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ltb4 elisa kit  (Cayman Chemical)


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    Cayman Chemical ltb4 elisa kit
    Ltb4 Elisa Kit, supplied by Cayman Chemical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ltb4+elisa/ltb4/bio_rxiv__2025__06__24__661434-64-5-8
    Average 90 stars, based on 1 article reviews
    ltb4 elisa kit - by Bioz Stars, 2026-09
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    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Validation of assays for inflammatory mediators in exhaled breath condensate.
    Article Snippet: The methods for LTB4 (GE Bioscience), SLPI and MPO have been described in detail previously [12]. .. The second commercial LTB4 ELISA (Cayman Chemical Company) was used according to the manufacturer’s instructions. .. 944 VOLUME 31 NUMBER 5 EUROPEAN RESPIRATORY JOURNAL IL-8 was measured by ELISA using a commercially available kit (R&D Systems Europe Ltd).

    Article Title: Development of a high-capacity homogeneous fluorescent assay for the measurement of leukotriene B4.
    Article Snippet: Current immunoassays for the measurement of leukotriene B4 (LTB4) typically utilize an enzyme-linked immunosorbent assay (ELISA) format that requires multiple incubations and washing steps and often expensive immunoassay kits.. We have developed a bead-based, mix and read, indirect fluorescence-linked immunosorbent assay utilizing fluorometric microvolume assay technology (FMAT).. The assay employs a monoclonal anti-LTB4 antibody-coated onto goat antimouse antibody coupled polystyrene beads and an AlexaFluor-647-coupled LTB4 ligand.

    Article Title: Immunomodulatory effects of tulathromycin on apoptosis, efferocytosis, and proinflammatory leukotriene B4 production in leukocytes from Actinobacillus pleuropneumoniae-or zymosan-challenged pigs.
    Article Snippet: From the Department of Biological Sciences, Inflammation Research Network (Duquette, Fischer, Williams, Sajedy, Feener, Bhargava, Reti, Morck, Buret), the Animal Health Unit (Muench, Morck), the Department of Comparative Biology and Experimental Medicine (Morck), Faculty of Veterinary Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada; Zoetis, 100 Campus Dr, Florham Park, NJ 07932 (Allison); and Veterinary Research and Development, Zoetis, 333 Portage St, Kalamazoo, MI 49001 (Lucas).

    Article Title: ATG5 suppresses type I IFN-dependent neutrophil effector functions during Mycobacterium tuberculosis infection in mice.
    Article Snippet: Inflammation is critical for controlling infections but can cause disease when unchecked.. During Mycobacterium tuberculosis (Mtb) infection, neutrophil-dominated inflammation is associated with exacerbated disease.. ATG5 expression by neutrophils mediates autophagy-independent control of infection but mechanistic understanding of how this regulates protective neutrophil function is lacking.

    other:

    Article Title: Multi-pronged inhibition of airway hyper-responsiveness and inflammation by lipoxin A(4).
    Article Snippet: Asthma is characterized by airway hyper-responsiveness and chronic airway inflammation.. Numerous eosinophils and T lymphocytes infiltrate peribronchial tissues in asthmatics, introducing into the lung an increased capacity to generate cysteinyl leukotrienes (CysLTs) and TH2 cytokines.. CysLTs have been associated with the asthmatic diathesis in both experimental models and patients with asthma.

    Article Title: Pharmacology of PF-4191834, a novel, selective non-redox 5-lipoxygenase inhibitor effective in inflammation and pain.
    Article Snippet: 5-Lipoxygenase (LOX) is an important arachidonic acidmetabolizing enzyme producing leukotrienes and other proinflammatory lipid mediators with potent pathophysiological functions in asthma and other inflammatory diseases.. 4-(3-(4-(1Methyl-1H-pyrazol-5-yl)phenylthio)phenyl)-tetrahydro-2H-pyran-4carboxamide (PF-4191834) is a novel, selective non-redox 5-lipoxygenase inhibitor effective in inflammation and pain.. In vitro and in vivo assays were developed for the evaluation of a novel 5-LOX inhibitor using conditions of maximal enzyme activity.

    Diff-Quik:

    Article Title: Immunomodulatory effects of tulathromycin on apoptosis, efferocytosis, and proinflammatory leukotriene B4 production in leukocytes from Actinobacillus pleuropneumoniae-or zymosan-challenged pigs.
    Article Snippet: From the Department of Biological Sciences, Inflammation Research Network (Duquette, Fischer, Williams, Sajedy, Feener, Bhargava, Reti, Morck, Buret), the Animal Health Unit (Muench, Morck), the Department of Comparative Biology and Experimental Medicine (Morck), Faculty of Veterinary Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada; Zoetis, 100 Campus Dr, Florham Park, NJ 07932 (Allison); and Veterinary Research and Development, Zoetis, 333 Portage St, Kalamazoo, MI 49001 (Lucas).

    Staining:

    Article Title: Immunomodulatory effects of tulathromycin on apoptosis, efferocytosis, and proinflammatory leukotriene B4 production in leukocytes from Actinobacillus pleuropneumoniae-or zymosan-challenged pigs.
    Article Snippet: From the Department of Biological Sciences, Inflammation Research Network (Duquette, Fischer, Williams, Sajedy, Feener, Bhargava, Reti, Morck, Buret), the Animal Health Unit (Muench, Morck), the Department of Comparative Biology and Experimental Medicine (Morck), Faculty of Veterinary Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada; Zoetis, 100 Campus Dr, Florham Park, NJ 07932 (Allison); and Veterinary Research and Development, Zoetis, 333 Portage St, Kalamazoo, MI 49001 (Lucas).

    Software:

    Article Title: Immunomodulatory effects of tulathromycin on apoptosis, efferocytosis, and proinflammatory leukotriene B4 production in leukocytes from Actinobacillus pleuropneumoniae-or zymosan-challenged pigs.
    Article Snippet: From the Department of Biological Sciences, Inflammation Research Network (Duquette, Fischer, Williams, Sajedy, Feener, Bhargava, Reti, Morck, Buret), the Animal Health Unit (Muench, Morck), the Department of Comparative Biology and Experimental Medicine (Morck), Faculty of Veterinary Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada; Zoetis, 100 Campus Dr, Florham Park, NJ 07932 (Allison); and Veterinary Research and Development, Zoetis, 333 Portage St, Kalamazoo, MI 49001 (Lucas).

    Imaging:

    Article Title: Immunomodulatory effects of tulathromycin on apoptosis, efferocytosis, and proinflammatory leukotriene B4 production in leukocytes from Actinobacillus pleuropneumoniae-or zymosan-challenged pigs.
    Article Snippet: From the Department of Biological Sciences, Inflammation Research Network (Duquette, Fischer, Williams, Sajedy, Feener, Bhargava, Reti, Morck, Buret), the Animal Health Unit (Muench, Morck), the Department of Comparative Biology and Experimental Medicine (Morck), Faculty of Veterinary Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada; Zoetis, 100 Campus Dr, Florham Park, NJ 07932 (Allison); and Veterinary Research and Development, Zoetis, 333 Portage St, Kalamazoo, MI 49001 (Lucas).

    Infection:

    Article Title: ATG5 suppresses type I IFN-dependent neutrophil effector functions during Mycobacterium tuberculosis infection in mice.
    Article Snippet: Inflammation is critical for controlling infections but can cause disease when unchecked.. During Mycobacterium tuberculosis (Mtb) infection, neutrophil-dominated inflammation is associated with exacerbated disease.. ATG5 expression by neutrophils mediates autophagy-independent control of infection but mechanistic understanding of how this regulates protective neutrophil function is lacking.

    Produced:

    Article Title: ATG5 suppresses type I IFN-dependent neutrophil effector functions during Mycobacterium tuberculosis infection in mice.
    Article Snippet: Inflammation is critical for controlling infections but can cause disease when unchecked.. During Mycobacterium tuberculosis (Mtb) infection, neutrophil-dominated inflammation is associated with exacerbated disease.. ATG5 expression by neutrophils mediates autophagy-independent control of infection but mechanistic understanding of how this regulates protective neutrophil function is lacking.



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    Global lipid profiling of healthy and asthmatic HBE cultures after exposure to h ‐BN and BNNTs indicates effects on the production of eicosanoid lipid intermediates. a) Summary of cellular eicosanoid signaling involving enzymes to target cell membrane lipids (PLA 2 , phospholipase A2) and to further process resulting arachidonic acids intracellularly to produce prostaglandins (using COX1/2) or leukotrienes (5‐lipooxygenase, also known as Alox‐5). b) Scatter plot of the first two components of the supervised sparse Partial Least Squares ‐ Discriminant Analysis (sPLS‐DA) model of global lipidomic data in healthy and asthmatic samples with a 95% confidence interval. c) Hierarchical clustering showing the top 100 most significantly altered lipid expression values based on One‐way ANOVA, and the additional Heatmap on the right side further shows the annotation of lipids within the highlighted cluster with FDR values < 0.05. d) Immunoblot indicating expression of Alox‐5 (an enzyme that produces <t>leukotriene</t> B4) in healthy HBE cultures. β‐actin was used as a reference for loading uniformity. Refer to Data file (Supporting Information) for full immunoblots. e) Densitometry analysis of the protein blot showing Alox‐5 expression with respect to β‐actin (loading control). f) diff‐HL60 cell migration after 24 h of exposure to conditioned medium from healthy (H) and asthmatic (As) HBE cell cultures in the presence or absence of <t>leukotriene</t> <t>B4</t> receptor inhibitor ( LY293111 , 25 n m ). Lipopolysaccharide (LPS, 100 ng mL −1 ) and fetal bovine serum (10%) were used as positive controls for chemotaxis‐mediated cell migration. The results in panels (e,f) are presented as mean + SD ( n = 3). The statistical significance was calculated using One‐Way ANOVA analysis with Tukey`s post hoc test. * p = 0.06 and *** p < 0.001 ‐ statistical significance with respect to negative control. ### p < 0.001 ‐ statistical significance between treatment groups (with and without inhibitor LY293111 ).
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    Global lipid profiling of healthy and asthmatic HBE cultures after exposure to h ‐BN and BNNTs indicates effects on the production of eicosanoid lipid intermediates. a) Summary of cellular eicosanoid signaling involving enzymes to target cell membrane lipids (PLA 2 , phospholipase A2) and to further process resulting arachidonic acids intracellularly to produce prostaglandins (using COX1/2) or leukotrienes (5‐lipooxygenase, also known as Alox‐5). b) Scatter plot of the first two components of the supervised sparse Partial Least Squares ‐ Discriminant Analysis (sPLS‐DA) model of global lipidomic data in healthy and asthmatic samples with a 95% confidence interval. c) Hierarchical clustering showing the top 100 most significantly altered lipid expression values based on One‐way ANOVA, and the additional Heatmap on the right side further shows the annotation of lipids within the highlighted cluster with FDR values < 0.05. d) Immunoblot indicating expression of Alox‐5 (an enzyme that produces <t>leukotriene</t> B4) in healthy HBE cultures. β‐actin was used as a reference for loading uniformity. Refer to Data file (Supporting Information) for full immunoblots. e) Densitometry analysis of the protein blot showing Alox‐5 expression with respect to β‐actin (loading control). f) diff‐HL60 cell migration after 24 h of exposure to conditioned medium from healthy (H) and asthmatic (As) HBE cell cultures in the presence or absence of <t>leukotriene</t> <t>B4</t> receptor inhibitor ( LY293111 , 25 n m ). Lipopolysaccharide (LPS, 100 ng mL −1 ) and fetal bovine serum (10%) were used as positive controls for chemotaxis‐mediated cell migration. The results in panels (e,f) are presented as mean + SD ( n = 3). The statistical significance was calculated using One‐Way ANOVA analysis with Tukey`s post hoc test. * p = 0.06 and *** p < 0.001 ‐ statistical significance with respect to negative control. ### p < 0.001 ‐ statistical significance between treatment groups (with and without inhibitor LY293111 ).
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    Global lipid profiling of healthy and asthmatic HBE cultures after exposure to h ‐BN and BNNTs indicates effects on the production of eicosanoid lipid intermediates. a) Summary of cellular eicosanoid signaling involving enzymes to target cell membrane lipids (PLA 2 , phospholipase A2) and to further process resulting arachidonic acids intracellularly to produce prostaglandins (using COX1/2) or leukotrienes (5‐lipooxygenase, also known as Alox‐5). b) Scatter plot of the first two components of the supervised sparse Partial Least Squares ‐ Discriminant Analysis (sPLS‐DA) model of global lipidomic data in healthy and asthmatic samples with a 95% confidence interval. c) Hierarchical clustering showing the top 100 most significantly altered lipid expression values based on One‐way ANOVA, and the additional Heatmap on the right side further shows the annotation of lipids within the highlighted cluster with FDR values < 0.05. d) Immunoblot indicating expression of Alox‐5 (an enzyme that produces <t>leukotriene</t> B4) in healthy HBE cultures. β‐actin was used as a reference for loading uniformity. Refer to Data file (Supporting Information) for full immunoblots. e) Densitometry analysis of the protein blot showing Alox‐5 expression with respect to β‐actin (loading control). f) diff‐HL60 cell migration after 24 h of exposure to conditioned medium from healthy (H) and asthmatic (As) HBE cell cultures in the presence or absence of <t>leukotriene</t> <t>B4</t> receptor inhibitor ( LY293111 , 25 n m ). Lipopolysaccharide (LPS, 100 ng mL −1 ) and fetal bovine serum (10%) were used as positive controls for chemotaxis‐mediated cell migration. The results in panels (e,f) are presented as mean + SD ( n = 3). The statistical significance was calculated using One‐Way ANOVA analysis with Tukey`s post hoc test. * p = 0.06 and *** p < 0.001 ‐ statistical significance with respect to negative control. ### p < 0.001 ‐ statistical significance between treatment groups (with and without inhibitor LY293111 ).
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    Global lipid profiling of healthy and asthmatic HBE cultures after exposure to h ‐BN and BNNTs indicates effects on the production of eicosanoid lipid intermediates. a) Summary of cellular eicosanoid signaling involving enzymes to target cell membrane lipids (PLA 2 , phospholipase A2) and to further process resulting arachidonic acids intracellularly to produce prostaglandins (using COX1/2) or leukotrienes (5‐lipooxygenase, also known as Alox‐5). b) Scatter plot of the first two components of the supervised sparse Partial Least Squares ‐ Discriminant Analysis (sPLS‐DA) model of global lipidomic data in healthy and asthmatic samples with a 95% confidence interval. c) Hierarchical clustering showing the top 100 most significantly altered lipid expression values based on One‐way ANOVA, and the additional Heatmap on the right side further shows the annotation of lipids within the highlighted cluster with FDR values < 0.05. d) Immunoblot indicating expression of Alox‐5 (an enzyme that produces <t>leukotriene</t> B4) in healthy HBE cultures. β‐actin was used as a reference for loading uniformity. Refer to Data file (Supporting Information) for full immunoblots. e) Densitometry analysis of the protein blot showing Alox‐5 expression with respect to β‐actin (loading control). f) diff‐HL60 cell migration after 24 h of exposure to conditioned medium from healthy (H) and asthmatic (As) HBE cell cultures in the presence or absence of <t>leukotriene</t> <t>B4</t> receptor inhibitor ( LY293111 , 25 n m ). Lipopolysaccharide (LPS, 100 ng mL −1 ) and fetal bovine serum (10%) were used as positive controls for chemotaxis‐mediated cell migration. The results in panels (e,f) are presented as mean + SD ( n = 3). The statistical significance was calculated using One‐Way ANOVA analysis with Tukey`s post hoc test. * p = 0.06 and *** p < 0.001 ‐ statistical significance with respect to negative control. ### p < 0.001 ‐ statistical significance between treatment groups (with and without inhibitor LY293111 ).
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    (A) Immunohistochemical images of mast cells, MCT, and EPX in rats of each group. The effects of FRP on (B) the number of mast cells, (C) the expression of MCT, and (D) the expression of EPX in rats. The effects of FRP on the levels of (E) IgE, (F) <t>LTB4,</t> and (G) HIS in the serum of rats. All data are presented as X ¯ ± SD deviation (n = 6/n = 3). Compared with the Control group, ### P < 0.001; compared with the model group, * P < 0.05, ** P < 0.01, *** P < 0.001.
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    Image Search Results


    Global lipid profiling of healthy and asthmatic HBE cultures after exposure to h ‐BN and BNNTs indicates effects on the production of eicosanoid lipid intermediates. a) Summary of cellular eicosanoid signaling involving enzymes to target cell membrane lipids (PLA 2 , phospholipase A2) and to further process resulting arachidonic acids intracellularly to produce prostaglandins (using COX1/2) or leukotrienes (5‐lipooxygenase, also known as Alox‐5). b) Scatter plot of the first two components of the supervised sparse Partial Least Squares ‐ Discriminant Analysis (sPLS‐DA) model of global lipidomic data in healthy and asthmatic samples with a 95% confidence interval. c) Hierarchical clustering showing the top 100 most significantly altered lipid expression values based on One‐way ANOVA, and the additional Heatmap on the right side further shows the annotation of lipids within the highlighted cluster with FDR values < 0.05. d) Immunoblot indicating expression of Alox‐5 (an enzyme that produces leukotriene B4) in healthy HBE cultures. β‐actin was used as a reference for loading uniformity. Refer to Data file (Supporting Information) for full immunoblots. e) Densitometry analysis of the protein blot showing Alox‐5 expression with respect to β‐actin (loading control). f) diff‐HL60 cell migration after 24 h of exposure to conditioned medium from healthy (H) and asthmatic (As) HBE cell cultures in the presence or absence of leukotriene B4 receptor inhibitor ( LY293111 , 25 n m ). Lipopolysaccharide (LPS, 100 ng mL −1 ) and fetal bovine serum (10%) were used as positive controls for chemotaxis‐mediated cell migration. The results in panels (e,f) are presented as mean + SD ( n = 3). The statistical significance was calculated using One‐Way ANOVA analysis with Tukey`s post hoc test. * p = 0.06 and *** p < 0.001 ‐ statistical significance with respect to negative control. ### p < 0.001 ‐ statistical significance between treatment groups (with and without inhibitor LY293111 ).

    Journal: Advanced Science

    Article Title: Boron Nitride Nanomaterials Trigger Immunomodulatory Effects in Human Broncho‐Epithelial Cells by Modulating Eicosanoid Lipid Signaling

    doi: 10.1002/advs.202516401

    Figure Lengend Snippet: Global lipid profiling of healthy and asthmatic HBE cultures after exposure to h ‐BN and BNNTs indicates effects on the production of eicosanoid lipid intermediates. a) Summary of cellular eicosanoid signaling involving enzymes to target cell membrane lipids (PLA 2 , phospholipase A2) and to further process resulting arachidonic acids intracellularly to produce prostaglandins (using COX1/2) or leukotrienes (5‐lipooxygenase, also known as Alox‐5). b) Scatter plot of the first two components of the supervised sparse Partial Least Squares ‐ Discriminant Analysis (sPLS‐DA) model of global lipidomic data in healthy and asthmatic samples with a 95% confidence interval. c) Hierarchical clustering showing the top 100 most significantly altered lipid expression values based on One‐way ANOVA, and the additional Heatmap on the right side further shows the annotation of lipids within the highlighted cluster with FDR values < 0.05. d) Immunoblot indicating expression of Alox‐5 (an enzyme that produces leukotriene B4) in healthy HBE cultures. β‐actin was used as a reference for loading uniformity. Refer to Data file (Supporting Information) for full immunoblots. e) Densitometry analysis of the protein blot showing Alox‐5 expression with respect to β‐actin (loading control). f) diff‐HL60 cell migration after 24 h of exposure to conditioned medium from healthy (H) and asthmatic (As) HBE cell cultures in the presence or absence of leukotriene B4 receptor inhibitor ( LY293111 , 25 n m ). Lipopolysaccharide (LPS, 100 ng mL −1 ) and fetal bovine serum (10%) were used as positive controls for chemotaxis‐mediated cell migration. The results in panels (e,f) are presented as mean + SD ( n = 3). The statistical significance was calculated using One‐Way ANOVA analysis with Tukey`s post hoc test. * p = 0.06 and *** p < 0.001 ‐ statistical significance with respect to negative control. ### p < 0.001 ‐ statistical significance between treatment groups (with and without inhibitor LY293111 ).

    Article Snippet: Leukotriene content in BAL fluid was determined by using LTB4 ELISA (R&D Systems, #KGE006B) and performed by following the manufacturer's instructions.

    Techniques: Membrane, Expressing, Western Blot, Control, Migration, Chemotaxis Assay, Negative Control

    Single‐cell immune profiling of primary human PBMCs using mass cytometry (CyToF) after exposure (24 h) to conditioned media (CM) from h‐ BN or BNNT‐treated healthy (H) and asthmatic (As) HBE cell cultures. a) Schematic representation of leukotriene–BLT1 lipid chemo‐attractant signaling and immune regulation in lungs: the extracellular release of leukotriene from lung epithelial cells could lead to the recruitment (by chemo‐attraction) and functional stimulation of BLT‐1 expressing immune cells from peripheral blood that subsequently sensitize airway tissues by releasing cytokine‐chemokine molecules and modulate disease progression. b) CyTOF results are represented in a T‐distributed stochastic neighbor embedding (tSNE) map with 12 clusters of cells identified in PBMCs with the most notable changes observed in NK cells, cytotoxic (CD8+) memory T cells, and naïve T cells (CD4+ and CD8+). c,d) Using the generalized linear model diffcyt‐DA‐EdgeR, we extracted the clusters that were significantly different between the conditions. Bar plots show the relative abundance of these clusters and that incubation of PBMCs with CM‐BNNT from asthmatic cultures triggered an increase in the number of NK cells and cytotoxic memory T cells (c), however, decreased the number of helper and cytotoxic naïve T cells (d). e) Heatmap showing median expression profiles of cell state‐specific markers across control and treatment groups for each donor using diffcyt‐DS‐limma ( n = 3).

    Journal: Advanced Science

    Article Title: Boron Nitride Nanomaterials Trigger Immunomodulatory Effects in Human Broncho‐Epithelial Cells by Modulating Eicosanoid Lipid Signaling

    doi: 10.1002/advs.202516401

    Figure Lengend Snippet: Single‐cell immune profiling of primary human PBMCs using mass cytometry (CyToF) after exposure (24 h) to conditioned media (CM) from h‐ BN or BNNT‐treated healthy (H) and asthmatic (As) HBE cell cultures. a) Schematic representation of leukotriene–BLT1 lipid chemo‐attractant signaling and immune regulation in lungs: the extracellular release of leukotriene from lung epithelial cells could lead to the recruitment (by chemo‐attraction) and functional stimulation of BLT‐1 expressing immune cells from peripheral blood that subsequently sensitize airway tissues by releasing cytokine‐chemokine molecules and modulate disease progression. b) CyTOF results are represented in a T‐distributed stochastic neighbor embedding (tSNE) map with 12 clusters of cells identified in PBMCs with the most notable changes observed in NK cells, cytotoxic (CD8+) memory T cells, and naïve T cells (CD4+ and CD8+). c,d) Using the generalized linear model diffcyt‐DA‐EdgeR, we extracted the clusters that were significantly different between the conditions. Bar plots show the relative abundance of these clusters and that incubation of PBMCs with CM‐BNNT from asthmatic cultures triggered an increase in the number of NK cells and cytotoxic memory T cells (c), however, decreased the number of helper and cytotoxic naïve T cells (d). e) Heatmap showing median expression profiles of cell state‐specific markers across control and treatment groups for each donor using diffcyt‐DS‐limma ( n = 3).

    Article Snippet: Leukotriene content in BAL fluid was determined by using LTB4 ELISA (R&D Systems, #KGE006B) and performed by following the manufacturer's instructions.

    Techniques: Single Cell, Mass Cytometry, Functional Assay, Expressing, Biomarker Discovery, Incubation, Control

    Leukotriene B4 biosynthesis pathway in mice lungs 28 days after pharyngeal aspiration to h ‐BN and BNNT (1 µg µL −1 ; total administered volume 30 µL). a) Evaluation of mRNA transcripts in lung tissue for the genes involved in lipid biosynthesis and phospholipid remodeling. b) Leukotriene B4 content in mouse BAL fluid. c,d) Alox‐5 protein expression in lung tissues with respect to β‐actin (loading control), (b) protein blots, and (c) corresponding densitometry plot, showing Alox‐5 expression in five individual mice from control and h ‐BN or BNNT exposures. The full protein blot for Alox‐5 and β‐actin can be found in Figure (Supporting Information). e) Evaluation of mRNA transcript levels for the asthma marker genes in lung tissue using RT‐qPCR. The data in (b) and (d) are presented as mean + SD ( n = 5) and statistical significance was calculated by One‐Way ANOVA analysis with Tukey`s post hoc test. * * p < 0.01 . The statistical analysis in (a) and (e) was performed by applying an unpaired t ‐test to compare the fold change between the negative control and individual treatments, n = 5; (*) p < 0.05, (**) p < 0.01.

    Journal: Advanced Science

    Article Title: Boron Nitride Nanomaterials Trigger Immunomodulatory Effects in Human Broncho‐Epithelial Cells by Modulating Eicosanoid Lipid Signaling

    doi: 10.1002/advs.202516401

    Figure Lengend Snippet: Leukotriene B4 biosynthesis pathway in mice lungs 28 days after pharyngeal aspiration to h ‐BN and BNNT (1 µg µL −1 ; total administered volume 30 µL). a) Evaluation of mRNA transcripts in lung tissue for the genes involved in lipid biosynthesis and phospholipid remodeling. b) Leukotriene B4 content in mouse BAL fluid. c,d) Alox‐5 protein expression in lung tissues with respect to β‐actin (loading control), (b) protein blots, and (c) corresponding densitometry plot, showing Alox‐5 expression in five individual mice from control and h ‐BN or BNNT exposures. The full protein blot for Alox‐5 and β‐actin can be found in Figure (Supporting Information). e) Evaluation of mRNA transcript levels for the asthma marker genes in lung tissue using RT‐qPCR. The data in (b) and (d) are presented as mean + SD ( n = 5) and statistical significance was calculated by One‐Way ANOVA analysis with Tukey`s post hoc test. * * p < 0.01 . The statistical analysis in (a) and (e) was performed by applying an unpaired t ‐test to compare the fold change between the negative control and individual treatments, n = 5; (*) p < 0.05, (**) p < 0.01.

    Article Snippet: Leukotriene content in BAL fluid was determined by using LTB4 ELISA (R&D Systems, #KGE006B) and performed by following the manufacturer's instructions.

    Techniques: Expressing, Control, Marker, Quantitative RT-PCR, Negative Control

    (A) Immunohistochemical images of mast cells, MCT, and EPX in rats of each group. The effects of FRP on (B) the number of mast cells, (C) the expression of MCT, and (D) the expression of EPX in rats. The effects of FRP on the levels of (E) IgE, (F) LTB4, and (G) HIS in the serum of rats. All data are presented as X ¯ ± SD deviation (n = 6/n = 3). Compared with the Control group, ### P < 0.001; compared with the model group, * P < 0.05, ** P < 0.01, *** P < 0.001.

    Journal: Frontiers in Pharmacology

    Article Title: Metabolomics combined with molecular docking and dynamics simulation to investigate the mechanism of action of Fibraurea recisa Pierre in the treatment of chronic urticaria

    doi: 10.3389/fphar.2025.1571819

    Figure Lengend Snippet: (A) Immunohistochemical images of mast cells, MCT, and EPX in rats of each group. The effects of FRP on (B) the number of mast cells, (C) the expression of MCT, and (D) the expression of EPX in rats. The effects of FRP on the levels of (E) IgE, (F) LTB4, and (G) HIS in the serum of rats. All data are presented as X ¯ ± SD deviation (n = 6/n = 3). Compared with the Control group, ### P < 0.001; compared with the model group, * P < 0.05, ** P < 0.01, *** P < 0.001.

    Article Snippet: The levels of immunoglobulin E (IgE, SEKR-0019), LTB4 (CSB-E08035r, Cusabio, Wuhan, China), and HIS (E-EL-0032c) in serum were detected at a wavelength of 450 nm using a microplate reader.

    Techniques: Immunohistochemical staining, Expressing, Control