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Pituitary Adenylyl Cyclase-activating Polypeptide Prevents Induced Cell Death in Retinal Tissue through Activation of Cyclic AMP-dependent Protein Kinase
2002; Elsevier BV; Volume: 277; Issue: 18 Linguagem: Inglês
10.1074/jbc.m110106200
ISSN1083-351X
AutoresMariana S. Silveira, Mariana R. Costa, Marcelo T. Bozza, Rafael Linden,
Tópico(s)Peptidase Inhibition and Analysis
ResumoMultiple neuroactive substances are secreted by neurons and/or glial cells and modulate the sensitivity to cell death. In the developing retina, it has been shown that increased intracellular levels of cAMP protect cells from degeneration. We tested the hypothesis that the neuroactive peptide pituitary adenylyl cyclase-activating polypeptide (PACAP) has neuroprotective effects upon the developing rat retina. PACAP38 prevented anisomycin-induced cell death in the neuroblastic layer (NBL) of retinal explants, and complete inhibition of induced cell death was obtained with 1 nm. A similar protective effect was observed with PACAP27 and with the specific PAC1 receptor agonist maxadilan but not with glucagon. Photoreceptor cell death induced by thapsigargin was also prevented by PACAP38. The neuroprotective effect of PACAP38 upon the NBL could be reverted by the competitive PACAP receptor antagonist PACAP6–38 and by the specific PAC1 receptor antagonist Maxd.4. Molecular and immunohistochemical analysis demonstrated PAC1 receptors, and treatment with PACAP38 induced phospho-cAMP-response element-binding protein immunoreactivity in the anisomycin-sensitive undifferentiated postmitotic cells within the NBL. PACAP38 produced an increase in cAMP but not inositol triphosphate, and treatment with the cAMP-dependent protein kinase inhibitorRp-cAMPS blocked the protective effect of PACAP38. The results indicate that activation of PAC1 receptors by PACAP38 modulates cell death in the developing retina through the intracellular cAMP/cAMP-dependent protein kinase pathway. Multiple neuroactive substances are secreted by neurons and/or glial cells and modulate the sensitivity to cell death. In the developing retina, it has been shown that increased intracellular levels of cAMP protect cells from degeneration. We tested the hypothesis that the neuroactive peptide pituitary adenylyl cyclase-activating polypeptide (PACAP) has neuroprotective effects upon the developing rat retina. PACAP38 prevented anisomycin-induced cell death in the neuroblastic layer (NBL) of retinal explants, and complete inhibition of induced cell death was obtained with 1 nm. A similar protective effect was observed with PACAP27 and with the specific PAC1 receptor agonist maxadilan but not with glucagon. Photoreceptor cell death induced by thapsigargin was also prevented by PACAP38. The neuroprotective effect of PACAP38 upon the NBL could be reverted by the competitive PACAP receptor antagonist PACAP6–38 and by the specific PAC1 receptor antagonist Maxd.4. Molecular and immunohistochemical analysis demonstrated PAC1 receptors, and treatment with PACAP38 induced phospho-cAMP-response element-binding protein immunoreactivity in the anisomycin-sensitive undifferentiated postmitotic cells within the NBL. PACAP38 produced an increase in cAMP but not inositol triphosphate, and treatment with the cAMP-dependent protein kinase inhibitorRp-cAMPS blocked the protective effect of PACAP38. The results indicate that activation of PAC1 receptors by PACAP38 modulates cell death in the developing retina through the intracellular cAMP/cAMP-dependent protein kinase pathway. neuroblastic layer pituitary adenylyl cyclase-activating polypeptide cAMP-dependent protein kinase cAMP-response element-binding protein vasoactive intestinal peptide terminal deoxynucleotidyltransferase-mediated dUTP nick end-labeling inositol triphosphate 5-bromo-2′-deoxyuridine adenosine 3′,5′-cyclic monophosphorothioate 6-Cl-PB, (±)-6-chloro-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-benzazepine postnatal Developmental cell death is a major event in neurogenesis, controlled by various secreted molecules, many of which play distinct roles in the mature nervous system. Identification of neuroprotective molecules is relevant both for embryogenesis as well as for studies of neurodegenerative diseases because the modes of cell death and many upstream control pathways appear to be conserved among both normal and pathological conditions (1Lockshin R.A. Zakeri Z.F. J. Gerontol. 1990; 45: B135-B140Crossref PubMed Scopus (81) Google Scholar). Classically, neuroprotection is attributed to neurotrophic proteins such as the neurotrophin family of growth factors (for a review, see Refs. 2Hefti F. Annu. Rev. Pharmacol. Toxicol. 1997; 37: 239-267Crossref PubMed Scopus (162) Google Scholar and 3Gu P. Casaccia-Bonnefil C. Chao M.V. Adv. Exp. Med. Biol. 1999; 468: 275-282Crossref PubMed Google Scholar), but many lines of evidence support the involvement of both classical neurotransmitters and neuropeptides in the control of cell death (4Kater S.B. Lipton A.S. Trends Neurosci. 1995; 18: 71-72Abstract Full Text PDF PubMed Scopus (26) Google Scholar, 5Journot L. Villalba M. Bockaert J. Ann. N. Y. Acad. Sci. 1998; 865: 100-110Crossref PubMed Scopus (33) Google Scholar). The retina of newborn rats is composed of two cellular strata separated by the inner plexiform layer. The innermost cellular stratum is the ganglion cell layer, the long axons of which form the optic nerve. On the opposite side of the inner plexiform layer, the outer cellular stratum contains a few rows of early developing amacrine cells in the inner nuclear layer. The remainder of the outer stratum constitutes the neuroblastic layer (NBL),1 which corresponds to the ventricular zone, in which high proliferative activity persists postnatally (6Alexiades M.R. Cepko C.L. Development. 1997; 124: 1119-1131PubMed Google Scholar). In addition to the proliferating neuroblasts, the NBL in newborn rats contains undifferentiated postmitotic cells that are migrating toward their final destinations across the depth of the retinal tissue as well as a row of regularly spaced, early differentiating horizontal cells. At about 4 days after birth, the outer plexiform layer separates the neuroblastic layer from an outer nuclear layer, which progressively concentrates at the outermost retinal tier the cell bodies of the photoreceptors (7Craft J.L. Fulton A.B. Silver J. Albert D.M. Curr. Eye Res. 1982; 2: 295-299Crossref PubMed Scopus (15) Google Scholar). More than 95% of the latter are of the rhodopsin-containing rod type. Evolution into the multilayered structure of the mature retina is accompanied by a wave of naturally occurring cell death that shapes the final cell populations, similar to other areas of the central nervous system. The period of naturally occurring cell death is closely associated with both neuronal differentiation and the encounter of both target and afferent partners and tends to precede the establishment of the mature morphology of synaptic connections. Reproducible timing and a close relation with the stage of maturation of the various cell populations imply tight regulation of sensitivity to programmed cell death. Indeed, a host of extracellular molecules that affect programmed cell death were identified in experimental models of chemically or otherwise induced cell death in the developing retina (8Arauéjo E.G. Linden R. Eur. J. Neurosci. 1993; 5: 1181-1188Crossref PubMed Scopus (63) Google Scholar, 9Rocha M. Martins R.A.P. Linden R. Brain Res. 1999; 827: 79-92Crossref PubMed Scopus (55) Google Scholar, 10Ary-Pires R. Nakatani M. Rehen S.K. Linden R. Int. J. Dev. Neurosci. 1997; 15: 239-255Crossref PubMed Scopus (24) Google Scholar, 11Guimaraes C. Assreuy J. Linden R. J. Neurochem. 2001; 76: 1233-1241Crossref PubMed Scopus (19) Google Scholar, 12Cui Q. Harvey A.R. Neuroreport. 2000; 11: 3921-3924Crossref PubMed Scopus (16) Google Scholar). Among those, we showed that dopamine protects the postmitotic undifferentiated retinal cells from degeneration induced by inhibition of protein synthesis through an increase in intracellular cAMP (13De Varella M.H. Mello F.G. Linden R. J. Neurochem. 1999; 73: 485-492Crossref PubMed Scopus (43) Google Scholar). The pituitary adenylyl cyclase-activating polypeptide (PACAP) is a neuroactive peptide of the secretin/glucagon/vasoactive intestinal peptide (VIP) superfamily. PACAP was first isolated for its ability to induce the production of cAMP in the anterior pituitary of rats (14Miyata A. Arimura A. Dahl R.R. Minamino N. Uehara A. Culler M.D. Jiang L. Coy D.H. Biochem. Biophys. Res. Commun. 1989; 164: 567-574Crossref PubMed Scopus (1711) Google Scholar). The PACAP precursor molecule is post-translationally processed into two biologically active products, PACAP38 and PACAP27 (14Miyata A. Arimura A. Dahl R.R. Minamino N. Uehara A. Culler M.D. Jiang L. Coy D.H. Biochem. Biophys. Res. Commun. 1989; 164: 567-574Crossref PubMed Scopus (1711) Google Scholar, 15Miyata A. Jiang L. Dahl R.R. Kitada C. Kubo K. Fujino M. Minamino N. Arimura A. Biochem. Biophys. Res. Commun. 1990; 170: 643-648Crossref PubMed Scopus (876) Google Scholar), which share high amino acid homology with VIP. In the nervous system, PACAP has been associated with proliferation (16Lu N. Zhou R. DiCicco-Bloom E. J. Neurosci. Res. 1998; 53: 651-662Crossref PubMed Scopus (79) Google Scholar), differentiation (17Lu N. DiCicco-Bloom E. Proc. Natl. Acad. Sci. U. S. A. 1997; 94: 3357-3362Crossref PubMed Scopus (167) Google Scholar,18Lu J. Suh N. Nicot A. Tatsuno I. Di DiCicco-Bloom E. Nat. Neurosci. 2001; 4: 1-2Crossref PubMed Scopus (3) Google Scholar), and cell survival (5Journot L. Villalba M. Bockaert J. Ann. N. Y. Acad. Sci. 1998; 865: 100-110Crossref PubMed Scopus (33) Google Scholar, 19Gonzalez B.J. Basille M. Vaudry D. Fournier A. Vaudry H. Neuroscience. 1997; 78: 419-430Crossref PubMed Scopus (163) Google Scholar, 21Vaudry D. Gonzalez B.J. Basille M. Fournier A. Vaudry H. Proc. Natl. Acad. Sci. U. S. A. 1999; 96: 9415-9420Crossref PubMed Scopus (140) Google Scholar, 22Tabuchi A. Koizumi M. Nakatsubo J. Yaguchi T. Tsuda M. Neurosci. Res. 2001; 36: 85-93Crossref Scopus (40) Google Scholar). Both PACAP and VIP act on receptors described pharmacologically as either type I (PACAP-specific) or type II (non-discriminative) (23Ishihara T. Shigemoto R. Mori K. Takahashi K. Nagata S. Neuron. 1992; 8: 811-819Abstract Full Text PDF PubMed Scopus (733) Google Scholar, 24Spengler D. Waeber C. Pantaloni C. Holsber F. Bockaert J. Seeburg P.H. Journot L. Nature. 1993; 356: 170-175Google Scholar, 25Lutz E.M. Sheward W.J. West K.M. Morrow J.A. Fink G. Harmar A.I. FEBS Lett. 1993; 334: 3-8Crossref PubMed Scopus (487) Google Scholar). Molecular cloning revealed three distinct receptors: PAC1, VPAC1, and VPAC2, of which the PAC1 receptor is selective for PACAP. The present study was designed to examine the effects of PACAP on induced cell death in the developing retina and the mechanisms that mediate its effects on retinal cell survival. Culture medium, fetal calf serum, and Trizol were from Invitrogen. Anisomycin was from Sigma. PACAP38 was from Peninsula Laboratories, San Carlos, CA. U73122, verapamil, nifedipine, and Rp-cAMPS were from Calbiochem. First-strand cDNA kit was from Amersham Biosciences. Maxadilan and Maxd.4 were kindly provided by Dr. Ethan Lerner from Harvard Medical School. Apoptag Tunel kit was from Intergen, Purchase, NY, and the antibody CM1 for activated caspase-3 was kindly provided by Dr. Anu Srinivasan (Idun Pharmaceuticals). All experimental procedures with animals were approved by the Committee on Animal Experimentation of the Institute of Biophysics Carlos Chagas Filho, based on the currently accepted international rules. Retinae were excised from the eyes of either 2-day-old or 6-day-old Lister hooded rat pups killed by instantaneous decapitation, and explants of ∼1 mm2 were maintained in an orbital shaker at 70–90 rpm in basal medium of Eagle supplemented with 5% fetal calf serum and 20 mm HEPES at pH 7.4 for 22 h except when noted. At the end of each experiment, the explants were fixed by immersion in 4% paraformaldehyde in sodium phosphate buffer, pH 7.4, for 2 h and then cryoprotected in 30% sucrose in phosphate buffer. Transverse 10-μm-thick sections through the retinal tissue were cut at −20 °C in a cryostat and stained either with neutral red (postnatal day 2 (P2) explants) or with a monoclonal antibody to the rod photoreceptor pigment rhodopsin (P6). Although there is a clear centro-peripheral gradient of development in the rat retina, previous work showed that responses to the induction of cell death upon either a given cell type or cells at a given stage of differentiation (i.e. either proliferating or postmitotic) are the same in both central and peripheral locations (26Rehen S.K. Neves D.D.C. Fragel-Madeira L. Britto L.R.G. Linden R. Eur. J. Neurosci. 1999; 11: 4349-4356Crossref PubMed Scopus (28) Google Scholar). In the current experiments, usually eight explants were cut from each retina, and explants from at least six distinct retinae were pooled irrespective of retinal location in each experimental group. Dead cells were recognized by their condensed homogeneously and deeply stained chromatin among normal neighboring cells when explant sections were stained with neutral red (27Rehen S.K. Varella M.H. Freitas F.G. Moraes M.O. Linden R. Development. 1996; 122: 1439-1448PubMed Google Scholar). Counts of pyknotic profiles were made at ×1000 magnification under oil immersion in three random fields of 0.0148 mm2 within the neuroblastic layer, and at least three randomly selected explants were analyzed for each group in each experiment. Photoreceptor cell death was identified by the round and condensed morphology of rhodopsin-positive profiles within the outer nuclear layer, wherein normal photoreceptors present an elongated shape at that age (33Chiarini L.B. Freitas F.G. Petrs-Silva H. Linden R. Cell Death Differ. 2000; 7: 272-281Crossref PubMed Scopus (34) Google Scholar). Counts were made at ×1000 magnification under oil immersion in three random fields of 0.0074 mm2 within the outer nuclear layer. At least three randomly selected explants were analyzed for each group in each of two independent experiments. Analysis of variance followed by planned comparisons using Duncan's multiple range test were done with an SPSSPC statistical package. The apoptotic form of cell death was selectively examined in some experiments by staining dead cell profiles with either the TUNEL technique using an Apoptag kit or the antibody CM1, which recognizes the activated form of caspase-3 (28Namura S. Zhu J. Fink K. Endres M. Srinivasan A. Tomaselli K.J. Yvan J. Moskowitz M.A. J. Neurosci. 1998; 18: 3659-3688Crossref PubMed Google Scholar). Total RNA was prepared from the retinas of rat pups at postnatal day 2 (P2) using Trizol (Invitrogen), and cDNA was synthesized and amplified using primers (5′-CACAGTATTCGCCTTCTCTCC-3′, 5′-GCCTATCCCTATCTCTCTCTT-3′) that recognize a region from the carboxyl-terminal intracellular domain common to all PAC1 receptor isoforms (29Braas K.M. May V. J. Biol. Chem. 1999; 274: 27702-27710Abstract Full Text Full Text PDF PubMed Scopus (108) Google Scholar). Newborn rats (postnatal day 1) were anesthetized by hypothermia and received a series of three 5-bromo-2′-deoxyuridine (BrdUrd) injections (60 mg/kg of body weight at 0, 5, and 19 h) to label all proliferating cells, and experiments were performed 1 h after the last injection (26Rehen S.K. Neves D.D.C. Fragel-Madeira L. Britto L.R.G. Linden R. Eur. J. Neurosci. 1999; 11: 4349-4356Crossref PubMed Scopus (28) Google Scholar). To locate the PAC1 receptor within retinal tissue, sections through the eye were immunostained using an affinity-purified rabbit anti-PAC1 antibody kindly provided by Dr. Victor May (University of Vermont, Vermont, ME) (29Braas K.M. May V. J. Biol. Chem. 1999; 274: 27702-27710Abstract Full Text Full Text PDF PubMed Scopus (108) Google Scholar). For phospho-CREB immunohistochemistry, retinal explants from rats injected with BrdUrd were maintained in vitro for various intervals either with or without PACAP38, and sections were processed with a rabbit anti-phospho-CREB antibody (Cell Signaling Technology, Inc., Beverly, MA) and a monoclonal antibody for BrdUrd (Amersham Biosciences). Photoreceptors were stained with monoclonal antibody rho4D2, kindly provided by Dr. Robert S. Molday, at 37 °C overnight at 1:50. PAC1 and rho4D2 immunoreactivity were developed with the appropriate rabbit or mouse horseradish peroxidase-ABC kits, respectively (Vector, Burlingame, CA) with diaminobenzidine as chromogen. Both BrdUrd and phospho-CREB immunoreactivity were developed with Alexa Fluor conjugate fluorescent antibodies from Molecular Probes (Eugene, OR) and analyzed in a Zeiss LSM310 confocal microscope. Cyclic AMP was quantitated according to the competitive binding assay of Gilman (30Gilman A.G. Proc. Natl. Acad. Sci. U. S. A. 1970; 67: 305-312Crossref PubMed Scopus (3376) Google Scholar) as described previously (13De Varella M.H. Mello F.G. Linden R. J. Neurochem. 1999; 73: 485-492Crossref PubMed Scopus (43) Google Scholar). Briefly, retinas from P2 rats were preincubated for 10 min at 37 °C in basal medium Eagle's buffered at pH 7.4, containing 0.5 mm isobutylmethylxanthine and 100 μm ascorbic acid, and stimulated for 15 min with either PACAP38 or 6-Cl-PB ([±]-6-chloro-7, 8-dihydroxy-1-phenyl-2, 3,4,5-tetrahydro-1H-3-benzazepine), a D1-like agonist that increases intracellular cAMP used as a positive control. The reaction was stopped with trichloroacetic acid, and after centrifugation, the supernatant was passed through an ion-exchange resin column (Dowex 50) to remove trichloroacetic acid and other nucleotides. The sample obtained was then used in a competition assay with the regulatory subunit of PKA with the addition of a fixed, trace amount of [3H]cAMP. Inositol triphosphate was assayed according to a modification (31Reis R.A.M. De Kubrusly R.C.C. Mello M.C.F. De Mello F.G. Neurochem. Int. 1995; 26: 375-380Crossref PubMed Scopus (17) Google Scholar) of the method described by Berridge et al. (32Berridge M.J. Dawson R.M.C. Downes P. Heslop J.P. Irvine R.F. Biochem. J. 1983; 212: 473-482Crossref PubMed Scopus (1613) Google Scholar). Retinal explants from P2 rats were preincubated for 8 h in inositol-free defined medium containing [3H]myoinositol. The cultures were then treated with either 10 nm PACAP38 or 500 μmkainate as a positive control for 15 min in 10 mm LiCl. The reaction was stopped by the addition of trichloroacetic acid, and following ether extraction, the supernatants were separated by ion-exchange chromatography (Dowex AG1-X8 resin, formate form; Bio-Rad). Inositol triphosphate (IP3) was quantified in a liquid scintillation analyzer. We have shown previously that inhibition of protein synthesis by anisomycin induces cell death within the NBL of retinal explants from newborn rats (27Rehen S.K. Varella M.H. Freitas F.G. Moraes M.O. Linden R. Development. 1996; 122: 1439-1448PubMed Google Scholar). The sensitive cells could be rescued by the increase of intracellular cAMP levels (27Rehen S.K. Varella M.H. Freitas F.G. Moraes M.O. Linden R. Development. 1996; 122: 1439-1448PubMed Google Scholar). Therefore, we investigated whether PACAP38, a potent cAMP inducer, affected retinal cell survival. PACAP38 protected cells from death induced by anisomycin with maximum effect at 1 nm (Fig.1, A–C). Retinal tissue treated with PACAP38 showed a very low density of pyknotic profiles, approximately the same as the density of control explants; part of these results, at least, are likely to be caused by slight mechanical damage to the tissue when preparing the explants. Protection against anisomycin-induced cell death was also observed with PACAP27 (data not shown). In contrast, glucagon, a peptide that belongs to the same family as PACAP, had no effect at a similar concentration range (Fig. 1C, inset). We specifically tested whether apoptosis could be prevented by PACAP38. Adjacent sections from the same explants were stained with neutral red (as in Fig. 1B), with the TUNEL procedure (Fig.1D), or with an antibody that detects the activated form of caspase-3 (Fig. 1E). Treatment with PACAP38 led to a reduction in the number of degenerating profiles identified with all three methods (Fig. 1F). The lower number of degenerating profiles detected with either TUNEL or the CM1 antibody may reflect the simultaneous occurrence of other forms of cell death besides apoptosis. Nevertheless, the data show that PACAP38 is effective against the caspase-3-dependent, apoptotic form of cell death. Previous work from our laboratory showed that thapsigargin selectively kills photoreceptors in the outer nuclear layer of retinal explants from 1-week-old rats (33Chiarini L.B. Freitas F.G. Petrs-Silva H. Linden R. Cell Death Differ. 2000; 7: 272-281Crossref PubMed Scopus (34) Google Scholar). The degeneration of rhodopsin-containing photoreceptors was also prevented by PACAP38 (Fig.2). Therefore, the protective effect of PACAP is not restricted to anisomycin-induced cell death. To test whether the neuroprotective effect was mediated by interaction of PACAP38 with its receptors, we used the competitive PACAP receptor antagonist PACAP6–38. Increasing amounts of PACAP6–38 prevented, in a dose-dependent fashion, the action of PACAP38 upon anisomycin-induced cell death (Fig.3A). The maximum inhibitory effect of PACAP6–38 was observed at 1 μm. To further characterize PACAP receptors involved in neuroprotection, we used the specific PAC1 receptor antagonist Maxd.4, which was developed based on the sequence of the PAC1 receptor-specific agonist maxadilan, originally cloned from sandfly salivary glands (34Moro O. Lerner E.A. J. Biol. Chem. 1997; 272: 966-970Abstract Full Text Full Text PDF PubMed Scopus (171) Google Scholar, 35Moro O. Wakita K. Ohnuma M. Denda S. Lerner E. Tajima M. J. Biol. Chem. 1999; 274: 23103-23110Abstract Full Text Full Text PDF PubMed Scopus (62) Google Scholar, 36Lerner E.A. Ribeiro J.M.C. Nelson R.J. Lerner M.R. J. Biol. Chem. 1991; 266: 11234-11236Abstract Full Text PDF PubMed Google Scholar). Treatment with increasing concentrations of Maxd.4 also prevented neuroprotection by PACAP38 (Fig. 3B) within a similar concentration range as that observed with PACAP6–38. In agreement with these results, 1 nm maxadilan also prevented anisomycin-induced cell death, and this protective effect was blocked by Maxd.4 (data not shown). The results obtained with both Maxd.4 and maxadilan suggested a major role for the PAC1 receptor on the neuroprotective effect of PACAP38 upon retinal cells. The presence of this receptor was then investigated both by reverse transcription-PCR and by immunohistochemistry with an anti-PAC1 antibody (Fig.4). Using primers for the carboxyl-terminal intracellular domain of the PAC1 receptor (29Braas K.M. May V. J. Biol. Chem. 1999; 274: 27702-27710Abstract Full Text Full Text PDF PubMed Scopus (108) Google Scholar), we amplified a product of the expected 449-bp size (Fig. 4A). Consistent with the latter result, immunoreactivity for the PAC1 receptor was found in all layers of the retina in P2 rat eyes, including the NBL (Fig. 4, B and C). We examined whether cells from the NBL responded to PACAP38 by testing for the induction of CREB phosphorylation. CREB is a transcriptional factor that may be activated by multiple stimuli, including intracellular cAMP (for a review, see Ref. 37Mayr B. Montminy M. Nat. Rev. Mol. Cell. Biol. 2001; 2: 599-609Crossref PubMed Scopus (2119) Google Scholar). Retinal explants were maintained for 2 h without stimulus, and then either PACAP38 or vehicle was added for 5, 20, or 60 min. Nuclei labeled for phospho-CREB were already detected at 5 min of treatment with PACAP38 in the neuroblastic layer (data not shown), but labeling was more intense after 20 min of incubation (Fig.5A, red), consistent with the detection of the PAC1 receptor (Fig. 4). In contrast, sections from explants maintained in control medium showed almost no detectable labeling for phospho-CREB within the NBL (Fig.5C). Phospho-CREB labeling of cells located in the outer half of the NBL was particularly strong. Cells within the NBL that degenerate following treatment with anisomycin are mainly located in the outer half of the neuroblastic layer and were identified as undifferentiated postmitotic cells because they neither incorporate BrdUrd following serial injections designed as to label the maximum possible number of proliferating neuroblasts nor can they be stained with various antibodies to retinal cell differentiation markers (26Rehen S.K. Neves D.D.C. Fragel-Madeira L. Britto L.R.G. Linden R. Eur. J. Neurosci. 1999; 11: 4349-4356Crossref PubMed Scopus (28) Google Scholar). We tested whether postmitotic cells were phospho-CREB-positive by prelabeling proliferating cells with BrdUrd injections identical to those used in our previous study (26Rehen S.K. Neves D.D.C. Fragel-Madeira L. Britto L.R.G. Linden R. Eur. J. Neurosci. 1999; 11: 4349-4356Crossref PubMed Scopus (28) Google Scholar). Confocal microscopic examination of sections from explants treated with PACAP38 (Fig. 5) showed that a large number of cells unlabeled for BrdUrd within the NBL (ingreen) were strongly labeled with phospho-CREB (inred). These data suggest that PACAP38 may affect directly the cells that are sensitive to cell death induced by the blockade of protein synthesis. The various PAC1 receptor isoforms can trigger several signal transduction mechanisms, including the activation of phospholipase C, adenylyl cyclase, or the modulation of voltage-dependent L-type Ca2+ channels. We tested whether one or more of these pathways were associated with the neuroprotective effect of PACAP38. No IP3 production was found in PACAP38-stimulated retinal explants (Fig. 6A). The PLC inhibitor, U73122, also failed to prevent the neuroprotective effect of PACAP38 upon anisomycin-induced cell death (Fig. 6B). At the concentration range tested, U73122 had no effect by itself (data not shown). The selective L-type Ca2+ channel inhibitors verapamil (30 μm) and nifedipine (10 μm) also did not prevent the neuroprotective effect of PACAP (data not shown). In contrast, PACAP38 at 1 and 10 nm induced a 2.5-fold and 6-fold increase in cAMP levels, respectively (Fig.7A), similar to the dopamine D1-like receptor agonist 6-Cl-PB, which was used as a positive control (13De Varella M.H. Mello F.G. Linden R. J. Neurochem. 1999; 73: 485-492Crossref PubMed Scopus (43) Google Scholar). Moreover, the PKA inhibitor, Rp-cAMPS, completely reverted the neuroprotective effect of PACAP38 (Fig.7B). These results clearly show a requirement of the cAMP/PKA signaling pathway for PACAP38-induced neuroprotection.Figure 7The cAMP/PKA pathway is required for modulation of anisomycin-induced cell death by PACAP38. A, relative levels of cAMP in retinal explants treated with either 1 or 10 nm PACAP38. The levels in control conditions were set to 1, and the dopamine D1-like receptor agonist 6-Cl-PB (100 μm) was used as a positive control. The data represent the mean ± S.E. of four experiments with at least two replicas per group. B, effect of the PKA inhibitorRp-cAMPS (100 μm) in explants treated with 1 μg/ml anisomycin plus 1 nm PACAP38. The rate of cell death is expressed as pyknotic profiles (PYK) per mm2 in the NBL, and data represent the means ± S.E. pooled from three experiments with three independent explants each. *, p < 0.01 versus anisomycin plus 1 nm PACAP38.View Large Image Figure ViewerDownload Hi-res image Download (PPT) This investigation showed that PACAP counteracts the induction of retinal cell death. Activation of PAC1 receptors expressed in the NBL of the neonatal rat retina resulted in production of cAMP and consequent activation of PKA, whereas a PKA inhibitor prevented the neuroprotective effect. PACAP38 also led to phosphorylation of CREB in the retinal tissue. In addition, PACAP38 counteracted photoreceptor cell death induced by thapsigargin. The detection of PACAP-induced effects upon both recent postmitotic cells of the neuroblastic layer as well as upon rhodopsin-containing photoreceptors suggest that both undifferentiated and differentiated cells may be subject to neuroprotection by PACAP. Both PACAP and VIP act on the same receptors, which were pharmacologically classified as types I and II by their relative affinity for the peptides. Subsequent molecular characterization showed three genes that encoded G-protein-coupled receptors responsive to these peptides with great functional heterogeneity (23Ishihara T. Shigemoto R. Mori K. Takahashi K. Nagata S. Neuron. 1992; 8: 811-819Abstract Full Text PDF PubMed Scopus (733) Google Scholar, 24Spengler D. Waeber C. Pantaloni C. Holsber F. Bockaert J. Seeburg P.H. Journot L. Nature. 1993; 356: 170-175Google Scholar, 25Lutz E.M. Sheward W.J. West K.M. Morrow J.A. Fink G. Harmar A.I. FEBS Lett. 1993; 334: 3-8Crossref PubMed Scopus (487) Google Scholar, 38Vaudry D. Gonzalez B.J. Basille M. Yon L. Fournier A. Vaudry H. Pharmacol. Rev. 2000; 52: 269-324PubMed Google Scholar). The PAC1 receptor is considered a PACAP-specific receptor and may present splicing variants that differ in the intracellular signaling pathways activated, which include adenylyl cyclase, phospholipase C, or modulation of L-type calcium channels (24Spengler D. Waeber C. Pantaloni C. Holsber F. Bockaert J. Seeburg P.H. Journot L. Nature. 1993; 356: 170-175Google Scholar, 38Vaudry D. Gonzalez B.J. Basille M. Yon L. Fournier A. Vaudry H. Pharmacol. Rev. 2000; 52: 269-324PubMed Google Scholar, 39Chaterjee T.K. Sharma R.V. Fisher R.A. J. Biol. Chem. 1996; 271: 32226-32232Abstract Full Text Full Text PDF PubMed Scopus (140) Google Scholar). In contrast with other regions of the central and peripheral nervous system, functional studies of PACAP peptides and their receptors in the developing retina are rare (42Shoge K. Mishima H.K. Saitoh T. Ishihara K. Tamura Y. Shiomi H. Sasa M. Brain Res. 1999; 839: 66-73Crossref PubMed Scopus (80) Google Scholar). Both PACAP as well as the mRNA and immunoreactivity for the PACAP receptor have been described in the retina of adult rats (43Seki T. Shioda S. Nakai Y. Arimura A. Koide R. Ann. N. Y. Acad. Sci. 1998; 865: 408-411Crossref PubMed Scopus (22) Google Scholar, 44Izumi S. Seki T. Shioda S. Zhou C.J. Arimura A. Koide R. Ann. N. Y. Acad. Sci. 2000; 921: 317-320Crossref PubMed Scopus (25) Google Scholar, 45Seki T Shioda S Izumi S Arimura A Koide R. Peptides (Elmsford). 2000; 21: 109-113Crossref PubMed Scopus (41) Google Scholar, 46Seki T. Shioda S. Ogino D. Nakai Y. Arimura A. Koide R. Neurosci. Lett. 1997; 238: 127-130Crossref PubMed Scopus (58) Google Scholar, 47Onali P. Olianas M.C. Brain Res. 1994; 641: 132-134Crossref PubMed Scopus (38) Google Scholar). Production of cAMP following activation of PACAP receptors was also described in the retinae of some mammalian species (47Onali P. Olianas M.C. Brain Res. 1994; 641: 132-134Crossref PubMed Scopus (38) Google Scholar, 48Olianas M.C. Ingianni A. Sogos V. Onali P. J. Neurochem. 1997; 69: 1213-1218Crossref PubMed Scopus (38) Google Scholar, 49D'Agata V. Cavallaro S. Mol. Brain Res. 1998; 54: 161-164Crossref PubMed Scopus (50) Google Scholar). In the present study, the PAC1 receptor was located in the developing retina and shown to be functional as well as participating in a neuroprotective signaling pathway. This is supported by the experiments showing that the specific antagonist Maxd.4 (35Moro O. Wakita K. Ohnuma M. Denda S. Lerner E. Tajima M. J. Biol. Chem. 1999; 274: 23103-23110Abstract Full Text Full Text PDF PubMed Scopus (62) Google Scholar) reverted (Fig. 3B), whereas the specific agonist maxadilan (34Moro O. Lerner E.A. J. Biol. Chem. 1997; 272: 966-970Abstract Full Text Full Text PDF PubMed Scopus (171) Google Scholar, 36Lerner E.A. Ribeiro J.M.C. Nelson R.J. Lerner M.R. J. Biol. Chem. 1991; 266: 11234-11236Abstract Full Text PDF PubMed Google Scholar) reproduced the neuroprotective effect of PACAP. Nonetheless, a contribution of VPAC1 and VPAC2 receptors cannot be discarded. Previous work in our laboratory has taken advantage of retinal explants in culture to study the sensitivity of developing nervous tissue to cell death (for a review, see Refs. 40Linden R. Rehen S.K. Chiarini L.B. Prog. in Retinal and Eye Res. 1999; 18: 133-165Crossref PubMed Scopus (105) Google Scholar and 41Linden R. Brain Res. Rev. 2000; 32: 146-158Crossref PubMed Scopus (28) Google Scholar). It was established that treatment of retinal explants with inhibitors of protein synthesis induces cell death in undifferentiated postmitotic cells (26Rehen S.K. Neves D.D.C. Fragel-Madeira L. Britto L.R.G. Linden R. Eur. J. Neurosci. 1999; 11: 4349-4356Crossref PubMed Scopus (28) Google Scholar, 27Rehen S.K. Varella M.H. Freitas F.G. Moraes M.O. Linden R. Development. 1996; 122: 1439-1448PubMed Google Scholar) and that an increase in intracellular cAMP levels, as well as dopamine-induced activation of a D1-like receptor (13De Varella M.H. Mello F.G. Linden R. J. Neurochem. 1999; 73: 485-492Crossref PubMed Scopus (43) Google Scholar), protected the neuroblastic layer from anisomycin-induced cell death. We tested the roles of PACAP signaling pathways in the neuroprotective effect. Activation of phospholipase C does not appear to be involved because neither was IP3 production detected following incubation of retinal tissue with PACAP at a maximally effective concentration (Fig. 6A) nor did treatment with the PLC inhibitor, U73122, prevent the effect (Fig. 6B). A role of L-type calcium channels (39Chaterjee T.K. Sharma R.V. Fisher R.A. J. Biol. Chem. 1996; 271: 32226-32232Abstract Full Text Full Text PDF PubMed Scopus (140) Google Scholar) was also ruled out in the present conditions. On the other hand, the PACAP-induced activation of PKA was required for neuroprotection (Fig. 7). We cannot discard the possibility that PACAP acts indirectly to promote neuroprotection, for example, inducing the secretion of neurotrophic factors or other intervening neuroactive substances. Indeed, previous work from our laboratory demonstrated paracrine neuroprotective effects of nitric oxide released from amacrine cells upon the neuroblastic layer (10Ary-Pires R. Nakatani M. Rehen S.K. Linden R. Int. J. Dev. Neurosci. 1997; 15: 239-255Crossref PubMed Scopus (24) Google Scholar). However, our data showed that CREB phosphorylation was also induced in postmitotic cells within the undifferentiated neuroblastic layer by PACAP38, which is consistent with a direct action of PKA upon the cells sensitive to anisomycin-induced degeneration. In conclusion, the overall data demonstrate that PACAP-induced activation of the cAMP/PKA pathway through the PAC1 receptor lowers the sensitivity of retinal cells to induced cell death. The results add PACAP to a growing list of intrinsic modulators of sensitivity to cell death within the developing central nervous system. Studies of the kinetics of neurodegenerative cell loss suggested that cell death in inherited neurodegenerations, rather than being caused by cumulative damage, may be due to single catastrophic events imposed on an altered homeostatic state (20Clarke G. Collins R.A. Leavitt B.R. Andrews D.F. Hayden M.R. Lumsden C.J. McInnes R.R. Nature. 2000; 406: 195-199Crossref PubMed Scopus (265) Google Scholar). The present data suggest that neuropeptides such as PACAP help to maintain retinal cells in a steady state removed from apoptosis execution pathways and may therefore be relevant for the control of inherited retinal dystrophies. We thank José Nilson dos Santos, José Francisco Tiburcio, and Gildo Brito de Souza for technical assistance, Dr. Victor May for the PAC1 antibody, Dr. Ethan Lerner for both maxadilan and Maxd.4, Dr. Anu Srinivasan (Idun Pharmaceuticals) for the CM1 antibody, Dr. Robert S. Molday for the rho4D2 antibody, and Dr. Fernando G. de Mello from the Instituto de Biofísica Carlos Chagas Filho for coaching with the cAMP and IP3measurements.
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