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Synaptic Systems
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GeneTex
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Image Search Results
Journal: bioRxiv
Article Title: Astrocyte GluN2C NMDA receptors control basal synaptic strengths of hippocampal CA1 pyramidal neurons in the stratum radiatum
doi: 10.1101/2021.05.28.446253
Figure Lengend Snippet: ( A ) Top: patch RT-PCR strategy. Bottom: representative voltage responses to current steps in CA1 pyramidal neuron (far left, black), and current responses to voltage steps in astrocytes in stratum radiatum (SR, green), stratum oriens (SO, yellow), and stratum lacunosum moleculare (SLM, blue). Scale bars: neuron, 40 mV, 500 ms; astrocytes, 6 nA, 200 ms. ( B ) Summary of I-V curves of astrocytes obtained before collecting RNA. N = 39 cells, 36 slices, 9 mice for each layer. ( C ) Summary of RT-PCR analysis for mRNA encoding indicated NMDAR subunits: GRIN1 (1), GRIN2A (2A), GRIN2B (2B), and GRIN2C (2C). Control samples (no patch) were obtained by inserting the electrode into the slice without patching cells. GRIN2D levels were undetectable in all cells examined (data not shown). ( D ) Western blots of co-immunoprecipitations performed using adult mouse hippocampal extracts with the indicated antibodies where anti-Cre antibody is used as a negative control. The blots are probed for GluN2A/2B (top row), GluN2C (middle row) or GluN1 (bottom row). ( E ) Representative brain sections of GRIN2C -Cre mice crossed to a tdTomato reporter line (Ai9), showing hippocampal area CA1 immunolabelled for GFAP, tdTomato and NeuN; scale bars, 160 μm (top), 25 μm (bottom). ( F ) Quantification of % cells that are positive for tdTomato amongst NeuN-labelled cells in stratum pyramidale (left) and SR (middle) and GFAP-labelled cells (right).
Article Snippet: Antibodies used were: mouse anti-NR1 (Synaptic Systems #114011),
Techniques: Reverse Transcription Polymerase Chain Reaction, Western Blot, Negative Control