed, and statistical significance was evaluated by the Tukey–Kramer post hoc test (p ≤ 0.05).

3. Results

3.1. Detection of PACAP, PAC1R and VPACRs in Corneal Epithelium

The expression of PACAP and its receptors in the eye has been widely reported [43,44,45]. PACAP-positive cells have been detected in the corneal endothelial layer [39,42], and PACAP-IR has been found in nerve terminals running through the stroma [29]. Here, we investigated the endogenous expression of PACAP and its receptors in the cornea of rabbits (n = 12) through IHC analysis. We found the positive expression of PACAP and its receptors in all examined sections. In particular, PACAP was expressed through the entire height of the corneal epithelium in all examined zones but showed higher signal intensity in the cells laying on the basement membrane. Weak expression of the peptide was detected in the stroma (Figure 1Aa). The labeling of PAC1R resembled the localization of PACAP, as the receptor was clearly expressed in both the basal epithelial layer as well as in the stroma (Figure 1Ab). The VPAC1 and VPAC2 receptors were found in all epithelial cell layers. The signal intensity of VPACRs differed in the stroma, where VPAC1R was highly expressed in comparison to VPAC2R (Figure 1Ac–d). The endogenous expression of PACAP, PAC1R, VPAC1R, and VPAC2R was also investigated in rabbit corneal epithelial cells. As shown in Figure 1B, the peptide and its receptors are expressed in SIRC cells.

3.2. Effect of PACAP Treatment on UV-B-Induced Apoptotic Cell Death

Studies showed that UV-B insult injures the cornea by causing apoptotic cell death [46,47,48,49]. Here, it was found that UV-B rays (20 mJ/cm2) significantly decreased cell viability in a time-dependent manner starting from 24 h following UV-B insult (**** p < 0.0001 vs. CTRL) (Figure 2A). Therefore, we chose this time point to investigate the effect of PACAP treatment on UV-B-exposed cells’ viability. As shown in Figure 2B, the peptide increased cell viability when compared with the UV-B group, confirming its protective role (#### p < 0.0001 vs. UV-B).
To further analyze the protective effect of PACAP on UV-B-mediated cell damage, the nuclei of SIRC cells exposed to UV-B were stained with Hoechst 33342. As shown in Figure 3, significant fragmentation and nuclear condensation, characteristic of apoptotic death, was observed in the UV-B-exposed group, in comparison with the control (**** p <0.0001 vs. CTRL). When the cells were treated with PACAP, the number of apoptotic nuclei in the UV-B-exposed cells was markedly reduced (#### p < 0.0001 vs. UV-B).
Considering that apoptotic cell death is regulated by Bcl-2 family proteins, key mediators, we investigated the role of PACAP to modulate the expression of the anti-apoptotic protein, Bcl-2, and pro-apoptotic protein, Bax. As shown in Figure 4, PACAP markedly increased the expression of Bcl-2 protein in UV-B-exposed cells (# p < 0.05 vs. UV-B). In contrast, the expression levels of the pro-apoptotic protein Bax, which drastically increased following UV-B exposure (**** p < 0.0001 vs. CTRL), were significantly downregulated by treatment with the peptide (#### p < 0.0001 vs. UV-B). These results confirmed that PACAP inhibits corneal epithelial cells’ apoptotic death activated by UV-B ray exposure.

3.3. PACAP Decreased the Production of ROS Induced by UV-B Rays on Corneal Epithelial Cells via the JNK Pathway Inhibition

Considering that corneal injuries induced by UV-B are predominantly triggered by oxidative stress [50,51], we analyzed the time-course of ROS generation in corneal epithelial cells after UV-B radiation exposure (20 mJ/cm2) by using the DCFDA assay and the Mito-SOX™ Red fluorescence indicator (Figure 5A,B). The cellular ROS production significantly increased in a time-dependent manner starting from 30 s after UV-B irradiation (**** p < 0.0001 vs. CTRL). Treatment with the peptide significantly counteracted ROS formation starting from one hour after UV-B irradiation (20 mJ/cm2 for 30 s) (Figure 5A). Similarly, a time-dependent increase in mitochondrial ROS formation was observed in cells exposed to UV-B irradiation (**** p < 0.0001 vs. CTRL) (Figure 5B). PACAP treatment strongly reduced UV-B-induced mitochondrial ROS formation at all time points considered.
The literature shows that JNK activation is crucial as it represents the signaling pathway downstream of ROS, leading to apoptotic cell death [50,51]. Therefore, to investigate whether this pathway was linked to UV-B ROS-generation-induced cell death, we first measured the phosphorylated JNK (p-JNK) and total JNK at different time points in cells exposed to UV-B rays, through Western blot analysis. The significant activation of JNK was observed starting from 6 h after UV-B irradiation (**** p < 0.0001 vs. CTRL) (Figure 6A), before assessing the PACAP effect on JNK phosphorylation after 6 h from UV-B insult. As observed in Figure 6B, PACAP treatment strongly reduced p-JNK (#### p < 0.0001 vs. UV-B).

4. Discussion

Ozone layer depletion causes a continuous and more pronounced exposure of the cornea to UV-B rays, which provokes the formation of ROS, including superoxide anion (O2−), hydrogen peroxide (H2O2), and hydroxyl (OH·) radicals. ROS overproduction is associated with different ocular disorders, e.g., cataracts, age-related macular degeneration, glaucoma, inflammation, and corneal alteration [52]. The human eye has several defense mechanisms, including enzymes and antioxidants (e.g., glutathione peroxidase and ascorbic acid) which protect ocular tissues against oxidative injury [53]. However, these are gradually reduced during UV-B irradiation, as opposed to the pro-oxidant enzymes such as xanthine oxidoreductase/xanthine oxidase, which remain at normal values or may even increase.
Many works demonstrated that PACAP exerts an important antioxidant and anti-apoptotic role in different cell types throughout the body [54,55,56]. The present study aimed to investigate the role of the peptide in corneal epithelium protection against UV-B radiation and elucidate the associated molecular mechanisms (Figure 7).
We first analyzed the endogenous expression of PACAP and its receptors in the corneal epithelium. PACAP and PAC1R are found in the rabbit corneal epithelium, specifically in basal cells. VPAC1R and VPAC2R were observed in the entire length of the epithelial layers as well as in the stroma (Figure 1).
To explore the role of PACAP in corneal epithelium, we exposed SIRC cells to UV-B insult. It is widely recognized that UV-B radiation leads to corneal cell apoptotic death due to DNA damage and the production of ROS [47,48,49]. Here, we confirmed this evidentially, as well as demonstrating that treatment with PACAP significantly increased cell viability (Figure 2B) by preventing UV-B-induced apoptotic death (Figure 3). These data were also confirmed by the analysis of proteins Bcl-2/Bax. High levels of Bax protein were detected in the UV-B group (Figure 4), consistent with previous findings showing that UV-B irradiation increased pro-apoptotic Bax gene expression [54,55]. PACAP treatment significantly increased Bcl-2 protein expression and reduced the pro-apoptotic protein Bax in SIRC cells exposed to UV-B insult, confirming the anti-apoptotic mechanism involved in the protective effect of PACAP against UV-B-induced corneal epithelial damage.
As previously shown, UV-B irradiation induced ROS formation on the ocular surface [56], leading to DNA and mitochondrial damage, mitochondrial membrane depolarization, lipid peroxidation, and protein denaturation [56]. Here, we showed that UV-B insult induced a time-dependent increase in cellular ROS formation, as well as mitochondrial superoxide anion generation, whereas treatment with PACAP significantly reversed these changes (Figure 5A,B). Therefore, PACAP reduced oxidative stress directly through ROS scavenging and protected cells against UV-B radiation through the modulation of the JNK pathway. ROS induces different pathways, including JNK [9], which serves a central role in the apoptotic event [57,58]. Accordingly, we showed that UV-B insult triggers the activation of the JNK pathway, whereas PACAP treatment counteracts its phosphorylation (Figure 6). Correspondingly, previous findings show that PACAP exerts important cytoprotective effects by suppressing the JNK pathway [59,60].
The therapeutic use of PACAP has some limitations due to its poor in vivo stability. In fact, the peptide is degraded by different peptidases in the blood, including the dipeptidyl peptidase IV, which binds PACAP 1-38 to the PAC1 receptor antagonist, and other enzymes such as carboxypeptidase, endopeptidase, and prohormone convertase [61,62]. However, a recent paper showed that PACAP in a water solution can be preserved for relatively long periods of time [62]. Consequently, the present findings, along with the aforementioned studies, demonstrate that PACAP protects the cornea from UV-B damage, encouraging new investigations. In fact, the main limitation of the present work is that it was executed on immortalized corneal epithelial cells that fail to perfectly replicate the complex architecture and organization of the epithelial corneal layer. Therefore, further in vivo studies will be needed to confirm the corneal protective effects displayed by PACAP.

Author Contributions

Conceptualization, G.M. (Grazia Maugeri) and V.D.; Funding Acquisition, G.M. (Grazia Maugeri) and S.G.; Investigation, G.M. (Grazia Maugeri), A.G.D., B.M., E.P. and C.G.; Resources, S.G., C.B. and G.M. (Giuseppe Musumeci); Visualization, C.B.; Writing, Grazia Maugeri, A.G.D. and V.D.; Supervision, V.D. All authors have read and agreed to the published version of the manuscript.

Funding

PIAno di inCEntivi per la RIcerca di Ateneo 2020/2022 Linea di Intervento 3 Starting. Grant “REPAIR” and Linea Intervento 2 “NanoRET”, University of Catania, Italy; Italian Ministry of University and Research (MUR) (grant number PRIN 2017TSHBXZ_003).

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Institution of Animal Care and Use Committee of Catania University (#303).

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available in article.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. (A) Immunodetection of PACAP (a), PAC1R (b), VPAC1R (c), and VPAC2R (d) in rabbit cornea: (1) epithelium, (2) Bowman’s membrane, (3) stroma. Original magnification ×200, scale bar: 20 μm. (B) Representative immunoblot of PACAP and its receptors in SIRC cells.
Figure 1. (A) Immunodetection of PACAP (a), PAC1R (b), VPAC1R (c), and VPAC2R (d) in rabbit cornea: (1) epithelium, (2) Bowman’s membrane, (3) stroma. Original magnification ×200, scale bar: 20 μm. (B) Representative immunoblot of PACAP and its receptors in SIRC cells.
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Figure 2. (A) MTT assay performed on SIRC cells at different time points. (B) Cell viability evaluated at 24 h on different experimental groups. **** p < 0.0001 vs. CTRL; #### p < 0.0001 vs. UV-B.
Figure 2. (A) MTT assay performed on SIRC cells at different time points. (B) Cell viability evaluated at 24 h on different experimental groups. **** p < 0.0001 vs. CTRL; #### p < 0.0001 vs. UV-B.
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Figure 3. Assessment of cell death using Hoechst 33342 staining. Scale bar: 20 μm. **** p < 0.0001 vs. CTRL; #### p < 0.0001 vs. UV-B.
Figure 3. Assessment of cell death using Hoechst 33342 staining. Scale bar: 20 μm. **** p < 0.0001 vs. CTRL; #### p < 0.0001 vs. UV-B.
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Figure 4. Expression of Bcl-2 and Bax proteins at 24 h in different experimental groups. **** p < 0.0001 vs. CTRL; # p < 0.05, and #### p < 0.0001 vs. UV-B.
Figure 4. Expression of Bcl-2 and Bax proteins at 24 h in different experimental groups. **** p < 0.0001 vs. CTRL; # p < 0.05, and #### p < 0.0001 vs. UV-B.
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Figure 5. Detection of intracellular ROS production in SIRC cells after UV-B exposure through DCFDA (A), or MitoSOX™ Red (B). **** p < 0.0001 vs. CTRL; #### p < 0.0001 vs. UV-B 30′; §§§ p < 0.001 and §§§§ p < 0.0001 vs. UV-B 1 h; ° p < 0.05 and °°°° p < 0.0001 vs. UV-B 6 h; ++ p < 0.01 and ++++ p < 0.0001 vs. UV-B 24 h.
Figure 5. Detection of intracellular ROS production in SIRC cells after UV-B exposure through DCFDA (A), or MitoSOX™ Red (B). **** p < 0.0001 vs. CTRL; #### p < 0.0001 vs. UV-B 30′; §§§ p < 0.001 and §§§§ p < 0.0001 vs. UV-B 1 h; ° p < 0.05 and °°°° p < 0.0001 vs. UV-B 6 h; ++ p < 0.01 and ++++ p < 0.0001 vs. UV-B 24 h.
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Figure 6. (A) JNK activation induced by UV-B at different time points. (B) JNK phosphorylation expression at 6 h. **** p < 0.0001 vs. CTRL; #### p < 0.0001 vs. UV-B.
Figure 6. (A) JNK activation induced by UV-B at different time points. (B) JNK phosphorylation expression at 6 h. **** p < 0.0001 vs. CTRL; #### p < 0.0001 vs. UV-B.
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Figure 7. Schematic representation of the protective effects exerted by PACAP on corneal epithelium against UV-B-induced apoptosis via ROS/JNK pathway inhibition.
Figure 7. Schematic representation of the protective effects exerted by PACAP on corneal epithelium against UV-B-induced apoptosis via ROS/JNK pathway inhibition.
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Maugeri, G.; D’Amico, A.G.; Magrì, B.; Pricoco, E.; Giallongo, C.; Musumeci, G.; Bucolo, C.; Giunta, S.; D’Agata, V. Pituitary Adenylate Cyclase-Activating Polypeptide Protects Corneal Epithelial Cells against UV-B-Induced Apoptosis via ROS/JNK Pathway Inhibition. Appl. Sci. 2022, 12, 3435. https://doi.org/10.3390/app12073435

AMA Style

Maugeri G, D’Amico AG, Magrì B, Pricoco E, Giallongo C, Musumeci G, Bucolo C, Giunta S, D’Agata V. Pituitary Adenylate Cyclase-Activating Polypeptide Protects Corneal Epithelial Cells against UV-B-Induced Apoptosis via ROS/JNK Pathway Inhibition. Applied Sciences. 2022; 12(7):3435. https://doi.org/10.3390/app12073435

Chicago/Turabian Style

Maugeri, Grazia, Agata Grazia D’Amico, Benedetta Magrì, Elisabetta Pricoco, Cesarina Giallongo, Giuseppe Musumeci, Claudio Bucolo, Salvatore Giunta, and Velia D’Agata. 2022. "Pituitary Adenylate Cyclase-Activating Polypeptide Protects Corneal Epithelial Cells against UV-B-Induced Apoptosis via ROS/JNK Pathway Inhibition" Applied Sciences 12, no. 7: 3435. https://doi.org/10.3390/app12073435

APA Style

Maugeri, G., D’Amico, A. G., Magrì, B., Pricoco, E., Giallongo, C., Musumeci, G., Bucolo, C., Giunta, S., & D’Agata, V. (2022). Pituitary Adenylate Cyclase-Activating Polypeptide Protects Corneal Epithelial Cells against UV-B-Induced Apoptosis via ROS/JNK Pathway Inhibition. Applied Sciences, 12(7), 3435. https://doi.org/10.3390/app12073435

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