Abstract
Laminin is a major structural element of the basal lamina consisting of an α-chain, a β-chain, and a γ-chain arranged in a cross-like structure, with their C-terminal inter-coiled. Laminin is abundantly expressed in the hippocampus of mature brain and is implicated in several psychiatric disorders, but its possible role involved in learning and memory function is not known. This issue was examined here. Our results revealed that water maze training significantly decreased laminin-β1 (LB1) expression in the rat hippocampal CA1 area. Transfection of LB1 WT plasmid to hippocampal CA1 neurons impaired water maze performance in rats. Meanwhile, it decreased the phosphorylation level of ERK/MAPK and protein kinase serum- and glucocorticoid-inducible kinase-1 (SGK1). By contrast, knockdown of endogenous LB1 expression using RNA interference (LB1 siRNA) enhanced water maze performance. Meanwhile, it increased the phosphorylation level of ERK/MAPK and SGK1. The enhancing effect of LB1 siRNA on spatial learning and on the phosphorylation of ERK/MAPK and SGK1 was blocked by co-treatment with the MEK inhibitor U0126 at a concentration that did not apparently affect spatial learning and ERK/MAPK phosphorylation alone. Further, the enhancing effect of LB1 siRNA on spatial learning and SGK1 phosphorylation was similarly blocked by co-transfection with SGK1 siRNA at a concentration that did not markedly affect spatial learning and SGK1 expression alone. These results together indicate that LB1 negatively regulates spatial learning in rats. In addition, LB1 impairs spatial learning through decreased activation of the ERK/MAPK–SGK1 signaling pathway in the rat hippocampus.
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References
Abdallah B, Hassan A, Benoist C, Goula D, Behr JP, Demeneix BA (1996). A powerful nonviral vector for in vivo gene transfer into the adult mammalian brain: polyethylenimine. Hum Gene Ther 7: 1947–1954.
Adams JP, Sweatt JD (2002). Molecular psychology: roles for the ERK MAP kinase cascade in memory. Annu Rev Pharmacol Toxicol 42: 135–163.
Alexander CM, Werb Z (1989). Proteinases and extracellular matrix remodeling. Curr Opin Cell Biol 1: 974–982.
Atkins CM, Selcher JC, Petraitis JJ, Trzaskos JM, Sweatt JD (1998). The MAPK cascade is required for mammalian associative learning. Nat Neurosci 1: 602–609.
Bruckner G, Hausen D, Hartig W, Drlicek M, Arendt T, Brauer K (1999). Cortical areas abundant in extracellular matrix chondroitin sulphate proteoglycans are less affected by cytoskeletal changes in Alzheimer's disease. Neuroscience 92: 791–805.
Bukalo O, Schachner M, Dityatev A (2001). Modification of extracellular matrix by enzymatic removal of chondroitin sulfate and by lack of tenascin-R differentially affects several forms of synaptic plasticity in the hippocampus. Neuroscience 104: 359–369.
Chan CS, Weeber EJ, Kurup S, Sweatt JD, Davis RL (2003). Integrin requirement for hippocampal synaptic plasticity and spatial memory. J Neurosci 23: 7107–7116.
Chao CC, Ma YL, Lee EHY (2011). BDNF enhances Bcl-xL expression through protein kinase CK2-activated and NF-κB-mediated pathway in rat hippocampus. Brain Pathol 21: 150–162.
Coccia EM, Del Russo N, Stellacci E, Testa U, Marziali G, Battistini A (1999). STAT1 activation during monocyte to macrophage maturation: role of adhesion molecules. Int Immunol 11: 1075–1083.
Coitinho AS, Freitas ARO, Lopes MH, Hajj GNM, Roesler R, Walz R et al (2006). The interaction between prion protein and laminin modulates memory consolidation. Eur J Neurosci 24: 3255–3264.
Colognato H, Yurchenco PD (2000). Form and function: the laminin family of heterotrimers. Dev Dyn 218: 213–234.
Dityatev A, Schachner M (2003). Extracellular matrix molecules and synaptic plasticity. Nat Rev 4: 456–468.
Easley CA, Faison MO, Kirsch TL, Lee JA, Seward ME, Tombes RM (2006). Laminin activates CaMK-II to stabilize nascent embryonic axons. Brain Res 1092: 59–68.
Egles C, Claudepierre T, Manglapus MK, Champliaud MF, Brunken WJ, Hunter DD (2007). Laminins containing the beta2 chain modulate the precise organization of CNS synapses. Mol Cell Neurosci 34: 288–298.
Ekblom P, Lonai P, Talts JF (2003). Expression and biological role of laminin-1. Matrix Biol 22: 35–47.
Gonzales M, Haan K, Baker SE, Fitchmun M, Todorov I, Weitzman S et al (1999). A cell signal pathway involving laminin-5, alpha3beta1 integrin, and mitogen-activated protein kinase can regulate epithelial cell proliferation. Mol Biol Cell 10: 259–270.
Graner E, Mercadante AF, Zanata SM, Forlenza OV, Cabral ALB, Veiga SS et al (2000). Cellular prion protein binds laminin and mediates neuritogenesis. Mol Brain Res 76: 85–92.
Hagg T, Muir D, Engvall E, Varon S, Manthorpe M (1989). Laminin-like antigen in rat CNS neurons: distribution and changes upon brain injury and nerve growth factor treatment. Neuron 3: 721–732.
Han JH, Kushner SA, Yiu AP, Cole CJ, Matynia A, Brown RA et al (2007). Neuronal competition and selection during memory formation. Science 316: 457–460.
Han JH, Kushner SA, Yiu AP, Hsiang HL, Buch T, Waisman A et al (2009). Selective erasure of a fear memory. Science 323: 1492–1495.
Hsu WL, Chiu TH, Tai DJ, Ma YL, Lee EH (2009). A novel defense mechanism that is activated on amyloid-beta insult to mediate cell survival: role of SGK1–STAT1/STAT2 signaling. Cell Death Differ 16: 1515–1529.
Huang AM, Wang HL, Tang YP, Lee EH (1998). Expression of integrin-associated protein gene associated with memory formation in rats. J Neurosci 18: 4305–4313.
Indyk JA, Chen ZL, Tsirka SE, Strickland S (2003). Laminin chain expression suggests that laminin-10 is a major isoform in the mouse hippocampus and is degraded by the tissue plasminogen activator/plasmin protease cascade during excitotoxic injury. Neuroscience 116: 359–371.
Kobayashi T, Cohen P (1999). Activation of serum- and glucocorticoid-regulated protein kinase by agonists that activate phosphotidylinositide 3-kinase is mediated by 3-phosphoinositide-dependent protein kinase-1 (PDK1) and PDK2. Biochem J 339: 319–328.
Kramar EA, Bernard JA, Gall CM, Lynch G (2002). Alpha3 integrin receptors contribute to the consolidation of long-term potentiation. Neuroscience 110: 29–39.
Laifenfeld D, Karry R, Grauer E, Klein E, Ben-Shachar D (2005a). Antidepressants and prolonged stress in rats modulate CAM-L1, laminin, and pCREB, implicated in neuronal plasticity. Neurobiol Dis 20: 432–441.
Laifenfeld D, Karry R, Klein E, Ben-Shachar D (2005b). Alterations in cell adhesion molecule L1 and functionally related genes in major depression: a postmortem study. Biol Psychiatry 57: 716–725.
Laifenfeld D, Klein E, Ben-Shachar D (2002). Norepinephrine alters the expression of genes involved in neuronal sprouting and differentiation: relevance for major depression and antidepressant mechanisms. J Neurochem 83: 1054–1064.
Lee CT, Tyan SW, Ma YL, Tsai MC, Yang YC, Lee EHY (2006). Serum- and glucocorticoid-inducible kinase (SGK) is a target of the MAPK/ERK signaling pathway that mediates memory formation in rats. Eur J Neurosci 23: 1311–1320.
Liang KC, Hu SJ, Chang SC (1996). Formation and retrieval of inhibitory avoidance memory: differential roles of glutamate receptors in the amygdala and medial prefrontal cortex. Chin J Physiol 39: 155–166.
Ma YL, Tsai MC, Hsu WL, Lee EHY (2006). SGK protein kinase facilitates the expression of long-term potentiation in hippocampal neurons. Learn Mem 13: 114–118.
Malberg JE, Eisch AJ, Nestler EJ, Duman RS (2000). Chronic antidepressant treatment increases neurogenesis in adult rat hippocampus. J Neurosci 20: 9104–9110.
Matsuda K, Tashiro K, Hayashi Y, Monji A, Yoshida I, Mitsuyama Y (2002). Measurement of laminins in the cerebrospinal fluid obtained from patients with Alzheimer's disease and vascular dementia using a modified enzyme-linked immunosorbent assay. Dement Geriatr Cogn Disord 14: 113–122.
McDearmon EL, Combs AC, Sekiguchi K, Fujiwara H, Ervasti JM (2006). Brain a-dystroglycan displays unique glycoepitopes and preferential binding to laminin-10/11. FEBS Lett 580: 3381–3385.
Meighan SE, Meighan PC, Choudhury P, Davis CJ, Olson ML, Zornes PA et al (2006). Effects of extracellular matrix-degrading proteases matrix metalloproteinases 3 and 9 on spatial learning and synaptic plasticity. J Neurochem 96: 1227–1241.
Michaluk P, Mikasova L, Groc L, Frischknecht R, Choquet D, Kaczmarek L (2009). Matrix metalloproteinase-9 controls NMDA receptor surface diffusion through integrin b1 signaling. J Neurosci 29: 6007–6012.
Murtomaki S, Risteli J, Risteli L, Koivisto UM, Johansson S, Liesi P (1992). Laminin and its neurite outgrowth-promoting domain in the brain in Alzheimer's disease and Down's syndrome patients. J Neurosci Res 32: 261–273.
Nagy V, Bozdagi O, Huntley GW (2007). The extracellular protease matrix metalloproteinase-9 is activated by inhibitory avoidance learning and required for long-term memory. Learn Mem 14: 655–664.
Nakagami Y, Abe K, Nishiyama N, Matsuki N (2000). Laminin degradation by plasmin regulates long-term potentiation. J Neurosci 20: 2003–2010.
Noakes PG, Gautam M, Mudd J, Sanes JR, Merlie JP (1995). Aberrant differentiation of neuromuscular junctions in mice lacking s-laminin/laminin beta 2. Nature 374: 258–262.
Okano R, Mita T, Matsui T (1992). Characterization of a novel promoter structure and its transcriptional regulation of the murine laminin β1 gene. Biochim Biophys Acta 1132: 49–57.
Palu E, Liesi P (2002). Differential distribution of laminins in Alzheimer disease and normal human brain tissue. J Neurosci Res 69: 243–256.
Sandi C (2004). Stress, cognitive impairment and cell adhesion molecules. Nat Rev 5: 917–930.
Sanes JR (1989). Extracellular matrix molecules that influence neural development. Ann Rev Neurosci 12: 491–516.
Sharif KA, Baker H, Gudas LJ (2004). Differential regulation of laminin β1 transgene expression in the neonatal and adult mouse brain. Neuroscience 126: 967–978.
Shi X, McGinty JF (2006). Extracellular signal-regulated mitogen-activated protein kinase inhibitors decrease amphetamine-induced behavior and neuropeptide gene expression. Neuroscience 138: 1289–1298.
Sobel RA, Ahmed AS (2001). White matter extracellular matrix chondroitin sulfate/dermatan sulfate proteoglycans in multiple sclerosis. J Neuropathol Exp Neurol 60: 1198–1207.
Tai DJC, Hsu WL, Liu YC, Ma YL, Lee EHY (2011). Novel role and mechanism of protein inhibitor of activated STAT1 in spatial learning. EMBO J 30: 205–220.
Timpl R (1996). Macromolecular organization of basement membranes. Curr Opin Cell Biol 8: 618–624.
Tsai KJ, Chen SK, Ma YL, Hsu WL, Lee EH (2002). Sgk, a primary glucocorticoid-induced gene, facilitates memory consolidation of spatial learning in rats. Proc Natl Acad Sci USA 99: 3990–3995.
Tunggal P, Smyth N, Paulsson M, Ott MC (2000). Laminins: structure and genetic regulation. Micros Res Tech 51: 214–227.
Vasios GW, Gold JD, Petkovich M, Chambon P, Gudas LJ (1989). A retinoic acid-responsive element is present in the 5′ flanking region of the laminin β1 gene. Proc Natl Acad Sci USA 86: 9099–9103.
Wang XB, Bozdagi O, Nikitczuk JS, Zhai ZW, Zhou Q, Huntley GW (2008). Extracellular proteolysis by matrix metalloproteinase-9 drives dendritic spine enlargement and long-term potentiation coordinately. Proc Natl Acad Sci USA 105: 19520–19525.
Woessner JF, Nagase H (2000). Matrix Metalloproteinases and TIMPs. Oxford UP: Oxford, New York.
Wright JW, Brown TE, Harding JW (2007). Inhibition of hippocampal matrix metalloproteinase-3 and -9 disrupts spatial memory. Neural Plast 2007: 73813–73820.
Xu R, Spencer VA, Groesser DL, Bissell MJ (2010). Laminin regulates PI3K basal localization and activation to sustain STAT5 activation. Cell Cycle 9: 4315–4322.
Yang YC, Lin CH, Lee EH (2006). Serum- and glucocorticoid-inducible kinase 1 (SGK1) increases neurite formation through microtubule depolymerization by SGK1 and by SGK1 phosphorylation of tau. Mol Cell Biol 26: 8357–8370.
Zamilpa R, Lopez EF, Chiao YA, Dai Q, Escobar GP, Hakala K et al (2010). Proteomic analysis identifies in vivo candidate matrix metalloproteinase-9 substrates in the left ventricle post-myocardial infarction. Proteomics 10: 2214–2223.
Zhang HT, Zhao Y, Huang Y, Dorairaj NR, Chandler LJ, O′Donnell JM (2004). Inhibition of the phosphodiesterase 4 (PDE4) enzyme reverses memory deficits produced by infusion of the MEK inhibitor U0126 into the CA1 subregion of the rat hippocampus. Neuropsychopharmacology 29: 1432–1439.
Zhao Z, Fan L, Frick KM (2010). Epigenetic alterations regulate estradiol-induced enhancement of memory consolidation. Proc Natl Acad Sci USA 107: 5605–5610.
Acknowledgements
This work was supported by research fund from the Institute of Biomedical Sciences (IBMS), Academia Sinica, Taiwan, and a Grant from the National Science Council of Taiwan (NSC98-2320-B-197-001). Part of this work was performed when Dr YC Yang was a postdoctoral fellow at IBMS.
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Yang, Y., Ma, Y., Liu, W. et al. Laminin-β1 Impairs Spatial Learning through Inhibition of ERK/MAPK and SGK1 Signaling. Neuropsychopharmacol 36, 2571–2586 (2011). https://doi.org/10.1038/npp.2011.148
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DOI: https://doi.org/10.1038/npp.2011.148
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