Src kinase up-regulates the ERK cascade through inactivation of protein phosphatase 2A following cerebral ischemia
- Xiaohan Hu†1, 2,
- Xiangyang Wu†1, 2, 3,
- Jiali Xu2, 4,
- Jin Zhou2, 3,
- Xiao Han1, 2 and
- Jun Guo1, 2, 4Email author
© Hu et al; licensee BioMed Central Ltd. 2009
Received: 25 March 2009
Accepted: 14 July 2009
Published: 14 July 2009
The regulation of protein phosphorylation requires a balance in the activity of protein kinases and protein phosphatases. Our previous data indicates that Src can increase ERK activity through Raf kinase in response to ischemic stimuli. This study examined the molecular mechanisms by which Src activates ERK cascade through protein phosphatases following cerebral ischemia.
Ischemia-induced Src activation is followed by phosphorylation of PP2A at Tyr307 leading to its inhibition in the rat hippocampus. SU6656, a Src inhibitor, up-regulates PP2A activity, resulting in a significant decreased activity in ERK and its targets, CREB and ERα. In addition, the PP2A inhibitor, cantharidin, led to an up-regulation of ERK activity and was able to counteract Src inhibition during ischemia.
Src induces up-regulation of ERK activity and its target transcription factors, CREB and ERα, through attenuation of PP2A activity. Therefore, activation of ERK is the result of a crosstalk between two pathways, Raf-dependent positive regulators and PP2A-dependent negative regulators.
When blood flow is decreased to the brain, cerebral ischemia, a complex signaling network is activated. Excitotoxicity can be induced by an increase in intraneuronal Ca2+ through calcium ion channels, such as the N-methyl-D-aspartic acid (NMDA) receptor, L-type voltage-gated calcium channels (L-VGCC) and IP3 receptor. An influx in intraneuronal Ca2+ is a key mediator in multiple intracellular signaling cascades after ischemia . Extracellular signal – regulated kinase (ERK), a member of the mitogen-activated protein kinase (MAPK) family, is activated in a Ca2+-dependent manner in cerebral ischemia [2–4]. ERK is regulated via phosphorylation at various motifs. Previous studies have demonstrated that ERK is activated by various upstream kinases, such as Akt and Src, by the Raf/MEK/ERK signaling cascade [5–7]. In response to ischemic stimuli, active Src kinase activates ERK through Raf phosphorylation at Tyr340/Tyr341 . Src is a non-receptor protein tyrosine kinase (PTK). The Src family of proteins contain a Src homology (SH) 2 domain and SH3 domain, a catalytic domain, and a C-terminal tail. Src maintains basal activity in normal cells by an auto-inhibitory mechanism, whereby Tyr527 in the C-terminal tail is phosphorylated allowing for association with the SH2 domain preventing catalytic activity. Src activation is initiated when Tyr527 is dephosphorylated and, subsequently, autophosphorylated at Tyr-416 .
In general, changes in protein phosphorylation require coordinate regulation of protein kinases and protein phosphatases. However, to date, the signaling mechanisms leading to dephosphorylation of ERK resulting in inactivation have not been well defined. Protein phosphotase 2A (PP2A) has been shown to be an ERK phosphatase. Furthermore, it has been suggested that PP2A dephosphorylates critical residues resulting in ERK inactivation [9–11]. PP2A is a Ser/Thr-specific phosphatase composed of two regulatory (A and B) and one catalytic subunit (C) . The catalytic subunit of PP2A (PP2AC) is regulated by phosphorylation at Tyr307 in the conserved C-terminal domain of the catalytic subunit resulting in inactivation of the enzyme [12, 13]. Active Src can directly phosphorylate PP2A C at Tyr307  and cerebral ischemia leads to up-regulation of Src activity . However, whether Src kinase induces ERK activation through inhibition of PP2A during cerebral ischemia is unclear.
Following ischemia, the activated ERK cascade regulates gene expression via upregulation of specific transcription factors . One of the upregulated targets is estrogen receptor α (ERα), a neuroprotector. It has been reported that ERα phosphorylation at Ser118 positively regulates its function and that phospho-ERK phosphorylates this residue [17–20]. Another neuroprotective protein induced by ERK activation is cyclic AMP response element-binding protein (CREB). Additionally, ERK phosphorylates CREB at Ser133, which is essential for CREB-mediated effects on transcription [21, 22]. Interestingly, this residue has been shown to be dephosphorylated by PP2A [23, 24].
Therefore, in the present study, we examine the involvement of PP2A in Src-dependent ERK phosphorylation in the rat hippocampus following ischemia. Through the use of SU6656 (SU), a Src inhibitor, we show that PP2A activity is upregulated, which may, in turn, attenuate ERK activation and its downstream proteins, CREB and ERα, in the post-ischemic hippocampus. Thus, we propose that Src induces ERK activation through downregulation of PP2A activity in cerebral ischemia.
Src inhibitor decreases activity of the ERK/CREB and ERα pathways post-ischemia
Activated ERK can facilitate the phosphorylation of a variety of transcription factors phosphorylation involved in gene expression . Two proteins regulated by ERK are CREB and ERα, which are activated by phosphorylation at the Ser133 residue  and at the Ser118 site , respectively. In this study, CREB and ERα nuclear activity were observed in response to cerebral ischemia. Compared with a sham group, both phospho-CREB and phospho-ERα are increased in the 24 h reperfusion groups (Figure. 1C and 1D; P < 0.05) and similar to ischemia-induced ERK activity. To determine whether Src might regulate CREB and ERα activity following ischemia, SU was employed. Levels of p-ERα and p-CREB in the 24 h reperfusion group showed obvious decrease in animals in which SU was administered (Figure. 1C and 1D; P < 0.05). These data suggest that Src kinase is required for activation of ERK and, subsequently, ERα and CREB post-ischemic hippocampus.
Src activation is correlated with an increase in PP2A phosphorylation and inhibition
Inhibition of Src activity results in PP2A increased activity in response to cerebral ischemia
Inhibition of PP2A compensates for inhibition of Src allowing for upregulation of ERK/CREB and ERα in the presence of SU
PP2A is also able to dephosphorylate ERK targets, CREB and ERα. To further assess the role of PP2A in regulation of signaling cascades during cerebral ischemia, intranuclear CREB and ERα immunoblot assays were performed using specific phosphorylation antibodies. Compared to samples treated with SU only, both ERα and CREB phosphorylations are increased in the Ct and SU co-administration samples (P < 0.05; Figure 1B). These data suggest that Src is required for up-regulation of CREB and ERα pathway through inhibition of PP2A activity. Total protein of ERK, CREB and ERα in each group remained unchanged (Figure 4A–B, P > 0.05).
PP2A is a Ser/Thr-specific phosphatase capable of dephosphorylating and inactivating ERK [9, 10, 29]. Induction of Src results in inactivation of PP2A resulting in up-regulation of ERK activity in cerebral ischemia. Several lines of evidence support the role of PP2A in regulation of the Src/ERK pathway. First, cerebral ischemia results in sustained activation of Src kinase after 6 h reperfusion post-ischemia, accompanied by continuous phosphorylation of Tyr307 and inhibition of PP2A. Second, SU6656, an effective Src inhibitor, prevents PP2A phosphorylation resulting in up-regulation of PP2A activity. Third, cantharidin is a specific inhibitor of PP2A, which has little effect on PP1. Treatment with cantharidin abrogates the effects of the Src inhibitor, SU6656, allowing for upregulation of ERK activity following ischemia. These results indicate that Src upregulation of the ERK pathway in ischemic neurons requires inhibition of PP2A.
Src-induced phosphorylation and inactivation of PP2A was thought to be closely associated with intracellular calcium signaling . In rat hippocampal neurons, the Src/ERK cascade is dependent on calcium influx elicited by upregulation of ion channels like NMDA receptor and IP3 receptor. In addition, inhibition of ion channels can inhibit Src and ERK activity after cerebral ischemia [2, 4, 31]. Our previous studies have also suggested that Src kinase can up-regulate the Raf/ERK cascade directly in a calcium-dependent manner following ischemia stroke . Apparently, Src can activate the ERK cascade via coordinated activation of protein kinases and inactivation of protein phosphatases in a calcium-dependent manner.
ERK exert their function through up-regulation of nuclear transcription factors resulting in changes in gene expression . Our present study indicates that there were no changes in subcellular localization of total protein levels of ERK in response to ischemic stimuli. Cerebral ischemia induced an increase in ERK phosphorylation and activity in membrane, cytoplasma, and nucleus in hippocampal neurons. Activated ERK in the nucleus is sufficient to target its intranuclear substrates like CREB and ERα. As transcription factors, CREB and ERα are localized primarily in the nucleus of rat hippocampal neurons and their activities are negatively regulated by PP2A. Therefore, CREB and ERα share similar mechanisms as downstream molecules of ERK, and are modulated by Src kinase through a complex signalling network dependent on PP2A inactivation. CREB and ERα are thought to be protective factors in the nucleus [20, 21]. Upregulation of intranuclear ERK/CREB and ERα pathway is involved in neuroprotective gene expression in response to Src signals following cerebral ischemia .
Activation of Src kinase in neurons during cerebral ischemia induces a complex signaling network leading to activation of ERK. In response to ischemia-induced upregulation of Src kinase, Raf, a positive regulator of the ERK signaling cascade, is activated. In addition induction of Src kinase activity also leads to inhibition of PP2A, a negative regulator of ERK activity. Activation of ERK through induction of Raf activity and inhibition of PP2A leads to activation of CREB and ERα, transcription factors, which is involved in neuronal protection from ischemic stress.
Transient cerebral ischemia
Adult male Sprague-Dawley rats weighing approximately 250 g (Shanghai Laboratory Animal Center, SLAC, China) were housed under natural conditions (12-h light/12-h dark cycle from 07:00 to 18:00 h) at a constant temperature of 25°C with food and water ad libitum. All animal surgery was performed in accordance with the Institutional Animal Care and Use Committee and conformed to international guidelines on the ethical use of animals (Guide for the Care and Use of Laboratory Animal, 1996). Before surgery, the animals were deprived of food and water overnight. Experimental rats were anesthetized with 20% chloral hydrate (300 mg/kg, i.p.) and subjected to four-vessel occlusion (4VO) according to the method of Pulsinelli et al., 1982. Briefly, in sterile conditions while animals were under deep anaesthesia, the bilateral vertebral arteries were occluded permanently by electrocauterization and the common carotid arteries were separated from connective tissue and nerves and marked with surgical thread. On the following day, ischemia was induced by bilateral occlusion of the common carotid arteries for 10 min using aneurysm clips. To minimize the experimental variations, all rats used had to satisfy the following criteria: (1) complete flat electroencephalogram throughout the duration of carotid occlusion, (2) maintenance of dilated pupils and an absence of cornea reflex during ischemia, (3) rigor of the extremities and vertebral column. Sham operated control rats received the same treatment without carotid artery occlusion. Body temperature was monitored using a rectal probe and maintained at approximately 37°C using a heating pad until the animal had fully recovered from anesthesia.
I.c.v. infusion and administration of inhibitors
Ten microliter microsyringes were used for injections. Polyethylene tubing was used to attach injection cannula to the microsyringe. A burr hole was drilled in the skull measured from bregma (0.8 mm posterior, 1.5 mm lateral and 3.5 mm deep) for administration of chemicals or vehicle before ischemia. Three microliters of cantharidin (Ct, 25 μg/μl; Biomol, Plymouth Meeting, PA) and SU6656 (SU, 5 μM; Calbiochem, La Jolla, CA, USA) (in DMSO) were administered, either individually or in combination, into the cerebral ventricle (i.c.v.). After the injection, the injector was retained in place for an additional 5 min in order to reduce any possible backflow of the liquid along with the injection void. Occlusion occurred 20 min post-injection.
Subcellular fractionation and sample preparation
Rats were euthanized by decapitation at various time points: 10 min after ischemia or 10 min, 1 h, 6 h, or 24 h post-reperfusion. The hippocampi were quickly removed on ice in a cold room [6, 33] and the separated brain regions were homogenized in 1:10 (w/v) ice-cold homogenization buffer A (HEPES 50, pH 7.4, KCl 100, Na3VO4 1, NaF 50, and PMSF 1 mM) supplemented with 1% mammalian protease inhibitor cocktail (Sigma-Aldrich Co., St. Louis, MO). Cytoplasmic and membrane proteins were extracted by centrifugation at 800 × g for 20 min at 4°C. Following centrifugation, the supernatant was transferred into the fresh tubes, which containing the membrane and cytoplasmic proteins (M and C). The resulting pellet was resuspended in homogenization buffer B (buffer A, 1 mM DTT, 1% cocktail and 10% NP-40), kept on ice for 30 min, intensely shaken for 15 min, and then centrifuged at 14,000 × g for 20 min at 4°C. The supernatant contains the nuclear protein (N). All of the supernatant was extracted and then stored at -80°C until assayed. The protein concentrations of the extracts were determined according to the Bradford assay protocol using bovine serum albumin (BSA) as a standard (Bradford, 1976).
Western blot analysis
Equivalent amounts of protein lysates were resolved by 10% SDS-PAGE, transferred to nitrocellulose membrane, incubated in a solution of 3% BSA-Block/TBST for 2 h at room temperature, and then incubated with primary antibody in 1% BSA with shaking at 4°C overnight. Following three 5–10 min washes in TBST, the membranes were incubated with secondary antibody conjugated to horseradish peroxidase in 1% BSA at room temperature for 2 h. Following the incubation, membranes were given three 10-min washes with TBST, and then developed using the Pierce SuperSignal® chemiluminescence kit (Pierce, Rockford, IL). The primary antibodies used were as follows: mouse anti-phospho-ERK (T202/Y204), rabbit anti-ERK, rabbit anti-Src, rabbit anti-PP2A C subunit, rabbit anti-phospho-CREB (Ser133), and rabbit anti-CREB purchased from Cell Signaling Technology (Beverly, MA); rabbit anti-phospho-ERα (Ser118) and rabbit anti-ERα purchased from Santa Cruz Biotechnology (Santa Cruz, CA); rabbit anti-phospho- PP2A (Y307) purchased from Abcom Biotechnology (Cambridge, UK), rabbit anti-phospho-Src (Tyr527) purchased from Sigma (St. Louis, MO); β-actin purchased from Boster Biotechnology (WuHan, HB, China). Blots were then washed four times for 15 min and visualized using enhanced chemiluminescence (ECL; Amersham Biosciences, Piscataway, NJ).
PP2A activity assay
PP2A activity was measured with a molybdate dye-based phosphatase assay kit (Promega, Madison, WI). Assays were performed according to the manufacturer's protocol. Briefly, the samples were homogenized in lysis buffer (Tris-HCl 50, pH 7.4, EDTA 0.1, DTT 1, PMSF 0.1 mM, 1% Triton X-100 and 1% protease inhibitor cocktail) in ice water. Samples were filtered through Sephadex G-25 columns to remove free phosphate. The samples were then added to a reaction premix which contained phosphopeptide substrate, 5 × PP2A reaction buffer (250 mM imidazole, pH 7.2, 1 mM EGTA, 0.1% β-mercaptoethanol, and 0.5 mg/ml BSA) and storage buffer in 96-well plates. The reactions were terminated by adding a molybdate dye/additive mixture and incubating at 37°C for 30 min. Finally, phosphotase activity in the samples were measured using a spectrophotometer (Molecular Devices, Sunnyvale, CA) at 630 nm wavelength.
In each case, for semi-quantitative analysis, the data from at least four animals are expressed as the mean ± standard deviation. Statistical analysis was conducted using an analysis of variance (ANOVA) followed by the Newman-Keuls test. Comparisons between two groups were performed using a t-test. P values less than 0.05 were considered significant.
Extracellular signal – regulated kinase
Protein phosphotase 2A
cyclic AMP response element-binding protein
estrogen receptor α
mitogen-activated protein kinase
L-type voltage-gated calcium channels
protein tyrosine kinase
bovine serum albumin
polyacrylamide gel electrophoresis
The work was supported by grants from the National Natural Science Foundation of China (No. 30871200) and Medical Foundation of Department of Health of Jiangsu Province (No. H200749).
- Starkov AA, Chinopoulos C, Fiskum G: Mitochondrial calcium and oxidative stress as mediators of ischemic brain injury. Cell Calcium. 2004, 36: 257-264. 10.1016/j.ceca.2004.02.012.View ArticlePubMedGoogle Scholar
- Gao J, Duan B, Wang DG, Deng XH, Zhang GY, Xu L, Xu TL: Coupling between NMDA Receptor and Acid-Sensing Ion Channel Contributes to Ischemic Neuronal Death. Neuron. 2005, 48: 635-646. 10.1016/j.neuron.2005.10.011.View ArticlePubMedGoogle Scholar
- Song B, Ma C, Gong S, Yuan Z, Li D, Liu W, Li W, Chen R, Zhu X, Zeng J, Han Y, Li M: Extracellular signal-regulated kinases are not involved in activity-dependent survival or apoptosis in cerebellar granule neurons. Neurosci. 2006, 407: 214-218.Google Scholar
- Mehta SL, Manhas N, Raghubir R: Molecular targets in cerebral ischemia for developing novel therapeutics. Brain Res Rev. 2007, 54: 34-66. 10.1016/j.brainresrev.2006.11.003.View ArticlePubMedGoogle Scholar
- Rusanescu G, Qi H, Thomas SM, Brugge JS, Halegoua S: Calcium influx induces neurite growth through a Src-Ras signaling cassette. Neuron. 1995, 15: 1415-1425. 10.1016/0896-6273(95)90019-5.View ArticlePubMedGoogle Scholar
- Guo J, Wu HW, Hu G, Han X, De W, Sun YJ: Sustained activation of Src-family tyrosine kinases by ischemia: a potential mechanism mediating extracellular signal-regulated kinase cascades in hippocampal dentate gyrus. Neurosci. 2006, 143: 827-836. 10.1016/j.neuroscience.2006.08.031.View ArticleGoogle Scholar
- Bełtowski J, Wójcicka G, Trzeciak J, Marciniak A: H2O2 and Src-dependent transactivation of the EGF receptor mediates the stimulatory effect of leptin on renal ERK and Na+, K+-ATPase. Peptides. 2006, 27 (12): 3234-3244. 10.1016/j.peptides.2006.08.010.View ArticlePubMedGoogle Scholar
- Moelling K, Schad K, Bosse M, Zimmermann S, Schweneker M: Regulation of Raf-Akt Cross-talk. J Biol Chem. 2002, 277 (34): 31099-106. 10.1074/jbc.M111974200.View ArticlePubMedGoogle Scholar
- Van Kanegan MJ, Adams DG, Wadzinski BE, Strack S: Distinct protein phosphatase 2A heterotrimers modulate growth factor signaling to extracellular signal-regulated kinases and Akt. J Biol Chem. 2005, 280: 36029-36036. 10.1074/jbc.M506986200.View ArticlePubMedGoogle Scholar
- Miglietta A, Bozzo F, Gabriel L, Bocca C, Canuto RA: Extracellular signal-regulated kinase 1/2 and protein phosphatase 2A are involved in the antiproliferative activity of conjugated linoleic acid in MCF-7 cells. Br J Nutr. 2006, 96: 22-27. 10.1079/BJN20061619.View ArticlePubMedGoogle Scholar
- Zhao J, Wu HW, Chen YJ, Tian HP, Li LX, Han X, Guo J: Protein phosphatase 2A-negative regulation of the protective signaling pathway of Ca2+/CaM-dependent ERK activation in cerebral ischemia. J Neurosci Res. 2008, 86 (12): 2733-45. 10.1002/jnr.21712.View ArticlePubMedGoogle Scholar
- Mao L, Yang L, Arora A, Choe ES, Zhang G, Liu Z, Fibuch EE, Wang JQ: Role of Protein Phosphatase 2A in mGluR5-regulated MEK/ERK Phosphorylation in Neurons. J Biol Chem. 2005, 280 (13): 12602-12610. 10.1074/jbc.M411709200.View ArticlePubMedGoogle Scholar
- Chung H, Nairn AC, Murata K, Brautigan DL: Mutation of Tyr307 and Leu309 in the protein phosphatase 2A catalytic subunit favors association with the alpha 4 subunit which promotes dephosphorylation of elongation factor-2. Biochemistry. 1999, 38 (32): 10371-10376. 10.1021/bi990902g.View ArticlePubMedGoogle Scholar
- Liu W, Akhand AA, Takeda K, Kawamoto Y, Itoigawa M, Kato M, Suzuki H, Ishikawa N, Nakashima I: Protein phosphatase 2A-linked and -unlinked caspase-dependent pathways for downregulation of Akt kinase triggered by 4-hydroxynonenal. Cell Death Differ. 2003, 10 (7): 772-781. 10.1038/sj.cdd.4401238.View ArticlePubMedGoogle Scholar
- Wu HW, Li HF, Guo J: Spry2-mediated inhibition of the Ras/ERK pathway through interaction with Src kinase following cerebral ischemia. Brain Inj. 2008, 22 (3): 275-281. 10.1080/02699050801911295.View ArticlePubMedGoogle Scholar
- Lee S, Yoon S, Kim DH: A high nuclear basal level of ERK2 phosphorylation contributes to the resistance of cisplatin-resistant human ovarian cancer cells. Gynecologic Oncology. 2007, 104: 338-344. 10.1016/j.ygyno.2006.08.040.View ArticlePubMedGoogle Scholar
- Xie W, Duan R, Safe S: Activation of adenosine deaminase in MCF-7 cells through IGF-estrogen receptor alpha crosstalk. J Mol Endocrinol. 2001, 26: 217-228. 10.1677/jme.0.0260217.View ArticlePubMedGoogle Scholar
- Tang HY, Lin HY, Zhang S, Davis FB, Davis PJ: Thyroid hormone causes mitogen-activated protein kinase-dependent phosphorylation of the nuclear estrogen receptor. Endocrinology. 2004, 145: 3265-3272. 10.1210/en.2004-0308.View ArticlePubMedGoogle Scholar
- Glaros S, Atanaskova N, Zhao C, Skafar DF, Reddy KB: Activation Function-1 Domain of Estrogen Receptor Regulates the Agonistic and Antagonistic Actions of Tamoxifen. Molecular Endocrinology. 2005, 20: 996-1008. 10.1210/me.2005-0285.View ArticleGoogle Scholar
- Zhao X, Lorenc H, Stephenson H, Wang YJ, Witherspoon D, Katzenellenbogen B, Pfaff D, Vasudevan N: Thyroid hormone can increase estrogen-mediated transcription from a consensus estrogen response element in neuroblastoma cells. Proc Natl Acad Sci USA. 2005, 102: 4890-4895. 10.1073/pnas.0501042102.PubMed CentralView ArticlePubMedGoogle Scholar
- Park EM, Joh TH, Volpe BT, Chu CK, Song G, Cho SA: Neuroprotective role of extracellular signal regulated kinase in N-acetyl-O-methyldopamine-treated hippocampal neurons after exposure to in vivo ischemia. Neurosci. 2004, 123: 147-154. 10.1016/j.neuroscience.2003.08.023.View ArticleGoogle Scholar
- D'Cruz BJ, Logue ES, Falke E, DeFranco DB, Callaway CW: Hypothermia and ERK activation after cardiac arrest. Brain Research. 2005, 1064: 108-118. 10.1016/j.brainres.2005.09.052.View ArticlePubMedGoogle Scholar
- Christen V, Treves S, Duong FH, Heim MH: Activation of endoplasmic reticulum stress response by hepatitis viruses up-regulates protein phosphatase 2A. Hepatology. 2007, 46 (2): 558-565. 10.1002/hep.21611.View ArticlePubMedGoogle Scholar
- Zhou XW, Gustafsson JA, Tanila H, Bjorkdahl C, Liu R, Winblad B, Pei JJ: Tau hyperphosphorylation correlates with reduced methylation of protein phosphatase 2A. Neurobiol Dis. 2008, 31 (3): 386-94. 10.1016/j.nbd.2008.05.013.View ArticlePubMedGoogle Scholar
- Li Z, Hosoi Y, Cai K, Tanno Y, Matsumoto Y, Enomoto A, Morita A, Nakagawa K, Miyagawa K: Src tyrosine kinase inhibitor PP2 suppresses ERK1/2 activation and epidermal growth factor receptor transactivation by X-irradiation. Biochem Biophys Res Commun. 2006, 341 (2): 363-368. 10.1016/j.bbrc.2005.12.193.View ArticlePubMedGoogle Scholar
- Choe ES, Parelkar NK, Kim JY, Cho HW, Kang HS, Mao L, Wang JQ: The protein phosphatase 1/2A inhibitor okadaic acid increases C REB and Elk-1 phosphorylation and c-fos expression in the rat striatum in vivo. J Neurochem. 2004, 89 (2): 383-390. 10.1111/j.1471-4159.2003.02334.x.View ArticlePubMedGoogle Scholar
- Kim SH, Seo MS, Jeon WJ, Yu HS, Park HG, Jung GA, Lee HY, Kang UG, Kim YS: Haloperidol regulates the phosphorylation level of the MEK-ERK-p90RSK signal pathway via protein phosphatase 2A in the rat frontal cortex. Int J Neuropsychopharmacol. 2008, 11 (4): 509-517. 10.1017/S1461145707008292.View ArticlePubMedGoogle Scholar
- Tan B, Long X, Nakshatri H, Nephew KP, Bigsby RM: Striatin-3 gamma inhibits estrogen receptor activity by recruiting a protein phosphatase. J Mol Endocrinol. 2008, 40 (5): 199-210. 10.1677/JME-07-0132.View ArticlePubMedGoogle Scholar
- Chen J, Martin BL, Brautigan DL: Regulation of protein serine-threonine phosphatase type-2A by tyrosine phosphorylation. Science. 1992, 257 (5074): 1261-4. 10.1126/science.1325671.View ArticlePubMedGoogle Scholar
- Zhu H, Yang H, Owen MR: Combined microarray analysis uncovers self-renewal related signaling in mouse embryonic stem cells. Syst Synth Biol. 2007, 1 (4): 171-81. 10.1007/s11693-008-9015-2.PubMed CentralView ArticlePubMedGoogle Scholar
- Thandi S, Blank JL, Challiss RA: Group-I metabotropic glutamate receptors, mGlu1a and mGlu5a, couple to extracellular signal-regulated kinase (ERK) activation via distinct, but overlapping, signalling pathways. J Neurochem. 2002, 83: 1139-53. 10.1046/j.1471-4159.2002.01217.x.View ArticlePubMedGoogle Scholar
- Miñano A, Xifró X, Pérez V, Barneda-Zahonero B, Saura CA, Rodríguez-Alvarez J: Estradiol facilitates neurite maintenance by a Src/Ras/ERK signalling pathway. Mol Cell Neurosci. 2008, 39 (2): 143-51. 10.1016/j.mcn.2008.06.001.View ArticlePubMedGoogle Scholar
- Hu BR, Liu CL, Park DJ: Alteration of MAP kinase pathways after transient forebrain ischemia. J Cereb Blood Flow Metab. 2000, 20: 1089-1095. 10.1097/00004647-200007000-00008.View ArticlePubMedGoogle Scholar