vo ohpic  (MedChemExpress)


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    MedChemExpress vo ohpic
    Cor modulates the PTEN-AKT-mTOR pathway for its inhibitory effects on Ang II-induced cardiac fibroblast migration. (A) Representative images of Western blot of p-PTEN (Ser380), PTEN, p-Akt (Ser473) and p-mTOR (Ser 2448) are shown. (B) Quantitative analysis of protein bands that are normalized to GAPDH (p-PTEN and PTEN), Akt (p-Akt) or mTOR (p-mTOR). The cardiac fibroblasts were stimulated with Ang II (1 μM) infusion, incubated for 48 hours, and then treated with Cor (50 μM) for 2 hours. Then, the <t>PTEN</t> <t>inhibitor</t> VO- <t>ohpic</t> (1 μM) was treated for 2 hours. (C) The mRNA expression of PTEN, AKT and mTOR was determined by RT-qPCR. GADPH served as an internal control. (D) The cell migrative capability of cardiac fibroblasts was determined by Transwell assay. (E) Quantification of the average number of migrated fibroblasts in each field. Data are shown as mean ± SD (n = 6 per group). Cor group cells were cotreated with Ang II and Cor; Cor+VO-ohpic group cells were cotreated with Ang II, Cor, and VO-ohpic. *** P < .001 vs control group; ### P < .001 vs Ang II group; $$$ P < .001 vs Cor group.
    Vo Ohpic, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Corilagin Alleviates Ang II-Induced Cardiac Fibrosis by Regulating the PTEN/AKT/mTOR Pathway"

    Article Title: Corilagin Alleviates Ang II-Induced Cardiac Fibrosis by Regulating the PTEN/AKT/mTOR Pathway

    Journal: Dose-Response

    doi: 10.1177/15593258241261198

    Cor modulates the PTEN-AKT-mTOR pathway for its inhibitory effects on Ang II-induced cardiac fibroblast migration. (A) Representative images of Western blot of p-PTEN (Ser380), PTEN, p-Akt (Ser473) and p-mTOR (Ser 2448) are shown. (B) Quantitative analysis of protein bands that are normalized to GAPDH (p-PTEN and PTEN), Akt (p-Akt) or mTOR (p-mTOR). The cardiac fibroblasts were stimulated with Ang II (1 μM) infusion, incubated for 48 hours, and then treated with Cor (50 μM) for 2 hours. Then, the PTEN inhibitor VO- ohpic (1 μM) was treated for 2 hours. (C) The mRNA expression of PTEN, AKT and mTOR was determined by RT-qPCR. GADPH served as an internal control. (D) The cell migrative capability of cardiac fibroblasts was determined by Transwell assay. (E) Quantification of the average number of migrated fibroblasts in each field. Data are shown as mean ± SD (n = 6 per group). Cor group cells were cotreated with Ang II and Cor; Cor+VO-ohpic group cells were cotreated with Ang II, Cor, and VO-ohpic. *** P < .001 vs control group; ### P < .001 vs Ang II group; $$$ P < .001 vs Cor group.
    Figure Legend Snippet: Cor modulates the PTEN-AKT-mTOR pathway for its inhibitory effects on Ang II-induced cardiac fibroblast migration. (A) Representative images of Western blot of p-PTEN (Ser380), PTEN, p-Akt (Ser473) and p-mTOR (Ser 2448) are shown. (B) Quantitative analysis of protein bands that are normalized to GAPDH (p-PTEN and PTEN), Akt (p-Akt) or mTOR (p-mTOR). The cardiac fibroblasts were stimulated with Ang II (1 μM) infusion, incubated for 48 hours, and then treated with Cor (50 μM) for 2 hours. Then, the PTEN inhibitor VO- ohpic (1 μM) was treated for 2 hours. (C) The mRNA expression of PTEN, AKT and mTOR was determined by RT-qPCR. GADPH served as an internal control. (D) The cell migrative capability of cardiac fibroblasts was determined by Transwell assay. (E) Quantification of the average number of migrated fibroblasts in each field. Data are shown as mean ± SD (n = 6 per group). Cor group cells were cotreated with Ang II and Cor; Cor+VO-ohpic group cells were cotreated with Ang II, Cor, and VO-ohpic. *** P < .001 vs control group; ### P < .001 vs Ang II group; $$$ P < .001 vs Cor group.

    Techniques Used: Migration, Western Blot, Incubation, Expressing, Quantitative RT-PCR, Control, Transwell Assay

    vo ohpic trihydrate  (MedChemExpress)


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    MedChemExpress vo ohpic trihydrate

    Vo Ohpic Trihydrate, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Images

    1) Product Images from "Epidermal growth factor augments the self-renewal capacity of aged hematopoietic stem cells"

    Article Title: Epidermal growth factor augments the self-renewal capacity of aged hematopoietic stem cells

    Journal: iScience

    doi: 10.1016/j.isci.2024.110306


    Figure Legend Snippet:

    Techniques Used: Purification, Recombinant, Enzyme-linked Immunosorbent Assay, Reverse Transcription, Sequencing, Software

    vo ohpic 10 840 µm selleckchem s8174  (Selleck Chemicals)


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    Selleck Chemicals vo ohpic 10 840 µm selleckchem s8174
    Vo Ohpic 10 840 µm Selleckchem S8174, supplied by Selleck Chemicals, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    vo ohpic 10 µm selleckchem s8174  (Selleck Chemicals)


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    Selleck Chemicals vo ohpic 10 µm selleckchem s8174
    Vo Ohpic 10 µm Selleckchem S8174, supplied by Selleck Chemicals, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Santa Cruz Biotechnology vo ohpic trihydrate
    Vo Ohpic Trihydrate, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Structured Review

    Millipore pten inhibitor vo ohpic
    ( A ) <t>PTEN</t> inhibitor <t>VO-OHpic</t> was used to disinhibit the PI3K/Akt/mTOR signaling pathway in CMT1A. ( B ) Example images of Schwann cell-dorsal root ganglia neuron co-cultures from wildtype (WT) and Pmp22 tg rats treated with DMSO as control (Ctrl) or PTEN inhibitor VO-OHpic (500 nM). Cells were stained for myelin basic protein (MBP) as a marker for myelinated segments (gray/ green) and TUJ1 for neurons (magenta) as well as DAPI for cell nuclei (blue). ( C ) Quantification of ( B ) shows a dose-dependent decrease of myelinated segments in WT co-cultures treated with DMSO and different concentrations of VO-OHpic (50 nM, 500 nM, 5 µM) and an increase of myelinated segments in Pmp22 tg co-cultures with 500 nM VO-OHpic (WT n = 5, CMT1A n = 7 animals). Groups were compared using two-way ANOVA with Sidak’s multiple comparison test (* p ≤ 0.05, **** p ≤ 0.0001). .
    Pten Inhibitor Vo Ohpic, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Targeting PI3K/Akt/mTOR signaling in rodent models of PMP22 gene-dosage diseases"

    Article Title: Targeting PI3K/Akt/mTOR signaling in rodent models of PMP22 gene-dosage diseases

    Journal: EMBO Molecular Medicine

    doi: 10.1038/s44321-023-00019-5

    ( A ) PTEN inhibitor VO-OHpic was used to disinhibit the PI3K/Akt/mTOR signaling pathway in CMT1A. ( B ) Example images of Schwann cell-dorsal root ganglia neuron co-cultures from wildtype (WT) and Pmp22 tg rats treated with DMSO as control (Ctrl) or PTEN inhibitor VO-OHpic (500 nM). Cells were stained for myelin basic protein (MBP) as a marker for myelinated segments (gray/ green) and TUJ1 for neurons (magenta) as well as DAPI for cell nuclei (blue). ( C ) Quantification of ( B ) shows a dose-dependent decrease of myelinated segments in WT co-cultures treated with DMSO and different concentrations of VO-OHpic (50 nM, 500 nM, 5 µM) and an increase of myelinated segments in Pmp22 tg co-cultures with 500 nM VO-OHpic (WT n = 5, CMT1A n = 7 animals). Groups were compared using two-way ANOVA with Sidak’s multiple comparison test (* p ≤ 0.05, **** p ≤ 0.0001). .
    Figure Legend Snippet: ( A ) PTEN inhibitor VO-OHpic was used to disinhibit the PI3K/Akt/mTOR signaling pathway in CMT1A. ( B ) Example images of Schwann cell-dorsal root ganglia neuron co-cultures from wildtype (WT) and Pmp22 tg rats treated with DMSO as control (Ctrl) or PTEN inhibitor VO-OHpic (500 nM). Cells were stained for myelin basic protein (MBP) as a marker for myelinated segments (gray/ green) and TUJ1 for neurons (magenta) as well as DAPI for cell nuclei (blue). ( C ) Quantification of ( B ) shows a dose-dependent decrease of myelinated segments in WT co-cultures treated with DMSO and different concentrations of VO-OHpic (50 nM, 500 nM, 5 µM) and an increase of myelinated segments in Pmp22 tg co-cultures with 500 nM VO-OHpic (WT n = 5, CMT1A n = 7 animals). Groups were compared using two-way ANOVA with Sidak’s multiple comparison test (* p ≤ 0.05, **** p ≤ 0.0001). .

    Techniques Used: Staining, Marker, Comparison

    Example images of SC-DRG co-cultures from wildtype (WT) and Pmp22 tg rats, treated with different dosages of the PTEN inhibitor VO-OHpic for 14 days. The number of myelinated segments (MBP; gray/green) decreases in WT cultures with increasing inhibitor dosage. In Pmp22 tg co-cultures an increase is observed up to 500 nM VO-OHpic but a decrease with 5 µM VO-OHpic. Scale bar is 50 µm. Images for 500 nM VO-OHpic treatment are the same as used in Fig. .
    Figure Legend Snippet: Example images of SC-DRG co-cultures from wildtype (WT) and Pmp22 tg rats, treated with different dosages of the PTEN inhibitor VO-OHpic for 14 days. The number of myelinated segments (MBP; gray/green) decreases in WT cultures with increasing inhibitor dosage. In Pmp22 tg co-cultures an increase is observed up to 500 nM VO-OHpic but a decrease with 5 µM VO-OHpic. Scale bar is 50 µm. Images for 500 nM VO-OHpic treatment are the same as used in Fig. .

    Techniques Used:

    vo ohpic  (OriGene)


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    OriGene vo ohpic
    Vo Ohpic, supplied by OriGene, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    vo ohpic trihydrate  (Selleck Chemicals)


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    Selleck Chemicals vo ohpic trihydrate

    Vo Ohpic Trihydrate, supplied by Selleck Chemicals, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "The myocardium utilizes a platelet-derived growth factor receptor alpha (Pdgfra)–phosphoinositide 3-kinase (PI3K) signaling cascade to steer toward the midline during zebrafish heart tube formation"

    Article Title: The myocardium utilizes a platelet-derived growth factor receptor alpha (Pdgfra)–phosphoinositide 3-kinase (PI3K) signaling cascade to steer toward the midline during zebrafish heart tube formation

    Journal: eLife

    doi: 10.7554/eLife.85930


    Figure Legend Snippet:

    Techniques Used: Transgenic Assay, Mutagenesis, Recombinant, Proliferation Assay, Software, Microscopy

    vo ohpic trihydrate  (Selleck Chemicals)


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    Selleck Chemicals vo ohpic trihydrate
    Vo Ohpic Trihydrate, supplied by Selleck Chemicals, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore vo ohpic treated microglia
    Vo Ohpic Treated Microglia, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    MedChemExpress vo ohpic
    Cor modulates the PTEN-AKT-mTOR pathway for its inhibitory effects on Ang II-induced cardiac fibroblast migration. (A) Representative images of Western blot of p-PTEN (Ser380), PTEN, p-Akt (Ser473) and p-mTOR (Ser 2448) are shown. (B) Quantitative analysis of protein bands that are normalized to GAPDH (p-PTEN and PTEN), Akt (p-Akt) or mTOR (p-mTOR). The cardiac fibroblasts were stimulated with Ang II (1 μM) infusion, incubated for 48 hours, and then treated with Cor (50 μM) for 2 hours. Then, the <t>PTEN</t> <t>inhibitor</t> VO- <t>ohpic</t> (1 μM) was treated for 2 hours. (C) The mRNA expression of PTEN, AKT and mTOR was determined by RT-qPCR. GADPH served as an internal control. (D) The cell migrative capability of cardiac fibroblasts was determined by Transwell assay. (E) Quantification of the average number of migrated fibroblasts in each field. Data are shown as mean ± SD (n = 6 per group). Cor group cells were cotreated with Ang II and Cor; Cor+VO-ohpic group cells were cotreated with Ang II, Cor, and VO-ohpic. *** P < .001 vs control group; ### P < .001 vs Ang II group; $$$ P < .001 vs Cor group.
    Vo Ohpic, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    MedChemExpress vo ohpic trihydrate

    Vo Ohpic Trihydrate, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Selleck Chemicals vo ohpic 10 840 µm selleckchem s8174

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    Santa Cruz Biotechnology vo ohpic trihydrate

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    Millipore pten inhibitor vo ohpic
    ( A ) <t>PTEN</t> inhibitor <t>VO-OHpic</t> was used to disinhibit the PI3K/Akt/mTOR signaling pathway in CMT1A. ( B ) Example images of Schwann cell-dorsal root ganglia neuron co-cultures from wildtype (WT) and Pmp22 tg rats treated with DMSO as control (Ctrl) or PTEN inhibitor VO-OHpic (500 nM). Cells were stained for myelin basic protein (MBP) as a marker for myelinated segments (gray/ green) and TUJ1 for neurons (magenta) as well as DAPI for cell nuclei (blue). ( C ) Quantification of ( B ) shows a dose-dependent decrease of myelinated segments in WT co-cultures treated with DMSO and different concentrations of VO-OHpic (50 nM, 500 nM, 5 µM) and an increase of myelinated segments in Pmp22 tg co-cultures with 500 nM VO-OHpic (WT n = 5, CMT1A n = 7 animals). Groups were compared using two-way ANOVA with Sidak’s multiple comparison test (* p ≤ 0.05, **** p ≤ 0.0001). .
    Pten Inhibitor Vo Ohpic, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    OriGene vo ohpic
    ( A ) <t>PTEN</t> inhibitor <t>VO-OHpic</t> was used to disinhibit the PI3K/Akt/mTOR signaling pathway in CMT1A. ( B ) Example images of Schwann cell-dorsal root ganglia neuron co-cultures from wildtype (WT) and Pmp22 tg rats treated with DMSO as control (Ctrl) or PTEN inhibitor VO-OHpic (500 nM). Cells were stained for myelin basic protein (MBP) as a marker for myelinated segments (gray/ green) and TUJ1 for neurons (magenta) as well as DAPI for cell nuclei (blue). ( C ) Quantification of ( B ) shows a dose-dependent decrease of myelinated segments in WT co-cultures treated with DMSO and different concentrations of VO-OHpic (50 nM, 500 nM, 5 µM) and an increase of myelinated segments in Pmp22 tg co-cultures with 500 nM VO-OHpic (WT n = 5, CMT1A n = 7 animals). Groups were compared using two-way ANOVA with Sidak’s multiple comparison test (* p ≤ 0.05, **** p ≤ 0.0001). .
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    Selleck Chemicals vo ohpic trihydrate

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    Millipore vo ohpic treated microglia

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    Image Search Results


    Cor modulates the PTEN-AKT-mTOR pathway for its inhibitory effects on Ang II-induced cardiac fibroblast migration. (A) Representative images of Western blot of p-PTEN (Ser380), PTEN, p-Akt (Ser473) and p-mTOR (Ser 2448) are shown. (B) Quantitative analysis of protein bands that are normalized to GAPDH (p-PTEN and PTEN), Akt (p-Akt) or mTOR (p-mTOR). The cardiac fibroblasts were stimulated with Ang II (1 μM) infusion, incubated for 48 hours, and then treated with Cor (50 μM) for 2 hours. Then, the PTEN inhibitor VO- ohpic (1 μM) was treated for 2 hours. (C) The mRNA expression of PTEN, AKT and mTOR was determined by RT-qPCR. GADPH served as an internal control. (D) The cell migrative capability of cardiac fibroblasts was determined by Transwell assay. (E) Quantification of the average number of migrated fibroblasts in each field. Data are shown as mean ± SD (n = 6 per group). Cor group cells were cotreated with Ang II and Cor; Cor+VO-ohpic group cells were cotreated with Ang II, Cor, and VO-ohpic. *** P < .001 vs control group; ### P < .001 vs Ang II group; $$$ P < .001 vs Cor group.

    Journal: Dose-Response

    Article Title: Corilagin Alleviates Ang II-Induced Cardiac Fibrosis by Regulating the PTEN/AKT/mTOR Pathway

    doi: 10.1177/15593258241261198

    Figure Lengend Snippet: Cor modulates the PTEN-AKT-mTOR pathway for its inhibitory effects on Ang II-induced cardiac fibroblast migration. (A) Representative images of Western blot of p-PTEN (Ser380), PTEN, p-Akt (Ser473) and p-mTOR (Ser 2448) are shown. (B) Quantitative analysis of protein bands that are normalized to GAPDH (p-PTEN and PTEN), Akt (p-Akt) or mTOR (p-mTOR). The cardiac fibroblasts were stimulated with Ang II (1 μM) infusion, incubated for 48 hours, and then treated with Cor (50 μM) for 2 hours. Then, the PTEN inhibitor VO- ohpic (1 μM) was treated for 2 hours. (C) The mRNA expression of PTEN, AKT and mTOR was determined by RT-qPCR. GADPH served as an internal control. (D) The cell migrative capability of cardiac fibroblasts was determined by Transwell assay. (E) Quantification of the average number of migrated fibroblasts in each field. Data are shown as mean ± SD (n = 6 per group). Cor group cells were cotreated with Ang II and Cor; Cor+VO-ohpic group cells were cotreated with Ang II, Cor, and VO-ohpic. *** P < .001 vs control group; ### P < .001 vs Ang II group; $$$ P < .001 vs Cor group.

    Article Snippet: For the inhibitor experiment, VO-ohpic (1 μM) (HY-110067, MedChemExpress) was used to inhibit PTEN activity.

    Techniques: Migration, Western Blot, Incubation, Expressing, Quantitative RT-PCR, Control, Transwell Assay

    Journal: iScience

    Article Title: Epidermal growth factor augments the self-renewal capacity of aged hematopoietic stem cells

    doi: 10.1016/j.isci.2024.110306

    Figure Lengend Snippet:

    Article Snippet: VO-Ohpic trihydrate , MedChemExpress , HY-13074.

    Techniques: Purification, Recombinant, Enzyme-linked Immunosorbent Assay, Reverse Transcription, Sequencing, Software

    ( A ) PTEN inhibitor VO-OHpic was used to disinhibit the PI3K/Akt/mTOR signaling pathway in CMT1A. ( B ) Example images of Schwann cell-dorsal root ganglia neuron co-cultures from wildtype (WT) and Pmp22 tg rats treated with DMSO as control (Ctrl) or PTEN inhibitor VO-OHpic (500 nM). Cells were stained for myelin basic protein (MBP) as a marker for myelinated segments (gray/ green) and TUJ1 for neurons (magenta) as well as DAPI for cell nuclei (blue). ( C ) Quantification of ( B ) shows a dose-dependent decrease of myelinated segments in WT co-cultures treated with DMSO and different concentrations of VO-OHpic (50 nM, 500 nM, 5 µM) and an increase of myelinated segments in Pmp22 tg co-cultures with 500 nM VO-OHpic (WT n = 5, CMT1A n = 7 animals). Groups were compared using two-way ANOVA with Sidak’s multiple comparison test (* p ≤ 0.05, **** p ≤ 0.0001). .

    Journal: EMBO Molecular Medicine

    Article Title: Targeting PI3K/Akt/mTOR signaling in rodent models of PMP22 gene-dosage diseases

    doi: 10.1038/s44321-023-00019-5

    Figure Lengend Snippet: ( A ) PTEN inhibitor VO-OHpic was used to disinhibit the PI3K/Akt/mTOR signaling pathway in CMT1A. ( B ) Example images of Schwann cell-dorsal root ganglia neuron co-cultures from wildtype (WT) and Pmp22 tg rats treated with DMSO as control (Ctrl) or PTEN inhibitor VO-OHpic (500 nM). Cells were stained for myelin basic protein (MBP) as a marker for myelinated segments (gray/ green) and TUJ1 for neurons (magenta) as well as DAPI for cell nuclei (blue). ( C ) Quantification of ( B ) shows a dose-dependent decrease of myelinated segments in WT co-cultures treated with DMSO and different concentrations of VO-OHpic (50 nM, 500 nM, 5 µM) and an increase of myelinated segments in Pmp22 tg co-cultures with 500 nM VO-OHpic (WT n = 5, CMT1A n = 7 animals). Groups were compared using two-way ANOVA with Sidak’s multiple comparison test (* p ≤ 0.05, **** p ≤ 0.0001). .

    Article Snippet: For PTEN inhibition in Pmp22 tg cultures, cells were treated with 1% DMSO (Sigma) as a control or with the PTEN inhibitor VO-OHpic (Rosivatz et al, ) (Sigma) at 50 nM, 500 nM and 5 μM, respectively.

    Techniques: Staining, Marker, Comparison

    Example images of SC-DRG co-cultures from wildtype (WT) and Pmp22 tg rats, treated with different dosages of the PTEN inhibitor VO-OHpic for 14 days. The number of myelinated segments (MBP; gray/green) decreases in WT cultures with increasing inhibitor dosage. In Pmp22 tg co-cultures an increase is observed up to 500 nM VO-OHpic but a decrease with 5 µM VO-OHpic. Scale bar is 50 µm. Images for 500 nM VO-OHpic treatment are the same as used in Fig. .

    Journal: EMBO Molecular Medicine

    Article Title: Targeting PI3K/Akt/mTOR signaling in rodent models of PMP22 gene-dosage diseases

    doi: 10.1038/s44321-023-00019-5

    Figure Lengend Snippet: Example images of SC-DRG co-cultures from wildtype (WT) and Pmp22 tg rats, treated with different dosages of the PTEN inhibitor VO-OHpic for 14 days. The number of myelinated segments (MBP; gray/green) decreases in WT cultures with increasing inhibitor dosage. In Pmp22 tg co-cultures an increase is observed up to 500 nM VO-OHpic but a decrease with 5 µM VO-OHpic. Scale bar is 50 µm. Images for 500 nM VO-OHpic treatment are the same as used in Fig. .

    Article Snippet: For PTEN inhibition in Pmp22 tg cultures, cells were treated with 1% DMSO (Sigma) as a control or with the PTEN inhibitor VO-OHpic (Rosivatz et al, ) (Sigma) at 50 nM, 500 nM and 5 μM, respectively.

    Techniques:

    Journal: eLife

    Article Title: The myocardium utilizes a platelet-derived growth factor receptor alpha (Pdgfra)–phosphoinositide 3-kinase (PI3K) signaling cascade to steer toward the midline during zebrafish heart tube formation

    doi: 10.7554/eLife.85930

    Figure Lengend Snippet:

    Article Snippet: The following inhibitors were used: LY294002 (LY, Millipore-Sigma 154447-36-6), Dactolisib (Dac, Millipore-Sigma 915019-65-7), Pictilisib (Pic, Millipore-Sigma 957054-30-7), Rapamycin (Rap, Selleckchem S1039), and VO-Ohpic trihydrate (VOOH, Selleckchem S8174).

    Techniques: Transgenic Assay, Mutagenesis, Recombinant, Proliferation Assay, Software, Microscopy