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Greer Laboratories alternaria alternata extract alt
CD4 + -specific PGI 2 signaling attenuates <t>Alternaria</t> -induced Th2 lung inflammation. (A) IP receptor expression (RT-PCR) in CD4 + T cells from CD4 Cre- IP flox (control) and CD4 Cre+ IP flox (IP-deficient) mice. (B) Experimental timeline: mice were intranasally sensitized/challenged daily with Alt on days 0 to 2 and 15 or 16, with mouse harvest on day 17. (C–E) IL-5, IL-13, and CCL11 levels in lung homogenates (ELISA). (F–J) BALF cellularity: total cells, eosinophils, lymphocytes, macrophages, and neutrophils. (K–L) PAS-stained mucus production (representative image and quantification). (K, M–N) Hematoxylin and eosin (H&E)–stained inflammation (representative image and scores for peribronchiolar/perivascular infiltration). Data represent 3 experiments (n = 5–18 mice/group). * P < 0.05 by 2-way analysis of variance.
Alternaria Alternata Extract Alt, supplied by Greer Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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1) Product Images from "PGI 2 signaling metabolically reprograms CD4 Th2 cells and represses allergic airway inflammation"

Article Title: PGI 2 signaling metabolically reprograms CD4 Th2 cells and represses allergic airway inflammation

Journal: The Journal of Immunology Author Choice

doi: 10.1093/jimmun/vkaf130

CD4 + -specific PGI 2 signaling attenuates Alternaria -induced Th2 lung inflammation. (A) IP receptor expression (RT-PCR) in CD4 + T cells from CD4 Cre- IP flox (control) and CD4 Cre+ IP flox (IP-deficient) mice. (B) Experimental timeline: mice were intranasally sensitized/challenged daily with Alt on days 0 to 2 and 15 or 16, with mouse harvest on day 17. (C–E) IL-5, IL-13, and CCL11 levels in lung homogenates (ELISA). (F–J) BALF cellularity: total cells, eosinophils, lymphocytes, macrophages, and neutrophils. (K–L) PAS-stained mucus production (representative image and quantification). (K, M–N) Hematoxylin and eosin (H&E)–stained inflammation (representative image and scores for peribronchiolar/perivascular infiltration). Data represent 3 experiments (n = 5–18 mice/group). * P < 0.05 by 2-way analysis of variance.
Figure Legend Snippet: CD4 + -specific PGI 2 signaling attenuates Alternaria -induced Th2 lung inflammation. (A) IP receptor expression (RT-PCR) in CD4 + T cells from CD4 Cre- IP flox (control) and CD4 Cre+ IP flox (IP-deficient) mice. (B) Experimental timeline: mice were intranasally sensitized/challenged daily with Alt on days 0 to 2 and 15 or 16, with mouse harvest on day 17. (C–E) IL-5, IL-13, and CCL11 levels in lung homogenates (ELISA). (F–J) BALF cellularity: total cells, eosinophils, lymphocytes, macrophages, and neutrophils. (K–L) PAS-stained mucus production (representative image and quantification). (K, M–N) Hematoxylin and eosin (H&E)–stained inflammation (representative image and scores for peribronchiolar/perivascular infiltration). Data represent 3 experiments (n = 5–18 mice/group). * P < 0.05 by 2-way analysis of variance.

Techniques Used: Expressing, Reverse Transcription Polymerase Chain Reaction, Control, Enzyme-linked Immunosorbent Assay, Staining

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Article Snippet: Where indicated, mice were treated i.n. with 5 μg anti-IL-17A blocking mAb (clone 17F3, Bioxcell) on days 7–11, treated i.v with 10 μg sST2-Fc (Catalog # 1004-MR-050, R&D Systems) on days 7–9, or treated i.p. with 100 μg of a mAb (clone V1.4C4.22) that specifically neutralizes IL-35 or 100 μg of a mAb (Catalog # AF1834, R&D Systems) that specifically neutralizes IL-27 on days 7 and 11. .. To induce allergic pulmonary inflammation to A. alternata , mice were anesthetized i.p. with Ketamine/Xylazine and challenged with 50 μg A. alternata extract ( Alternaria alternata extracts, Greer Laboratories) in 30 μl of sterile PBS on days 0, 1 and 17–19. ..

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Article Snippet: .. Alternaria model. Seven- and 8-week-old BALB/c mice were sensitized intranasally with Alternaria alternata extracts (Greer Laboratories, Lenoir, NC; 50 mg of dry weight/10 mg of protein in 50 mL of saline) at day 0 and 1, and challenged intranasally with Alternaria extracts (25 mg of dry weight/5 mg of protein in 50 mL) at day 17, 18, and 19.26 OM-85 (1 mg in 50 mL, 25 mL per nostril) was administered every 2 days for 14 times from day 210. ..

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Article Title: Allergen-induced activation of epithelial P2Y 2 receptors promotes ATP exocytosis and type 2 immunity in airways.
Article Snippet: This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record.. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article.. Please note that, during the production process, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

Article Title: CD52-targeted depletion by Alemtuzumab ameliorates allergic airway hyperreactivity and lung inflammation
Article Snippet: The mice were intranasally challenged via rmIL-33 (BioLegend, San Diego, Calif), Alternaria alternata extracts (Greer Laboratories, Lenoir, North Carolina), House Dust Mite (Greer Laboratories, Lenoir, North Carolina), as shown in the experimental schemes.



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CD4 + -specific PGI 2 signaling attenuates <t>Alternaria</t> -induced Th2 lung inflammation. (A) IP receptor expression (RT-PCR) in CD4 + T cells from CD4 Cre- IP flox (control) and CD4 Cre+ IP flox (IP-deficient) mice. (B) Experimental timeline: mice were intranasally sensitized/challenged daily with Alt on days 0 to 2 and 15 or 16, with mouse harvest on day 17. (C–E) IL-5, IL-13, and CCL11 levels in lung homogenates (ELISA). (F–J) BALF cellularity: total cells, eosinophils, lymphocytes, macrophages, and neutrophils. (K–L) PAS-stained mucus production (representative image and quantification). (K, M–N) Hematoxylin and eosin (H&E)–stained inflammation (representative image and scores for peribronchiolar/perivascular infiltration). Data represent 3 experiments (n = 5–18 mice/group). * P < 0.05 by 2-way analysis of variance.
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CD4 + -specific PGI 2 signaling attenuates <t>Alternaria</t> -induced Th2 lung inflammation. (A) IP receptor expression (RT-PCR) in CD4 + T cells from CD4 Cre- IP flox (control) and CD4 Cre+ IP flox (IP-deficient) mice. (B) Experimental timeline: mice were intranasally sensitized/challenged daily with Alt on days 0 to 2 and 15 or 16, with mouse harvest on day 17. (C–E) IL-5, IL-13, and CCL11 levels in lung homogenates (ELISA). (F–J) BALF cellularity: total cells, eosinophils, lymphocytes, macrophages, and neutrophils. (K–L) PAS-stained mucus production (representative image and quantification). (K, M–N) Hematoxylin and eosin (H&E)–stained inflammation (representative image and scores for peribronchiolar/perivascular infiltration). Data represent 3 experiments (n = 5–18 mice/group). * P < 0.05 by 2-way analysis of variance.
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CD4 + -specific PGI 2 signaling attenuates <t>Alternaria</t> -induced Th2 lung inflammation. (A) IP receptor expression (RT-PCR) in CD4 + T cells from CD4 Cre- IP flox (control) and CD4 Cre+ IP flox (IP-deficient) mice. (B) Experimental timeline: mice were intranasally sensitized/challenged daily with Alt on days 0 to 2 and 15 or 16, with mouse harvest on day 17. (C–E) IL-5, IL-13, and CCL11 levels in lung homogenates (ELISA). (F–J) BALF cellularity: total cells, eosinophils, lymphocytes, macrophages, and neutrophils. (K–L) PAS-stained mucus production (representative image and quantification). (K, M–N) Hematoxylin and eosin (H&E)–stained inflammation (representative image and scores for peribronchiolar/perivascular infiltration). Data represent 3 experiments (n = 5–18 mice/group). * P < 0.05 by 2-way analysis of variance.
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CD4 + -specific PGI 2 signaling attenuates <t>Alternaria</t> -induced Th2 lung inflammation. (A) IP receptor expression (RT-PCR) in CD4 + T cells from CD4 Cre- IP flox (control) and CD4 Cre+ IP flox (IP-deficient) mice. (B) Experimental timeline: mice were intranasally sensitized/challenged daily with Alt on days 0 to 2 and 15 or 16, with mouse harvest on day 17. (C–E) IL-5, IL-13, and CCL11 levels in lung homogenates (ELISA). (F–J) BALF cellularity: total cells, eosinophils, lymphocytes, macrophages, and neutrophils. (K–L) PAS-stained mucus production (representative image and quantification). (K, M–N) Hematoxylin and eosin (H&E)–stained inflammation (representative image and scores for peribronchiolar/perivascular infiltration). Data represent 3 experiments (n = 5–18 mice/group). * P < 0.05 by 2-way analysis of variance.
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(A) Schematic of the intranasal allergic esophagus inflammation model using the protease allergen <t>Alternaria</t> <t>alternata</t> (ALT). (B) Mouse Grimace Scale (MGS) measurements taken immediately prior to intranasal allergen challenges. Allergen treated (n=6) vs. Control (n=6). Day 14 Allergen (red) vs. Day 14 Control (gray), grimace *p<0.05 allergen vs saline at the same time point, two-way ANOVA with Holm-Sidak‘s post hoc, n=6 per group mean±SEM. #p<0.05 AUC allergen vs saline overall, student’s t-test, n=6 per group. (C) MGS measurements on day 26 immediately prior (Pre) and 20 minutes after (Post) intranasal allergen administration. *p<0.05. Two-Way ANOVA with Multiple Comparisons. Mean ± SEM. (D) Schematic of the calcium assay beginning with the allergic esophagus inflammation model outlined in with Pirt-GCAMP6 mice. Dissection, dissociation, and culturing of VG and T1-T4 DRG is completed two days after final ALT treatment. Imaging of cells completed <24 hours after dissection. (E-F) ATP responsive (E) and capsaicin responsive (F) DRG neurons shown in red as a percentage of total KCl-responsive neurons shown in black (left), fluorescence intensity changes (middle), and representative calcium transients from sensory neurons of PBS and ALT treated mice in response to capsaicin (1 um) or ATP (150 um) stimulation. The arrow indicates when the stimulus was added. Each dot represents one cell. (right) *p<0.05, **p<0.01, ****p<0.0001, percent responders: chi squared test, fluorescent intensity changes: unpaired T-test; DRG n>25 from ≥3 Pirt-GCAMP6 mice. Data shown as mean +/- SEM.
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Image Search Results


CD4 + -specific PGI 2 signaling attenuates Alternaria -induced Th2 lung inflammation. (A) IP receptor expression (RT-PCR) in CD4 + T cells from CD4 Cre- IP flox (control) and CD4 Cre+ IP flox (IP-deficient) mice. (B) Experimental timeline: mice were intranasally sensitized/challenged daily with Alt on days 0 to 2 and 15 or 16, with mouse harvest on day 17. (C–E) IL-5, IL-13, and CCL11 levels in lung homogenates (ELISA). (F–J) BALF cellularity: total cells, eosinophils, lymphocytes, macrophages, and neutrophils. (K–L) PAS-stained mucus production (representative image and quantification). (K, M–N) Hematoxylin and eosin (H&E)–stained inflammation (representative image and scores for peribronchiolar/perivascular infiltration). Data represent 3 experiments (n = 5–18 mice/group). * P < 0.05 by 2-way analysis of variance.

Journal: The Journal of Immunology Author Choice

Article Title: PGI 2 signaling metabolically reprograms CD4 Th2 cells and represses allergic airway inflammation

doi: 10.1093/jimmun/vkaf130

Figure Lengend Snippet: CD4 + -specific PGI 2 signaling attenuates Alternaria -induced Th2 lung inflammation. (A) IP receptor expression (RT-PCR) in CD4 + T cells from CD4 Cre- IP flox (control) and CD4 Cre+ IP flox (IP-deficient) mice. (B) Experimental timeline: mice were intranasally sensitized/challenged daily with Alt on days 0 to 2 and 15 or 16, with mouse harvest on day 17. (C–E) IL-5, IL-13, and CCL11 levels in lung homogenates (ELISA). (F–J) BALF cellularity: total cells, eosinophils, lymphocytes, macrophages, and neutrophils. (K–L) PAS-stained mucus production (representative image and quantification). (K, M–N) Hematoxylin and eosin (H&E)–stained inflammation (representative image and scores for peribronchiolar/perivascular infiltration). Data represent 3 experiments (n = 5–18 mice/group). * P < 0.05 by 2-way analysis of variance.

Article Snippet: CD4 Cre- IP flox and CD4 Cre+ IP flox mice were sensitized intranasally with Alternaria alternata extract (Alt) (Greer Laboratories; 2 μg in 40 μL PBS per mouse) or PBS as a control for 3 d. After a 13-d rest period, mice were challenged with Alt (0.125 μg in 40 μL PBS per mouse) for 2 consecutive days.

Techniques: Expressing, Reverse Transcription Polymerase Chain Reaction, Control, Enzyme-linked Immunosorbent Assay, Staining

(A) Schematic of the intranasal allergic esophagus inflammation model using the protease allergen Alternaria alternata (ALT). (B) Mouse Grimace Scale (MGS) measurements taken immediately prior to intranasal allergen challenges. Allergen treated (n=6) vs. Control (n=6). Day 14 Allergen (red) vs. Day 14 Control (gray), grimace *p<0.05 allergen vs saline at the same time point, two-way ANOVA with Holm-Sidak‘s post hoc, n=6 per group mean±SEM. #p<0.05 AUC allergen vs saline overall, student’s t-test, n=6 per group. (C) MGS measurements on day 26 immediately prior (Pre) and 20 minutes after (Post) intranasal allergen administration. *p<0.05. Two-Way ANOVA with Multiple Comparisons. Mean ± SEM. (D) Schematic of the calcium assay beginning with the allergic esophagus inflammation model outlined in with Pirt-GCAMP6 mice. Dissection, dissociation, and culturing of VG and T1-T4 DRG is completed two days after final ALT treatment. Imaging of cells completed <24 hours after dissection. (E-F) ATP responsive (E) and capsaicin responsive (F) DRG neurons shown in red as a percentage of total KCl-responsive neurons shown in black (left), fluorescence intensity changes (middle), and representative calcium transients from sensory neurons of PBS and ALT treated mice in response to capsaicin (1 um) or ATP (150 um) stimulation. The arrow indicates when the stimulus was added. Each dot represents one cell. (right) *p<0.05, **p<0.01, ****p<0.0001, percent responders: chi squared test, fluorescent intensity changes: unpaired T-test; DRG n>25 from ≥3 Pirt-GCAMP6 mice. Data shown as mean +/- SEM.

Journal: bioRxiv

Article Title: Identification of a Neuroimmune Circuit that Regulates Allergic Inflammation in the Esophagus

doi: 10.1101/2024.11.16.623883

Figure Lengend Snippet: (A) Schematic of the intranasal allergic esophagus inflammation model using the protease allergen Alternaria alternata (ALT). (B) Mouse Grimace Scale (MGS) measurements taken immediately prior to intranasal allergen challenges. Allergen treated (n=6) vs. Control (n=6). Day 14 Allergen (red) vs. Day 14 Control (gray), grimace *p<0.05 allergen vs saline at the same time point, two-way ANOVA with Holm-Sidak‘s post hoc, n=6 per group mean±SEM. #p<0.05 AUC allergen vs saline overall, student’s t-test, n=6 per group. (C) MGS measurements on day 26 immediately prior (Pre) and 20 minutes after (Post) intranasal allergen administration. *p<0.05. Two-Way ANOVA with Multiple Comparisons. Mean ± SEM. (D) Schematic of the calcium assay beginning with the allergic esophagus inflammation model outlined in with Pirt-GCAMP6 mice. Dissection, dissociation, and culturing of VG and T1-T4 DRG is completed two days after final ALT treatment. Imaging of cells completed <24 hours after dissection. (E-F) ATP responsive (E) and capsaicin responsive (F) DRG neurons shown in red as a percentage of total KCl-responsive neurons shown in black (left), fluorescence intensity changes (middle), and representative calcium transients from sensory neurons of PBS and ALT treated mice in response to capsaicin (1 um) or ATP (150 um) stimulation. The arrow indicates when the stimulus was added. Each dot represents one cell. (right) *p<0.05, **p<0.01, ****p<0.0001, percent responders: chi squared test, fluorescent intensity changes: unpaired T-test; DRG n>25 from ≥3 Pirt-GCAMP6 mice. Data shown as mean +/- SEM.

Article Snippet: Allergic esophageal inflammation was induced by intranasal administration of Alternaria alternata extract (Greer Laboratories, Inc.; 2 mg/dose in 30 ul of sterile phosphate-buffered saline [PBS]) three times a week for a total of 11-12 injections.

Techniques: Control, Saline, Calcium Assay, Dissection, Imaging, Fluorescence

Increased esophageal sensory neuron innervation density in the lamina propria of allergen-treated mice. (A) Representative immunofluorescence images of BIII-tubulin in longitudinal esophageal cuts from NaV1.8-Cre R26CAG-floxStop-tdTomato mice treated with PBS and intranasal ALT. (B) Murine Esophageal NaV1.8-tdT+ nerve area; LP tissue control vs Alternaria treated, ****p<0.0001. Data were obtained from 3 independent experiments; allergen treated (n=8) vs. Control (n=4). (C) Murine Esophageal BIII-tubulin nerve density. Data were obtained from 2 independent experiments; allergen treated (n=6) vs. Control (n=5). Individual data points represent a separate section of esophagus. Two-way ANOVA with multiple comparisons, horizontal line shows mean.

Journal: bioRxiv

Article Title: Identification of a Neuroimmune Circuit that Regulates Allergic Inflammation in the Esophagus

doi: 10.1101/2024.11.16.623883

Figure Lengend Snippet: Increased esophageal sensory neuron innervation density in the lamina propria of allergen-treated mice. (A) Representative immunofluorescence images of BIII-tubulin in longitudinal esophageal cuts from NaV1.8-Cre R26CAG-floxStop-tdTomato mice treated with PBS and intranasal ALT. (B) Murine Esophageal NaV1.8-tdT+ nerve area; LP tissue control vs Alternaria treated, ****p<0.0001. Data were obtained from 3 independent experiments; allergen treated (n=8) vs. Control (n=4). (C) Murine Esophageal BIII-tubulin nerve density. Data were obtained from 2 independent experiments; allergen treated (n=6) vs. Control (n=5). Individual data points represent a separate section of esophagus. Two-way ANOVA with multiple comparisons, horizontal line shows mean.

Article Snippet: Allergic esophageal inflammation was induced by intranasal administration of Alternaria alternata extract (Greer Laboratories, Inc.; 2 mg/dose in 30 ul of sterile phosphate-buffered saline [PBS]) three times a week for a total of 11-12 injections.

Techniques: Immunofluorescence, Control