BioMed Research International

BioMed Research International / 2019 / Article

Research Article | Open Access

Volume 2019 |Article ID 3238719 | 10 pages |

N-Methyl-N-Nitrosourea-Induced Photoreceptor Degeneration Is Inhibited by Nicotinamide via the Blockade of Upstream Events before the Phosphorylation of Signalling Proteins

Academic Editor: Arianna Scuteri
Received06 Feb 2019
Revised09 Apr 2019
Accepted15 Apr 2019
Published23 Apr 2019


N-methyl-N-nitrosourea (MNU), a known carcinogen, is generally used in animal models to chemically induce photoreceptor degeneration. It has been reported that nicotinamide (NAM) exerts a protective effect on MNU-induced photoreceptor degeneration. We investigated the molecular mechanisms on MNU-induced photoreceptor degeneration. Intraperitoneal MNU injection (75 mg/kg) in rats induced selective photoreceptor degeneration in 7 days. NAM administration completely inhibited photoreceptor degeneration. Photoreceptor layer abnormality was observed within 6 hours after MNU injection, whereas it was restored in the NAM-treated retina, as detected by optical coherence tomography. One day following MNU administration, phosphorylation of the cell death-associated signalling proteins c-Jun N-terminal kinase (JNK) and p38 mitogen-activated protein kinase (p38) increased, while the apoptosis-related proteins, full-length poly(ADP-ribose) polymerase (PARP) and apoptosis-inducing factor (AIF), were depleted. These changes were not observed in the NAM-treated retinas. Cell survival signalling, such as extracellular signal-regulated kinase (ERK), Akt, and cAMP response element binding protein (CREB) phosphorylation, increased in the MNU- but not in the NAM-treated rat retinas. Increased phosphorylated ERK (p-ERK) levels were observed within 6 hours after MNU administration, suggestive of cell survival signalling activation. This did not occur in NAM-treated retinas. These results indicate that NAM regulates upstream cellular events prior to the activation of cell death-related signalling events, such as JNK and p38 phosphorylation.

1. Introduction

Photoreceptor degenerative diseases, such as retinitis pigmentosa (RP) and age-related macular degeneration (AMD), are a major cause of blindness. Although these two conditions present with similar pathological symptoms with respect to photoreceptor degeneration, they have different causative mechanisms. RP is a genetic disorder with various associated genetic mutations having been identified, mainly in relation to phototransduction pathways ( On the contrary, the development of age-related macular degeneration (AMD) has been mainly associated with various environmental factors, such as smoking, obesity, and vitamin deficiencies with only a few disease-associated mutations having been identified to date [1].

There are various types of photoreceptor degeneration animal models that simulate human pathology and represent important tools for investigating the molecular mechanisms behind RP and AMD and potential treatment targets. Rodent models of photoreceptor degeneration can be classified into two types: rat models, such as P23H [2], S334ter [3], and the one developed by the Royal College of Surgeons [4, 5], that harbour degenerative genetic mutations, and the models of photoreceptor degeneration that are induced by light [6, 7] or chemically [811]. Although various genetic mutations that lead to RP have been identified, they all eventually lead to photoreceptor cell apoptosis [12, 13]. Photoreceptor degeneration induced by light or chemicals is also associated with cellular apoptosis. Apoptosis is the final common pathway in the photoreceptor degeneration though some differences of molecular mechanisms involve in between gene- and light- or chemical-induced photoreceptor degenerations.

Nicotinamide (NAM), a water-soluble B-group vitamin (vitamin B3), exerts protective effects against light- [14, 15] and N-methyl-nitrosourea (MNU)-induced [16] photoreceptor cell apoptosis. A better understanding of the molecular mechanisms involved in the photoreceptor degeneration and NAM-mediated cellular protection will aid in the identification of successful therapeutic approaches against retinal degenerative diseases.

2. Materials and Methods

2.1. Animals

All animal experiments were conducted in accordance with the guidelines of the Animal Experiment Committee of Iwate University, Japan. Male Sprague-Dawley rats were obtained from CLEA Japan, Inc. (Tokyo, Japan). The rats were housed in a 12 h/12 h light/dark cycle with access to water ad libitum.

2.2. Antibodies

Antibodies against extracellular signal-regulated kinase (ERK; Cat No. 4695S), phosphorylated ERK (pERK; Cat No. 9101S), Akt (Cat No. 9272), pAkt (Cat No. 9271L), cAMP response element binding protein (CREB; Cat No. 9197S), and pCREB (Cat No. 9198S) were obtained from Cell Signalling Technology (Tokyo). The anti-glutamine synthetase (GS) antibody (Cat No. MAB302) was obtained from Millipore (Tokyo). The anti-c-Jun N-terminal kinase (JNK; Cat No. sc-571) and phosphorylated JNK (Cat No. sc-6254) were obtained from Santa Cruz Biotechnology. Secondary antibodies against rabbit (Cat No. S3731) and mouse immunoglobulin (Ig) G (IgG; Cat No. S3721) were obtained from Promega (Tokyo).

2.3. MNU and NAM Administration

Rats were administered a single intraperitoneal injection of MNU (Fujifilm Wako Pure Chemical Corp., Osaka, Japan) at a dose of 75 mg/kg body weight. The MNU solution was freshly prepared with sterile physiological saline containing 0.05% acetic acid immediately prior to use and stored at 4°C in the dark. NAM (Nacalai Tesque, Kyoto, Japan) was freshly dissolved in sterile physiological saline and subcutaneously injected at a dose of 1000 mg/kg, 30 minutes prior to MNU administration.

2.4. Histology

Seven days following MNU injection, rats were sacrificed using carbon dioxide, and eyes were enucleated. Eyes were immersed in 4% paraformaldehyde in phosphate buffered saline (PBS) overnight at 4°C and then embedded in paraffin. Serial sections (4 μm) of the whole eye were cut sagittally through the cornea and parallel to the optic nerve, stained against haematoxylin and eosin, and visualised by microscopy (AxioImager A1; Carl Zeiss, Tokyo, Japan).

2.5. Optical Coherence Tomography (OCT)

Rats were anaesthetized by intramuscular injection of ketamine (75 mg/kg) and medetomidine (0.5 mg/kg) and their pupils were dilated with tropicamide (Midrin-P, Santen Co., Ltd., Osaka, Japan). The eye was placed under local anaesthesia using oxybuprocaine (Santen Co., Ltd., Osaka, Japan) and covered with a contact lens. Image acquisition of 1.1 mm length of the rat retina including the optic disk was performed using the line scan mode on an OCT imaging device equipped with a special ordered lens (RS-3000, NIDEK Co., Ltd., Aichi, Japan).

2.6. Western Blot Analysis

Western blot analysis was performed as previously described [17]. Briefly, the retinas were isolated from the eyes 1 and 3 days after MNU or MNU/NAM administration. Proteins were extracted from the samples with a lysis buffer containing 10 mM Tris-HCl (pH 7.5), 1% Triton X-100, 0.5% NP-40, 1 mM EDTA, 150 mM NaCl, 1x protease inhibitor cocktail (Thermo Scientific, Tokyo), and 1x Halt™ phosphatase inhibitor cocktail (Thermo Scientific, Tokyo). The lysate was quantified using a bicinchoninic acid assay (BCA) protein assay kit (Pierce, Rockford, IL). Thirty micrograms of protein was loaded for electrophoresis on 4–15 % Mini-PROTEIN TGX gels (Bio-Rad, Tokyo) and transferred onto a polyvinylidene difluoride (PVDF) membrane. After blocking with Block Ace (DS Pharma Biomedical, Osaka, Japan), the membrane was incubated with the appropriate primary antibody. Following washing, the membrane was incubated with the appropriate alkaline phosphatase-conjugated secondary antibody. Chemiluminescence detection (CDP-Star Detection Reagent; GE Healthcare, Tokyo) was performed according to the standard procedure. Band densities were measured using ImageQuant software (GE Healthcare, Tokyo) and the density of each band was normalised to that of β-actin.

2.7. Immunohistochemistry

Immunohistochemistry was performed on the retina 6 hours and 1 day after MNU or MNU/NAM administration. Paraffin-embedded sections were deparaffinized according to the standard procedure. The sections were treated in citrate buffer (pH 6.0) in a microwave for antigen retrieval. After blocking, the sections were incubated with anti-pERK (dilution 1:200) and GS antibodies as a marker of Müller cells or with a control solution of anti-rabbit and anti-mouse IgGs overnight at 4°C. The sections were then washed three times with PBS containing 0.01% Tween-20 and incubated with Alexa 488- or Alexa 594-conjugated anti-rabbit and anti-mouse IgG solution at room temperature for 1 h. Following washing, the sections were covered with mounting media including 4′,6-diamidino-2-phenylindole (DAPI; VECTASHIELD: Funakoshi, Tokyo).

Statistical Analysis. Statistical analysis was performed using GraphPad Prism 4 (GraphPad software, San Diego, CA). The statistical method used was Tukey’s multiple comparison test.

3. Results

3.1. Histology

Seven days following the intraperitoneal injection of MNU in rats, the outer nuclear layer (ONL) of the retina was not detectable (Figure 1(b)) and photoreceptor degeneration occurred in the whole retina (Figure 1(e)). The MNU-induced degeneration was localised to the ONL and did not affect any of the other retinal layers (Figure 1(d)). On the contrary, the retinal morphology was maintained in NAM-treated animals (Figures 1(c) and 1(e)), similar to that in controls (Figure 1(a)).

3.2. OCT

The early phase of photoreceptor degeneration was evaluated by OCT (Figure 2(a)). The ONL was poorly marginated at 6 hours and 1 day after MNU administration and its thickness significantly increased at 6 hours, but decreased 1 day and 3 days after MNU administration (Figure 2(b)). This ONL thinning induced by MNU was completely blocked by NAM coadministration and the retinal architecture remained unchanged at all time points following NAM treatment.

3.3. Signalling Protein Expression

We sought to evaluate possible expression changes in cell death-related proteins. The phosphorylation of JNK (Figure 3(a); 54 kDa and 48 kDa) and p38 mitogen-activated protein kinase (p38; Figure 3(b)) was significantly increased 1 day after MNU administration. The increase in phosphorylated JNKs (pJNKs) was maintained for 3 days following MNU injection (Figure 3(a)). The expression levels of both poly(ADP-ribose) polymerase (PARP; Figure 3(c)) and the apoptosis-inducing factor (AIF; Figure 3(d)) were decreased after MNU injection. These changes were not observed in the retinas of the animals cotreated with NAM. Next, we examined the expression of various markers of cellular proliferation and survival. The levels of pERK (Figure 4(a)) and pAkt (Figure 4(b)) increased at 1 day, and the pCREB (Figure 4(c)) significantly increased after MNU injection. This MNU-induced protein phosphorylation was completely abolished by NAM coadministration (Figures 4(a), 4(b) and 4(c)).

3.4. Phospho-ERK and GS Immunohistochemistry

Phospho-ERK is a well-known marker of retinal stress with protective effects against retinal injuries [1719]. We evaluated the early cellular responses following MNU administration. Phospho-ERK immunoreactivity (IR) was mainly observed in the inner nuclear layer and partly in the ganglion cell layer in control retinas (Figure 5(a)). However, six hours after MNU injection, pERK IR was mainly localised in the inner limiting membrane and the cell bodies of the inner nuclear layer (Figure 5(b)). Phospho-ERK IR was subsequently detected in the outer nuclear layer and the outer limiting membrane 1 day after MNU administration (Figure 5(c)), with predominant nuclear localisation. GS IR was consistently detected from the inner limiting membrane to the outer limiting membrane in control retinas. GS IR significantly increased 1 day after MNU injection in the outer nuclear layer (Figure 5(c)). When NAM was coadministered, retinal GS IR was slightly increased, as compared to controls, but no changes were observed in pERK levels (Figures 5(d) and 5(e)).

4. Discussion

MNU induced selective retinal photoreceptor degeneration in our rat model. Photoreceptor cell death was completely induced 7 days after MNU injection. OCT revealed photoreceptor layer degeneration as early as 6 hours after MNU injection, indicating the quick activation of the cell death signalling pathway (within 6 hours; Figure 2(a)). However, NAM cotreated retinas were indistinguishable from controls in OCT, as early as 6 hours following administration. We hypothesized that NAM regulates the early phase of photoreceptor degeneration to induce such protective responses against MNU-induced toxicity.

Previously, the JNK/stress-activated protein kinase (SAPK) signalling pathway has been associated with MNU-induced photoreceptor cell death [20] and is known to induce neuronal apoptosis [21, 22]. It has also been reported that the cell death pathway induced by the phosphorylation of p38 plays an important role in light-induced photoreceptor degeneration [23]. We detected MNU-mediated increases in pJNK and p-p38. NAM administration completely abolished these changes (Figures 3(a) and 3(b)) and blocked the MNU-induced photoreceptor degeneration (Figures 1(c), 1(d), and 1(e)). Nevertheless, there is little evidence supporting the direct inhibition of pJNKs or p-p38 by NAM. MNU is an alkylating agent that causes DNA damage [24]. PARP is a known immediate cellular response activator following alkylating agent-induced DNA damage [25]. We demonstrated that MNU leads to the depletion of full-length PARP within a day after its administration (Figure 3(c)) and a subsequent decrease in AIF expression (Figure 3(d)). Uehara N. et al. previously showed the increased PARP in the photoreceptor cells with the same model [20]. Our results seemed to be controversial. However, the MNU concentration used in this study was higher than that they used, indicating that more severe retinal damage was induced in our model. The PARP would be cleaved by the MNU administration, and PARP and AIF were possibly translocated into the nucleus. Subsequently, the full-length PARP and AIF levels in the cellular component were decreased. These results, at least, indicate that the PARP/AIF-associated cell death pathway [26] is involved in MNU-induced photoreceptor degeneration. The nuclear translocation of PARP leads to the depletion of nicotinamide adenine dinucleotide (NAD+) and a decrease in cellular ATP levels, which in turn induce cell death [27]. Taking all these into consideration, it is likely that NAM acts as a NAD+ supplier or a PARP inhibitor as NAM is a precursor for NAD+, a known PARP inhibitor by pretreatment of NAM [28].

To further explore the effects of NAM on cellular signalling, pERK [18], pAkt [29], and pCREB [30] were evaluated with respect to their potential protective effects against retinal injuries. NAM administration did not affect the phosphorylation levels of these signalling proteins (Figures 4(a), 4(b) and 4(c)). On the contrary, MNU administration led to a significant increase in pERK and pAkt, as well as pCREB at later time points. Likewise, we have previously reported that Akt also contributes in photoreceptor survival and maintenance in light-induced photoreceptor degeneration [31]. Increased pERK IR was mainly observed in Müller cells, as early as 6 hours after MNU administration. It has been reported that the phosphorylation of signal transducer and activator of transcription 3 (STAT3) and ERK in Müller cells plays an important role in ciliary neurotrophic factor (CNTF)-mediated photoreceptor rescue in the retinal degeneration [32]. The observed MNU-mediated pERK increase in Müller cells might reflect an intrinsic retinal protection mechanism against injuries.

In this study, we evaluated potential changes in the expression patterns of various signalling proteins following MNU administration. The expression levels of all signalling proteins evaluated in this study were altered within one day after MNU injection. The immunohistochemical evaluation of pERK revealed the activation of self-protective retinal responses within 6 hours of MNU injection, which was not the case in the NAM cotreated retinas.

5. Conclusions

NAM is likely to regulate upstream signalling pathways, such as NAD+ consumption or PARP inhibition, to induce retinal protection against photoreceptor degeneration prior to the phosphorylation of signalling proteins that occurs in later stages. The results of this study provide a better understanding of the molecular mechanisms underlying retinal degeneration and aid in the identification of novel therapeutic targets against photoreceptor degenerations.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that they have no conflicts of interest.


This work was supported by Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology, Japan (Grant Nos. 16H05485, 16K11314, 18K09433, and 17H06330). We express our heartfelt appreciation to Ms. Miho Sato of Laboratory of Visual Neuroscience for preparing the histological sections used in this study.


  1. L. S. Lim, P. Mitchell, J. M. Seddon, F. G. Holz, and T. Y. Wong, “Age-related macular degeneration,” The Lancet, vol. 379, no. 9827, pp. 1728–1738, 2012. View at: Publisher Site | Google Scholar
  2. A. S. Lewin, K. A. Drenser, W. W. Hauswirth et al., “Ribozyme rescue of photoreceptor cells in a transgenic rat model of autosomal dominant retinitis pigmentosa,” Nature Medicine, vol. 4, no. 8, pp. 967–971, 1998. View at: Publisher Site | Google Scholar
  3. C. Liu, Y. Li, M. Peng, A. M. Laties, and R. Wen, “Activation of caspase-3 in the retina of transgenic rats with the rhodopsin mutation S334ter during photoreceptor degeneration,” The Journal of Neuroscience, vol. 19, no. 12, pp. 4778–4785, 1999. View at: Publisher Site | Google Scholar
  4. M. M. LaVail, R. L. Sidman, and C. O. Gerhardt, “Congenic strains of RCS rats with inherited retinal dystrophy,” Journal of Heredity, vol. 66, no. 4, pp. 242–244, 1975. View at: Publisher Site | Google Scholar
  5. H. Tomita, E. Sugano, H. Yawo et al., “Restoration of visual response in aged dystrophic RCS rats using AAV-mediated channelopsin-2 gene transfer,” Investigative Ophthalmology & Visual Science, vol. 48, no. 8, pp. 3821–3826, 2007. View at: Publisher Site | Google Scholar
  6. W. K. Noell and R. Albrecht, “Irreversible effects of visible light on the retina: Role of vitamin A,” Science, vol. 172, no. 3978, pp. 76–80, 1971. View at: Publisher Site | Google Scholar
  7. H. Tomita, Y. Kotake, and R. E. Anderson, “Mechanism of protection from light-induced retinal degeneration by the synthetic antioxidant phenyl-N-tert-butylnitrone,” Investigative Ophthalmology & Visual Science, vol. 46, no. 2, pp. 427–434, 2005. View at: Publisher Site | Google Scholar
  8. E. L. Pautler, K. T. Wheeler, R. E. Sheridan, and B. Hon, “The effect of iodoacetate on the retinal cell DNA in rabbit,” Experimental Eye Research, vol. 14, no. 3, pp. 183–IN1, 1972. View at: Publisher Site | Google Scholar
  9. A. Hara, M. Niwa, H. Aoki et al., “A new model of retinal photoreceptor cell degeneration induced by a chemical hypoxia-mimicking agent, cobalt chloride,” Brain Research, vol. 1109, no. 1, pp. 192–200, 2006. View at: Publisher Site | Google Scholar
  10. K. Yuge, H. Nambu, H. Senzaki et al., “N-methyl-n-nitrosourea-induced photoreceptor apoptosis in the Mouse retina,” In Vivo, vol. 10, no. 5, pp. 483–488, 1996. View at: Google Scholar
  11. H. Isago, E. Sugano, N. Murayama, M. Tamai, and H. Tomita, “Establishment of monocular-limited photoreceptor degeneration models in rabbits,” BMC Ophthalmology, vol. 13, no. 1, 2013. View at: Google Scholar
  12. F. Doonan and T. G. Cotter, “Apoptosis: a potential therapeutic target for retinal degenerations,” Current Neurovascular Research, vol. 1, no. 1, pp. 41–53, 2004. View at: Publisher Site | Google Scholar
  13. G.-Q. Chang, Y. Hao, and F. Wong, “Apoptosis: Final common pathway of photoreceptor death in rd, rds, and mutant mice,” Neuron, vol. 11, no. 4, pp. 595–605, 1993. View at: Publisher Site | Google Scholar
  14. C. T. Sheline, Y. Zhou, and S. Bai, “Light-induced photoreceptor and RPE degeneration involve zinc toxicity and are attenuated by pyruvate, nicotinamide, or cyclic light,” Molecular Vision, vol. 16, pp. 2639–2652, 2010. View at: Google Scholar
  15. S. Bai and C. T. Sheline, “NAD+ maintenance attenuates light induced photoreceptor degeneration,” Experimental Eye Research, vol. 108, pp. 76–83, 2013. View at: Publisher Site | Google Scholar
  16. K. Kiuchi, K. Yoshizawa, N. Shikata, M. Matsumura, and A. Tsubura, “Nicotinamide prevents N-methyl-N-nitrosourea-induced photoreceptor cell apoptosis in Sprague-Dawley rats and C57BL mice,” Experimental Eye Research, vol. 74, no. 3, pp. 383–392, 2002. View at: Publisher Site | Google Scholar
  17. Y. Hayashi, Y. Kitaoka, Y. Munemasa et al., “Neuroprotective effect of 17β-estradiol against N-methyl-D-aspartate- induced retinal neurotoxicity via p-ERK induction,” Journal of Neuroscience Research, vol. 85, no. 2, pp. 386–394, 2007. View at: Publisher Site | Google Scholar
  18. H. Akiyama, T. Nakazawa, M. Shimura, H. Tomita, and M. Tamai, “Presence of mitogen-activated protein kinase in retinal Müller cells and its neuroprotective effect ischemia-reperfusion injury,” NeuroReport, vol. 13, no. 16, pp. 2103–2107, 2002. View at: Publisher Site | Google Scholar
  19. Y. Munemasa, R. Ohtani-Kaneko, Y. Kitaoka et al., “Contribution of mitogen-activated protein kinases to NMDA-induced neurotoxicity in the rat retina,” Brain Research, vol. 1044, no. 2, pp. 227–240, 2005. View at: Publisher Site | Google Scholar
  20. N. Uehara, K. Miki, R. Tsukamoto, Y. Matsuoka, and A. Tsubura, “Nicotinamide blocks N-methyl-N-nitrosourea-induced photoreceptor cell apoptosis in rats through poly (ADP-ribose) polymerase activity and Jun N-terminal kinase/activator protein-1 pathway inhibition,” Experimental Eye Research, vol. 82, no. 3, pp. 488–495, 2006. View at: Publisher Site | Google Scholar
  21. S. Estus, W. J. Zaks, R. S. Freeman, M. Gruda, R. Bravo, and E. M. Johnson Jr., “Altered gene expression in neurons during programmed cell death: Identification of c-jun as necessary for neuronal apoptosis,” The Journal of Cell Biology, vol. 127, no. 6 I, pp. 1717–1727, 1994. View at: Publisher Site | Google Scholar
  22. Z. Xia, M. Dickens, J. Raingeaud, R. J. Davis, and M. E. Greenberg, “Opposing effects of ERK and JNK-p38 MAP kinases on apoptosis,” Science, vol. 270, no. 5240, pp. 1326–1331, 1995. View at: Publisher Site | Google Scholar
  23. L. Yang, X. Zhu, and M. O. Tso, “Role of NF-kappaB and MAPKs in light-induced photoreceptor apoptosis,” Investigative Opthalmology & Visual Science, vol. 48, no. 10, p. 4766, 2007. View at: Publisher Site | Google Scholar
  24. Y. Fujiwara, “Postreplication repair of alkylation damage to DNA of mammalian cells in culture,” Cancer Research, vol. 35, no. 10, pp. 2780–2789, 1975. View at: Google Scholar
  25. A. Bürkle, “Poly(APD-ribosyl)ation, a DNA damage-driven protein modification and regulator of genomic instability,” Cancer Letters, vol. 163, no. 1, pp. 1–5, 2001. View at: Publisher Site | Google Scholar
  26. S. W. Yu, H. Wang, M. F. Poitras et al., “Mediation of poly (ADP-ribose) polymerase-1-dependent cell death by apoptosis-inducing factor,” Science, vol. 297, no. 5579, pp. 259–263, 2002. View at: Publisher Site | Google Scholar
  27. D. A. Carson, S. Seto, D. B. Wasson, and C. J. Carrera, “DNA strand breaks, NAD metabolism, and programmed cell death,” Experimental Cell Research, vol. 164, no. 2, pp. 273–281, 1986. View at: Publisher Site | Google Scholar
  28. M. R. Purnell and W. J. Whish, “Novel inhibitors of poly(ADP-ribose) synthetase,” Biochemical Journal, vol. 185, no. 3, pp. 775–777, 1980. View at: Publisher Site | Google Scholar
  29. T. Nakazawa, M. Shimura, H. Tomita et al., “Intrinsic activation of PI3K/Akt signaling pathway and its neuroprotective effect against retinal injury,” Current Eye Research, vol. 26, no. 1, pp. 55–63, 2003. View at: Publisher Site | Google Scholar
  30. J. Sancho-Pelluz, B. Arango-Gonzalez, S. Kustermann et al., “Photoreceptor cell death mechanisms in inherited retinal degeneration,” Molecular Neurobiology, vol. 38, no. 3, pp. 253–269, 2008. View at: Publisher Site | Google Scholar
  31. G. Li, R. E. Anderson, H. Tomita et al., “Nonredundant role of Akt2 for neuroprotection of rod photoreceptor cells from light-induced cell death,” The Journal of Neuroscience, vol. 27, no. 1, pp. 203–211, 2007. View at: Publisher Site | Google Scholar
  32. K. D. Rhee, S. Nusinowitz, K. Chao, F. Yu, D. Bok, and X.-J. Yang, “CNTF-mediated protection of photoreceptors requires initial activation of the cytokine receptor gp130 in Müller glial cells,” Proceedings of the National Acadamy of Sciences of the United States of America, vol. 110, no. 47, pp. E4520–E4529, 2013. View at: Publisher Site | Google Scholar

Copyright © 2019 Eriko Sugano et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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