Journal: The Journal of Clinical Investigation

Article Title: Spinal α 2 δ -1 induces GluA3 degradation to regulate assembly of calcium-permeable AMPA receptors and pain hypersensitivity

doi: 10.1172/JCI193349

Figure Lengend Snippet: ( A – C ) Representative current-voltage (I-V) plots of glutamate-elicited currents ( A and B ) and quantification ( C ) show the differential effect of coexpression of α2δ-1, α2δ-2, or α2δ-3 on GluA3 currents in HEK29 cells ( n = 11 cells for GluA3/empty vector [pcDNA], GluA3/α2δ-1, and GluA3/α2δ-2; n = 12 cells for GluA3/α2δ-3). ( D – F ) Representative I-V plots of glutamate-elicited currents ( D ) and mean current density ( E ) and rectification index ( F ) in HEK293 cells transfected with GluA2/A3 with either pcDNA or α2δ-1 ( n = 12 cells for GluA2/GluA3; n = 13 cells for GluA2/GluA3/α2δ-1). * P < 0.05, *** P < 0.001; 1-way ANOVA followed by Dunnett’s post hoc test in C ; 2-tailed Student’s t test in E and F . Data are expressed as means ± SEM. ( G and H ) Original confocal immunofluorescence images show the distribution of GluA3 (red) and GFP-tagged α2δ-1 (green) in HEK293 cells transfected with either GluA3/pcDNA or GluA3/α2δ-1-GFP. Areas in yellow boxes in G are magnified in H . Scale bars: 50 μm ( G ), 10 μm ( H ).

Article Snippet: After a brief rinse, the cells were blocked with 4% normal goat serum (Vector Laboratories), followed by immunolabeling with a rabbit anti-GluA3 antibody (1:100; 5117, Cell Signaling Technology) overnight at 4°C.

Techniques: Plasmid Preparation, Transfection, Immunofluorescence

Journal: The Journal of Clinical Investigation

Article Title: Spinal α 2 δ -1 induces GluA3 degradation to regulate assembly of calcium-permeable AMPA receptors and pain hypersensitivity

doi: 10.1172/JCI193349

Figure Lengend Snippet: ( A and B ) Representative immunoblot images ( A ) and quantification ( B ) show the distinct effect of coexpression of HA-tagged α2δ-1, α2δ-2, or α2δ-3 on GluA3 protein levels in HEK293 cells ( n = 8 independent experiments per group). GAPDH was used as the internal control for normalizing the protein levels on the same gel. *** P < 0.001; 1-way ANOVA followed by Dunnett’s post hoc test.

Article Snippet: After a brief rinse, the cells were blocked with 4% normal goat serum (Vector Laboratories), followed by immunolabeling with a rabbit anti-GluA3 antibody (1:100; 5117, Cell Signaling Technology) overnight at 4°C.

Techniques: Western Blot, Control

Journal: The Journal of Clinical Investigation

Article Title: Spinal α 2 δ -1 induces GluA3 degradation to regulate assembly of calcium-permeable AMPA receptors and pain hypersensitivity

doi: 10.1172/JCI193349

Figure Lengend Snippet: ( A ) Representative immunoblot images and quantification show the concentration-dependent reduction in GluA3 protein levels induced by α2δ-1 coexpression in HEK293 cells ( n = 7 independent experiments per group). ( B ) Representative immunoblot images and quantification show the effect of coexpression with GFP on GluA3 protein levels in HEK293 cells ( n = 7 independent experiments per group). ( C ) Representative immunoblot images and quantification show the protein levels of GluA2 and GluA3 in HEK293 cells expressing GluA2/GluA3 with either empty vectors or α2δ-1 ( n = 6 independent experiments per group). ( D ) Representative immunoblot images and quantification show the protein levels of GluA3 and α2δ-1 in HEK293 cells expressing GluA3 with either empty vectors or α2δ-1 ( n = 6 independent experiments per group). GAPDH was used as the internal control for normalizing the protein levels on the same gel. ** P < 0.01, *** P < 0.001; 1-way ANOVA followed by Dunnett’s post hoc test in A and B ; 2-tailed Student’s t test in C and D . Data are expressed as means ± SEM.

Article Snippet: After a brief rinse, the cells were blocked with 4% normal goat serum (Vector Laboratories), followed by immunolabeling with a rabbit anti-GluA3 antibody (1:100; 5117, Cell Signaling Technology) overnight at 4°C.

Techniques: Western Blot, Concentration Assay, Expressing, Control

Journal: The Journal of Clinical Investigation

Article Title: Spinal α 2 δ -1 induces GluA3 degradation to regulate assembly of calcium-permeable AMPA receptors and pain hypersensitivity

doi: 10.1172/JCI193349

Figure Lengend Snippet: ( A ) Original confocal images show the distribution of GluA3 (green), IB4 (red), and NeuN (blue) in the spinal dorsal horn of sham control and SNL rats. Scale bars: 100 μm (upper panels), 50 μm (lower panels). ( B and C ) Representative immunoblot images ( B ) and quantification ( C ) show the protein levels of α2δ-1 and GluA3 in the dorsal spinal cord of sham control and SNL rats. β-Actin served as the internal control for normalizing the protein levels on the same gel ( n = 8 mice per group). ( D and E ) Representative immunoblot images ( D ) and quantification ( E ) show the protein levels of GluA3 and GluA2/GluA3 complexes in the dorsal spinal cord from sham and SNL rats treated intrathecally with vehicle or 10 μg pregabalin (PGB; n = 9 rats per group) 3 weeks after surgery. Protein extracts from rat spinal cord tissues were immunoprecipitated using a rabbit GluA2 antibody or IgG. Immunoblotting was then performed using mouse GluA2, mouse GluA3, and mouse β-actin antibodies. β-Actin served as the internal control for normalizing GluA3 protein levels in the input. The corresponding immunoprecipitated GluA2 protein bands were used for normalizing GluA2/GluA3 protein complex levels. * P < 0.05, ** P < 0.01, *** P < 0.001; 2-tailed Student’s t test in C ; 2-way ANOVA followed by Tukey’s post hoc test in E . Data are expressed as means ± SEM.

Article Snippet: After a brief rinse, the cells were blocked with 4% normal goat serum (Vector Laboratories), followed by immunolabeling with a rabbit anti-GluA3 antibody (1:100; 5117, Cell Signaling Technology) overnight at 4°C.

Techniques: Control, Western Blot, Immunoprecipitation

Journal: The Journal of Clinical Investigation

Article Title: Spinal α 2 δ -1 induces GluA3 degradation to regulate assembly of calcium-permeable AMPA receptors and pain hypersensitivity

doi: 10.1172/JCI193349

Figure Lengend Snippet: Representative immunoblot images ( A and C ) and quantification show the total ( B ) and synaptosome ( D ) protein levels of GluA3 and α2δ-1 in the dorsal spinal cord of naive rats injected intrathecally with control lentiviruses or lentiviruses expressing Cacna2d1 ( n = 6 rats per group). β-Actin served as the internal control for normalizing the GluA3 and α2δ-1 protein levels on the same gel. PSD-95, a synaptic protein marker, served as the internal control for normalizing the GluA3 and α2δ-1 protein levels in synaptosome fractions. *** P < 0.001; 2-tailed Student’s t test. Data are expressed as means ± SEM.

Article Snippet: After a brief rinse, the cells were blocked with 4% normal goat serum (Vector Laboratories), followed by immunolabeling with a rabbit anti-GluA3 antibody (1:100; 5117, Cell Signaling Technology) overnight at 4°C.

Techniques: Western Blot, Injection, Control, Expressing, Marker

Journal: The Journal of Clinical Investigation

Article Title: Spinal α 2 δ -1 induces GluA3 degradation to regulate assembly of calcium-permeable AMPA receptors and pain hypersensitivity

doi: 10.1172/JCI193349

Figure Lengend Snippet: ( A and B ) Representative immunoblot images ( A ) and quantification ( B ) show the basal protein levels of GluA3 in the dorsal spinal cord of WT and Cana2d1- KO mice ( n = 6 mice per group). ( C and D ) Representative immunoblot images ( C ) and quantification ( D ) show the protein levels of GluA3 and α2δ-1 in dorsal spinal cord tissues from WT and Cana2d1- KO mice subjected to sham or SNI surgery ( n = 11 mice per group). β-Actin served as the internal control for normalizing the GluA3 and α2δ-1 protein levels on the same gel. ** P < 0.01; 2-tailed Student’s t test. Data are expressed as means ± SEM.

Article Snippet: After a brief rinse, the cells were blocked with 4% normal goat serum (Vector Laboratories), followed by immunolabeling with a rabbit anti-GluA3 antibody (1:100; 5117, Cell Signaling Technology) overnight at 4°C.

Techniques: Western Blot, Control

Journal: The Journal of Clinical Investigation

Article Title: Spinal α 2 δ -1 induces GluA3 degradation to regulate assembly of calcium-permeable AMPA receptors and pain hypersensitivity

doi: 10.1172/JCI193349

Figure Lengend Snippet: ( A and B ) Representative immunoblot images ( A ) and quantification ( B ) show GluA3 and α2δ-1 protein levels in HEK293 cells coexpressing GluA3 with YFP-tagged WT α2δ-1 or chimeric constructs [α2δ-1CT (α2δ-2) and α2δ-1CT (α2δ-3) ] ( n = 8 independent experiments per group). ( C and D ) Representative immunoblot images ( C ) and quantification ( D ) show the effects of treatment with control peptide (1 μM), α2δ-1CT peptide (1 μM), pregabalin (PGB; 20 μM), and MG132 (10 μM) on the GluA3 protein levels in HEK293 cells coexpressing α2δ-1 and GluA3 ( n = 9 independent experiments per group). PT, peptide. GAPDH was used as an internal control for normalizing the GluA3 protein levels on the same gel. *** P < 0.001; 1-way ANOVA followed by Dunnett’s post hoc test. Data are expressed as means ± SEM.

Article Snippet: After a brief rinse, the cells were blocked with 4% normal goat serum (Vector Laboratories), followed by immunolabeling with a rabbit anti-GluA3 antibody (1:100; 5117, Cell Signaling Technology) overnight at 4°C.

Techniques: Western Blot, Construct, Control

Journal: The Journal of Clinical Investigation

Article Title: Spinal α 2 δ -1 induces GluA3 degradation to regulate assembly of calcium-permeable AMPA receptors and pain hypersensitivity

doi: 10.1172/JCI193349

Figure Lengend Snippet: ( A ) Time-course effects of intrathecal injection of 20 μg MG132 or vehicle (Veh) on hindpaw nociceptive thresholds in sham and SNL rats 3 weeks after surgery ( n = 9 rats per group). * P < 0.05, ** P < 0.01, *** P < 0.001 versus baseline (time 0); # P < 0.05, ### P < 0.001 versus Veh-SNL group at the same time point; 2-way ANOVA followed by Tukey’s post hoc test. ( B ) Representative immunoblot images and quantification show the effect of MG132 treatment on GluA3 protein levels in dorsal spinal cord tissues from SNL and sham rats ( n = 9 rats per group). * P < 0.05, *** P < 0.001; 1-way ANOVA followed by Tukey’s post hoc test. Data are expressed as means ± SEM.

Article Snippet: After a brief rinse, the cells were blocked with 4% normal goat serum (Vector Laboratories), followed by immunolabeling with a rabbit anti-GluA3 antibody (1:100; 5117, Cell Signaling Technology) overnight at 4°C.

Techniques: Injection, Western Blot

Journal: The Journal of Clinical Investigation

Article Title: Spinal α 2 δ -1 induces GluA3 degradation to regulate assembly of calcium-permeable AMPA receptors and pain hypersensitivity

doi: 10.1172/JCI193349

Figure Lengend Snippet: ( A ) Representative immunoblot images show the ubiquitin protein levels in GluA3 precipitates from HEK293 cells expressing GluA3 with either pcDNA or α2δ-1 (similar data were obtained from 4 independent experiments). ( B ) Representative immunoblot images and quantification show the ubiquitin protein levels in GluA3 precipitates from the dorsal spinal cord of sham control and SNL rats ( n = 9 rats per group). Protein extracts from HEK293 cells or spinal cord tissues were immunoprecipitated using a rabbit GluA3 antibody or IgG. Immunoblotting was then conducted using mouse ubiquitin or mouse GluA3 antibodies. The corresponding GluA3 protein bands were used as the internal control on the same gel. ( C and D ) Representative immunoblot images ( C ) and quantification ( D ) show GluA3 protein levels in HEK293 cells expressing WT GluA3 or GluA3 mutants (K710R, K861R, and K887R) with and without α2δ-1 ( n = 12 independent experiments per group). GAPDH was used as the internal control for normalizing GluA3 and α2δ-1 protein levels on the same gel. ** P < 0.01, *** P < 0.001; 2-tailed Student’s t test in B ; 1-way ANOVA followed by Tukey’s post hoc test in D . Data are expressed as means ± SEM.

Article Snippet: After a brief rinse, the cells were blocked with 4% normal goat serum (Vector Laboratories), followed by immunolabeling with a rabbit anti-GluA3 antibody (1:100; 5117, Cell Signaling Technology) overnight at 4°C.

Techniques: Western Blot, Ubiquitin Proteomics, Expressing, Control, Immunoprecipitation

Journal: The Journal of Clinical Investigation

Article Title: Spinal α 2 δ -1 induces GluA3 degradation to regulate assembly of calcium-permeable AMPA receptors and pain hypersensitivity

doi: 10.1172/JCI193349

Figure Lengend Snippet: ( A ) Changes in the hindpaw withdrawal thresholds of sham control and SNL rats 2 and 3 weeks after intrathecal injection of control (Cont) lentiviral vectors or lentiviral vectors expressing Gria3 ( n = 13 rats per group). ** P < 0.01, *** P < 0.001; 2-way ANOVA followed by Tukey’s post hoc test. ( B and C ) Representative immunoblot images ( B ) and quantification ( C ) show the protein levels of GluA3 and GluA2/GluA3 complexes in the dorsal spinal cords of sham control and SNL rats treated with intrathecal control lentiviruses or Gria3 -expressing lentiviruses ( n = 8 rats per group). Protein extracts from spinal cord tissues were immunoprecipitated (IP) using a GluA2 antibody or IgG. Immunoblotting was then conducted using GluA2, GluA3, and β-actin antibodies. β-Actin protein bands were used as the internal control on the same gel. ** P < 0.01, *** P < 0.001; 2-way ANOVA followed by Tukey’s post hoc test. ( D and E ) Representative recording traces ( D ) and quantification ( E ) show the differential effect of bath application of IEM-1460 (50 μM) on the amplitude of monosynaptic AMPAR-EPSCs in spinal lamina II neurons from SNL rats treated with intrathecal injection of control lentiviruses or Gria3 -expressing lentiviruses ( n = 18 neurons from 4 rats per group). Data were normalized to the baseline value (100%) before IEM-1460 application. * P < 0.05, ** P < 0.01 versus control vector group at the same time point; 2-way ANOVA followed by Tukey’s post hoc test. Data are presented as mean ± SEM.

Article Snippet: After a brief rinse, the cells were blocked with 4% normal goat serum (Vector Laboratories), followed by immunolabeling with a rabbit anti-GluA3 antibody (1:100; 5117, Cell Signaling Technology) overnight at 4°C.

Techniques: Control, Injection, Expressing, Western Blot, Immunoprecipitation, Plasmid Preparation

Journal: iScience

Article Title: The decreased astrocyte-microglia interaction reflects the early characteristics of Alzheimer’s disease

doi: 10.1016/j.isci.2024.109281

Figure Lengend Snippet:

Article Snippet: Primary antibodies used were: anti-Iba1 (1:1000, rabbit, 019–19741, Wako), anti-GFAP (1:1000, rabbit, goat, ab53554, Abcam), anti-6E10 (1:1000, mouse, 803014, biolegends), anti- Synaptophysin (1:1000, rabbit, ab14692, Abcam), anti-Gria1 (1:20000, mouse, 67642-1-IG, proteintech), anti-Gria2 (1:500, rabbit, 11994-1-IG, proteintech), anti-Gria3 (1:1000, rabbit, 29588-1-IG, proteintech), anti-Gria4 (1:500, rabbit, 23350-1-IG, proteintech), anti-PSD95 (1:2000, rabbit, 20665-1-IG, proteintech), anti-Vglut1 (1:1000, rabbit, 12331, Cell signaling), anti-Vim (1:1000, rabbit, YT4880, immunoway), anti-C1qa (1:1000, rabbit, YN0612, immunoway), anti-Lcp1 (1:1000, rabbit, YN0002, immunoway), anti-Anxa3 (1:1000, rabbit, YT0237, immunoway), anti-Anxa5 (1:1000, rabbit, ab14196, Abcam), anti- Ctsb (1:1000, goat, AF965, RD), anti-β-actin (1:5000, mouse, A5441, sigma), Confocal fluorescence images were acquired using a Nikon A1 confocal laser scanning microscope with ×20 objectives for imaging stained or autofluorescent neurons.

Techniques: Virus, Bicinchoninic Acid Protein Assay, Mass Spectrometry, Software

Journal: Nature Communications

Article Title: The intellectual disability protein RAB39B selectively regulates GluA2 trafficking to determine synaptic AMPAR composition

doi: 10.1038/ncomms7504

Figure Lengend Snippet: Representative immunofluorescence images of COS7 cells ( a ) single, ( b – f ) double or ( g , h ) triple transfected with flag-RAB39B (red), myc-PICK1 (blue), GFP-GluA1 (green) or GFP-GluA2 (green). Scale bar represents 10 μm. ( i ) Histogram shows the Pearson’s correlation coefficients (PCC; means±s.e.m.) for each transfection. PCC was calculated between proteins highlighted with a bold ‘+’. Significant statistical differences were found comparing: flag-RAB39B/GFP-GluA1 PCC ( n =26 cells; three experimental replicates; PCC=0.09, P adj.=1.8E−08) and flag-RAB39B/GFP-GluA2 PCC ( n =22 cells; three experimental replicates; PCC=0.06, P adj.=1.8E−08) to flag-RAB39B/myc-PICK1 PCC ( n =14 cells; three experimental replicates; PCC=0.70); myc-PICK1/GFP-GluA1 PCC ( n =29 cells; three experimental replicates; PCC=−0.01, P adj.=1.8E−08) to myc-PICK1/GFP-GluA2 PCC ( n =38 cells; three experimental replicates; PCC=0.66); flag-RAB39B/GFP-GluA2 PCC in the absence or presence of PICK1 (PCC in the presence of PICK1=0.71; n =12 cells; three experimental replicates; P adj.=1.8E−08). Benjamini–Hochberg procedure used to test statistical significance. *** P <0.001.

Article Snippet: GluA1, GluA2 and GluA3 were detected using a anti-GluA1 polyclonal antibody (SySy, #182003, 1:1,000 WB), anti-GluA2 polyclonal antibody (SySy; #182103, 1:1,000 WB) and anti-GluA3 polyclonal antibody (made into the laboratory of Professor R. Huganir Johns Hopkins University, Baltimore, MD, USA, 1:1,000 WB).

Techniques: Immunofluorescence, Transfection

Journal: Nature Communications

Article Title: The intellectual disability protein RAB39B selectively regulates GluA2 trafficking to determine synaptic AMPAR composition

doi: 10.1038/ncomms7504

Figure Lengend Snippet: Representative TIRF and epifluorescence images of COS7 cells transfected with flag-RAB39B (red) and GFP-GluA1 (green) or GFP-GluA2 (green), in the absence ( a – b ) or presence ( c , d ) of PICK1 (blue). Scale bar, 10 μm. ( e ) Representative western blots ( n =3 experimental replicates) of immunoprecipitation from WT and Pick1 KO mouse brain lysates (Input). The 31-kDa contaminant bands reacting with the anti-RAB39B correspond to the protein G as shown in the mock elution of protein G Sepharose-4 fast flow beads (in conditions of elution adopted as described in Methods ).

Article Snippet: GluA1, GluA2 and GluA3 were detected using a anti-GluA1 polyclonal antibody (SySy, #182003, 1:1,000 WB), anti-GluA2 polyclonal antibody (SySy; #182103, 1:1,000 WB) and anti-GluA3 polyclonal antibody (made into the laboratory of Professor R. Huganir Johns Hopkins University, Baltimore, MD, USA, 1:1,000 WB).

Techniques: Transfection, Western Blot, Immunoprecipitation

Journal: Nature Communications

Article Title: The intellectual disability protein RAB39B selectively regulates GluA2 trafficking to determine synaptic AMPAR composition

doi: 10.1038/ncomms7504

Figure Lengend Snippet: ( a ) Quantification of PICK1 (shScramble n =21 cells; shRab39b n =21 cells; Rab39b-rescue n =8 cells; Student’s t -test shScramble versus shRab39b P =0.009; Rab39b-rescue versus shRab39b P =0.002), GluA1 (shScramble n =10 cells; shRab39b n =10 cells; Rab39b-rescue n =9 cells), GluA2 (shScramble n =9 cells; shRab39b n =5 cells; Rab39b-rescue n =11 cells; Student’s t -test shScramble versus shRab39b P =0.003; Rab39b-rescue versus shRab39b P =0.004) and GluA3 (shScramble n =6 cells; shRab39b n =7 cells; Rab39b-rescue n =9 cells; Student’s t -test shScramble versus shRab39b P =0.03; Rab39b-rescue versus shRab39b P =0.04) cell body density in shScramble-, shRab39b- and Rab39b-rescue-treated mouse hippocampal neurons. ( b ) Quantification of the ratio between mature (1) and immature (2) forms of AMPARs in shRab39b- compared with shScramble-treated neurons after PNGasef or EndoHf digestion. NT: non-treated neurons. Representative western blots (lower panels) showing the maturation ratio for GluA1 ( n =3 experimental replicates), GluA2 ( n =3 experimental replicates; Student’s t -test P =0.002) and GluA3 ( n =3 experimental replicates; Student’s t -test P =1.28E−04). ( c ) Quantification of PICK1 (shScramble n =14 cells; shRab39b n =15 cells; Rab39b-rescue n =8 cells; Student’s t -test shScramble versus shRab39b P =0.03; Rab39b-rescue versus shRab39b P =0.01), GluA1 (shScramble n =10 cells; shRab39b n =10 cells; Rab39b-rescue n =9 cells; Student’s t -test shScramble versus shRab39b P =7.4E−04; Rab39b-rescue versus shRab39b P =8.1E−04), GluA2 (shScramble n =10 cells; shRab39b n =5 cells; Rab39b-rescue n =9 cells; Student’s t -test shScramble versus shRab39b P =2.8E−07; Rab39b-rescue versus shRab39b P =3.1E−05) and GluA3 (shScramble n =6 cells; shRab39b n =7 cells; Rab39b-rescue n =9 cells; Student’s t -test shScramble versus shRab39b P =1.5E−05; Rab39b-rescue versus shRab39b P =4.7E−05) dendrite density in shScramble-, shRab39b- and Rab39b-rescue-treated mouse hippocampal neurons. ( d ) Representative images of shRab39b, shScramble and Rab39b-rescue neurons immunostained without permeabilization for the extracellular N-terminal region of GluA1 and GluA2. Quantification of positive puncta at cell surface shows a significant increase of GluA1 (shScramble n =41 cells; shRab39b n =40 cells; Rab39b-rescue n =10; Student’s t -test shScramble versus shRab39b P =0.03; Rab39b-rescue versus shRab39b P =0.006) and significant decrease of GluA2 (shScramble n =89 cells; shRab39b n =70 cells; Rab39b-rescue n =8; Student’s t -test shScramble versus shRab39b P =0.006; Rab39b-rescue versus shRab39b P =0.01) subunits. The number of cells belongs from a minimum of three experimental replicates. * P <0.05; ** P <0.01; *** P <0.001.

Article Snippet: GluA1, GluA2 and GluA3 were detected using a anti-GluA1 polyclonal antibody (SySy, #182003, 1:1,000 WB), anti-GluA2 polyclonal antibody (SySy; #182103, 1:1,000 WB) and anti-GluA3 polyclonal antibody (made into the laboratory of Professor R. Huganir Johns Hopkins University, Baltimore, MD, USA, 1:1,000 WB).

Techniques: Western Blot

Journal: Nature Communications

Article Title: The intellectual disability protein RAB39B selectively regulates GluA2 trafficking to determine synaptic AMPAR composition

doi: 10.1038/ncomms7504

Figure Lengend Snippet: Proposed model of RAB39B-PICK1-GluA2 complex on a 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) coarse grained liposome model with a 40 nm diameter (grey dots are the atoms of DOPC) emphasizing RAB39B-driven traffic of GluA2 cargo between the ER and Golgi compartment.

Article Snippet: GluA1, GluA2 and GluA3 were detected using a anti-GluA1 polyclonal antibody (SySy, #182003, 1:1,000 WB), anti-GluA2 polyclonal antibody (SySy; #182103, 1:1,000 WB) and anti-GluA3 polyclonal antibody (made into the laboratory of Professor R. Huganir Johns Hopkins University, Baltimore, MD, USA, 1:1,000 WB).

Techniques:

Journal: Frontiers in Molecular Neuroscience

Article Title: Somatic Accumulation of GluA1-AMPA Receptors Leads to Selective Cognitive Impairments in Mice

doi: 10.3389/fnmol.2018.00199

Figure Lengend Snippet: Expression of the L-α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR) subunits and subunit assemblies in WT and Gria1 R/R mice. (A) Hippocampal expression of GluA1–3, GluN1, αCaMKII and ß-actin in WT and Gria1 R/R mice from P2 till P90. (B) Co-immunoprecipitations (IPs) using polyclonal anti-GluA1 and anti-GluA2/3 antibodies show the presence of GluA1–3 in AMPAR assemblies from hippocampal membrane preparations at P > 60 of WT , Gria1 R/R (R/R) and Gria1 −/− (−/−) mice. (C) Schematic representation of the Gria1 R “knock-in” ( Gria1 tm1Erk ) allele and the Gria1 + allele ( WT ). Below the gene segments, the putative AMPAR subtypes, that can operate at CA3-to-CA1 synapses in Gria1 R/R and WT mice, are schematically depicted (GluA1(R) = GluA1(Q600R)). Large AMPAR symbols for high abundance; small symbols for low abundance; transparent for AMPARs with low single channel conductance. The inset shows the position of the Q600R mutations (R) in two out of the four P-loop segments that form the ion pore of an AMPAR. Exons are in boxes, loxP sites in black triangles and the M1 and P-loop coding sequence in black squares. The position of the mutated codon Q600R codon and codon Q600 in Gria1 tm1Erk and Gria1 are indicated, respectively (see Sprengel et al., ). High resolution images of (A,B) are accessible at https://dx.doi.org/10.17617/3.1i .

Article Snippet: The blotted proteins were probed with polyclonal antibodies against GluA1 (Merck Millipore 0.1 μg/ml), anti-GluA2 (Merck Millipore 0.16 μg/ml), anti-GluN1 (Merck Millipore, 0.25 μg/ml, monoclonal anti-GluA3 (ThermoFisher, 1:250), anti-CaMKII (MAB 8699 Merck Millipore 0.1 μg/ml) and anti-ß-actin (AC-15 Ascites, Sigma, 1:25,000), followed by peroxidase-linked anti-rabbit or -mouse secondary antibodies (Jackson Immuno Res., 1:20,000).

Techniques: Expressing, Knock-In, Sequencing