HUGO ID Detailed Result 10940


HUGO ID 10940
Symbol SLC1A2
Name solute carrier family 1 (glial high affinity glutamate transporter), member 2
#Occurrence 68
#Paper 9

 


PMID Match String Actual String Score Flanking text Edited by Edit
11173059EAAT2EAAT-20.3transporters have already been cloned the glial transporters EAAT-1 and EAAT-2 and the neuronal transporters EAAT-3 EAAT-4 and EAAT-5 (the the 
11173059EAAT2EAAT-20.3originates from a decreased expression of the glial glutamate transporter EAAT-2 ( Rothstein et al. 1995 
11173059EAAT2EAAT-20.3The loss of EAAT-2 is not related to genomic mutations and selective EAAT 2 
11173059EAAT2EAAT-20.3Alternatively EAAT-2 deficiency could derive from defective translational or post-translational mechanisms secondary 
15210305EAAT2EAAT21.3receptors and of the excitatory amino acid transporter 2 (EAAT2) EAAT2 (which which is involved in the removal of glutamate from 
15210305EAAT2EAAT21.3expression studies have highlighted the early focal loss of the EAAT2 glutamate transporter in the ventral horn of the G93A TG 
15210305EAAT2EAAT21.3pattern of steady increase of gliosis paralleled with a 90% EAAT2 loss in the ventral horn is also reported suggesting a 
15572176EAAT2EAAT22.8(COX-2), COX-2 display nitrotyrosine immunoreactivity and downregulate the glutamate transporter EAAT2 
15572176GLT-1GLT-12.8of SOD1-containing aggregates and decreased expression of glial glutamate transporter GLT-1 18 
15572176GLT-1GLT-12.8the neuropil and with a striking focal loss of the GLT-1 glutamate transporter in the ventral horn 
15572176EAAT2EAAT22.8fluid and a selective reduction of the astrocytic glutamate transporter EAAT2 (GLT1), GLT1 giving support to the excitotoxic hypothesis of motor 
15572176GLT1GLT12.8a selective reduction of the astrocytic glutamate transporter EAAT2 (GLT1), GLT1 giving support to the excitotoxic hypothesis of motor neuron degeneration 
15572176EAAT2EAAT22.8In patients with ALS EAAT2 transporters are decreased or defective 108 and 114 which is 
15572176EAAT2EAAT22.8Significant loss of the EAAT2 transporters has also been documented in the spinal cord of 
15572176EAAT2EAAT22.8In contrast neither EAAT1 nor EAAT2 transporters seem to be affected in presymptomatic or symptomatic mice 
15572176EAAT2EAAT22.8The presence of aberrant mRNA splice variants for EAAT2 in ALS has been hypothesized as a putative cause of 
15572176EAAT2EAAT22.8in ALS has been hypothesized as a putative cause of EAAT2 loss 6 and 79 
16179515EAAT2EAAT21.0stroma-derived factor-1 (SDF-1), SDF-1 and excitatory amino acid transporter-2 (EAAT2) EAAT2 
16624536EAAT2EAAT21.0been observed to have decreased expression of the glutamate transporter EAAT2 potentially leading to decreased glutamate transport and subsequent increases in 
16624536EAAT2EAAT21.0this decrease in expression resulting from alternately spliced variants of EAAT2 has been demonstrated in normal controls in addition to ALS 
17008387GLT-1GLT-11.0that PDTC treatment prevented the reduction of the glutamate transporter GLT-1 a potential therapeutic target verified in numerous animal studies of 
17008387GLT-1GLT-11.0in models of ALS by increasing expression of glutamate transporter GLT-1 (Rothstein Rothstein et al. 2005 beta-lactams because it significantly increases 
17008387GLT-1GLT-11.0al. 2005 beta-lactams because it significantly increases the expression of GLT-1 and Cu concentration in the spinal cord We hypothesize that 
17008387GLT-1GLT-11.0though beta-lactams and PDTC might both be able to modulate GLT-1 and Cu concentration only PDTC but not beta-lactams inhibits immunoproteasome 
17008387GLT-1GLT-11.0as an antioxidant and activating Akt-GSK3 beta pathway also induces GLT-1 a potential drug target in brain diseases 
17008387GLT-1GLT-11.0PDTC led to decreased immunoproteasome levels and increased GLT-1 levels in TG rats at the end stage whereas PDTC 
17008387GLT-1GLT-11.0no effect on the levels of constitutive proteasome immunoproteasome or GLT-1 in WT rats 
17008387GLT-1GLT-11.0effect on the levels of astrocyte specific glutamate transporter (GLT-1) GLT-1 
17008387GLT-1GLT-11.0the spinal cords of untreated TG rats the levels of GLT-1 were decreased whereas in PDTC-treated TG rats the levels of 
17008387GLT-1GLT-11.0were decreased whereas in PDTC-treated TG rats the levels of GLT-1 were at the same levels as in WT rats p 
17008387GLT-1GLT-11.0PDTC also increased the levels of astrocyte-specific glutamate transporter (GLT-1) GLT-1 
17008387GLT-1GLT-11.0the spinal cords of untreated TG rats the levels of GLT-1 were decreased whereas in PDTC-treated TG rats the levels of 
17008387GLT-1GLT-11.0were decreased whereas in PDTC-treated TG rats the levels of GLT-1 were at the same levels as in WT rats ( 
17015226EAAT2EAAT22.8caspase-3 activation in glial cells proteolytically inactivates the glutamate transporter EAAT2 ( Boston-Howes et_amp_#xa0 al. 2006 
17015226EAAT2EAAT22.8Since EAAT2 is selectively lost during the disease process and is considered 
17015226EAAT2EAAT22.8synaptic glutamate through the action of the glial glutamate transporter EAAT2 (also also referred to as GLT-1 in rodents 
17015226GLT-1GLT-12.8the glial glutamate transporter EAAT2 (also also referred to as GLT-1 in rodents 
17015226EAAT2EAAT22.8ALS patients ( Rothstein et_amp_#xa0 al. 1992 and levels of EAAT2 are reduced in the motor cortex and spinal cord of 
17015226EAAT2EAAT22.8for familial ALS in that hSOD1 G93A mice heterozygous for EAAT2 develop earlier-onset disease ( Pardo et_amp_#xa0 al. 2006 while drugs 
17015226EAAT2EAAT22.8disease ( Pardo et_amp_#xa0 al. 2006 while drugs that increase EAAT2 activity extend survival ( Ganel et_amp_#xa0 al. 2006 and Rothstein 
17015226EAAT2EAAT22.8Indeed screening of FDA-approved drugs for those that_amp_#xa0 could elevate EAAT2 activity has identified_amp_#xa0 a CNS-penetrating _amp_#x3b2 -lactam antibiotic ceftriaxone as_amp_#xa0 
17015226EAAT2EAAT22.8activation in response to neuronal damage induces loss of the EAAT2 glutamate transporter reducing rapid recovery of synaptic glutamate and driving 
17015226EAAT2EAAT22.8Loss of EAAT2 glutamate transporters from astrocytes drives repetitive firing of glutamate receptors 
18464925GLT-1GLT-12.8agonist L-796 449 induced a concentration-dependent increase in glutamate transporter GLT-1 expression and 3 H glutamate uptake in rat astrocytes 
18464925GLT1GLT13.1identified six putative PPREs in the promoter region of GLT1/EAAT2 GLT1 EAAT2 gene suggesting GLT1/EAAT2 GLT1 EAAT2 glutamate transporter is a 
18464925EAAT2EAAT23.3six putative PPREs in the promoter region of GLT1/EAAT2 GLT1 EAAT2 gene suggesting GLT1/EAAT2 GLT1 EAAT2 glutamate transporter is a novel 
18464925GLT1GLT13.1the promoter region of GLT1/EAAT2 GLT1 EAAT2 gene suggesting GLT1/EAAT2 GLT1 EAAT2 glutamate transporter is a novel PPAR-_amp_#x003b3 target gene 56 
18464925EAAT2EAAT23.3promoter region of GLT1/EAAT2 GLT1 EAAT2 gene suggesting GLT1/EAAT2 GLT1 EAAT2 glutamate transporter is a novel PPAR-_amp_#x003b3 target gene 56 
18598679EAAT2EAAT21.0Corroborating this view are the elevated levels of EAAT2 after exposure to LPS ( Persson et al. 2005 and 
15210305excitatory amino acid transporter 2excitatory amino acid transporter 21.0for this reason the expression of glutamate receptors and of the excitatory amino acid transporter 2 eaat2 which is involved in the removal of glutamate from the synapse in spinal cord have been extensively investigated [ 92 and 107 ].  
15572176glt 1glt 11.0g85r sod 1 mutation astrocytes display major morphological and functional changes characterized by the appearance of sod1 containing aggregates and decreased expression of glial glutamate transporter glt 1 [ 18 ].  
15572176glt 1glt 11.0howland et al. [ 62 ] found that gliosis coincided with early vacuolization of the neuropil and with a striking focal loss of the glt 1 glutamate transporter in the ventral horn.  
15572176glt 1glt11.0many als patients have elevated glutamate levels in cerebrospinal fluid and a selective reduction of the astrocytic glutamate transporter eaat2 glt1 giving support to the excitotoxic hypothesis of motor neuron degeneration [ 107 ].  
16179515excitatory amino acid transporter 2excitatory amino acid transporter 21.0however it did upregulate 3 genes unaffected by the presence of the g93a/sod1 mutation: glial fibrillary acidic protein gfap stroma derived factor 1 sdf 1 and excitatory amino acid transporter 2 eaat2 .  
17008387glt 1glt 11.0structions and immunostained using rabbit polyclonal anti proteasome 20s lmp7 dilution 1:1000; abcam cambridge uk rabbit polyclonal anti proteasome 20s x dilution 1:1000; abcam rabbit polyclonal anti glt 1 dilution 1:1000; calbiochem la jolla ca monoclonal anti beta actin dilution 1:4000 sigma or rabbit polyclonal anti ubiquitin antibodies dilution 1:1000; dakocytomation denmark a/s glostrup denmark an 
17008387glt 1glt 11.0the fact that pdtc treatment prevented the reduction of the glutamate transporter glt 1 a potential therapeutic target verified in numerous animal studies of als gurney et al. 1996 ; howland et al. 2002 and that pdtc treatment did not induce toxic side effects in the tg or wt rats the n 
17008387glt 1glt 11.0ducts in rat peripheral nerves calviello et al. 2005 beta lactams such as ceftriaxone which have been reported to be neuroprotective in models of als by increasing expression of glutamate transporter glt 1 rothstein et al. 2005 beta lactams because it significantly increases the expression of glt 1 and cu concentration in the spinal cord we hypothesize that even though beta lactams and pdtc might both  
17008387glt 1glt 11.0 rothstein et al. 2005 beta lactams because it significantly increases the expression of glt 1 and cu concentration in the spinal cord we hypothesize that even though beta lactams and pdtc might both be able to modulate glt 1 and cu concentration only pdtc but not beta lactams inhibits immunop 
17008387glt 1glt 11.0 and cu concentration in the spinal cord we hypothesize that even though beta lactams and pdtc might both be able to modulate glt 1 and cu concentration only pdtc but not beta lactams inhibits immunoproteasome because induction of immunoproteasome may be a rather selective characteristic for als models compared with models of isc 
17008387glt 1glt 11.0in summary we report that pdtc a multipotent drug providing protection in various animal models by inhibiting nf kappab acting as an antioxidant and activating akt gsk3 beta pathway also induces glt 1 a potential drug target in brain diseases.  
17008387glt 1glt 11.0pdtc led to decreased immunoproteasome levels and increased glt 1 levels in tg rats at the end stage whereas pdtc had no effect on the levels of constitutive proteasome immunoproteasome or glt 1 in wt rats.  
17008387glt 1glt 11.0pdtc also had an effect on the levels of astrocyte specific glutamate transporter glt 1 .  
17008387glt 1glt 11.0a and c in the spinal cords of untreated tg rats the levels of glt 1 were decreased whereas in pdtc treated tg rats the levels of glt 1 were at the same levels as in wt rats. p _lt_ 0.05 n = 5 results shown are mean _amp_#177; s.d.  
17008387glt 1glt 11.0the changes in immunoproteasome levels after pdtc treatment were not due to common reduction of astroglial functions because pdtc also increased the levels of astrocyte specific glutamate transporter glt 1 .  
17008387glt 1glt 11.0in the spinal cords of untreated tg rats the levels of glt 1 were decreased whereas in pdtc treated tg rats the levels of glt 1 were at the same levels as in wt rats fig 5 a and c .  
17015226glt 1glt 11.0ential partners of motor neurons providing them with trophic support and mediating rapid recovery of synaptic glutamate through the action of the glial glutamate transporter eaat2 also referred to as glt 1 in rodents .  
18464925glt 1glt 11.0in addition rosiglitazone and the non tzd agonist l 796 449 induced a concentration dependent increase in glutamate transporter glt 1 expression and [ 3 h] glutamate uptake in rat astrocytes.  
18464925glt 1glt11.0in addition the authors identified six putative ppres in the promoter region of glt1/eaat2 gene suggesting glt1/eaat2 glutamate transporter is a novel ppar _amp_#x003b3; target gene [ 56 ].