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ATCC melanoma cell lines mel624
Galectin-9 depletion reduces DC 3D migration. (A) Left: schematic representation of the 3D collagen migration assay used. Right: representative single-cell tracking paths of WT or gal9 KD moDCs embedded in a 3D collagen matrix. Lines represent the tracking path covered by each cell from their initial position (time = 0 min). Scale bar = 150 µm. (B) Mature WT or gal9 KD moDCs were embedded within a 3D collagen matrix as per (A). The mean cell velocity of a representative donor is shown. (C–E) Mean ± SEM cell velocity (C), MSD (D), and Euclidean distance (E) of four independent donors. 20 cells were analyzed per donor and transfection. Lines in C connect matched WT and gal9 KD moDCs. Graph in E depicts relative Euclidean distance in gal9 KD moDCs after 60 min of tracking with respect to control cells. (F) Individual trajectory plots of WT and gal9 KD moDCs of one representative donor out of four analyzed. End points of tracks are indicated by red dots. The black line indicates the overall movement in x and y direction (µm). (G) Representative single-cell tracking paths of WT or gal9 KD moDCs embedded in a 3D collagen matrix together with a <t>MEL624</t> malignant melanoma spheroid. Dots indicate cell position at the specified time point, whereas lines represent the tracking path covered by each cell from their initial position (time = 0 min). Scale bar = 150 µm. (H–J) Cell velocity (H), the MSD (I), and the Euclidean distance migrated after 1 h (J) are depicted. Data represent the mean value ± SEM of three independent donors. The Euclidean distance is depicted as the mean value for galectin-9–depleted moDCs relative to the control group after 60 min of tracking. A one-way t test was performed. In (H), lines connect matched WT and gal9 KD moDCs. (K) Collagen matrices from (G) were fixed and stained for actin, and the number of DCs surrounding (left graph) and infiltrated (right graph) in the spheroid was calculated. Measurements were taken at the same tumor spheroid z-plane across conditions. Images are representative of the tumor spheroid and surrounding DCs. Graphs show the mean ± SEM of four independent donors. Unpaired Student’s t test was conducted to compare WT and gal9 KD cells except for E and J, where a one-way t test was performed. *P < 0.05; **P < 0.01; ***P < 0.0001.
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Galectin-9 depletion reduces DC 3D migration. (A) Left: schematic representation of the 3D collagen migration assay used. Right: representative single-cell tracking paths of WT or gal9 KD moDCs embedded in a 3D collagen matrix. Lines represent the tracking path covered by each cell from their initial position (time = 0 min). Scale bar = 150 µm. (B) Mature WT or gal9 KD moDCs were embedded within a 3D collagen matrix as per (A). The mean cell velocity of a representative donor is shown. (C–E) Mean ± SEM cell velocity (C), MSD (D), and Euclidean distance (E) of four independent donors. 20 cells were analyzed per donor and transfection. Lines in C connect matched WT and gal9 KD moDCs. Graph in E depicts relative Euclidean distance in gal9 KD moDCs after 60 min of tracking with respect to control cells. (F) Individual trajectory plots of WT and gal9 KD moDCs of one representative donor out of four analyzed. End points of tracks are indicated by red dots. The black line indicates the overall movement in x and y direction (µm). (G) Representative single-cell tracking paths of WT or gal9 KD moDCs embedded in a 3D collagen matrix together with a <t>MEL624</t> malignant melanoma spheroid. Dots indicate cell position at the specified time point, whereas lines represent the tracking path covered by each cell from their initial position (time = 0 min). Scale bar = 150 µm. (H–J) Cell velocity (H), the MSD (I), and the Euclidean distance migrated after 1 h (J) are depicted. Data represent the mean value ± SEM of three independent donors. The Euclidean distance is depicted as the mean value for galectin-9–depleted moDCs relative to the control group after 60 min of tracking. A one-way t test was performed. In (H), lines connect matched WT and gal9 KD moDCs. (K) Collagen matrices from (G) were fixed and stained for actin, and the number of DCs surrounding (left graph) and infiltrated (right graph) in the spheroid was calculated. Measurements were taken at the same tumor spheroid z-plane across conditions. Images are representative of the tumor spheroid and surrounding DCs. Graphs show the mean ± SEM of four independent donors. Unpaired Student’s t test was conducted to compare WT and gal9 KD cells except for E and J, where a one-way t test was performed. *P < 0.05; **P < 0.01; ***P < 0.0001.
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Galectin-9 depletion reduces DC 3D migration. (A) Left: schematic representation of the 3D collagen migration assay used. Right: representative single-cell tracking paths of WT or gal9 KD moDCs embedded in a 3D collagen matrix. Lines represent the tracking path covered by each cell from their initial position (time = 0 min). Scale bar = 150 µm. (B) Mature WT or gal9 KD moDCs were embedded within a 3D collagen matrix as per (A). The mean cell velocity of a representative donor is shown. (C–E) Mean ± SEM cell velocity (C), MSD (D), and Euclidean distance (E) of four independent donors. 20 cells were analyzed per donor and transfection. Lines in C connect matched WT and gal9 KD moDCs. Graph in E depicts relative Euclidean distance in gal9 KD moDCs after 60 min of tracking with respect to control cells. (F) Individual trajectory plots of WT and gal9 KD moDCs of one representative donor out of four analyzed. End points of tracks are indicated by red dots. The black line indicates the overall movement in x and y direction (µm). (G) Representative single-cell tracking paths of WT or gal9 KD moDCs embedded in a 3D collagen matrix together with a <t>MEL624</t> malignant melanoma spheroid. Dots indicate cell position at the specified time point, whereas lines represent the tracking path covered by each cell from their initial position (time = 0 min). Scale bar = 150 µm. (H–J) Cell velocity (H), the MSD (I), and the Euclidean distance migrated after 1 h (J) are depicted. Data represent the mean value ± SEM of three independent donors. The Euclidean distance is depicted as the mean value for galectin-9–depleted moDCs relative to the control group after 60 min of tracking. A one-way t test was performed. In (H), lines connect matched WT and gal9 KD moDCs. (K) Collagen matrices from (G) were fixed and stained for actin, and the number of DCs surrounding (left graph) and infiltrated (right graph) in the spheroid was calculated. Measurements were taken at the same tumor spheroid z-plane across conditions. Images are representative of the tumor spheroid and surrounding DCs. Graphs show the mean ± SEM of four independent donors. Unpaired Student’s t test was conducted to compare WT and gal9 KD cells except for E and J, where a one-way t test was performed. *P < 0.05; **P < 0.01; ***P < 0.0001.
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Image Search Results


Galectin-9 depletion reduces DC 3D migration. (A) Left: schematic representation of the 3D collagen migration assay used. Right: representative single-cell tracking paths of WT or gal9 KD moDCs embedded in a 3D collagen matrix. Lines represent the tracking path covered by each cell from their initial position (time = 0 min). Scale bar = 150 µm. (B) Mature WT or gal9 KD moDCs were embedded within a 3D collagen matrix as per (A). The mean cell velocity of a representative donor is shown. (C–E) Mean ± SEM cell velocity (C), MSD (D), and Euclidean distance (E) of four independent donors. 20 cells were analyzed per donor and transfection. Lines in C connect matched WT and gal9 KD moDCs. Graph in E depicts relative Euclidean distance in gal9 KD moDCs after 60 min of tracking with respect to control cells. (F) Individual trajectory plots of WT and gal9 KD moDCs of one representative donor out of four analyzed. End points of tracks are indicated by red dots. The black line indicates the overall movement in x and y direction (µm). (G) Representative single-cell tracking paths of WT or gal9 KD moDCs embedded in a 3D collagen matrix together with a MEL624 malignant melanoma spheroid. Dots indicate cell position at the specified time point, whereas lines represent the tracking path covered by each cell from their initial position (time = 0 min). Scale bar = 150 µm. (H–J) Cell velocity (H), the MSD (I), and the Euclidean distance migrated after 1 h (J) are depicted. Data represent the mean value ± SEM of three independent donors. The Euclidean distance is depicted as the mean value for galectin-9–depleted moDCs relative to the control group after 60 min of tracking. A one-way t test was performed. In (H), lines connect matched WT and gal9 KD moDCs. (K) Collagen matrices from (G) were fixed and stained for actin, and the number of DCs surrounding (left graph) and infiltrated (right graph) in the spheroid was calculated. Measurements were taken at the same tumor spheroid z-plane across conditions. Images are representative of the tumor spheroid and surrounding DCs. Graphs show the mean ± SEM of four independent donors. Unpaired Student’s t test was conducted to compare WT and gal9 KD cells except for E and J, where a one-way t test was performed. *P < 0.05; **P < 0.01; ***P < 0.0001.

Journal: The Journal of Cell Biology

Article Title: Galectin-9 regulates dendritic cell polarity and uropod contraction by modulating RhoA activity

doi: 10.1083/jcb.202404079

Figure Lengend Snippet: Galectin-9 depletion reduces DC 3D migration. (A) Left: schematic representation of the 3D collagen migration assay used. Right: representative single-cell tracking paths of WT or gal9 KD moDCs embedded in a 3D collagen matrix. Lines represent the tracking path covered by each cell from their initial position (time = 0 min). Scale bar = 150 µm. (B) Mature WT or gal9 KD moDCs were embedded within a 3D collagen matrix as per (A). The mean cell velocity of a representative donor is shown. (C–E) Mean ± SEM cell velocity (C), MSD (D), and Euclidean distance (E) of four independent donors. 20 cells were analyzed per donor and transfection. Lines in C connect matched WT and gal9 KD moDCs. Graph in E depicts relative Euclidean distance in gal9 KD moDCs after 60 min of tracking with respect to control cells. (F) Individual trajectory plots of WT and gal9 KD moDCs of one representative donor out of four analyzed. End points of tracks are indicated by red dots. The black line indicates the overall movement in x and y direction (µm). (G) Representative single-cell tracking paths of WT or gal9 KD moDCs embedded in a 3D collagen matrix together with a MEL624 malignant melanoma spheroid. Dots indicate cell position at the specified time point, whereas lines represent the tracking path covered by each cell from their initial position (time = 0 min). Scale bar = 150 µm. (H–J) Cell velocity (H), the MSD (I), and the Euclidean distance migrated after 1 h (J) are depicted. Data represent the mean value ± SEM of three independent donors. The Euclidean distance is depicted as the mean value for galectin-9–depleted moDCs relative to the control group after 60 min of tracking. A one-way t test was performed. In (H), lines connect matched WT and gal9 KD moDCs. (K) Collagen matrices from (G) were fixed and stained for actin, and the number of DCs surrounding (left graph) and infiltrated (right graph) in the spheroid was calculated. Measurements were taken at the same tumor spheroid z-plane across conditions. Images are representative of the tumor spheroid and surrounding DCs. Graphs show the mean ± SEM of four independent donors. Unpaired Student’s t test was conducted to compare WT and gal9 KD cells except for E and J, where a one-way t test was performed. *P < 0.05; **P < 0.01; ***P < 0.0001.

Article Snippet: The melanoma cell lines MEL624 (ATCC) (RRID:CVCL_8054) and BLM (AIMM Therapeutics) (RRID:CVCL_7035) were cultured in Gibco DMEM high-glucose medium (Life Technologies) supplemented with 10% FBS and 0.5% antibiotics (100 U/ml penicillin, 100 μg/ml streptomycin, and 0.25 μg/ml amphotericin B; Life Technologies).

Techniques: Migration, Single Cell Tracking, Transfection, Control, Staining

Galectin-9 depletion diminishes DC 3D migration. (A and B) WT or gal9 KD moDCs were matured and embedded within a 3D collagen matrix containing either a MEL624 or a BLM melanoma cell spheroid. The median cell velocity (A) and the MSD (B) were calculated. Data represent the mean value ± SEM of a representative donor. At least 20 cells were analyzed per condition. (C–E) Migration pattern of WT or gal9 KD moDCs either immature (at day 6 of DC differentiation), mature (at day 8), and mature in the presence of a tumor spheroid (at day 8) was analyzed for one representative donor. The median cell velocity (C), the MSD (D), and the Euclidean distance reached after 60 min of tracking (E) were assessed. In D, m = mature DCs; i = immature DCs. Graphs represent the mean value ± SEM of one representative donor. At least 25 cells were analyzed per condition. One-way ANOVA was performed to compare WT and gal9 KD moDCs. n.s., P > 0.05; *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001.

Journal: The Journal of Cell Biology

Article Title: Galectin-9 regulates dendritic cell polarity and uropod contraction by modulating RhoA activity

doi: 10.1083/jcb.202404079

Figure Lengend Snippet: Galectin-9 depletion diminishes DC 3D migration. (A and B) WT or gal9 KD moDCs were matured and embedded within a 3D collagen matrix containing either a MEL624 or a BLM melanoma cell spheroid. The median cell velocity (A) and the MSD (B) were calculated. Data represent the mean value ± SEM of a representative donor. At least 20 cells were analyzed per condition. (C–E) Migration pattern of WT or gal9 KD moDCs either immature (at day 6 of DC differentiation), mature (at day 8), and mature in the presence of a tumor spheroid (at day 8) was analyzed for one representative donor. The median cell velocity (C), the MSD (D), and the Euclidean distance reached after 60 min of tracking (E) were assessed. In D, m = mature DCs; i = immature DCs. Graphs represent the mean value ± SEM of one representative donor. At least 25 cells were analyzed per condition. One-way ANOVA was performed to compare WT and gal9 KD moDCs. n.s., P > 0.05; *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001.

Article Snippet: The melanoma cell lines MEL624 (ATCC) (RRID:CVCL_8054) and BLM (AIMM Therapeutics) (RRID:CVCL_7035) were cultured in Gibco DMEM high-glucose medium (Life Technologies) supplemented with 10% FBS and 0.5% antibiotics (100 U/ml penicillin, 100 μg/ml streptomycin, and 0.25 μg/ml amphotericin B; Life Technologies).

Techniques: Migration

(a) Entire cohort; (b) Development cohort; (c) Test Cohort. MACE – major adverse cardiovascular event; MI: non-fatal myocardial infarction.

Journal: medRxiv

Article Title: Risk of Cardiovascular Events Using the SMART Polyvascular Disease Risk Score

doi: 10.1101/2025.09.05.25335208

Figure Lengend Snippet: (a) Entire cohort; (b) Development cohort; (c) Test Cohort. MACE – major adverse cardiovascular event; MI: non-fatal myocardial infarction.

Article Snippet: We accessed the Baylor Scott & White EPIC informatics and data warehouse to identify patients at their first outpatient cardiology evaluation between April 2014 and October 2023 to estimate up to 10-year risk of MACE, a composite of all-cause death, ischemic stroke, and non-fatal myocardial infarction (MI).

Techniques: