Proteome profiling of different rat brain regions reveals the modulatory effect of prolonged maternal separation on proteins involved in cell death-related processes

. 2021 Feb 08 ; 54 (1) : 4. [epub] 20210208

Jazyk angličtina Země Anglie, Velká Británie Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid33557947

Grantová podpora
16-13399S Grantová Agentura České Republiky
SVV-260871/2020 Univerzita Karlova v Praze

Odkazy

PubMed 33557947
PubMed Central PMC7871601
DOI 10.1186/s40659-021-00327-5
PII: 10.1186/s40659-021-00327-5
Knihovny.cz E-zdroje

BACKGROUND: Early-life stress in the form of maternal separation can be associated with alterations in offspring neurodevelopment and brain functioning. Here, we aimed to investigate the potential impact of prolonged maternal separation on proteomic profiling of prefrontal cortex, hippocampus and cerebellum of juvenile and young adult rats. A special attention was devoted to proteins involved in the process of cell death and redox state maintenance. METHODS: Long-Evans pups were separated from their mothers for 3 h daily over the first 3 weeks of life (during days 2-21 of age). Brain tissue samples collected from juvenile (22-day-old) and young adult (90-day-old) rats were used for label-free quantitative (LFQ) proteomic analysis. In parallel, selected oxidative stress markers and apoptosis-related proteins were assessed biochemically and by Western blot, respectively. RESULTS: In total, 5526 proteins were detected in our proteomic analysis of rat brain tissue. Approximately one tenth of them (586 proteins) represented those involved in cell death processes or regulation of oxidative stress balance. Prolonged maternal separation caused changes in less than half of these proteins (271). The observed alterations in protein expression levels were age-, sex- and brain region-dependent. Interestingly, the proteins detected by mass spectrometry that are known to be involved in the maintenance of redox state were not markedly altered. Accordingly, we did not observe any significant differences between selected oxidative stress markers, such as the levels of hydrogen peroxide, reduced glutathione, protein carbonylation and lipid peroxidation in brain samples from rats that underwent maternal separation and from the corresponding controls. On the other hand, a number of changes were found in cell death-associated proteins, mainly in those involved in the apoptotic and autophagic pathways. However, there were no detectable alterations in the levels of cleaved products of caspases or Bcl-2 family members. Taken together, these data indicate that the apoptotic and autophagic cell death pathways were not activated by maternal separation either in adolescent or young adult rats. CONCLUSION: Prolonged maternal separation can distinctly modulate expression profiles of proteins associated with cell death pathways in prefrontal cortex, hippocampus and cerebellum of juvenile rats and the consequences of early-life stress may last into adulthood and likely participate in variations in stress reactivity.

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Vaiserman AM. Epigenetic programming by early-life stress: evidence from human populations. Dev Dyn. 2015;244(3):254–265. doi: 10.1002/dvdy.24211. PubMed DOI

Tractenberg SG, Levandowski ML, de Azeredo LA, Orso R, Roithmann LG, Hoffmann ES, Brenhouse H, Grassi-Oliveira R. An overview of maternal separation effects on behavioural outcomes in mice: evidence from a four-stage methodological systematic review. Neurosci Biobehav Rev. 2016;68:489–503. doi: 10.1016/j.neubiorev.2016.06.021. PubMed DOI

Jawahar MC, Murgatroyd C, Harrison EL, Baune BT. Epigenetic alterations following early postnatal stress: a review on novel aetiological mechanisms of common psychiatric disorders. Clin Epigenet. 2015;7:122. doi: 10.1186/s13148-015-0156-3. PubMed DOI PMC

Haller J, Harold G, Sandi C, Neumann ID. Effects of adverse early-life events on aggression and anti-social behaviours in animals and humans. J Neuroendocrinol. 2014;26(10):724–738. doi: 10.1111/jne.12182. PubMed DOI

Brunton PJ. Programming the brain and behaviour by early-life stress: a focus on neuroactive steroids. J Neuroendocrinol. 2015;27(6):468–480. doi: 10.1111/jne.12265. PubMed DOI

van Bodegom M, Homberg JR, Henckens MJAG. Modulation of the hypothalamic-pituitary-adrenal axis by early life stress exposure. Front Cell Neurosci. 2017 doi: 10.3389/fncel.2017.00087. PubMed DOI PMC

Nederhof E, Schmidt MV. Mismatch or cumulative stress: toward an integrated hypothesis of programming effects. Physiol Behav. 2012;106(5):691–700. doi: 10.1016/j.physbeh.2011.12.008. PubMed DOI

Rice D, Barone S., Jr Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models. Environ Health Perspect. 2000;108(Suppl 3):511–533. doi: 10.1289/ehp.00108s3511. PubMed DOI PMC

Watson RE, Desesso JM, Hurtt ME, Cappon GD. Postnatal growth and morphological development of the brain: a species comparison. Birth Defects Res B Dev Reprod Toxicol. 2006;77(5):471–484. doi: 10.1002/bdrb.20090. PubMed DOI

Galas L, Benard M, Lebon A, Komuro Y, Schapman D, Vaudry H, Vaudry D, Komuro H. Postnatal migration of cerebellar interneurons. Brain Sci. 2017;7(6):62. doi: 10.3390/brainsci7060062. PubMed DOI PMC

Stagni F, Giacomini A, Guidi S, Ciani E, Bartesaghi R. Timing of therapies for Down syndrome: the sooner, the better. Front Behav Neurosci. 2015;9:265. doi: 10.3389/fnbeh.2015.00265. PubMed DOI PMC

Rice D, Barone S. Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models. Environ Health Persp. 2000;108(Suppl 3):511–533. doi: 10.1289/ehp.00108s3511. PubMed DOI PMC

Ryu JR, Hong CJ, Kim JY, Kim EK, Sun W, Yu SW. Control of adult neurogenesis by programmed cell death in the mammalian brain. Mol Brain. 2016 doi: 10.1186/s13041-016-0224-4. PubMed DOI PMC

Elmore S. Apoptosis: a review of programmed cell death. Toxicol Pathol. 2007;35(4):495–516. doi: 10.1080/01926230701320337. PubMed DOI PMC

Yamaguchi Y, Miura M. Programmed cell death in neurodevelopment. Dev Cell. 2015;32(4):478–490. doi: 10.1016/j.devcel.2015.01.019. PubMed DOI

Galluzzi L, Vitale I, Aaronson SA, Abrams JM, Adam D, Agostinis P, Alnemri ES, Altucci L, Amelio I, Andrews DW, et al. Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018. Cell Death Differ. 2018;25(3):486–541. doi: 10.1038/s41418-017-0012-4. PubMed DOI PMC

Bonneau B, Prudent J, Popgeorgiev N, Gillet G. Non-apoptotic roles of Bcl-2 family: the calcium connection. Bba-Mol Cell Res. 2013;1833(7):1755–1765. PubMed

Dekkers MPJ, Nikoletopoulou V, Barde YA. Death of developing neurons: new insights and implications for connectivity. J Cell Biol. 2013;203(3):385–393. doi: 10.1083/jcb.201306136. PubMed DOI PMC

White LD, Barone S., Jr Qualitative and quantitative estimates of apoptosis from birth to senescence in the rat brain. Cell Death Differ. 2001;8(4):345–356. doi: 10.1038/sj.cdd.4400816. PubMed DOI

Ghavami S, Shojaei S, Yeganeh B, Ande SR, Jangamreddy JR, Mehrpour M, Christoffersson J, Chaabane W, Moghadam AR, Kashani HH, et al. Autophagy and apoptosis dysfunction in neurodegenerative disorders. Prog Neurobiol. 2014;112:24–49. doi: 10.1016/j.pneurobio.2013.10.004. PubMed DOI

Blomgren K, Leist M, Groc L. Pathological apoptosis in the developing brain. Apoptosis. 2007;12(5):993–1010. doi: 10.1007/s10495-007-0754-4. PubMed DOI

Mattson MP, Gleichmann M, Cheng A. Mitochondria in neuroplasticity and neurological disorders. Neuron. 2008;60(5):748–766. doi: 10.1016/j.neuron.2008.10.010. PubMed DOI PMC

Schiavone S, Colaianna M, Curtis L. Impact of early life stress on the pathogenesis of mental disorders: relation to brain oxidative stress. Curr Pharm Des. 2015;21(11):1404–1412. doi: 10.2174/1381612821666150105143358. PubMed DOI

Singh A, Kukreti R, Saso L, Kukreti S. Oxidative stress: a key modulator in neurodegenerative diseases. Molecules. 2019;24(8):1583. doi: 10.3390/molecules24081583. PubMed DOI PMC

Ursini F, Maiorino M, Forman HJ. Redox homeostasis: the golden mean of healthy living. Redox Biol. 2016;8:205–215. doi: 10.1016/j.redox.2016.01.010. PubMed DOI PMC

Uysal N, Gonenc S, Acikgoz O, Petcetin C, Kayatekin BM, Sonmez A, Semin I. Age-dependent effects of maternal deprivation on oxidative stress in infant rat brain. Neurosci Lett. 2005;384(1–2):98–101. doi: 10.1016/j.neulet.2005.04.052. PubMed DOI

Uysal N, Sisman AR, Gonenc S, Acikgoz O, Kayatekin BM, Yalaz G. Effects of repeated maternal separation on oxidative stress in adolescent male and female rat brains. J Neurol Sci-Turkish. 2008;25(3#15):150–157.

Diehl LA, Pereira NDC, Laureano DP, Benitz AND, Noschang C, Ferreira AGK, Scherer EB, Machado FR, Henriques TP, Wyse ATS, et al. Contextual fear conditioning in maternal separated rats: the amygdala as a site for alterations. Neurochem Res. 2014;39(2):384–393. doi: 10.1007/s11064-013-1230-x. PubMed DOI

Markovic B, Radonjic NV, Jevtic G, Stojkovic T, Velimirovic M, Aksic M, Poleksic J, Nikolic T, Aleksic D, Radonjic V, Filipovic B, Petronijevic ND. Long-term effects of maternal deprivation on redox regulation in rat brain: involvement of NADPH oxidase. Oxid Med Cell Longev. 2017;2017:7390516. PubMed PMC

Diehl LA, Alvares LO, Noschang C, Engelke D, Andreazza AC, Goncalves CAS, Quillfeldt JA, Dalmaz C. Long-lasting effects of maternal separation on an animal model of post-traumatic stress disorder: effects on memory and hippocampal oxidative stress. Neurochem Res. 2012;37(4):700–707. doi: 10.1007/s11064-011-0660-6. PubMed DOI

Semple BD, Blomgren K, Gimlin K, Ferriero DM, Noble-Haeusslein LJ. Brain development in rodents and humans: identifying benchmarks of maturation and vulnerability to injury across species. Prog Neurobiol. 2013;106–107:1–16. doi: 10.1016/j.pneurobio.2013.04.001. PubMed DOI PMC

van Bodegom M, Homberg JR, Henckens M. Modulation of the hypothalamic-pituitary-adrenal axis by early life stress exposure. Front Cell Neurosci. 2017;11:87. PubMed PMC

Du X, Pang TY. Is dysregulation of the HPA-axis a core pathophysiology mediating co-morbid depression in neurodegenerative diseases? Front Psychiatry. 2015;6:32. doi: 10.3389/fpsyt.2015.00032. PubMed DOI PMC

Lupien SJ, McEwen BS, Gunnar MR, Heim C. Effects of stress throughout the lifespan on the brain, behaviour and cognition. Nat Rev Neurosci. 2009;10(6):434–445. doi: 10.1038/nrn2639. PubMed DOI

Zhang LX, Levine S, Dent G, Zhan YT, Xing GQ, Okimoto D, Gordon MK, Post RM, Smith MA. Maternal deprivation increases cell death in the infant rat brain. Dev Brain Res. 2002;133(1):1–11. doi: 10.1016/S0926-6410(01)00118-5. PubMed DOI

Coccurello R, Bielawski A, Zelek-Molik A, Vetulani J, Kowalska M, D'Amato FR, Nalepa I. Brief maternal separation affects brain alpha(1)-adrenoceptors and apoptotic signaling in adult mice. Prog Neuropsychopharmacol Biol Psychiatry. 2014;48:161–169. doi: 10.1016/j.pnpbp.2013.10.004. PubMed DOI

Rappsilber J, Mann M, Ishihama Y. Protocol for micro-purification, enrichment, pre-fractionation and storage of peptides for proteomics using StageTips. Nat Protoc. 2007;2(8):1896–1906. doi: 10.1038/nprot.2007.261. PubMed DOI

Hebert AS, Richards AL, Bailey DJ, Ulbrich A, Coughlin EE, Westphall MS, Coon JJ. The one hour yeast proteome. Mol Cell Proteomics. 2014;13(1):339–347. doi: 10.1074/mcp.M113.034769. PubMed DOI PMC

Cox J, Hein MY, Luber CA, Paron I, Nagaraj N, Mann M. Accurate proteome-wide label-free quantification by delayed normalization and maximal peptide ratio extraction, termed MaxLFQ. Mol Cell Proteomics. 2014;13(9):2513–2526. doi: 10.1074/mcp.M113.031591. PubMed DOI PMC

Tyanova S, Temu T, Sinitcyn P, Carlson A, Hein MY, Geiger T, Mann M, Cox J. The Perseus computational platform for comprehensive analysis of (prote)omics data. Nature Meth. 2016;13(9):731–740. doi: 10.1038/nmeth.3901. PubMed DOI

Novotny J, Bourova L, Kolar F, Svoboda P. Membrane-bound and cytosolic forms of heterotrimeric G proteins in young and adult rat myocardium: influence of neonatal hypo- and hyperthyroidism. J Cell Biochem. 2001;82(2):215–224. doi: 10.1002/jcb.1157. PubMed DOI

Samarghandian S, Azimi-Nezhad M, Samini F. Preventive effect of safranal against oxidative damage in aged male rat brain. Exp Anim. 2015;64(1):65–71. doi: 10.1538/expanim.14-0027. PubMed DOI PMC

Skrabalova J, Karlovska I, Hejnova L, Novotny J. Protective effect of morphine against the oxidant-induced injury in H9c2 cells. Cardiovasc Toxicol. 2018;18(4):374–385. doi: 10.1007/s12012-018-9448-0. PubMed DOI

Jiang ZY, Woollard AC, Wolff SP. Lipid hydroperoxide measurement by oxidation of Fe2+ in the presence of xylenol orange. Comparison with the TBA assay and an iodometric method. Lipids. 1991;26(10):853–856. doi: 10.1007/BF02536169. PubMed DOI

Levine RL, Garland D, Oliver CN, Amici A, Climent I, Lenz AG, Ahn BW, Shaltiel S, Stadtman ER. Determination of carbonyl content in oxidatively modified proteins. Meth Enzymol. 1990;186:464–478. doi: 10.1016/0076-6879(90)86141-H. PubMed DOI

Flohe L, Gunzler WA. Assays of glutathione peroxidase. Meth Enzymol. 1984;105:114–121. doi: 10.1016/S0076-6879(84)05015-1. PubMed DOI

Rosenkrantz TS, Hussain Z, Fitch RH. Sex differences in brain injury and repair in newborn infants: clinical evidence and biological mechanisms. Front Pediatr. 2019;7:211. doi: 10.3389/fped.2019.00211. PubMed DOI PMC

VanRyzin JW, Pickett LA, McCarthy MM. Microglia: driving critical periods and sexual differentiation of the brain. Dev Neurobiol. 2018;78(6):580–592. doi: 10.1002/dneu.22569. PubMed DOI PMC

McCarthy MM, Auger AP, Bale TL, De Vries GJ, Dunn GA, Forger NG, Murray EK, Nugent BM, Schwarz JM, Wilson ME. The epigenetics of sex differences in the brain. J Neurosci. 2009;29(41):12815–12823. doi: 10.1523/JNEUROSCI.3331-09.2009. PubMed DOI PMC

Llorente R, Miguel-Blanco C, Aisa B, Lachize S, Borcel E, Meijer OC, Ramirez MJ, De Kloet ER, Viveros MP. Long term sex-dependent psychoneuroendocrine effects of maternal deprivation and juvenile unpredictable stress in rats. J Neuroendocrinol. 2011;23(4):329–344. doi: 10.1111/j.1365-2826.2011.02109.x. PubMed DOI

Mela V, Diaz F, Vazquez MJ, Argente J, Tena-Sempere M, Viveros MP, Chowen JA. Interaction between neonatal maternal deprivation and serum leptin levels on metabolism, pubertal development, and sexual behavior in male and female rats. Biol Sex Differ. 2016;7:2. doi: 10.1186/s13293-015-0054-6. PubMed DOI PMC

Tower J, Pomatto LCD, Davies KJA. Sex differences in the response to oxidative and proteolytic stress. Redox Biol. 2020;31:101488. doi: 10.1016/j.redox.2020.101488. PubMed DOI PMC

Waters EM, Simerly RB. Estrogen induces caspase-dependent cell death during hypothalamic development. J Neurosci. 2009;29(31):9714–9718. doi: 10.1523/JNEUROSCI.0135-09.2009. PubMed DOI PMC

Ahern TH, Krug S, Carr AV, Murray EK, Fitzpatrick E, Bengston L, McCutcheon J, De Vries GJ, Forger NG. Cell death atlas of the postnatal mouse ventral forebrain and hypothalamus: effects of age and sex. J Comp Neurol. 2013;521(11):2551–2569. doi: 10.1002/cne.23298. PubMed DOI PMC

Gross A, Yin XM, Wang K, Wei MC, Jockel J, Milliman C, Erdjument-Bromage H, Tempst P, Korsmeyer SJ. Caspase cleaved BID targets mitochondria and is required for cytochrome c release, while BCL-XL prevents this release but not tumor necrosis factor-R1/Fas death. J Biol Chem. 1999;274(2):1156–1163. doi: 10.1074/jbc.274.2.1156. PubMed DOI

Kale J, Osterlund EJ, Andrews DW. BCL-2 family proteins: changing partners in the dance towards death. Cell Death Differ. 2018;25(1):65–80. doi: 10.1038/cdd.2017.186. PubMed DOI PMC

Sung YH, Shin MS, Cho S, Baik HH, Jin BK, Chang HK, Lee EK, Kim CJ. Depression-like state in maternal rats induced by repeated separation of pups is accompanied by a decrease of cell proliferation and an increase of apoptosis in the hippocampus. Neurosci Lett. 2010;470(1):86–90. doi: 10.1016/j.neulet.2009.12.063. PubMed DOI

Chocyk A, Dudys D, Przyborowska A, Majcher I, Mackowiak M, Wedzony K. Maternal separation affects the number, proliferation and apoptosis of glia cells in the substantia nigra and ventral tegmental area of juvenile rats. Neuroscience. 2011;173:1–18. doi: 10.1016/j.neuroscience.2010.11.037. PubMed DOI

Piubelli C, Carboni L, Becchi S, Mathe AA, Domenici E. Regulation of cytoskeleton machinery, neurogenesis and energy metabolism pathways in a rat gene-environment model of depression revealed by proteomic analysis. Neuroscience. 2011;176:349–380. doi: 10.1016/j.neuroscience.2010.12.043. PubMed DOI

Irles C, Nava-Kopp AT, Moran J, Zhang L. Neonatal maternal separation up-regulates protein signalling for cell survival in rat hypothalamus. Stress. 2014;17(3):275–284. doi: 10.3109/10253890.2014.913017. PubMed DOI

Li B, Zani A, Lee C, Zani-Ruttenstock E, Zhang ZY, Li XP, Wan IP, Gonska T, Pierro A. Endoplasmic reticulum stress is involved in the colonic epithelium damage induced by maternal separation. J Pediatr Surg. 2016;51(6):1001–1004. doi: 10.1016/j.jpedsurg.2016.02.073. PubMed DOI

Yang SJ, Li JY, Han L, Zhu GQ. Early maternal separation promotes apoptosis in dentate gyrus and alters neurological behaviors in adolescent rats. Int J Clin Exp Pathol. 2017;10(11):10812–10820. PubMed PMC

Chen M, He G, Li Q. Maternal deprivation promotes hippocampal neuronal apoptosis via ERK1/2 signaling. Front Biosci. 2018;23:1923–1932. doi: 10.2741/4665. PubMed DOI

Favaloro B, Allocati N, Graziano V, Di Ilio C, De Laurenzi V. Role of apoptosis in disease. Aging-US. 2012;4(5):330–349. doi: 10.18632/aging.100459. PubMed DOI PMC

Csaszar-Nagy N, Bokkon I. Mother-newborn separation at birth in hospitals: a possible risk for neurodevelopmental disorders? Neurosci Biobehav Rev. 2018;84:337–351. doi: 10.1016/j.neubiorev.2017.08.013. PubMed DOI

Wu HL, Xing KY, Lou MF. Glutaredoxin 2 prevents H2O2-induced cell apoptosis by protecting complex I activity in the mitochondria. Biochim Biophys Acta-Bioenerget. 2010;1797(10):1705–1715. doi: 10.1016/j.bbabio.2010.06.003. PubMed DOI PMC

Antolak A, Bodzon-Kulakowska A, Cetnarska E, Pietruszka M, Marszalek-Grabska M, Kotlinska J, Suder P. Proteomic data in morphine addiction versus real protein activity: metabolic enzymes. J Cell Biochem. 2017;118(12):4323–4330. doi: 10.1002/jcb.26085. PubMed DOI

Bodzon-Kulakowska A, Suder P, Drabik A, Kotlinska JH, Silberring J. Constant activity of glutamine synthetase after morphine administration versus proteomic results. Anal Bioanal Chem. 2010;398(7–8):2939–2942. doi: 10.1007/s00216-010-4244-0. PubMed DOI PMC

You ZB, Ouyang H, Lopatin D, Polver PJ, Wang CY. Nuclear factor-kappa B-inducible death effector domain-containing protein suppresses tumor necrosis factor-mediated apoptosis by inhibiting caspase-8 activity. J Biol Chem. 2001;276(28):26398–26404. doi: 10.1074/jbc.M102464200. PubMed DOI

Pietsch EC, Sykes SM, McMahon SB, Murphy ME. The p53 family and programmed cell death. Oncogene. 2008;27(50):6507–6521. doi: 10.1038/onc.2008.315. PubMed DOI PMC

Gorman AM. Neuronal cell death in neurodegenerative diseases: recurring themes around protein handling. J Cell Mol Med. 2008;12(6A):2263–2280. doi: 10.1111/j.1582-4934.2008.00402.x. PubMed DOI PMC

Green DR, Llambi F. Cell death signaling. Cold Spring Harbor Perspect Biol. 2015 doi: 10.1101/cshperspect.a006080. PubMed DOI PMC

Zamaraev AV, Kopeina GS, Prokhorova EA, Zhivotovsky B, Lavrik IN. Post-translational modification of caspases: the other side of apoptosis regulation. Trends Cell Biol. 2017;27(5):322–339. doi: 10.1016/j.tcb.2017.01.003. PubMed DOI

Basanez G, Hardwick JM. Unravelling the bcl-2 apoptosis code with a simple model system. PLoS Biol. 2008;6(6):e154. doi: 10.1371/journal.pbio.0060154. PubMed DOI PMC

Shamas-Din A, Kale J, Leber B, Andrews DW. Mechanisms of action of Bcl-2 family proteins. Cold Spring Harbor Perspect Biol. 2013;5(4):a00871. doi: 10.1101/cshperspect.a008714. PubMed DOI PMC

Harder JM, Ding Q, Fernandes KA, Cherry JD, Gan L, Libby RT. BCL2L1 (BCL-X) promotes survival of adult and developing retinal ganglion cells. Mol Cell Neurosci. 2012;51(1–2):53–59. doi: 10.1016/j.mcn.2012.07.006. PubMed DOI PMC

Xiao Q, Ford AL, Xu J, Yan P, Lee KY, Gonzales E, West T, Holtzman DM, Lee JM. Bcl-x pre-mRNA splicing regulates brain injury after neonatal hypoxia-ischemia. J Neurosci. 2012;32(39):13587–13596. doi: 10.1523/JNEUROSCI.2617-12.2012. PubMed DOI PMC

Saraiva L, Silva RD, Pereira G, Goncalves J, Corte-Real M. Specific modulation of apoptosis and Bcl-xL phosphorylation in yeast by distinct mammalian protein kinase C isoforms. J Cell Sci. 2006;119(Pt 15):3171–3181. doi: 10.1242/jcs.03033. PubMed DOI

Baek SB, Bahn G, Moon SJ, Lee J, Kim KH, Ko IG, Kim SE, Sung YH, Kim BK, Kim TS, et al. The phosphodiesterase type-5 inhibitor, tadalafil, improves depressive symptoms, ameliorates memory impairment, as well as suppresses apoptosis and enhances cell proliferation in the hippocampus of maternal-separated rat pups. Neurosci Lett. 2011;488(1):26–30. doi: 10.1016/j.neulet.2010.10.074. PubMed DOI

Lopatniuk P, Witkowski JM. Conventional calpains and programmed cell death. Acta Biochim Pol. 2011;58(3):287–296. doi: 10.18388/abp.2011_2238. PubMed DOI

Ferreira A. Calpain dysregulation in Alzheimer's disease. ISRN Biochem. 2012;2012:728571. doi: 10.5402/2012/728571. PubMed DOI PMC

Luo T, Wu W-H, Chen BS. NMDA receptor signaling: death or survival? Front Biol (Beijing) 2011;6(6):468–479. doi: 10.1007/s11515-011-1187-6. PubMed DOI PMC

Zhou X, Ding Q, Chen Z, Yun H, Wang H. Involvement of the GluN2A and GluN2B subunits in synaptic and extrasynaptic N-methyl-d-aspartate receptor function and neuronal excitotoxicity. J Biol Chem. 2013;288(33):24151–24159. doi: 10.1074/jbc.M113.482000. PubMed DOI PMC

Roceri M, Hendriks W, Racagni G, Ellenbroek BA, Riva MA. Early maternal deprivation reduces the expression of BDNF and NMDA receptor subunits in rat hippocampus. Mol Psych. 2002;7(6):609–616. doi: 10.1038/sj.mp.4001036. PubMed DOI

Reshetnikov VV, Lepeshko AA, Ryabushkina YA, Studenikina AA, Merkulova TI, Bondar NP. The long-term effects of early postnatal stress on cognitive abilities and expression of genes of the glutamatergic system in mice. Neurochem J. 2018;12(2):142–151. doi: 10.1134/S1819712418020095. DOI

Borodezt K, D'Mello SR. Decreased expression of the metabotropic glutamate receptor-4 gene is associated with neuronal apoptosis. J Neurosci Res. 1998;53(5):531–541. doi: 10.1002/(SICI)1097-4547(19980901)53:5<531::AID-JNR3>3.0.CO;2-A. PubMed DOI

Mukherjee A, Williams DW. More alive than dead: non-apoptotic roles for caspases in neuronal development, plasticity and disease. Cell Death Diff. 2017;24(8):1411–1421. doi: 10.1038/cdd.2017.64. PubMed DOI PMC

Hollville E, Deshmukh M. Physiological functions of non-apoptotic caspase activity in the nervous system. Semin Cell Dev Biol. 2018;82:127–136. doi: 10.1016/j.semcdb.2017.11.037. PubMed DOI PMC

Kipanyula MJ, Kimaro WH, Seke Etet PF. The emerging roles of the calcineurin-nuclear factor of activated T-lymphocytes pathway in nervous system functions and diseases. J Aging Res. 2016;2016:5081021. doi: 10.1155/2016/5081021. PubMed DOI PMC

Sala C, Vicidomini C, Bigi I, Mossa A, Verpelli C. Shank synaptic scaffold proteins: keys to understanding the pathogenesis of autism and other synaptic disorders. J Neurochem. 2015;135(5):849–858. doi: 10.1111/jnc.13232. PubMed DOI

Uemura T, Mori H, Mishina M. Direct interaction of GluRdelta2 with Shank scaffold proteins in cerebellar Purkinje cells. Mol Cell Neurosci. 2004;26(2):330–341. doi: 10.1016/j.mcn.2004.02.007. PubMed DOI

Contractor T, Harris CR. p53 negatively regulates transcription of the pyruvate dehydrogenase kinase Pdk2. Cancer Res. 2012;72(2):560–567. doi: 10.1158/0008-5472.CAN-11-1215. PubMed DOI

Brustovetsky T, Antonsson B, Jemmerson R, Dubinsky JM, Brustovetsky N. Activation of calcium-independent phospholipase A(2) (iPLA(2)) in brain mitochondria and release of apoptogenic factors by BAX and truncated BID. J Neurochem. 2005;94(4):980–994. doi: 10.1111/j.1471-4159.2005.03248.x. PubMed DOI

Balsinde J, Perez R, Balboa MA. Calcium-independent phospholipase A2 and apoptosis. Biochim Biophys Acta. 2006;1761(11):1344–1350. doi: 10.1016/j.bbalip.2006.07.013. PubMed DOI

Barbour SE, Nguyen PT, Park M, Emani B, Lei X, Kambalapalli M, Shultz JC, Wijesinghe D, Chalfant CE, Ramanadham S. Group VIA phospholipase A2 (iPLA2beta) modulates Bcl-x 5'-splice site selection and suppresses anti-apoptotic Bcl-x(L) in beta-cells. J Biol Chem. 2015;290(17):11021–11031. doi: 10.1074/jbc.M115.648956. PubMed DOI PMC

Pena-Blanco A, Garcia-Saez AJ. Bax, Bak and beyond - mitochondrial performance in apoptosis. Febs J. 2018;285(3):416–431. doi: 10.1111/febs.14186. PubMed DOI

Nakamura A, Swahari V, Plestant C, Smith I, McCoy E, Smith S, Moy SS, Anton ES, Deshmukh M. Bcl-xL Is Essential for the survival and function of differentiated neurons in the cortex that control complex behaviors. J Neurosci. 2016;36(20):5448–5461. doi: 10.1523/JNEUROSCI.4247-15.2016. PubMed DOI PMC

Ryeom S, Greenwald RJ, Sharpe AH, McKeon F. The threshold pattern of calcineurin-dependent gene expression is altered by loss of the endogenous inhibitor calcipressin. Nat Immunol. 2003;4(9):874–881. doi: 10.1038/ni966. PubMed DOI

Neumar RW, Xu YA, Gada H, Guttmann RP, Siman R. Cross-talk between calpain and caspase proteolytic systems during neuronal apoptosis. J Biol Chem. 2003;278(16):14162–14167. doi: 10.1074/jbc.M212255200. PubMed DOI

McIlwain DR, Berger T, Mak TW. Caspase functions in cell death and disease. Cold Spring Harb Perspect Biol. 2013;5(4):a008656. doi: 10.1101/cshperspect.a008656. PubMed DOI PMC

Nelson WB, Smuder AJ, Hudson MB, Talbert EE, Powers SK. Cross-talk between the calpain and caspase-3 proteolytic systems in the diaphragm during prolonged mechanical ventilation. Crit Care Med. 2012;40(6):1857–1863. doi: 10.1097/CCM.0b013e318246bb5d. PubMed DOI PMC

Mullen TD, Hannun YA, Obeid LM. Ceramide synthases at the centre of sphingolipid metabolism and biology. Biochem J. 2012;441(3):789–802. doi: 10.1042/BJ20111626. PubMed DOI PMC

Wang Z, Wen L, Zhu F, Wang Y, Xie Q, Chen Z, Li Y. Overexpression of ceramide synthase 1 increases C18-ceramide and leads to lethal autophagy in human glioma. Oncotarget. 2017;8(61):104022–104036. doi: 10.18632/oncotarget.21955. PubMed DOI PMC

Cooper DM. The balance between life and death: defining a role for apoptosis in aging. J Clin & Exp Pathol. 2012;S4:001. doi: 10.4172/2161-0681.S4-001. DOI

Selimi F, Lohof AM, Heitz S, Lalouette A, Jarvis CI, Bailly Y, Mariani J. Lurcher GRID2-induced death and depolarization can be dissociated in cerebellar Purkinje cells. Neuron. 2003;37(5):813–819. doi: 10.1016/S0896-6273(03)00093-X. PubMed DOI

Armstrong CL, Duffin CA, McFarland R, Vogel M. Mechanisms of compartmental purkinje cell death and survival in the lurcher mutant mouse. Cerebellum. 2011;10(3):504–514. doi: 10.1007/s12311-010-0231-4. PubMed DOI

Kalkan Z, Durasi IM, Sezerman U, Atasever-Arslan B. Potential of GRID2 receptor gene for preventing TNF-induced neurodegeneration in autism. Neurosci Lett. 2016;620:62–69. doi: 10.1016/j.neulet.2016.03.043. PubMed DOI

Pei DS, Wang XT, Liu Y, Sun YF, Guan QH, Wang W, Yan JZ, Zong YY, Xu TL, Zhang GY. Neuroprotection against ischaemic brain injury by a GluR6-9c peptide containing the TAT protein transduction sequence. Brain. 2006;129:465–479. doi: 10.1093/brain/awh700. PubMed DOI

Ameri K, Jahangiri A, Rajah AM, Tormos KV, Nagarajan R, Pekmezci M, Nguyen V, Wheeler ML, Murphy MP, Sanders TA, Jeffrey SS, Yeghiazarians Y, Rinaudo PF, Costello JF, Aghi MA, Maltepe E. HIGD1A regulates oxygen consumption, ROS production, and AMPK activity during glucose deprivation to modulate cell survival and tumor growth. Cell Rep. 2015;10(6):891–899. doi: 10.1016/j.celrep.2015.01.020. PubMed DOI PMC

An HJ, Shin H, Jo SG, Kim YJ, Lee JO, Paik SG, Lee H. The survival effect of mitochondrial Higd-1a is associated with suppression of cytochrome C release and prevention of caspase activation. Biochim Biophys Acta. 2011;1813(12):2088–2098. doi: 10.1016/j.bbamcr.2011.07.017. PubMed DOI

Liu B, Barbosa-Sampaio H, Jones PM, Persaud SJ, Muller DS. The CaMK4/CREB/IRS-2 cascade stimulates proliferation and inhibits apoptosis of beta-cells. Plos One. 2012;7(9):e45711. doi: 10.1371/journal.pone.0045711. PubMed DOI PMC

Baquedano E, Burgos-Ramos E, Canelles S, Gonzalez-Rodriguez A, Chowen JA, Argente J, Barrios V, Valverde AM, Frago LM. Increased oxidative stress and apoptosis in the hypothalamus of diabetic male mice in the insulin receptor substrate-2 knockout model. Dis Model Mech. 2016;9(5):573–583. doi: 10.1242/dmm.023515. PubMed DOI PMC

Zhang Z, Zheng X, Luan Y, Liu Y, Li X, Liu C, Lu H, Chen X, Liu Y. Activity of metabotropic glutamate receptor 4 suppresses proliferation and promotes apoptosis with inhibition of gli-1 in human glioblastoma cells. Front Neurosci. 2018;12:320. doi: 10.3389/fnins.2018.00320. PubMed DOI PMC

Lei L, Han D, Gong S, Zheng J, Xu J. Mpz gene suppression by shRNA increases Schwann cell apoptosis in vitro. Neurol Sci. 2010;31(5):603–608. doi: 10.1007/s10072-010-0341-2. PubMed DOI

Kong Q, Wang M, Liao Z, Camden JM, Yu S, Simonyi A, Sun GY, Gonzalez FA, Erb L, Seye CI, Weisman GA. P2X(7) nucleotide receptors mediate caspase-8/9/3-dependent apoptosis in rat primary cortical neurons. Purinergic Signal. 2005;1(4):337–347. doi: 10.1007/s11302-005-7145-5. PubMed DOI PMC

McLarnon JG, Ryu JK, Walker DG, Choi HB. Upregulated expression of purinergic P2X(7) receptor in Alzheimer disease and amyloid-beta peptide-treated microglia and in peptide-injected rat hippocampus. J Neuropathol Exp Neurol. 2006;65(11):1090–1097. doi: 10.1097/01.jnen.0000240470.97295.d3. PubMed DOI

Illes P, Rubini P. Regulation of neural stem/progenitor cell functions by P2X and P2Y receptors. Neural Regen Res. 2017;12(3):395–396. doi: 10.4103/1673-5374.202937. PubMed DOI PMC

Savio LEB, de Andrade Mello P, da Silva CG, Coutinho-Silva R. The P2X7 receptor in inflammatory diseases: angel or demon. Front Pharmacol. 2018;9:52. doi: 10.3389/fphar.2018.00052. PubMed DOI PMC

Li A, Li L, Sun X, Ni Y, Chen X, Guo A, Chen X. Increased expression of mitochondrial inner-membrane protein Mpv17 after intracerebral hemorrhage in adult rats. Neurochem Res. 2015;40(8):1620–1630. doi: 10.1007/s11064-015-1644-8. PubMed DOI

Traba J, Satrustegui J, del Arco A. Adenine nucleotide transporters in organelles: novel genes and functions. Cell Mol Life Sci. 2011;68(7):1183–1206. doi: 10.1007/s00018-010-0612-3. PubMed DOI PMC

Harashima SI, Harashima C, Nishimura T, Hu Y, Notkins AL. Overexpression of the autoantigen IA-2 puts beta cells into a pre-apoptotic state: autoantigen-induced, but non-autoimmune-mediated, tissue destruction. Clin Exp Immunol. 2007;150(1):49–60. doi: 10.1111/j.1365-2249.2007.03455.x. PubMed DOI PMC

Jiang W, Guo M, Gong M, Chen L, Bi Y, Zhang Y, Shi Y, Qu P, Liu Y, Chen J, Li T. Vitamin A bio-modulates apoptosis via the mitochondrial pathway after hypoxic-ischemic brain damage. Mol Brain. 2018;11(1):14. doi: 10.1186/s13041-018-0360-0. PubMed DOI PMC

Foskolou IP, Jorgensen C, Leszczynska KB, Olcina MM, Tarhonskaya H, Haisma B, D'Angiolella V, Myers WK, Domene C, Flashman E, Flashman EM. Ribonucleotide reductase requires subunit switching in hypoxia to maintain DNA replication. Mol Cell. 2017;2017(2):206–220 e209. doi: 10.1016/j.molcel.2017.03.005. PubMed DOI PMC

Kuo ML, Lee MB, Tang M, den Besten W, Hu S, Sweredoski MJ, Hess S, Chou CM, Changou CA, Su M, Jia W, Su L, Yen Y. PYCR1 and PYCR2 interact and collaborate with RRM2B to protect cells from overt oxidative stress. Sci Rep. 2016;6:18846. doi: 10.1038/srep18846. PubMed DOI PMC

Tebbi A, Guittet O, Tuphile K, Cabrie A, Lepoivre M. Caspase-dependent proteolysis of human ribonucleotide reductase small subunits R2 and p53R2 during apoptosis. J Biol Chem. 2015;290(22):14077–14090. doi: 10.1074/jbc.M115.649640. PubMed DOI PMC

Jackson TC, Du L, Janesko-Feldman K, Vagni VA, Dezfulian C, Poloyac SM, Jackson EK, Clark RS, Kochanek PM. The nuclear splicing factor RNA binding motif 5 promotes caspase activation in human neuronal cells, and increases after traumatic brain injury in mice. J Cereb Blood Flow Metab. 2015;35(4):655–666. doi: 10.1038/jcbfm.2014.242. PubMed DOI PMC

Inoue A, Yamamoto N, Kimura M, Nishio K, Yamane H, Nakajima K. RBM10 regulates alternative splicing. FEBS Lett. 2014;588(6):942–947. doi: 10.1016/j.febslet.2014.01.052. PubMed DOI

Loiselle JJ, Roy JG, Sutherland LC. RBM10 promotes transformation-associated processes in small cell lung cancer and is directly regulated by RBM5. PLoS One. 2017;12(6):e0180258. doi: 10.1371/journal.pone.0180258. PubMed DOI PMC

Hand TW, Cui W, Jung YW, Sefik E, Joshi NS, Chandele A, Liu Y, Kaech SM. Differential effects of STAT5 and PI3K/AKT signaling on effector and memory CD8 T-cell survival. Proc Natl Acad Sci U S A. 2010;107(38):16601–16606. doi: 10.1073/pnas.1003457107. PubMed DOI PMC

Stankiewicz TR, Loucks FA, Schroeder EK, Nevalainen MT, Tyler KL, Aktories K, Bouchard RJ, Linseman DA. Signal transducer and activator of transcription-5 mediates neuronal apoptosis induced by inhibition of Rac GTPase activity. J Biol Chem. 2012;287(20):16835–16848. doi: 10.1074/jbc.M111.302166. PubMed DOI PMC

Ma R, Hu J, Huang C, Wang M, Xiang J, Li G. JAK2/STAT5/Bcl-xL signalling is essential for erythropoietin-mediated protection against apoptosis induced in PC12 cells by the amyloid beta-peptide Abeta25-35. Br J Pharmacol. 2014;171(13):3234–3245. doi: 10.1111/bph.12672. PubMed DOI PMC

Samuels-Lev Y, O'Connor DJ, Bergamaschi D, Trigiante G, Hsieh JK, Zhong S, Campargue I, Naumovski L, Crook T, Lu X. ASPP proteins specifically stimulate the apoptotic function of p53. Mol Cell. 2001;8(4):781–794. doi: 10.1016/S1097-2765(01)00367-7. PubMed DOI

Chen T, Yang I, Irby R, Shain KH, Wang HG, Quackenbush J, Coppola D, Cheng JQ, Yeatman TJ. Regulation of caspase expression and apoptosis by adenomatous polyposis coli. Cancer Res. 2003;63(15):4368–4374. PubMed

Lee JS, Kim HY, Jeong NY, Lee SY, Yoon YG, Choi YH, Yan C, Chu IS, Koh H, Park HT, Yoo YH. Expression of alphaB-crystallin overrides the anti-apoptotic activity of XIAP. Neuro Oncol. 2012;14(11):1332–1345. doi: 10.1093/neuonc/nos247. PubMed DOI PMC

Mao YW, Liu JP, Xiang H, Li DW. Human alphaA- and alphaB-crystallins bind to Bax and Bcl-X(S) to sequester their translocation during staurosporine-induced apoptosis. Cell Death Differ. 2004;11(5):512–526. doi: 10.1038/sj.cdd.4401384. PubMed DOI

Watanabe G, Kato S, Nakata H, Ishida T, Ohuchi N, Ishioka C. alphaB-crystallin: a novel p53-target gene required for p53-dependent apoptosis. Cancer Sci. 2009;100(12):2368–2375. doi: 10.1111/j.1349-7006.2009.01316.x. PubMed DOI PMC

Sahara S, Aoto M, Eguchi Y, Imamoto N, Yoneda Y, Tsujimoto Y. Acinus is a caspase-3-activated protein required for apoptotic chromatin condensation. Nature. 1999;401(6749):168–173. doi: 10.1038/43678. PubMed DOI

Kipanyula MJ, Woodhoo A, Rahman M, Payne D, Jessen KR, Mirsky R. Calcineurin-nuclear factor of activated T cells regulation of Krox-20 expression in Schwann cells requires elevation of intracellular cyclic AMP. J Neurosci Res. 2013;91(1):105–115. PubMed PMC

Sproston NR, Ashworth JJ. Role of C-Reactive Protein at Sites of Inflammation and Infection. Front Immunol. 2018;9:754. doi: 10.3389/fimmu.2018.00754. PubMed DOI PMC

Maddigan A, Truitt L, Arsenault R, Freywald T, Allonby O, Dean J, Narendran A, Xiang J, Weng A, Napper S, Freywald A. EphB receptors trigger akt activation and suppress fas receptor-induced apoptosis in malignant T lymphocytes. J Immunol. 2011;187(11):5983–5994. doi: 10.4049/jimmunol.1003482. PubMed DOI

Stetler RA, Gao Y, Signore AP, Cao G, Chen J. HSP27: mechanisms of cellular protection against neuronal injury. Curr Mol Med. 2009;9(7):863–872. doi: 10.2174/156652409789105561. PubMed DOI PMC

Kennedy D, Jager R, Mosser DD, Samali A. Regulation of apoptosis by heat shock proteins. IUBMB Life. 2014;66(5):327–338. doi: 10.1002/iub.1274. PubMed DOI

Xiong WC, Parsons JT. Induction of apoptosis after expression of PYK2, a tyrosine kinase structurally related to focal adhesion kinase. J Cell Biol. 1997;139(2):529–539. doi: 10.1083/jcb.139.2.529. PubMed DOI PMC

Zamostiano R, Pinhasov A, Gelber E, Steingart RA, Seroussi E, Giladi E, Bassan M, Wollman Y, Eyre HJ, Mulley JC, Brenneman DE, Gozes I. Cloning and characterization of the human activity-dependent neuroprotective protein. J Biol Chem. 2001;276(1):708–714. doi: 10.1074/jbc.M007416200. PubMed DOI

Idan-Feldman A, Ostritsky R, Gozes I. Tau and caspase 3 as targets for neuroprotection. Int J Alzheimers Dis. 2012;2012:493670. PubMed PMC

Merenlender-Wagner A, Malishkevich A, Shemer Z, Udawela M, Gibbons A, Scarr E, Dean B, Levine J, Agam G, Gozes I. Autophagy has a key role in the pathophysiology of schizophrenia. Mol Psychiatr. 2015;20(1):126–132. doi: 10.1038/mp.2013.174. PubMed DOI PMC

Pugazhenthi S, Nesterova A, Sable C, Heidenreich KA, Boxer LM, Heasley LE, Reusch JEB. Akt/protein kinase B up-regulates Bcl-2 expression through cAMP-response element-binding protein. J Biol Chem. 2000;275(15):10761–10766. doi: 10.1074/jbc.275.15.10761. PubMed DOI

Wang C, Kaufmann JA, Sanchez-Ross MG, Johnson KM. Mechanisms of N-methyl-D-aspartate-induced apoptosis in phencyclidine-treated cultured forebrain neurons. J Pharmacol Exp Ther. 2000;294(1):287–295. PubMed

Liu YT, Wong TP, Aarts M, Rooyakkers A, Liu LD, Lai TW, Wu DC, Lu J, Tymianski M, Craig AM, Wang YT. NMDA receptor subunits have differential roles in mediating excitotoxic neuronal death both in vitro and in vivo. J Neurosci. 2007;27(11):2846–2857. doi: 10.1523/JNEUROSCI.0116-07.2007. PubMed DOI PMC

Chen BS, Roche KW. Growth factor-dependent trafficking of cerebellar NMDA receptors via protein kinase B/Akt phosphorylation of NR2C. Neuron. 2009;62(4):471–478. doi: 10.1016/j.neuron.2009.04.015. PubMed DOI PMC

Kumazawa T, Nishimura K, Katagiri N, Hashimoto S, Hayashi Y, Kimura K. Gradual reduction in rRNA transcription triggers p53 acetylation and apoptosis via MYBBP1A. Sci Rep. 2015;5:10854. doi: 10.1038/srep10854. PubMed DOI PMC

Mori S, Bernardi R, Laurent A, Resnati M, Crippa A, Gabrieli A, Keough R, Gonda TJ, Blasi F. Myb-binding protein 1A (MYBBP1A) Is essential for early embryonic development, controls cell cycle and mitosis, and acts as a tumor suppressor. Plos One. 2012;7(10):e39723. doi: 10.1371/journal.pone.0039723. PubMed DOI PMC

Cotteret S, Jaffer ZM, Beeser A. Chernoff J.xiao p21-Activated kinase 5 (Pak5) localizes to mitochondria and inhibits apoptosis by phosphorylating BAD. Mol Cell Biol. 2003;23(16):5526–5539. doi: 10.1128/MCB.23.16.5526-5539.2003. PubMed DOI PMC

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