Journal: Molecular Cancer

Article Title: Lipid phosphate phosphatase-3 regulates tumor growth via β-catenin and Cyclin-D1 signaling

doi: 10.1186/1476-4598-10-51

Figure Lengend Snippet: LPP3 regulates glioblastoma cell proliferation . (A) The time line indicates when glioblastoma cell lines were plated, shRNA (retrovirus) mediated knockdown was conducted, cells were growth factor and serum starved, fresh medium was added, BrdU (1.0 μg/ml) was added, and the proliferation assay was performed. (B) Quantification of glioblastoma cell proliferation assay. The data represent the mean ± s.e.m. n = 5-7 from five to seven independent experiments, ¥ P < 0.05 vs. control untreated; ¶ P < 0.05 vs. control shRNA treated group. (C-F) Representative images of the BrdU assay. Arrows indicate BrdU positive cells. Scale bar, 150 μm. (G) The efficiency of knockdown of LPP3 was assessed by western blotting with the indicated antibodies. Figure 3G (top panel, last lane, anti-LPP3), a partial band is likely produced by over flow from the neighboring well. All experiments are representative of those obtained in at least three separate experiments with similar results.

Article Snippet: Control and LPP shRNA retroviral constructs were purchased from Origene (Rockville, MD).

Techniques: shRNA, Knockdown, Proliferation Assay, Control, BrdU Staining, Western Blot, Produced

Journal: Molecular Cancer

Article Title: Lipid phosphate phosphatase-3 regulates tumor growth via β-catenin and Cyclin-D1 signaling

doi: 10.1186/1476-4598-10-51

Figure Lengend Snippet: LPP3 regulates glioblastoma cell migration . (A) The time line indicates when glioblastoma cell lines were plated, shRNA (retrovirus) mediated knockdown was conducted, medium was added, and the migration assay was performed as described in materials and methods. (B) Quantification of glioblastoma cell migration through the Boyden chamber. The data represent the mean ± s.e.m. n = 5-7, ¥ P < 0.05 vs. control shRNA treated group. (C) Efficiency of knockdown of LPP3 was assessed by western blotting with the indicated antibodies. All experiments are representative of those obtained in at least three separate experiments with similar results.

Article Snippet: Control and LPP shRNA retroviral constructs were purchased from Origene (Rockville, MD).

Techniques: Migration, shRNA, Knockdown, Control, Western Blot

Journal: Molecular Cancer

Article Title: Lipid phosphate phosphatase-3 regulates tumor growth via β-catenin and Cyclin-D1 signaling

doi: 10.1186/1476-4598-10-51

Figure Lengend Snippet: LPP3 regulates glioblastoma tumor growth . (A) Stable clones of U87 and U118 were selected and efficiency of knockdown was determined by western blotting with the indicated antibodies. LPP3 -knockdown decreased total β-catenin, CYCLIN-D1, and CD133 proteins, whereas it had no effect on LPP2 or GAPDH. (B) Conditioned media were collected and subjected to ELISA for VEGF, IL-8, and TIMP-2. LPP3 -knockdown in U87 and U118 cells reduced the concentration of VEGF and IL-8, whereas TIMP-2 was unaffected. (C) In the xenograft assay, mice receiving cells that expressed control shRNA showed increased tumor growth (n = 12, ¥ P < 0.05) after 14 and 28 days. LPP3 -knockdown reduced U87 and U118 tumor growth (n = 12, ¶ P < 0.05). (D) Representative images from the xenograft assay. Dotted circles indicate the location of tumor implants.

Article Snippet: Control and LPP shRNA retroviral constructs were purchased from Origene (Rockville, MD).

Techniques: Clone Assay, Knockdown, Western Blot, Enzyme-linked Immunosorbent Assay, Concentration Assay, Xenograft Assay, Control, shRNA

Journal: Molecular Cancer

Article Title: Lipid phosphate phosphatase-3 regulates tumor growth via β-catenin and Cyclin-D1 signaling

doi: 10.1186/1476-4598-10-51

Figure Lengend Snippet: Forced expression of LPP3 potentiates SW480 tumor growth in the xenograft assay . (A) pLNCX2-based retroviral constructs expressing vector alone, hLPP1, hLPP2, hLPP3 or mLpp3 cDNAs. (B) The comparable levels of hLPP1, hLPP2, hLPP3 and mLpp3 proteins were confirmed by western blotting with anti-HA antibody. (C) Xenograft assay: there was minimal tumor growth after 14 and 28 days in mice receiving LPP3-deficient SW480 cells (2 × 10 4 tumor cells/site) that expressed vector alone, hLPP1, or hLPP2 constructs. In contrast, tumor volume was significantly increased in mice receiving SW480 cells that expressed hLPP3 or mLpp3 (n = 12, ¥ P < 0.01 vs. hLPP1 group; n = 12, ¶ P < 0.005 vs. hLPP1 group) at 14 and 28 days.

Article Snippet: Control and LPP shRNA retroviral constructs were purchased from Origene (Rockville, MD).

Techniques: Expressing, Xenograft Assay, Retroviral, Construct, Plasmid Preparation, Western Blot

Journal: Molecular Cancer

Article Title: Lipid phosphate phosphatase-3 regulates tumor growth via β-catenin and Cyclin-D1 signaling

doi: 10.1186/1476-4598-10-51

Figure Lengend Snippet: Domains involved in the regulation of SW480 tumor growth . (A) Schematics of pLNCX2-based retroviral constructs (a-e). Empty red and blue circles indicate the relative positions of lipid phosphatase and RGD cell adhesion domains, respectively. Filled red and blue circles indicate phosphatase-inactive (PI) and RAD (adhesion defective) domains, respectively. Black boxes represent transmembrane segments. Three copies of hemagglutinin (HA) epitopes were fused to the N-terminal and in-frame to the open reading frame of the cDNAs. (B) Equivalent protein expression and phosphorylation states of β-catenin and CYCLIN-D1 proteins were analyzed by immunoblotting with anti-HA, anti-β-catenin, anti-p-β-catenin, and anti-CYCLIN-D1 antibodies. Equal loading of proteins across the lanes were determined with the anti-GRB-2 antibody. All blots are representative of those obtained in at least three separate experiments with similar results. (C) LPP3 expression potentiates SW480 tumor growth. Nude mice were injected subcutaneously with SW480 cells (~ 2 × 10 4 ) expressing the indicated constructs. After 21 days, the tumor outgrowths were measured and photographed. (n = 12, ¶ P < 0.005 vs. vector alone group). (D) Representative pictures of primary tumors in nude mice injected with SW480 cells expressing the indicated constructs.

Article Snippet: Control and LPP shRNA retroviral constructs were purchased from Origene (Rockville, MD).

Techniques: Retroviral, Construct, Expressing, Phospho-proteomics, Western Blot, Injection, Plasmid Preparation

Journal: Frontiers in Microbiology

Article Title: Lily polysaccharides alleviate colitis through the microbiota–N8-acetylspermidine–cGAS–STING signaling axis

doi: 10.3389/fmicb.2025.1686902

Figure Lengend Snippet: The therapeutic effect of lily polysaccharide on colitis. (a) Changes of mice weight. (Day x/Day 0 *100%, n = 5). (b) Disease activity index. ( n = 4). (c,d) Quantified lengths of colonic tissues isolated from mice after treatment ( n = 5). (e) H&E-stained histological sections of colons. Representative digital photos. (f) The pathology score of colons from mice in the different treatment group ( n = 5). (g–i) The levels of pro-inflammatory cytokines IL-1 β , IL-6 and TNF- α in colon of mice were detected by ELISA ( n = 5). (j) The expression levels of MUC2 were determined by immunofluorescence staining in the mouse colon. Representative digital photos. Data are presented as the mean ± SEM. Statistically significant differences are indicated; * p < 0.05, ** p < 0.01, *** p < 0.001.

Article Snippet: Subsequently, the samples were washed again with PBST and incubated overnight at 4 °C with a primary antibody against MUC2 (Rabbit polyclonal IgG, Proteintech, Catalog No. 27675-1-AP, unconjugated; 1:200 dilution).

Techniques: Activity Assay, Isolation, Staining, Enzyme-linked Immunosorbent Assay, Expressing, Immunofluorescence

Journal: Frontiers in Microbiology

Article Title: Lily polysaccharides alleviate colitis through the microbiota–N8-acetylspermidine–cGAS–STING signaling axis

doi: 10.3389/fmicb.2025.1686902

Figure Lengend Snippet: Fecal bacteria transplantation experiments showed that LP could positively regulate the gut microbiota. (a) Changes of mice weight. (Day x/Day 0 *100%, n = 5). (b) Disease activity index ( n = 5). (c,d) Quantified lengths of colonic tissues isolated from mice after treatment ( n = 5). (e) H&E-stained histological sections of colons. Representative digital photos. (f) The pathology score of colons from mice in the different treatment group ( n = 5). (g–i) The levels of pro-inflammatory cytokines IL-1β, IL-6 and TNF-α in colon of mice were detected by ELISA ( n = 5). (j) The expression levels of MUC2 were determined by immunofluorescence staining in the mouse colon. Representative digital photos. Data are presented as the mean ± SEM. Statistically significant differences are indicated; * p < 0.05, ** p < 0.01, *** p < 0.001.

Article Snippet: Subsequently, the samples were washed again with PBST and incubated overnight at 4 °C with a primary antibody against MUC2 (Rabbit polyclonal IgG, Proteintech, Catalog No. 27675-1-AP, unconjugated; 1:200 dilution).

Techniques: Bacteria, Transplantation Assay, Activity Assay, Isolation, Staining, Enzyme-linked Immunosorbent Assay, Expressing, Immunofluorescence

Journal: Frontiers in Microbiology

Article Title: Lily polysaccharides alleviate colitis through the microbiota–N8-acetylspermidine–cGAS–STING signaling axis

doi: 10.3389/fmicb.2025.1686902

Figure Lengend Snippet: Replenishing N8AS can effectively alleviate enteritis. (a) Changes of mice weight.(Day x/Day 0 *100%, n = 5). (b) Disease activity index. ( n = 5). (c,d) Quantified lengths of colonic tissues isolated from mice after treatment ( n = 5). (e) H&E-stained histological sections of colons. Representative digital photos. (f) The pathology score of colons from mice in the different treatment group ( n = 5). (g–i) The levels of pro-inflammatory cytokines IL-1β, IL-6 and TNF-α in colon of mice were detected by ELISA ( n = 5). (j) The expression levels of MUC2 were determined by immunofluorescence staining in the mouse colon. Representative digital photos. (k–o) The protein expression levels of cGAS, STING, p-TBK, p-IRF3 were assessed by western blot analysis. Data are presented as the mean ± SEM. Statistically significant differences are indicated; * p < 0.05, ** p < 0.01, *** p < 0.001.

Article Snippet: Subsequently, the samples were washed again with PBST and incubated overnight at 4 °C with a primary antibody against MUC2 (Rabbit polyclonal IgG, Proteintech, Catalog No. 27675-1-AP, unconjugated; 1:200 dilution).

Techniques: Activity Assay, Isolation, Staining, Enzyme-linked Immunosorbent Assay, Expressing, Immunofluorescence, Western Blot

Journal: Frontiers in Microbiology

Article Title: Lily polysaccharides alleviate colitis through the microbiota–N8-acetylspermidine–cGAS–STING signaling axis

doi: 10.3389/fmicb.2025.1686902

Figure Lengend Snippet: In vitro verification, lily polysaccharide can inhibit the cGAS-STING pathway and play an anti-inflammatory role. (a) IL-1β mRNA expression. (b) TNF-α mRNA expression level. (c) IL-6 mRNA expression level. (d) ZO-1 mRNA expression level. (e) occludin mRNA expression level. (f) MUC2 mRNA expression level. (g–k) The protein expression levels of cGAS, STING, p-TBK, p-IRF3 were assessed by western blot analysis. Data are presented as the mean ± SEM. Statistically significant differences are indicated; * p < 0.05, ** p < 0.01, *** p < 0.001.

Article Snippet: Subsequently, the samples were washed again with PBST and incubated overnight at 4 °C with a primary antibody against MUC2 (Rabbit polyclonal IgG, Proteintech, Catalog No. 27675-1-AP, unconjugated; 1:200 dilution).

Techniques: In Vitro, Expressing, Western Blot