Journal: Cell metabolism

Article Title: Comprehensive Proteomics Analysis of Stressed Human Islets Identifies GDF15 as a Target for Type 1 Diabetes Intervention

doi: 10.1016/j.cmet.2019.12.005

Figure Lengend Snippet: (A) GDF15 and SPP1 levels in human islets treated with the combination of cytokines IL-1β+IFN-γ were measured by label-free proteomics, western blot, and qPCR. The western blot image is shown in Figure S2.

Article Snippet: To study the protective effect of GDF15 and SPP1, we pretreated EndoC βH1 cells and human islets with human recombinant 100 ng/mL GDF15 (Sino Biologicals) and 50 ng/mL SPP1 (GenTex), followed by cytokine treatment for 24 h. Recombinant GDF15 was previously tested for TGF-β contamination by ELISA, confirming absence of TGF-β in the sample.

Techniques: Western Blot

Journal: Cell metabolism

Article Title: Comprehensive Proteomics Analysis of Stressed Human Islets Identifies GDF15 as a Target for Type 1 Diabetes Intervention

doi: 10.1016/j.cmet.2019.12.005

Figure Lengend Snippet: (A) Network analysis using MetaCore of downstream signaling of GDF15 and SPP1. Note that both GDF15 and SPP1 regulate the apoptotic pathway by different but overlapping signaling.

Article Snippet: To study the protective effect of GDF15 and SPP1, we pretreated EndoC βH1 cells and human islets with human recombinant 100 ng/mL GDF15 (Sino Biologicals) and 50 ng/mL SPP1 (GenTex), followed by cytokine treatment for 24 h. Recombinant GDF15 was previously tested for TGF-β contamination by ELISA, confirming absence of TGF-β in the sample.

Techniques:

Journal: Cell metabolism

Article Title: Comprehensive Proteomics Analysis of Stressed Human Islets Identifies GDF15 as a Target for Type 1 Diabetes Intervention

doi: 10.1016/j.cmet.2019.12.005

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: To study the protective effect of GDF15 and SPP1, we pretreated EndoC βH1 cells and human islets with human recombinant 100 ng/mL GDF15 (Sino Biologicals) and 50 ng/mL SPP1 (GenTex), followed by cytokine treatment for 24 h. Recombinant GDF15 was previously tested for TGF-β contamination by ELISA, confirming absence of TGF-β in the sample.

Techniques: Plasmid Preparation, Recombinant, Modification, Produced, Enzyme-linked Immunosorbent Assay, LAL Assay, Caspase-Glo Assay, Expressing, Software

Journal: Frontiers in Immunology

Article Title: Osteopontin regulates right ventricular failure through integrin ανβ3/PERK/CHOP-dependent inflammatory and apoptotic pathways

doi: 10.3389/fimmu.2025.1569210

Figure Lengend Snippet: Clinical significance of serum OPN levels in right ventricular failure patients. (A) Serum OPN concentrations measured by ELISA in patients with normal right ventricular function (NF-RV, n=10) and pulmonary arterial hypertension-associated right heart failure (HF-RV, n=10). (B) Pearson correlation analysis between serum OPN and NT-proBNP levels in the HF-RV group (n=8). Solid line: linear regression fit; dashed lines: 95% confidence intervals. (C) Receiver Operating Characteristic (ROC) curve evaluating the diagnostic performance of serum OPN for right ventricular dysfunction. OPN, Osteopontin; NF-RV, Normal Right Ventricular Function; HF-RV, Right Heart Failure; PAH, Pulmonary Arterial Hypertension; NT-proBNP, N-terminal pro-Brain Natriuretic Peptide; ROC, Receiver Operating Characteristic; AUC, Area Under the Curve. Data presentation: Mean ± SD. Statistical significance: ** P < 0.01.

Article Snippet: Serum OPN levels were measured using the Human OPN ELISA Kit (EK0482, BOSTER) according to the manufacturer’s instructions.

Techniques: Enzyme-linked Immunosorbent Assay, Diagnostic Assay

Journal: Laboratory investigation; a journal of technical methods and pathology

Article Title: Osteopontin Isoforms Differentially Promote Arteriogenesis in Response to Ischemia via Macrophage Accumulation and Survival

doi: 10.1038/s41374-018-0094-8

Figure Lengend Snippet: A. Illustration of OPN isoform primary domain structure. Each block corresponds to an exon (numbered). OPNa is full length (top), OPNb lacks exon 5 (middle), and OPNc lacks exon 4 (bottom). Expanded amino acid sequences of exons 4 and 5, absent in OPNc and OPNb, respectively, are included. B. OPN primers were used to measure OPNa (277bp), OPNb (235bp), and OPNc (196bp) mRNA levels in tissue samples from non-ischemic tissues and tissues from PAD patients with critical limb ischemia by RT-PCR (n=3–5). Isoform plasmid DNA controls and beta actin for loading are both shown. C. To investigate if OPN isoforms differentially affect collateral vessel formation in vivo , the hindlimb ischemia was performed on the following groups: WT, OPN −/− , or OPN −/− mice treated (trx) with lentivirus (LV) to overexpress GFP, OPNa, OPNb, or OPNc. Perfusion was measured by Laser Doppler perfusion imaging (LDPI). Representative LDPI images 14 days post-HLI are shown. D. Ischemic limb (IL) perfusion was quantified and normalized to the contralateral non-ischemic limb (NIL) and compared across groups. * p<0.05, † p<0.001 vs. GFP; d14, n=6. E. To determine if the OPN isoform effects on perfusion translate to increased functional limb use, animals were given free access to a running wheel (d7 post-HLI) and allowed to run for 7 days. Total distance run (meters) by was plotted for all groups as a measure of limb function. *p<0.05, † p<0.001 vs. GFP; n=9–10.

Article Snippet: For macrophage polarization studies, 3 hours after plating cells were stimulated with 10% FBS-RPMI with 100 ng/mL purified recombinant human OPNa, OPNb, or OPNc (cat# TP304803, TP305118, and TP31059; Origene, Rockville, MD), or were stimulated with 20 ng/mL of either interferon gamma (INFγ) or interleukin (IL)-4 for 48 hours (cat# 554587 and 550067; BD Biosciences) as positive controls for macrophage polarization.

Techniques: Blocking Assay, Reverse Transcription Polymerase Chain Reaction, Plasmid Preparation, In Vivo, Imaging, Functional Assay

Journal: Laboratory investigation; a journal of technical methods and pathology

Article Title: Osteopontin Isoforms Differentially Promote Arteriogenesis in Response to Ischemia via Macrophage Accumulation and Survival

doi: 10.1038/s41374-018-0094-8

Figure Lengend Snippet: To determine if OPN isoforms differentially affect arteriogenesis, tissue sections from animals 14 days post-HLI treated (trx) with lentivirus (LV) to overexpress OPN isoform a, b, or c were stained with α smooth muscle actin (α-SMA). α-SMA positive vessel numbers and sizes were quantified as a readout for arteriogenesis. A. The number of α-SMA positive vessels was counted across treatment groups and plotted (p = ns). B. α-SMA positive vessel sizes were measured in WT or OPN −/− mice treated (trx) with lentivirus (LV) to overexpress GFP, OPNa, OPNb, or OPNc. The number of vessels measured within the arteriole (10 – 200 μm 2 ), small artery (200 – 700 μm 2 ) and large artery (1000 – 2500 μm 2 ) size ranges were compared across all animal groups. Data are expressed as % change compared to +LV-GFP (control). *p<0.05 vs. OPNa, † p<0.001 vs. OPNb; n=8–10. C. Representative histology images from 14 days post-HLI stained with α-SMA are shown. α-SMA stain is red and counterstain is violet. Scale bars = 500 μm.

Article Snippet: For macrophage polarization studies, 3 hours after plating cells were stimulated with 10% FBS-RPMI with 100 ng/mL purified recombinant human OPNa, OPNb, or OPNc (cat# TP304803, TP305118, and TP31059; Origene, Rockville, MD), or were stimulated with 20 ng/mL of either interferon gamma (INFγ) or interleukin (IL)-4 for 48 hours (cat# 554587 and 550067; BD Biosciences) as positive controls for macrophage polarization.

Techniques: Staining

Journal: Cells

Article Title: Involvement of Cyclooxygenase-2 in Establishing an Immunosuppressive Microenvironment in Tumorspheres Derived from TMZ-Resistant Glioblastoma Cell Lines and Primary Cultures

doi: 10.3390/cells13030258

Figure Lengend Snippet: List of primary antibodies used in the present study.

Article Snippet: rabbit monoclonal anti-osteopontin , 1:1000 , Boster Biological Technology, Pleasanton, CA, USA.

Techniques:

Journal: Journal of Oral & Maxillofacial Research

Article Title: Evaluation of the Effects of Topical Ellagic Acid and Graft Application on Bone Regeneration: an Experimental Study

doi: 10.5037/jomr.2022.13203

Figure Lengend Snippet: Biochemical measurement values in bone defect between test and control groups

Article Snippet: Enzyme-linked immunosorbent assay In this study, enzyme-linked immunosorbent assay (ELISA) kits were used: osteonectin (MyBioSource Inc.; San Diego, California, USA) and osteopontin (Shanghai Korain Biotech Co., Ltd; Shanghai, China).

Techniques:

Journal: Journal of Oral & Maxillofacial Research

Article Title: Evaluation of the Effects of Topical Ellagic Acid and Graft Application on Bone Regeneration: an Experimental Study

doi: 10.5037/jomr.2022.13203

Figure Lengend Snippet: Biochemical measurement values in serum of rats between test and control groups

Article Snippet: Enzyme-linked immunosorbent assay In this study, enzyme-linked immunosorbent assay (ELISA) kits were used: osteonectin (MyBioSource Inc.; San Diego, California, USA) and osteopontin (Shanghai Korain Biotech Co., Ltd; Shanghai, China).

Techniques: