pgl3 mmp2  (Addgene inc)

Journal: The Journal of Biological Chemistry

Article Title: Acid sphingomyelinase recruits palmitoylated CD36 to membrane rafts and enhances lipid uptake

doi: 10.1016/j.jbc.2025.110213

Figure Lengend Snippet: CD36 interacts with ASMase in membrane of oxLDL-induced cells. A , schematic representation of the steps for identification of CD36-associated proteins in the membrane. RAW264.7 cells transfected with Flag-CD36 are incubated with oxLDL (50 μg/ml). Plasma LR are isolated, and CD36-associated proteins are purified using an anti-Flag affinity column. The protein complex is analyzed by mass spectrometry. B , immunoblotting analysis of presence of ASMase in eluates immunoprecipitated with anti-Flag-CD36 antibodies. Blank vector used as control. C , cells transfected with Flag-CD36 and HA-ASM undergo immunoprecipitation with anti-Flag agarose gel, followed by immunoblotting with CD36 and ASMase antibodies. D , co-immunoprecipitation assay shows the association of endogenous CD36 and ASMase. E and F , purified GST-CD36 is incubated with HA-ASM and cell lysates, and the complexes are subjected to a pull-down assay. G and H , schematic diagram of full-length and deletion mutants of ASMase, and the domain responsible for interaction with CD36 was identified by using co-immunoprecipitation. I , immunofluorescence staining shows Flag-CD36 ( red ) and HA-ASM ( green ). Percentages of Flag-CD36/HA-ASM colocalization cells in total cells were from eight separated fields. J and K , Flag-CD36 and HA-ASM intensities in randomly selected 30 cells. L , Spearman analysis for the relationship between CD36 and ASMase intensities. M , cell lysate were centrifugated and fractionized. The ASMase in the raft and nonraft fractions were detected by Western blot. Representative blots and images were from three independent experiments. Data are analyzed by Student's t test in ( C , I – K , M ), by one-way ANOVA followed by Tukey’s post hoc test in ( D ) and by Spearman Correlation Analysis in ( L ), mean ± SD, n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001.

Article Snippet: RAW264.7 cells were co-transfected with an ASMase promoter-driven firefly luciferase construct (pGL3-MMP2, Promega) and a Renilla luciferase-expressing plasmid (pRL-TK, Promega).

Techniques: Membrane, Transfection, Incubation, Clinical Proteomics, Isolation, Purification, Affinity Column, Mass Spectrometry, Western Blot, Immunoprecipitation, Plasmid Preparation, Control, Agarose Gel Electrophoresis, Co-Immunoprecipitation Assay, Pull Down Assay, Immunofluorescence, Staining

Journal: The Journal of Biological Chemistry

Article Title: Acid sphingomyelinase recruits palmitoylated CD36 to membrane rafts and enhances lipid uptake

doi: 10.1016/j.jbc.2025.110213

Figure Lengend Snippet: ASMase promotes lipid recruitment of palmitoylated CD36 during foam cell formation. A , the ABE assay measures CD36 palmitoylation in oxLDL-incubated peritoneal macrophages isolated from wild-type and ASMase−/− mice (Student's t test, n = 6 mice per group). B , LR localization of CD36 in wild-type and ASMase deficient macrophages (Student's t test, n = 6 mice per group). C , LR localization of CD36 in RAW264.7 macrophages with ASMase knockdown via shRNA (two-way ANOVA with Tukey’s test, n = 3). D , RAW264.7 macrophages are stained with anti-CD36 antibody ( red ) and FITC-CTxB ( green ) (two-way ANOVA with Tukey’s test, n = 3). E , Western blot analysis of CD36 localization in LR in oxLDL-treated cells treated with ASM-IN-1 (3 μM), an ASMase inhibitor, for 24 h. (one-way ANOVA with Tukey’s test, n = 3). F , Western blot analysis of CD36 localization in LR in oxLDL-treated cells transfected with adenovirus-mediated ASMase expressing vector. (Student's t test, n = 3). G and H , CD36 palmitoylation and LR localization in oxLDL-treated cells treated with recombinant ASMase (20 μg/ml) for 24 h and with or without MβCD (5 mmol/L) for 2 h. (one-way ANOVA with Tukey’s test, n = 3). I , immunofluorescence staining shows CD36 ( red ) and FITC-CTxB ( green ) in oxLDL-treated cells treated with ASMase and ASMase + MβCD (one-way ANOVA with Tukey’s test, n = 3). ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001. ns, not significant.

Article Snippet: RAW264.7 cells were co-transfected with an ASMase promoter-driven firefly luciferase construct (pGL3-MMP2, Promega) and a Renilla luciferase-expressing plasmid (pRL-TK, Promega).

Techniques: Incubation, Isolation, Knockdown, shRNA, Staining, Western Blot, Transfection, Expressing, Plasmid Preparation, Recombinant, Immunofluorescence

Journal: The Journal of Biological Chemistry

Article Title: Acid sphingomyelinase recruits palmitoylated CD36 to membrane rafts and enhances lipid uptake

doi: 10.1016/j.jbc.2025.110213

Figure Lengend Snippet: Reduced membrane AMSase inhibits CD36-mediated downstream signaling in RAW264.7 macrophages. A , co-immunoprecipitation assay measures CD36/Fyn/Lyn association in cells with ASMase knockdown. Cells are transfected with sh-ASMase and incubated with oxLDL for 24 h (Student's t test, n = 3). B – D , phosphorylation levels of Fyn, Lyn, and JNK1/2 are analyzed in oxLDL-treated cells with ASMase knockdown (Student's t test, n = 3). E , cells transfected with sh-ASMase are incubated with DiI-oxLDL (30 μg/ml) for 6 h. DiI-oxLDL uptake is measured by flow cytometry (Student's t test, n = 3). F , cells transfected with sh-ASMase are incubated with oxLDL for 24 h and stained with Oil Red O (Student's t test, n = 3). G , total cholesterol is measured in cells transfected with sh-ASMase and incubated with oxLDL (Student's t test, n = 3). H , LR localization of CD36 and ASMase is analyzed in cells incubated with oxLDL with or without Sortilin inhibitor AF38469 (one-way ANOVA followed by Tukey’s post hoc test, n = 3). I , cells incubated with oxLDL with or without AF38469 are stained with anti-CD36 antibody ( red ) and FITC-CTxB ( green ). J , DiI-oxLDL uptake is measured in cells incubated with or without AF38469 (Student's t test, n = 3). ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001.

Article Snippet: RAW264.7 cells were co-transfected with an ASMase promoter-driven firefly luciferase construct (pGL3-MMP2, Promega) and a Renilla luciferase-expressing plasmid (pRL-TK, Promega).

Techniques: Membrane, Co-Immunoprecipitation Assay, Knockdown, Transfection, Incubation, Phospho-proteomics, Flow Cytometry, Staining

Journal: The Journal of Biological Chemistry

Article Title: Acid sphingomyelinase recruits palmitoylated CD36 to membrane rafts and enhances lipid uptake

doi: 10.1016/j.jbc.2025.110213

Figure Lengend Snippet: Reduced CD36 palmitoylation inhibits ASMase-mediated CD36 LR localization. A , CD36 palmitoylation is analyzed in cells treated with oxLDL and with or without 2-BP. B , CD36 LR localization is measured in oxLDL-incubated cells treated with ASMase or ASMase + 2-BP. C , CD36 palmitoylation is analyzed in oxLDL-induced cells transfected with Flag-wCD36 (wild-type) or Flag-mCD36 (mutant). D , CD36 LR localization is measured in cells transfected with Flag-wCD36 or Flag-mCD36, following oxLDL incubation. E and F , RAW264.7 macrophages were stimulated with oxLDL and treated as indicated. The cells were then stained with CD36 and CTxB, and percentage of cells with CD36/CTxB co-localization in total cells were counted. G , inhibited association of ASMase and CD36 in LR after CD36 palmitoylation were blocked by 2-BP ( left ) or transfection with mCD36 ( right ) in oxLDL-treated cells. H , immunofluorescence staining assay shows reduced co-localization of ASMase with CD36 of palmitoylation inhibited by 2-BP or mutation in oxLDL-treated cells. CD36 appears red and ASMase appears green. All data are analyzed by Student's t test, mean ± SD, n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001.

Article Snippet: RAW264.7 cells were co-transfected with an ASMase promoter-driven firefly luciferase construct (pGL3-MMP2, Promega) and a Renilla luciferase-expressing plasmid (pRL-TK, Promega).

Techniques: Incubation, Transfection, Mutagenesis, Staining, Immunofluorescence

Journal: The Journal of Biological Chemistry

Article Title: Acid sphingomyelinase recruits palmitoylated CD36 to membrane rafts and enhances lipid uptake

doi: 10.1016/j.jbc.2025.110213

Figure Lengend Snippet: ASMase deficiency reduces CD36 LR recruitment and aortic lipid accumulation in atherosclerotic plaques ASM+/+ApoE−/− and ASM−/−ApoE−/− mice are fed a high-fat diet beginning at 8 weeks of age for 16. A , peritoneal macrophages isolated from ASM+/+ApoE−/− and ASM−/−ApoE−/− mice are incubated with DiI-oxLDL for 6 h, and DiI-oxLDL uptake is measured by flow cytometry. B , intracellular cholesterol levels in peritoneal macrophages are quantified. C , peritoneal macrophages are incubated with oxLDL for 24 h and stained with Oil Red O. D , whole aorta from ASM+/+ApoE−/− and ASM−/−ApoE−/− mice are stained with Oil Red O to assess plaque formation. E , CD36 LR localization is analyzed in macrophages isolated from high-fat diet ASM+/+ApoE−/− and ASM−/−ApoE−/− mice. F and G , Oil Red O staining of aortic root sections is performed in ASM+/+ApoE−/− and ASM−/−ApoE−/− mice. Positive staining in total plaque area was calculated. H and I , sections of the aortic roots are stained with HE and anti-CD68 antibodies. All data are analyzed by Student's t test, mean ± SD, n = 6. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001.

Article Snippet: RAW264.7 cells were co-transfected with an ASMase promoter-driven firefly luciferase construct (pGL3-MMP2, Promega) and a Renilla luciferase-expressing plasmid (pRL-TK, Promega).

Techniques: Isolation, Incubation, Flow Cytometry, Staining

Journal: The Journal of Biological Chemistry

Article Title: Acid sphingomyelinase recruits palmitoylated CD36 to membrane rafts and enhances lipid uptake

doi: 10.1016/j.jbc.2025.110213

Figure Lengend Snippet: OxLDL increases ASMase expression and promotes sphingomyelin (SM) catabolism. A , schematic illustration of SM catabolism. SM is hydrolyzed by ASMase to generate ceramide and phosphatidylcholine. Ceramidases convert ceramides into sphingosine and fatty acids. B , Western blot detection of ASMase expression is performed in cells treated with varying concentrations of oxLDL (50–120 μg/ml; one-way ANOVA followed by Tukey’s post hoc test, n = 3). C , RT-qPCR analysis measures ASMase mRNA levels in oxLDL (50 μg/ml) treated macrophages. D , ASMase enzymatic activity is assessed in cells treated with oxLDL at concentration of 50 μg/ml. E , OxLDL-treated cells are seeded on coverslip and incubated with SM-binding protein, lysenin-His (1 μg/ml). Membrane SM is detected using immunofluorescence staining and quantified by flow cytometry. F – H , total cellular levels of SM and ceramides, and SM/ceramide ratio are measured by LC-MS/MS in oxLDL-treated cells (50 μg/ml). I and J , lipidomics analysis of specific SM and ceramide species in cells treated with oxLDL (50 μg/ml). All comparisons were conducted with Student's t test except in ( B ) (mean ± SD, n = 3). ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001. ns, not significant.

Article Snippet: RAW264.7 cells were co-transfected with an ASMase promoter-driven firefly luciferase construct (pGL3-MMP2, Promega) and a Renilla luciferase-expressing plasmid (pRL-TK, Promega).

Techniques: Expressing, Western Blot, Quantitative RT-PCR, Activity Assay, Concentration Assay, Incubation, Binding Assay, Membrane, Immunofluorescence, Staining, Flow Cytometry, Liquid Chromatography with Mass Spectroscopy

Journal: The Journal of Biological Chemistry

Article Title: Acid sphingomyelinase recruits palmitoylated CD36 to membrane rafts and enhances lipid uptake

doi: 10.1016/j.jbc.2025.110213

Figure Lengend Snippet: ASMase is upregulated by activating ERKs/Sp-1 signaling in oxLDL-induced macrophages. A , schematic illustration shows the ASMase promoter containing an SP-1 binding site. Primers P1 and P2 are used for the ChIP assay. The primer sequences used are listed in the Experimental procedures section. B , the ChIP assay detects SP-1 binding to the ASMase promoter (two-way ANOVA followed by Tukey’s post hoc test). C , EMSA detects SP-1/ASMase promoter binding. D , luciferase reporter assay of truncated ASMase promoter activity. Student's t test. E , Western blot analysis measures SP-1 phosphorylation. Macrophages are treated with oxLDL and incubated with SCH772984, VX-702, or SP600125, which are specific inhibitors of ERK1/2, p38, and JNK1/2, respectively (one-way ANOVA followed by Tukey’s post hoc test). ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001. ns, not significant, mean ± SD, n = 3.

Article Snippet: RAW264.7 cells were co-transfected with an ASMase promoter-driven firefly luciferase construct (pGL3-MMP2, Promega) and a Renilla luciferase-expressing plasmid (pRL-TK, Promega).

Techniques: Binding Assay, Luciferase, Reporter Assay, Activity Assay, Western Blot, Phospho-proteomics, Incubation

Journal: The Journal of Biological Chemistry

Article Title: Acid sphingomyelinase recruits palmitoylated CD36 to membrane rafts and enhances lipid uptake

doi: 10.1016/j.jbc.2025.110213

Figure Lengend Snippet: Model for ASMase-mediated palmitoylated CD36 membrane rafts recruitment .

Article Snippet: RAW264.7 cells were co-transfected with an ASMase promoter-driven firefly luciferase construct (pGL3-MMP2, Promega) and a Renilla luciferase-expressing plasmid (pRL-TK, Promega).

Techniques: Membrane

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research

Article Title: BMI1 drives metastasis of prostate cancer in Caucasian and African-American men and is a potential therapeutic target: hypothesis tested in race-specific models

doi: 10.1158/1078-0432.CCR-18-1394

Figure Lengend Snippet: (Ai–ii) pictomicrographs show the expression of BMI1 ( pointing to brown staining) in CaP tissues of African- American and Caucasian by the IHC analysis and box plot shows the comparative average BMI1-postive staining score in Caucasian and African-American tumor specimens (Bi) Box plots shows the mRNA expression in matched samples of normal vs. tumor in African American patients. (Bii) pictomicrographs show the expression of BMI1 in the lymph node metastatic tissues (Mets) of CaP patients shows as assessed by (IHC) analysis (Biii) Dot plots show correlation of BMI1 with metastasis of CaP in a large cohort of patients as analyzed using mining of oncomine and GEO data (Ci–ii) box plot graphs show the mRNA expression of BMI1, AR, PTEN, INK4A/p16 and metastatic genes (Cyclin D1, VEGF, c-MYC) in the metastatic tissues (Mets) of African-American and Caucasian patients as assessed by quantitative real-time PCR (qRT-PCR) analysis. (Di–ii) histograms showing the recruitment of BMI1 on the promoter of PTEN gene in African-American indolent CaP model (RCC7/T) and Caucasian CRPC (22Rν1) and brain metastasis model (DU145) as assessed by chromatin-immunoprecipitation (ChIP) analysis. (Ei–v) histograms showing the effect of BMI1-targeting (by siRNA) on the promoter activities of VEGF, MMP2, MMP9, BCl2 genes and transcriptional activity of NFκB transcriptional factor in bone metastasis CaP model of African-Americans as assessed by dual-luciferase reporter assays.

Article Snippet: We used following plasmids pTK-TCF-Luc (Upstate Laboratories, Lake Placid, NY); pGL3-MMP2, pGL3-VEGF, pGL3-MYC (Addgene, Cambridge, MA) and pGL3-BMI1 (gifted by Goberdhan Dimri, George Washington University, Washington DC).

Techniques: Expressing, Staining, Real-time Polymerase Chain Reaction, Quantitative RT-PCR, Chromatin Immunoprecipitation, Activity Assay, Luciferase