Journal: Frontiers in Pharmacology

Article Title: USP7 Inhibition Alleviates H 2 O 2 -Induced Injury in Chondrocytes via Inhibiting NOX4/NLRP3 Pathway

doi: 10.3389/fphar.2020.617270

Figure Lengend Snippet: H 2 O 2 increased USP7 expression and caused damage in rat chondrocytes. (A) Representative immunohistochemical staining for collagen II and SOX9 in rat chondrocytes. Rat chondrocytes were treated with different concentrations of H 2 O 2 ; (B,C) ROS production, (D) cell proliferation, and (E) USP7 expression was measured by flow cytometry, CCK8, and Western blot, respectively. Scale bar, 100 μm *** p < 0.001 vs. 0 μM.

Article Snippet: In addition, rat chondrocytes were treated with 100 μM H 2 O 2 and transduced with USP7-silencing vector or USP7 inhibitor 5 μM P22077 (Selleck, Houston, TX, United States) treatment.

Techniques: Expressing, Immunohistochemical staining, Staining, Flow Cytometry, Western Blot

Journal: Frontiers in Pharmacology

Article Title: USP7 Inhibition Alleviates H 2 O 2 -Induced Injury in Chondrocytes via Inhibiting NOX4/NLRP3 Pathway

doi: 10.3389/fphar.2020.617270

Figure Lengend Snippet: USP7 KD inhibited H 2 O 2 -induced injury in rat chondrocytes. Rat chondrocytes were treated with 100 μM H 2 O 2 and transduced with USP7 shRNA vector or treated with USP7 inhibitor 5 μM P22077, and (A) pyroptosis (B) ROS production, (C) IL-1β and IL-18 levels, and (D and E) expression levels of USP7, NLRP3, GSDMD-N, active caspase-1, pro-caspase-1, MMP1, and MMP13 was measured by flow cytometry, ELISA, and Western blot, respectively. *** p < 0.001 vs control; ++ + p < 0.001 vs H 2 O 2 + shNC + vehicle.

Article Snippet: In addition, rat chondrocytes were treated with 100 μM H 2 O 2 and transduced with USP7-silencing vector or USP7 inhibitor 5 μM P22077 (Selleck, Houston, TX, United States) treatment.

Techniques: Transduction, shRNA, Plasmid Preparation, Expressing, Flow Cytometry, Enzyme-linked Immunosorbent Assay, Western Blot, Control

Journal: Frontiers in Pharmacology

Article Title: USP7 Inhibition Alleviates H 2 O 2 -Induced Injury in Chondrocytes via Inhibiting NOX4/NLRP3 Pathway

doi: 10.3389/fphar.2020.617270

Figure Lengend Snippet: USP7 overexpression promoted injury in rat chondrocytes through increasing ROS production. Rat chondrocytes were transduced with the USP7 expression vector and treated with ROS inhibitor 50 μM apocynin, and (A) pyroptosis, (B) ROS production, (C) IL-1β and IL-18 levels, and (D) expression levels of NLRP3, GSDMD-N, active caspase-1, pro-caspase-1, MMP1, and MMP13 was measured by flow cytometry, ELISA, and Western blot, respectively. ### p < 0.001 vs vector; ^ ^ ^ p < 0.001 vs oeUSP7 + vehicle.

Article Snippet: In addition, rat chondrocytes were treated with 100 μM H 2 O 2 and transduced with USP7-silencing vector or USP7 inhibitor 5 μM P22077 (Selleck, Houston, TX, United States) treatment.

Techniques: Over Expression, Transduction, Expressing, Plasmid Preparation, Flow Cytometry, Enzyme-linked Immunosorbent Assay, Western Blot

Journal: Frontiers in Pharmacology

Article Title: USP7 Inhibition Alleviates H 2 O 2 -Induced Injury in Chondrocytes via Inhibiting NOX4/NLRP3 Pathway

doi: 10.3389/fphar.2020.617270

Figure Lengend Snippet: USP7 interacted with NOX4 and inhibited NOX4 ubiquitinylation. Rat chondrocytes were treated with 100 μM H 2 O 2 and transduced with USP7 shRNA vector or treated with USP7 inhibitor P22077, and (A) mRNA and (B) protein expression levels of USP7 and NOX4 were measured by qRT-PCR and western blot. (C) Immunoprecipitation was carried out with IgG control, anti-USP7, or anti-NOX4 antibody. (D) USP7-silencing rat chondrocytes were immunoprecipitated with NOX4 or IgG antibodies and ubiquitination was evaluated by Western blot. (E) Expression levels of USP7 and NOX4 in the cartilage of OA patients ( n = 12) and healthy controls ( n = 4) were measured by qRT-PCR. *** p < 0.001 vs. control; ### p < 0.001 vs. H 2 O 2 + shNC + vector; +++ p < 0.001 vs. healthy.

Article Snippet: In addition, rat chondrocytes were treated with 100 μM H 2 O 2 and transduced with USP7-silencing vector or USP7 inhibitor 5 μM P22077 (Selleck, Houston, TX, United States) treatment.

Techniques: Transduction, shRNA, Plasmid Preparation, Expressing, Quantitative RT-PCR, Western Blot, Immunoprecipitation, Control, Ubiquitin Proteomics

Journal: Frontiers in Pharmacology

Article Title: USP7 Inhibition Alleviates H 2 O 2 -Induced Injury in Chondrocytes via Inhibiting NOX4/NLRP3 Pathway

doi: 10.3389/fphar.2020.617270

Figure Lengend Snippet: The effect of USP7 overexpression was abolished by inhibition of NOX4. Rat chondrocytes were transduced with USP7 expression vector and treated with the NOX4 inhibitor GLX351322 (10 μM), and (A) pyroptosis, (B) ROS levels, (C) IL-1β and IL-18 levels, and (D) expression levels of NLRP3, GSDMD-N, active caspase-1, and pro-caspase-1 was measured by flow cytometry, ELISA and Western blot, respectively. ### p < 0.001 vs vector; ^ ^ ^ p < 0.001 vs oeUSP7 + vehicle.

Article Snippet: In addition, rat chondrocytes were treated with 100 μM H 2 O 2 and transduced with USP7-silencing vector or USP7 inhibitor 5 μM P22077 (Selleck, Houston, TX, United States) treatment.

Techniques: Over Expression, Inhibition, Transduction, Expressing, Plasmid Preparation, Flow Cytometry, Enzyme-linked Immunosorbent Assay, Western Blot

Journal: Frontiers in Pharmacology

Article Title: USP7 Inhibition Alleviates H 2 O 2 -Induced Injury in Chondrocytes via Inhibiting NOX4/NLRP3 Pathway

doi: 10.3389/fphar.2020.617270

Figure Lengend Snippet: USP7 inhibition suppressed the OA process in vivo . Rats were injected with monosodium iodoacetate (MIA) to establish an OA model with or without P22077 treatment, and (A) H and E staining, (B) IL-1β and IL-18 levels, and (C,D) expression levels of USP7, NOX4, NLRP3, GSDMD-N, active caspase-1, pro-caspase-1, MMP1, and MMP13 were measured. ### p < 0.001 vs control; ^ ^ ^ p < 0.001 vs OA + vehicle.

Article Snippet: In addition, rat chondrocytes were treated with 100 μM H 2 O 2 and transduced with USP7-silencing vector or USP7 inhibitor 5 μM P22077 (Selleck, Houston, TX, United States) treatment.

Techniques: Inhibition, In Vivo, Injection, Staining, Expressing, Control

Journal: Cell Biology and Toxicology

Article Title: Gomisin B promotes RSL3-induced ferroptosis in neuroblastoma by inhibiting the ESR1/USP7/SREBF1 axis

doi: 10.1007/s10565-026-10155-6

Figure Lengend Snippet: USP7 deubiquitinated SREBF1. ( A ) Co-IP was performed to test the binding relationship between USP7 and SREBF1 in SH-SY5Y and IMR-32 cells. ( B ) Localization of USP7 and SREBF1 in SH-SY5Y ans IMR-32 cells detected by immunofluorescence (25 μm). ( C ) Co-IP was adopted to assess SREBF1 expression and ubiquitination level in USP7 knockdown SH-SY5Y cells with MG-132 treatment. ( D ) The SREBF1 expression level was analyzed by western blot in SH-SY5Y cells following 3-MA treatment. ( E ) After knocking down USP7 and treating with CHX, the half-life of SREBF1 in SH-SY5Y cells was detected by western blot. ( F ) HEK293T cells were co-transfected with FLAG‑tagged USP7 (FLAG‑USP7), HA‑tagged SREBF1 (HA‑SREBF1), and Myc‑tagged ubiquitin variants (Myc‑Ub, Myc‑Ub‑K48, or Myc‑Ub‑K63). Cell lysates were immunoprecipitated (IP) with anti‑HA antibody and probed with anti‑Myc antibody to detect ubiquitinated SREBF1. N = 3, ** p < 0.01

Article Snippet: ESR1 (OE-ESR1) and USP7 (OE-USP7) overexpression vectors were acquired from Sango Biotech (Shanghai, China).

Techniques: Co-Immunoprecipitation Assay, Binding Assay, Immunofluorescence, Expressing, Ubiquitin Proteomics, Knockdown, Western Blot, Transfection, Immunoprecipitation

Journal: Cell Biology and Toxicology

Article Title: Gomisin B promotes RSL3-induced ferroptosis in neuroblastoma by inhibiting the ESR1/USP7/SREBF1 axis

doi: 10.1007/s10565-026-10155-6

Figure Lengend Snippet: ESR1 inhibited ferroptosis in NB cells by transcriptionally activating USP7. ( A ) JASPAR ( http://jaspar.genereg.net ) was applied to predict the binding site between ESR1 and USP7 promoter. ( B ) The binding relationship between ESR1 and promoter of USP7 was verified using a dual-luciferase reporter. ( C ) ChIP was utilized to confirm the binding relationship between ESR1 and the upstream promoter region of USP7. SH-SY5Y and IMR-32 cells were transfected with sh-ESR1 or OE-USP7, and RSL3 was used to induce ferroptosis in NB cells. ( D ) RT-qPCR was carried out to measure ESR1 and USP7 levels. ( E ) CCK-8 was implemented to examine cell viability. ( F ) GSH, MDA and LPO levels were tested via commercial kits. ( G ) C-11 BODIPY 581/591 fluorescent probe was deployed to assess lipid ROS level (100 μm). (H) ESR1, USP7, SREBF1 and SCD1 expressions were calculated by western blot. N = 3, * p < 0.05, ** p < 0.01, *** p < 0.001

Article Snippet: ESR1 (OE-ESR1) and USP7 (OE-USP7) overexpression vectors were acquired from Sango Biotech (Shanghai, China).

Techniques: Binding Assay, Luciferase, Transfection, Quantitative RT-PCR, CCK-8 Assay, Western Blot

Journal: Cell Biology and Toxicology

Article Title: Gomisin B promotes RSL3-induced ferroptosis in neuroblastoma by inhibiting the ESR1/USP7/SREBF1 axis

doi: 10.1007/s10565-026-10155-6

Figure Lengend Snippet: Gomisin B promoted ferroptosis in NB cells by regulating the ESR1/USP7/SREBF1 axis. After OE-USP7 or sh-SREBF1 was transfected into the SH-SY5Y and IMR-32 cell lines, NB cells were treated with RSL3 or Gomisin B. The experimental groups were: Control, RSL3, RSL3 + GB, RSL3 + GB + OE-USP7, RSL3 + GB + OE-USP7 + sh-SREBF1. ( A ) USP7 and SREBF1 mRNA expressions were examined by RT-qPCR. ( B ) Cell viability was visualized by CCK-8 assay. ( C ) The commercial kits were administered to analyze GSH, MDA and LPO levels in each group of cells. ( D ) Intracellular lipid ROS level measured by the C-11 BODIPY 581/591 fluorescent probe (100 μm). ( E ) Western blot was adopted to test ESR1, USP7, SREBF1 and SCD1 expressions. N = 3, * p < 0.05, ** p < 0.01, *** p < 0.001

Article Snippet: ESR1 (OE-ESR1) and USP7 (OE-USP7) overexpression vectors were acquired from Sango Biotech (Shanghai, China).

Techniques: Transfection, Control, Quantitative RT-PCR, CCK-8 Assay, Western Blot

Journal: Cell Biology and Toxicology

Article Title: Gomisin B promotes RSL3-induced ferroptosis in neuroblastoma by inhibiting the ESR1/USP7/SREBF1 axis

doi: 10.1007/s10565-026-10155-6

Figure Lengend Snippet: Gomisin B promoted ferroptosis and inhibited tumor growth in NB tumor-bearing nude mice. NB cells were injected subcutaneously into BALB/c nude mice to construct NB tumor-bearing nude mice, and then Gomisin B or RSL3 was injected intraperitoneally every other day. The experimental groups were: Control, DMSO, RSL3, RSL3 + GB. ( A ) Representative pictures of different tumor tissues were taken. ( B ) Tumor growth curves were plotted, and the tumor weight was recorded. ( C ) The commercial kits were utilized to test tumor tissue GSH, MDA and LPO levels. ( D ) C-11 BODIPY 581/591 fluorescent probe was performed to estimate tissue lipid ROS level (50 μm). ( E ) ESR1, USP7, SREBF1 and SCD1 expressions were examined using western blot. N = 5, * p < 0.05, ** p < 0.01, *** p < 0.001

Article Snippet: ESR1 (OE-ESR1) and USP7 (OE-USP7) overexpression vectors were acquired from Sango Biotech (Shanghai, China).

Techniques: Injection, Construct, Control, Western Blot

Journal: Cell Biology and Toxicology

Article Title: Gomisin B promotes RSL3-induced ferroptosis in neuroblastoma by inhibiting the ESR1/USP7/SREBF1 axis

doi: 10.1007/s10565-026-10155-6

Figure Lengend Snippet: Graphical abstract: Gomisin B inhibits the transcriptional activation of USP7 by downregulating ESR1 to suppress the deubiquitination of SREBF1, thereby enhancing NB ferroptosis

Article Snippet: ESR1 (OE-ESR1) and USP7 (OE-USP7) overexpression vectors were acquired from Sango Biotech (Shanghai, China).

Techniques: Activation Assay

Journal: iScience

Article Title: Role of the DUB enzyme USP7 in dendritic arborization, neuronal migration, and autistic-like behaviors in mice

doi: 10.1016/j.isci.2022.104595

Figure Lengend Snippet: Expression and subcellular distribution of USP7 in neurons (A) Immunostaining of USP7 and GFAP in rat hippocampal cultures at DIV15. Scale bar = 50 μm. (B) Immunostaining of USP7 and GAD67 in rat hippocampal cultures at DIV15. (C) Lysates of cultured neurons were collected on DIV15, and USP7 levels were measured by Westerns. GAPDH was probed as a loading control. (D) Lysates of different brain regions were collected from rats of embryonic day 18. USP7 levels were measured by Western blot. (E) Cultured neurons were treated with USP7 inhibitor HBX41108 (10 μM) for 2 or 4 h at DIV15, and the lysates were probed for ubiquitination. (F) Quantification showed an increase in ubiquitination intensity in the HBX41108 treated group (F(2,9) = 33.13, p < 0.01, One-way ANOVA). (G) Developmental time course of USP7 expression in the brain. Cortical tissues were collected from mice of ages from E10 to P90. Data are represented as mean ± SEM. Error bars represent SEM, ∗∗p < 0.01.

Article Snippet: Full length USP7 fragment from pCI-neo Flag HAUSP/USP7 (addgene, #16655) were inserted into the AAV-ReaChR-citrine vector.

Techniques: Expressing, Immunostaining, Cell Culture, Control, Western Blot, Ubiquitin Proteomics

Journal: iScience

Article Title: Role of the DUB enzyme USP7 in dendritic arborization, neuronal migration, and autistic-like behaviors in mice

doi: 10.1016/j.isci.2022.104595

Figure Lengend Snippet: USP7 regulates dendritic growth and arborization (A–D) Hippocampal neurons were transfected with a control vector or USP7 plasmid at DIV 7, and imaged for morphology at DIV 11 (A). Scale bar = 100 μm. Dendritic arborization was analyzed by Sholl analysis (F(1,56) = 3.865, p = 0.054, Repeated measures ANOVA) (B). The total number of dendritic branches and the sum length of dendrites showed no significant difference between the control (n = 24) and the USP7 group (n = 28) at DIV11 (p > 0.05, t -test) (C and D). (E–H) Neurons were transfected with USP7 or a vector as control at DIV 11, and imaged for morphology at DIV 15 (E). Scale bar = 100 μm. Dendritic arborization was analyzed by sholl analysis (F(1,44) = 13.037, p = 0.001, Repeated measure ANOVA) (F). The total number of dendrites and total length of dendrites were increased in USP7-transfected neurons on DIV15 (Ctrl: n = 18; USP7: n = 22. Number of dendrites, p < 0.01, t -test; sum length of dendrites, p < 0.01, t -test) (G, H). Scale bar = 100 μm. (I–M) Knockdown of USP7 results in a reduction of dendritic arborization. (I) Cortical neurons were transfected with vector (Control, n = 16) or shUSP7 (n = 31) at DIV 11 and imaged for morphology on DIV 15. Scale bar = 100 μm. (J) Sholl analysis of dendritic arborization at DIV 15 (F(1,46) = 7.497, p = 0.009, Repeated measure ANOVA). (K and L) Total number of dendrites and total length of dendrites were decreased in shUSP7 neurons on DIV15 (Number of dendrites, p < 0.05, t -test; sum length of dendrites, p < 0.01, t -test). (M) Mean length of dendrites was decreased in shUSP7 neurons on DIV15 (p < 0.05, t -test). Data are represented as mean ± SEM. Error bars represent SEM, ∗p < 0.05, ∗∗p < 0.01.

Article Snippet: Full length USP7 fragment from pCI-neo Flag HAUSP/USP7 (addgene, #16655) were inserted into the AAV-ReaChR-citrine vector.

Techniques: Transfection, Control, Plasmid Preparation, Knockdown

Journal: iScience

Article Title: Role of the DUB enzyme USP7 in dendritic arborization, neuronal migration, and autistic-like behaviors in mice

doi: 10.1016/j.isci.2022.104595

Figure Lengend Snippet: Caspase-3 and microtubules are the downstream effectors mediating the USP7 effect on dendritic arborization (A) Primary hippocampal neurons were transfected with USP7 and immunostained for the cleaved caspase 3. Arrows indicate the transfected neurons. Scale bar = 50 μm. (B) Quantification showed a decrease in cleaved caspase-3 intensity in USP7 overexpressing neurons (Ctrl: n = 15; USP7: n = 19, t -test). (C) HEK cells were transfected with USP7 and shUSP7. Cell lysates were collected to determine the cleaved caspase-3 levels by Westerns. (D) Quantification of Western blot intensities of cleaved caspase-3 (F(2,6) = 16.56, p < 0.01, one-way ANOVA, Tukey). (E) Primary neurons were infected with AAV-USP7 at DIV 0, and neuron lysates were collected for western blot to detect changes in microtubule cleavage. (F) Quantification showed a significant decrease in cleaved microtubules in neurons with USP7 virus infection (Ctrl: n = 3; USP7: n = 3, t -test). (G) Primary neurons were infected with AAV-USP7 at DIV 0 and immunostained at DIV 15 with TubΔCasp6 antibodies. Scale bar = 50 μm. (H and I) Quantification showed that USP7-infected neurons had a decrease in microtubule cleavage intensity (Ctrl: n = 15; USP7: n = 18, t -test), but not in the number of cleavage sites along the dendrite (Ctrl: n = 20; USP7: n = 18, t -test). Data are represented as mean ± SEM. Error bars represent SEM, ∗p < 0.05, ∗∗p < 0.01.

Article Snippet: Full length USP7 fragment from pCI-neo Flag HAUSP/USP7 (addgene, #16655) were inserted into the AAV-ReaChR-citrine vector.

Techniques: Transfection, Western Blot, Infection, Virus

Journal: iScience

Article Title: Role of the DUB enzyme USP7 in dendritic arborization, neuronal migration, and autistic-like behaviors in mice

doi: 10.1016/j.isci.2022.104595

Figure Lengend Snippet: USP7 regulates XIAP protein accumulation in neurons (A) Lysates were collected from primary cortical neurons of DIV 0 to DIV 20. Expression levels of USP7 and XIAP were measured by Western blot. GAPDH was probed as a loading control. (B) Quantification of USP7 and XIAP intensity (n = 3). (C–E) Cortical neurons were infected with AAV-GFP or AAV-USP7 on DIV 0 for 15 days, and USP7 and XIAP levels were measured by Western blot. An increased level for both USP7 and XIAP was detected in neurons infected with USP7 virus (GFP-AAV: n = 4; USP7-AAV: n = 4. p < 0.05, t -test). (F and G) Cortical neurons were treated with HBX41108 (USP7 inhibitor) for 2 and 4 h and the lysates were collected to probe for XIAP. Inhibition of USP7 led to a decrease in XIAP amount. (Ctrl: n = 4; HBX 2 h: n = 4; HBX 4 h: n = 4. F(2,9) = 30.88, p < 0.01, one-way ANOVA, Dunnett). (H) Cortical neurons were transfected with USP7 at DIV 11 and immunostained for XIAP at DIV 15. Scale bar = 50 μm. (I) Quantification showed an increase in endogenous XIAP intensity in neurons transfected with USP7 (Ctrl: n = 13; USP7: n = 13. p < 0.01, t -test). (J) Hippocampal neurons were transfected with shUSP7 at DIV 8 and immunostained for XIAP at DIV 15. Scale bar = 50 μm. (K) Quantification showed a decrease in endogenous XIAP in neurons with USP7 knockdown (Ctrl: n = 14; USP7: n = 14. p < 0.01, t -test). Data are represented as mean ± SEM. Error bars represent SEM, ∗p < 0.05, ∗∗p < 0.01.

Article Snippet: Full length USP7 fragment from pCI-neo Flag HAUSP/USP7 (addgene, #16655) were inserted into the AAV-ReaChR-citrine vector.

Techniques: Expressing, Western Blot, Control, Infection, Virus, Inhibition, Transfection, Knockdown

Journal: iScience

Article Title: Role of the DUB enzyme USP7 in dendritic arborization, neuronal migration, and autistic-like behaviors in mice

doi: 10.1016/j.isci.2022.104595

Figure Lengend Snippet: USP7 causes XIAP deubiquitination and stabilization (A) XIAP ubiquitination assay. HEK293 cells were transfected with FLAG-XIAP, HA-ubiquitin, and USP7 for 2 days. XIAP was immunoprecipitated and probed for ubiquitin (ubi). Cell lysates (input) were used to detect protein levels. (B and C) Quantification of Western blot intensities. USP7 caused a decrease in XIAP ubiquitination and a decrease in XIAP protein levels (Ubiquitination Signal: F(2,9) = 20.95, p < 0.01, one-way ANOVA, Tukey; XIAP Signal: F(2,9) = 22.20, p < 0.01, one-way ANOVA, Tukey. XIAP: n = 4; XIAP + Ubi: n = 4; XIAP + Ubi + USP7: n = 4). (D) Degradation assay of XIAP with or without USP7. Transfected HEK cells were treated with cycloheximide (CHX) for various time periods and cell lysates were collected to examine XIAP levels by Western blot. (E) Quantification of the degradation rate of XIAP over time (Treatment: F(1,4) = 10.14, p < 0.05, repeated measure ANOVA). (F) Morphology of primary neurons transfected with USP7 or XIAP alone, or both. Scale bar = 100 μm. (G and H) Dendrite branch number and the total length of dendrite were increased in neurons overexpressing USP7 or XIAP. Co-transfection of USP7 and XIAP had no additional effects compared with USP7 alone or XIAP only group (Ctrl: n = 35; USP7: n = 25; XIAP: n = 34; XIAP + USP7: n = 31. Number of dendrites: F(3,121) = 13.83, p < 0.01, one-way ANOVA, Tukey; Sum dendrite length: F(3,121) = 8.82, p < 0.01. one-way ANOVA, Tukey). Data are represented as mean ± SEM. Error bars represent SEM, ∗p < 0.05, ∗∗p < 0.01.

Article Snippet: Full length USP7 fragment from pCI-neo Flag HAUSP/USP7 (addgene, #16655) were inserted into the AAV-ReaChR-citrine vector.

Techniques: Ubiquitin Proteomics, Transfection, Immunoprecipitation, Western Blot, Degradation Assay, Cotransfection

Journal: iScience

Article Title: Role of the DUB enzyme USP7 in dendritic arborization, neuronal migration, and autistic-like behaviors in mice

doi: 10.1016/j.isci.2022.104595

Figure Lengend Snippet: Knockdown of XIAP blocks the effect of USP7 on dendritic arborization (A) Cultured neurons were transfected with shXIAP at DIV 7 and immunostained for XIAP at DIV 11. Scale bar = 50 μm. (B) Quantification of XIAP expression (Ctrl: n = 36; shXIAP: n = 36. p < 0.01, t -test). (C) Morphology of primary neurons transfected with USP7 or shXIAP alone, or both at DIV11. Scale bar = 100 μm. (D and E) Dendrite branch number and the total length of dendrite were decreased in XIAP knockdown neurons. Co-transfection of USP7 and shXIAP had no additional effects compared with shXIAP alone group, but decreased significantly compared with USP7 only group (Ctrl: n = 35; USP7: n = 46; shXIAP: n = 46; USP7+shXIAP: n = 35. Number of dendrites: F(3,148) = 10.69, p < 0.01, one-way ANOVA, Tukey; Sum dendrite length: F(3,148) = 10.01, p < 0.01. one-way ANOVA, Tukey). (F) Sholl analysis of dendritic arborization at DIV 11 (Group: F (3, 154) = 11.23, p < 0.01. Ctrl vs. shXIAP: p < 0.01; Ctrl vs. USP7: p > 0.05; USP7+shXIAP vs. USP7: p < 0.01; USP7+shXIAP vs. shXIAP: p > 0.05. Repeated measures ANOVA, Tukey). Data are represented as mean ± SEM. Error bars represent SEM, ∗p < 0.05, ∗∗p < 0.01.

Article Snippet: Full length USP7 fragment from pCI-neo Flag HAUSP/USP7 (addgene, #16655) were inserted into the AAV-ReaChR-citrine vector.

Techniques: Knockdown, Cell Culture, Transfection, Expressing, Cotransfection

Journal: iScience

Article Title: Role of the DUB enzyme USP7 in dendritic arborization, neuronal migration, and autistic-like behaviors in mice

doi: 10.1016/j.isci.2022.104595

Figure Lengend Snippet: USP7 antagonizes E6AP effect on dendritic arborization via control of XIAP ubiquitination (A) HEK293 cells were transfected with FLAG-XIAP, HA-ubiquitin, and USP7 with or without E6AP for 2 d. XIAP was immunoprecipitated and probed for HA-ubiquitin (HA-ubi). Cell lysates (input) were also probed to detect the total protein levels. (B and C) Quantification of western blot intensities. E6AP caused an increase in XIAP ubiquitination (F(3,12) = 19.62, p < 0.01, one-way ANOVA, Tukey) and a decrease in XIAP protein levels in the input (F(3,8) = 43.69, p < 0.01, one-way ANOVA, Tukey). USP7 blocked the effect of E6AP on XIAP protein accumulation and XIAP ubiquitination. (D) Morphology of primary neurons transfected with USP7, E6AP, and USP7+E6AP (DIV 11 - DIV 15). Scale bar = 100 μm. (E and F) Dendritic branch number (F(3,81) = 17.28, p < 0.01, one-way ANOVA, Tukey) and the total length of dendrites (F(3,81) = 17.92, p < 0.01, one-way ANOVA, Tukey) were decreased in neurons with E6AP overexpression (E6AP: n = 19; Ctrl: n = 20. one-way ANOVA, Tukey). USP7 abolished the effect caused by E6AP expression (E6AP + USP7: n = 21; E6AP: n = 19. one-way ANOVA, Tukey). (G) Sholl analysis showed a reduction in the complexity of dendritic arborization in E6AP neurons, which was blocked by co-expression with USP7 in neurons (Group: F(3,77) = 16.833, p < 0.01. Repeated measures ANOVA, Tukey). Data are represented as mean ± SEM. Error bars represent SEM, ∗p < 0.05, ∗∗p < 0.01.

Article Snippet: Full length USP7 fragment from pCI-neo Flag HAUSP/USP7 (addgene, #16655) were inserted into the AAV-ReaChR-citrine vector.

Techniques: Control, Ubiquitin Proteomics, Transfection, Immunoprecipitation, Western Blot, Over Expression, Expressing

Journal: iScience

Article Title: Role of the DUB enzyme USP7 in dendritic arborization, neuronal migration, and autistic-like behaviors in mice

doi: 10.1016/j.isci.2022.104595

Figure Lengend Snippet: USP7 overexpression in the brain affects neuron migration and dendritic arborization (A) Schematic illustration of the procedures for in utero electroporation (IUE) performed at E15 and P0, P15. (B) Brain slices taken at P0 following IUE of DsRed control (Ctrl) or GFP-USP7 at E15. Scale bar = 200 μm. (C) Analysis of neuronal migration at P0 showed that less neurons were distributed in the upCP and more in the loCP and VZ regions compared with controls (Ctrl: n = 12; USP7: n = 14. t -test). More than 1200 GFP + neurons from four brains were analyzed in each group. 15 slices from five brains were analyzed in each group, and more than 3000 GFP + neurons were analyzed totally. (D) Representative images showing dendritic arborizations of control and USP7 groups. Scale bar = 50 μm. (E) Sholl analysis of dendritic structure at P15 after IUE showed a significant change in branching (Group: F(1, 48) = 17.06, p < 0.01, Repeated measures ANOVA. Ctrl: n = 27; USP7: n = 22). (F and G) Dendrite numbers and the total length of dendrites were increased in the USP7 overexpressing group compared with the control (Ctrl: n = 27; USP7: n = 22. t -test). Data are represented as mean ± SEM. Error bars represent SEM, ∗p < 0.05, ∗∗p < 0.01.

Article Snippet: Full length USP7 fragment from pCI-neo Flag HAUSP/USP7 (addgene, #16655) were inserted into the AAV-ReaChR-citrine vector.

Techniques: Over Expression, Migration, In Utero, Electroporation, Control

Journal: iScience

Article Title: Role of the DUB enzyme USP7 in dendritic arborization, neuronal migration, and autistic-like behaviors in mice

doi: 10.1016/j.isci.2022.104595

Figure Lengend Snippet: USP7 overexpression in vivo in mouse brain at P0 leads to dendrite morphological changes (A) Schematic illustration of the procedures for virus injection at P0 and schedule for behavior tests performed at P30-P55. AAV-USP7 and AAV-GFP were injected into the lateral ventricles in mice at P0, and the mice were perfused around P30 to P60 for cryostat to show the validity of the virus. The expression of GFP (B) or GFP-fused USP7 (left: Scale bar = 1000 μm; right: Scale bar = 200 μm) (C) can be detected in the whole brain around P30 to P60 ( left: Scale bar = 500 μm; right: Scale bar = 100 μm). (D) Western blot showed that the expression of USP7 in the cortex of the AAV USP7 group is significantly higher than in the control group, as well as XIAP. (E–I) Sholl analysis shows the morphological changes. Scale bar = 50 μm. 19 cortical neurons from 5 control mice and 27 neurons from 5 AAV USP7 mice were analyzed. The number of dendrites and the mean and total length of dendrites were all increased significantly in the AAV USP7 group (F, Number of dendrites: Ctrl: n = 19, USP7: n = 27, p < 0.01, t -test; G,Sum length: Ctrl: n = 19, USP7: n = 27, p < 0.01, t -test; H, Mean length: Ctrl: n = 19, USP7: n = 27, p < 0.01. t -test). I, The dendritic arborization was more complex in the AAV USP7 group compared with the control group (Group: F(1, 44) = 37.91, p < 0.01, Repeated measures ANOVA). Data are represented as mean ± SEM. Error bars represent SEM, ∗p < 0.05, ∗∗p < 0.01.

Article Snippet: Full length USP7 fragment from pCI-neo Flag HAUSP/USP7 (addgene, #16655) were inserted into the AAV-ReaChR-citrine vector.

Techniques: Over Expression, In Vivo, Virus, Injection, Expressing, Western Blot, Control

Journal: iScience

Article Title: Role of the DUB enzyme USP7 in dendritic arborization, neuronal migration, and autistic-like behaviors in mice

doi: 10.1016/j.isci.2022.104595

Figure Lengend Snippet: Behavior changes in mice following USP7 overexpression in the brain at P0. Behavioral tests were performed at P30-P55 (A and B) Homecage activities including grooming, rearing, digging, climbing, circling, and jumping (Ctrl: n = 9; USP7: n = 13, t -test). Counts of grooming and digging (A), as well as the overall activity events (B), were increased significantly in USP7 infected mice. (C) Track length in the open field test showed no difference between two groups ( t -test). (D) A representative example of the test arena at the end of the Marble burying test. (E) USP7 mice buried more marbles during the test (F(1,20) = 13.46, p < 0.01. Ctrl: n = 9; USP7: n = 13, repeated measures ANOVA). (F) Quantification of the number of marbles buried at the end of the test (30 min). (G and J) Paradigm for the social preference test (G) and social novelty test (J), and representative tracing. (H and K) Quantification of time spent in each chamber in the social preference test (H) (Ctrl: n = 8; USP7: n = 12, t -test) and social novelty test (K) (Ctrl: n = 8; USP7: n = 12, t -test). (I and L) Quantification of the preference index in the social preference test (I) and social novelty test (L). The preference for social interaction was increased in USP7 animals compared with the control ( t -test) (I). (M and N) The novel object recognition test showed no difference in discrimination index between the two groups (Ctrl: n = 8; USP7: n = 13, t -test). (O and P) Hot plate test. The withdrawal latency was decreased in USP7 mice compared with the control (Ctrl: n = 8; USP7: n = 13, t -test). Data are represented as mean ± SEM. Error bars represent SEM, ∗p < 0.05, ∗∗p < 0.01.

Article Snippet: Full length USP7 fragment from pCI-neo Flag HAUSP/USP7 (addgene, #16655) were inserted into the AAV-ReaChR-citrine vector.

Techniques: Over Expression, Activity Assay, Infection, Control, Hot Plate Test

Journal: iScience

Article Title: Role of the DUB enzyme USP7 in dendritic arborization, neuronal migration, and autistic-like behaviors in mice

doi: 10.1016/j.isci.2022.104595

Figure Lengend Snippet:

Article Snippet: Full length USP7 fragment from pCI-neo Flag HAUSP/USP7 (addgene, #16655) were inserted into the AAV-ReaChR-citrine vector.

Techniques: Virus, Transfection, Recombinant, Sequencing, Software