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Figure 2. NPTX2 in dorsal hippocampal pyramidal neurons directionally regulates the extinction of cocaine-associated context memory. (A) Experimental procedure of the extinction of cocaine-associated context memory. (B, C) Representative Western blots (B) and quantification (C) of NPTX2 protein level across the extinction process. F = 4.680, p , .05, one-way analysis of variance by Tukey’s post hoc analysis. (D, E) Representative confocal images (D) and quantification (E) of the single-molecule fluorescence in situ hybridization (smFISH) intensity of Nptx2 in CamkIIa1 neurons across the extinction process. Green: Nptx2; red: CamkIIa. Scale bar: 200 mm. c2 = 11.241, p = .002, Kruskal–Wallis H test with Dunn’s post hoc test. (F–I) <t>AAV-CaMKIIa-CreERT2</t> mixed with either AAV-Flex-scramble-shRNA-EGFP or AAV-Flex-Nptx2-shRNA-EGFP was bilaterally injected into dorsal hippocampus of C57BL/6J mice, and the mice were injected with tamoxifen (TAM) (100 mg/kg) for 3 consecutive days after three pairs of cocaine conditioning. Experimental procedure of the extinction (F). Representative confocal images show short hairpin RNA (shRNA) enhanced green fluorescent protein (EGFP) expression (G) and quantitative real-time po- lymerase chain reaction analysis (H) of the relative messenger RNA (mRNA) level of Nptx2. p = .005, two-tailed unpaired t test. Green: EGFP; blue: DAPI. Scale bar: 1 mm. (I) Downregulating Nptx2 in dorsal hippocampal pyramidal neurons impaired the extinction of the cocaine-associated context memory. FTreatment3Ext(3,63) = 4.411, p = .007, two-way repeated-measures analysis of variance by Bonferroni post hoc analysis. (J–M) Experimental procedure of the
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Figure 2. NPTX2 in dorsal hippocampal pyramidal neurons directionally regulates the extinction of cocaine-associated context memory. (A) Experimental procedure of the extinction of cocaine-associated context memory. (B, C) Representative Western blots (B) and quantification (C) of NPTX2 protein level across the extinction process. F = 4.680, p , .05, one-way analysis of variance by Tukey’s post hoc analysis. (D, E) Representative confocal images (D) and quantification (E) of the single-molecule fluorescence in situ hybridization (smFISH) intensity of Nptx2 in CamkIIa1 neurons across the extinction process. Green: Nptx2; red: CamkIIa. Scale bar: 200 mm. c2 = 11.241, p = .002, Kruskal–Wallis H test with Dunn’s post hoc test. (F–I) <t>AAV-CaMKIIa-CreERT2</t> mixed with either AAV-Flex-scramble-shRNA-EGFP or AAV-Flex-Nptx2-shRNA-EGFP was bilaterally injected into dorsal hippocampus of C57BL/6J mice, and the mice were injected with tamoxifen (TAM) (100 mg/kg) for 3 consecutive days after three pairs of cocaine conditioning. Experimental procedure of the extinction (F). Representative confocal images show short hairpin RNA (shRNA) enhanced green fluorescent protein (EGFP) expression (G) and quantitative real-time po- lymerase chain reaction analysis (H) of the relative messenger RNA (mRNA) level of Nptx2. p = .005, two-tailed unpaired t test. Green: EGFP; blue: DAPI. Scale bar: 1 mm. (I) Downregulating Nptx2 in dorsal hippocampal pyramidal neurons impaired the extinction of the cocaine-associated context memory. FTreatment3Ext(3,63) = 4.411, p = .007, two-way repeated-measures analysis of variance by Bonferroni post hoc analysis. (J–M) Experimental procedure of the
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Figure 2. NPTX2 in dorsal hippocampal pyramidal neurons directionally regulates the extinction of cocaine-associated context memory. (A) Experimental procedure of the extinction of cocaine-associated context memory. (B, C) Representative Western blots (B) and quantification (C) of NPTX2 protein level across the extinction process. F = 4.680, p , .05, one-way analysis of variance by Tukey’s post hoc analysis. (D, E) Representative confocal images (D) and quantification (E) of the single-molecule fluorescence in situ hybridization (smFISH) intensity of Nptx2 in CamkIIa1 neurons across the extinction process. Green: Nptx2; red: CamkIIa. Scale bar: 200 mm. c2 = 11.241, p = .002, Kruskal–Wallis H test with Dunn’s post hoc test. (F–I) <t>AAV-CaMKIIa-CreERT2</t> mixed with either AAV-Flex-scramble-shRNA-EGFP or AAV-Flex-Nptx2-shRNA-EGFP was bilaterally injected into dorsal hippocampus of C57BL/6J mice, and the mice were injected with tamoxifen (TAM) (100 mg/kg) for 3 consecutive days after three pairs of cocaine conditioning. Experimental procedure of the extinction (F). Representative confocal images show short hairpin RNA (shRNA) enhanced green fluorescent protein (EGFP) expression (G) and quantitative real-time po- lymerase chain reaction analysis (H) of the relative messenger RNA (mRNA) level of Nptx2. p = .005, two-tailed unpaired t test. Green: EGFP; blue: DAPI. Scale bar: 1 mm. (I) Downregulating Nptx2 in dorsal hippocampal pyramidal neurons impaired the extinction of the cocaine-associated context memory. FTreatment3Ext(3,63) = 4.411, p = .007, two-way repeated-measures analysis of variance by Bonferroni post hoc analysis. (J–M) Experimental procedure of the
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Image Search Results


Journal: STAR Protocols

Article Title: Analyzing engram reactivation and long-range connectivity

doi: 10.1016/j.xpro.2024.102840

Figure Lengend Snippet:

Article Snippet: pFosCreER , Addgene , #46388.

Techniques: Virus, Plasmid Preparation, Recombinant, Software

Figure 2. NPTX2 in dorsal hippocampal pyramidal neurons directionally regulates the extinction of cocaine-associated context memory. (A) Experimental procedure of the extinction of cocaine-associated context memory. (B, C) Representative Western blots (B) and quantification (C) of NPTX2 protein level across the extinction process. F = 4.680, p , .05, one-way analysis of variance by Tukey’s post hoc analysis. (D, E) Representative confocal images (D) and quantification (E) of the single-molecule fluorescence in situ hybridization (smFISH) intensity of Nptx2 in CamkIIa1 neurons across the extinction process. Green: Nptx2; red: CamkIIa. Scale bar: 200 mm. c2 = 11.241, p = .002, Kruskal–Wallis H test with Dunn’s post hoc test. (F–I) AAV-CaMKIIa-CreERT2 mixed with either AAV-Flex-scramble-shRNA-EGFP or AAV-Flex-Nptx2-shRNA-EGFP was bilaterally injected into dorsal hippocampus of C57BL/6J mice, and the mice were injected with tamoxifen (TAM) (100 mg/kg) for 3 consecutive days after three pairs of cocaine conditioning. Experimental procedure of the extinction (F). Representative confocal images show short hairpin RNA (shRNA) enhanced green fluorescent protein (EGFP) expression (G) and quantitative real-time po- lymerase chain reaction analysis (H) of the relative messenger RNA (mRNA) level of Nptx2. p = .005, two-tailed unpaired t test. Green: EGFP; blue: DAPI. Scale bar: 1 mm. (I) Downregulating Nptx2 in dorsal hippocampal pyramidal neurons impaired the extinction of the cocaine-associated context memory. FTreatment3Ext(3,63) = 4.411, p = .007, two-way repeated-measures analysis of variance by Bonferroni post hoc analysis. (J–M) Experimental procedure of the

Journal: Biological psychiatry

Article Title: Retrieval-Driven Hippocampal NPTX2 Plasticity Facilitates the Extinction of Cocaine-Associated Context Memory.

doi: 10.1016/j.biopsych.2019.10.009

Figure Lengend Snippet: Figure 2. NPTX2 in dorsal hippocampal pyramidal neurons directionally regulates the extinction of cocaine-associated context memory. (A) Experimental procedure of the extinction of cocaine-associated context memory. (B, C) Representative Western blots (B) and quantification (C) of NPTX2 protein level across the extinction process. F = 4.680, p , .05, one-way analysis of variance by Tukey’s post hoc analysis. (D, E) Representative confocal images (D) and quantification (E) of the single-molecule fluorescence in situ hybridization (smFISH) intensity of Nptx2 in CamkIIa1 neurons across the extinction process. Green: Nptx2; red: CamkIIa. Scale bar: 200 mm. c2 = 11.241, p = .002, Kruskal–Wallis H test with Dunn’s post hoc test. (F–I) AAV-CaMKIIa-CreERT2 mixed with either AAV-Flex-scramble-shRNA-EGFP or AAV-Flex-Nptx2-shRNA-EGFP was bilaterally injected into dorsal hippocampus of C57BL/6J mice, and the mice were injected with tamoxifen (TAM) (100 mg/kg) for 3 consecutive days after three pairs of cocaine conditioning. Experimental procedure of the extinction (F). Representative confocal images show short hairpin RNA (shRNA) enhanced green fluorescent protein (EGFP) expression (G) and quantitative real-time po- lymerase chain reaction analysis (H) of the relative messenger RNA (mRNA) level of Nptx2. p = .005, two-tailed unpaired t test. Green: EGFP; blue: DAPI. Scale bar: 1 mm. (I) Downregulating Nptx2 in dorsal hippocampal pyramidal neurons impaired the extinction of the cocaine-associated context memory. FTreatment3Ext(3,63) = 4.411, p = .007, two-way repeated-measures analysis of variance by Bonferroni post hoc analysis. (J–M) Experimental procedure of the

Article Snippet: The coding sequence of CreERT2 obtained from p-FosCreERT2 (Addgene: No. 46388) was subcloned into pAAV-CaMKIIahChR2(H134R)-EGFP (Addgene: No. 26969) (26,27) to generate pAAV-CaMKIIa-CreERT2.

Techniques: Western Blot, In Situ Hybridization, shRNA, Injection, Expressing, Two Tailed Test