mouse anti gal3  (Santa Cruz Biotechnology)

Journal: bioRxiv

Article Title: Galectin-3 recruitment at the Mycobacterium tuberculosis -containing phagosome is critical in macrophage but dispensable in epithelial cells

doi: 10.64898/2026.06.04.730029

Figure Lengend Snippet: Galectin-3 recruitment to intracellular bacteria and associated cellular phenotypes during infection. THP-1 cells were grown in 384-well plates, infected with Mtb H37Rv pMRF1 (MOI = 1) or heat-killed (HK) H37Rv pMRF1 for 5 days and imaged by automated confocal microscopy. (A) Representative images of THP-1 (nucleus; blue) infected with H37Rv pMRF1 (yellow) over 5 days. Scale bar = 50 μm (20X). (B) Representative images of THP-1 infected with live and HK H37Rv pMRF1 (MOI = 1; yellow) and labelled by immunofluorescence for Galectin-3 (Gal3; red) at day 3 post-infection. (Left) The focused image highlights a live bacterium colocalized with a Gal3 spot, indicating phagosomal membrane damage, while (right) no colocalization of HK bacterium with Gal3 spot is shown. The magnified inset of bystander cells under conditions of infection with both live and HK bacteria show Gal3 spots, suggesting cellular damage. Scale bar = 50 μm (20X). (C, D, E, F, G) Quantitative image analysis of infected and bystander HPAEpiC cells infected with live and HK H37Rv pMRF1 and in non-infected conditions over 5 days. (C) Percentage of bacteria colocalizing with Gal3 spots. Live bacteria display significantly higher rate of colocalization with Gal3 than HK bacteria from day 1 post-infection (Mann-Whitney, P≤0.05). (D) Intracellular bacterial area (pixel²) per infected cells containing at least one bacterium that is positive for Gal3 (Gal3+, rupture) compared to cells infected with bacteria not colocalized with Gal3 spot (Gal3-, non-rupture). The cells exhibiting colocalization with Gal3 show significantly greater bacterial area from 1 day after infection (Wilcoxon test, P≤0.05). (E) Total cell number. No significant difference is detected on day 0, while cell numbers obtained for live-infection conditions and HK controls are significantly different from day 1 post-infection (One-way Anova, P≤0.05). (F) Percentage of infected and bystander Gal3-positive THP-1 cells for infection with live bacteria. Infected cells show significant higher rate of Gal3-positive cells than bystander cells (Paired t-test, P≤0.05). (G) Percentage of infected and bystander Gal3-positive THP-1 cells for infection with HK bacteria. Infected cells exhibit a significantly higher proportion of Gal3-positive cells up to the first day following infection, whereas no significant difference is observed from the day 2 (Paired t-test, P≤0.05). (H) Mean cellular Gal3 fluorescence intensity. Infected cells exhibit significantly reduced Gal3 intensity relative to bystanders from day 1 (Paired t-test, P≤0.05), whereas bystander and uninfected cells do not differ (Unpaired t-test). (I) Mean cellular Gal3 fluorescence intensity over time in infected and bystander cells obtained for infection with HK H37Rv pMRF1, and in uninfected controls. No significant differences (paired and unpaired t-test, P≤0.05).

Article Snippet: We analyzed Gal3 dynamics over a five-day infection course in THP-1 differentiated human macrophages with a virulent red fluorescent strain of Mtb (H37Rv) followed by immunostaining with an anti-Galectin 3 (Gal3) antibody and nuclear labeling with DAPI ( ).

Techniques: Bacteria, Infection, Confocal Microscopy, Immunofluorescence, Membrane, MANN-WHITNEY, Fluorescence

Journal: bioRxiv

Article Title: Galectin-3 recruitment at the Mycobacterium tuberculosis -containing phagosome is critical in macrophage but dispensable in epithelial cells

doi: 10.64898/2026.06.04.730029

Figure Lengend Snippet: ESX-1–dependent phagosomal damage using BCG and BCG::ESX-1 Mmar strains. THP-1 cells were grown in 384-well plates, infected with BCG pMRF1 and BCG::ESX-1 Mmar pMRF1 (MOI = 2) for 6 days and imaged with confocal microscope. (A) Representative images of THP-1 (nuclei; blue) infected with BCG and BCG::ESX-1Mmar (yellow), showing bacterial colocalization of BCG::ESX-1 Mmar with a Gal3 spot (red). Scale bar = 10 μm (60X). (B) Percentage of bacteria colocalizing with Gal3 spots over 6 days. BCG::ESX-1 Mmar display a significantly higher rate of colocalization with Gal3 than BCG from day 2 post-infection (Mann-Whitney test, P≤0.05). (C) Quantification of total cell number under conditions of BCG and BCG::ESX-1 Mmar infection. No significant difference is observed between the two bacterial strains (Unpaired t-test). (D) Flow cytometry gating strategy for BCG and BCG::ESX-1 Mmar -infected samples. Singlet cells were first selected based on size (Forward Scatter, FSC) vs. granularity (Side Scatter, SSC) and on FSC-H vs. FSC-A, followed by separation of infected populations (DsRed+) displaying two distinct phenotypes based on blue and green fluorescence signals of the CCF4-AM staining. (E): Percentage of CCF4-positive (blue) infected cells at 3 days post-infection, which is significantly increased under BCG::ESX-1 Mmar infection conditions than under BCG infection conditions (Unpaired t-test, P≤0.05).

Article Snippet: We analyzed Gal3 dynamics over a five-day infection course in THP-1 differentiated human macrophages with a virulent red fluorescent strain of Mtb (H37Rv) followed by immunostaining with an anti-Galectin 3 (Gal3) antibody and nuclear labeling with DAPI ( ).

Techniques: Infection, Microscopy, Bacteria, MANN-WHITNEY, Flow Cytometry, Fluorescence, Staining

Journal: bioRxiv

Article Title: Galectin-3 recruitment at the Mycobacterium tuberculosis -containing phagosome is critical in macrophage but dispensable in epithelial cells

doi: 10.64898/2026.06.04.730029

Figure Lengend Snippet: Functional impact of LGALS3 silencing on Galectin-3 levels and infection phenotypes. THP-1 cells were transfected with SiRNA in 384-well plates, infected with H37Rv pMRF1 (MOI = 1) for 3 days and imaged by automated confocal microscopy. (A) Representative images of THP-1 cells transfected with scramble control (left), siLGALS3 (middle) and siVPS18 (right) and infected. Scale bar = 50 μm (20X). (B, C, D, E) Quantitative image analysis of non-transfected (NT), scramble, siLGALS3 and siVPS18 conditions on day 3 post-infection. (B) Mean Gal3 fluorescence intensity. Gal3 signal is 4-fold reduced for siLGALS3-treated cells relative to scramble and siVPS18-treated ones (Brown–Forsythe ANOVA, P≤0.01). (C) Intracellular bacterial area (pixel²) per infected cells containing at least one bacterium that is positive for Gal3 (Gal3+, rupture) compared to cells infected with bacteria not colocalized with Gal3 spot (Gal3-, non-rupture). Bacterial area is significantly increased under both siLGALS3 and siVPS18 conditions by comparison with scramble condition (Unpaired t-test, P≤0.05). (D) Percentage of bacteria colocalizing with Gal3 spots. No significant difference is observed between NT and scramble controls. Bacteria and Gal3 colocalization is significantly decreased for siLGALS3-transfected cells and significantly increased for siVPS18-transfected ones relative to scramble condition (Mann-Whitney test, P≤0.05). (E) Total cell number for transfected and non transfected conditions. No significant difference is observed (Unpaired t-test).

Article Snippet: We analyzed Gal3 dynamics over a five-day infection course in THP-1 differentiated human macrophages with a virulent red fluorescent strain of Mtb (H37Rv) followed by immunostaining with an anti-Galectin 3 (Gal3) antibody and nuclear labeling with DAPI ( ).

Techniques: Functional Assay, Infection, Transfection, Confocal Microscopy, Control, Fluorescence, Bacteria, Comparison, MANN-WHITNEY

Journal: bioRxiv

Article Title: Galectin-3 recruitment at the Mycobacterium tuberculosis -containing phagosome is critical in macrophage but dispensable in epithelial cells

doi: 10.64898/2026.06.04.730029

Figure Lengend Snippet: Infection phenotype and Galectin-3 distribution in human alveolar epithelial cells (HPAEpiC). HPAEpiC cells were grown in 384-well plates, infected with Mtb H37Rv pMRF1 (MOI = 5) for 3 days and imaged by automated confocal microscopy. (A) Representative image of HPAEpiC cells infected with live H37Rv pMRF1 bacteria (yellow) and labelled by immunofluorescence for Galectin-3 (Gal3; red). The focused image shows a bacterium which colocalized with a Gal3 spot. Scale bar = 20 μm (40X). (B, C, D, E) Quantitative image analysis of infected and bystander HPAEpiC cells infected with live H37Rv pMRF1 or uninfected over 3 days. (B) Percentage of infected, bystander and uninfected Gal3-positive HPAEpiC cells. No significant difference is observed between infected and bystander cells (Paired t-test) and between uninfected and bystander cells or uninfected and infected cells (Mann-Whitney test). (C) Mean Gal3 fluorescence intensity in infected, bystander and uninfected HPAEpiC cells. No significant difference is observed between cells infected with H37Rv pMRF1 and bystander cells (Paired t-tests) or uninfected conditions (Unpaired t-test). (D) Intracellular bacterial area (pixel²) per infected cells containing at least one bacterium that is positive for Gal3 (rupture) versus infected cells without colocalization of bacterium with Gal3 spot (non-rupture). The cells exhibiting colocalization with Gal3 or not show non significant difference of bacterial area from 2 days after infection. (Mann-Whitney test). (E) Total cell number for infected and non infected conditions. No significant difference observed between the conditions (Unpaired t-test).

Article Snippet: We analyzed Gal3 dynamics over a five-day infection course in THP-1 differentiated human macrophages with a virulent red fluorescent strain of Mtb (H37Rv) followed by immunostaining with an anti-Galectin 3 (Gal3) antibody and nuclear labeling with DAPI ( ).

Techniques: Infection, Confocal Microscopy, Bacteria, Immunofluorescence, MANN-WHITNEY, Fluorescence

Journal: bioRxiv

Article Title: Galectin-3 recruitment at the Mycobacterium tuberculosis -containing phagosome is critical in macrophage but dispensable in epithelial cells

doi: 10.64898/2026.06.04.730029

Figure Lengend Snippet: Human alveolus-on-chip (AoC) model and Galectin-3 responses to infection. HPAEpiC cells and human lung endothelial cells were seeded in in-house AoC devices, respectively in top and bottom channels, and grown over 7 days to reconstitute the alveolar interface. Human macrophages were introduced into the top channel on the day 7 (M-AoC) and then infected with Mtb H37Rv pMRF1 (MOI = 5) on day 8. M-AoC was imaged at 1 and 5 days post-infection by confocal microscopy and analyzed using a 3D image analysis software (IMARIS v10, Oxford Instruments). (A) Photograph of the in-house alveolus-on-chip (AoC) device. (B) Representative 3D-imaging of infected M-AoC at 1 day post-infection, used for the determination of H37Rv pMRF1 infection (red) inside the alveolar barrier model (nuclei, blue; actin, gray; macrophages, green). Scale bar = 50 μm (20X). (C) Representative immunofluorescence image of the alveolar barrier co-cultured with macrophages (CFSE labeled, green) and infected with H37Rv pMRF1 (yellow). The focused image highlights a bacterium within a macrophage colocalized with a strong Gal3 signal (red), consistent with phagosomal rupture. (D) Percentage of infected Gal3-positive HPAEpiC cells and macrophages in AoC and M-AoC models at days 1 and 5 post-infection. Infected macrophages exhibit significant higher rate than epithelial cells in M-AoC (Paired t-test) and epithelial cells in AoC models (Unpaired t-test, P≤0.05). Quantifications were obtained from pooled datasets comprising ∼10 infected macrophages and ∼40 infected epithelial cells per experiment.

Article Snippet: We analyzed Gal3 dynamics over a five-day infection course in THP-1 differentiated human macrophages with a virulent red fluorescent strain of Mtb (H37Rv) followed by immunostaining with an anti-Galectin 3 (Gal3) antibody and nuclear labeling with DAPI ( ).

Techniques: Infection, Confocal Microscopy, Software, 3D Imaging, Immunofluorescence, Cell Culture, Labeling

Journal: Neuroprotection

Article Title: Environmental enrichment modulates chronic poststroke inflammation and links white matter TREM2‐positive microglia in recovery in mice

doi: 10.1002/nep3.70028

Figure Lengend Snippet: Infarct size correlations with peri‐infarct immunofluorescence analysis of ionized calcium binding adaptor molecule 1 (Iba1), galectin‐3 (Gal3), and purinergic receptor P2Y12 (P2RY12). (A) Representative immunostaining of 4′,6‐diamidino‐2‐phenylindole (DAPI), Iba1, P2RY12, and Gal3 in a standard environment (SE) mouse at peri‐infarct area (at ×20 magnification). (B) Representative immunostaining of DAPI, Iba1, P2RY12, and Gal3 in an enriched environment (EE) mouse at peri‐infarct area (at ×20 magnification). (C) Quantification of indirect infarct area measurements. (D) Correlation of infarct area with Neuroscore per group. (E) Iba1 coverage quantification measured as the percentage of image covered by Iba1 area (%area). (F) Correlation of infarct area with Iba1 coverage. (G) Gal3 coverage quantification measured as the percentage of image covered by Iba1 + Gal3 + area (%area). (H) Correlation of infarct area with Gal3 coverage. (I) P2RY12 coverage quantification measured as the percentage of image covered by Iba1 + P2RY12 + area (%area). (J) Correlation of infarct area with P2RY12 coverage. Peri‐infarct area is shown as dashed red lines in A and B. In (C, E, G, and I), values are expressed as individual experimental replicates with mean ± SEM. In (D, F, H, and J), values are expressed as individual experimental replicates with simple linear regression lines; Pearson correlation's r value with p ‐value are also shown. In (C, E, G, and I), unpaired t ‐test was performed. n = 4/6 mice in SE and n = 7 mice in EE (2 mice in SE were not behaviorally characterized). P ‐values and r values are expressed with 3 decimals. P ‐values were not corrected for multiple comparisons.

Article Snippet: They were then incubated at 4°C overnight with one of the following antibodies: Iba1 (1:500, rabbit, Cat# 016‐26721; Wako), Gal3 (1:750, goat, Cat# AF1197; R&D Systems) P2RY12 (1:200, rat, Cat# S16007D; Biolegend).

Techniques: Immunofluorescence, Binding Assay, Immunostaining

Journal: Neuroprotection

Article Title: Environmental enrichment modulates chronic poststroke inflammation and links white matter TREM2‐positive microglia in recovery in mice

doi: 10.1002/nep3.70028

Figure Lengend Snippet: Infarct size correlations with white matter immunofluorescence analysis of ionized calcium binding adaptor molecule 1 (Iba1), galectin‐3 (Gal3), and purinergic receptor P2Y12 (P2RY12). (A) Representative immunostaining of 4′,6‐diamidino‐2‐phenylindole (DAPI), Iba1, P2RY12, and Gal3 (at ×20 magnification) in a standard environment (SE) mouse at white matter area (corpus callosum + external capsule). (B) Representative immunostaining of DAPI, Iba1, P2RY12, and Gal3 in an enriched environment (EE) mouse at white matter area (at ×20 magnification). (C) Iba1 coverage quantification measured as the percentage of image covered by Iba1 area (%area). (D) Gal3 coverage quantification measured as the percentage of image covered by Iba1 + Gal3 + area (%area). (E) P2RY12 coverage quantification measured as the percentage of image covered by Iba1 + P2RY12 + area (%area). (F) Correlation of infarct area with Iba1 coverage. (G) Correlation of infarct area with Gal3 coverage. (H) Correlation of infarct area with P2RY12 coverage. White matter area is shown as dashed red lines in (A, B). In (C–E) values are expressed as individual experimental replicates with mean ± SEM. In (F–H) values are expressed as individual experimental replicates with simple linear regression lines; Pearson correlation's r value with p ‐value are also shown. In (C–E) unpaired t ‐test was performed n = 6 mice in SE and n = 7 mice in EE. p ‐Values and r values are expressed with 3 decimals. p ‐Values were not corrected for multiple comparisons.

Article Snippet: They were then incubated at 4°C overnight with one of the following antibodies: Iba1 (1:500, rabbit, Cat# 016‐26721; Wako), Gal3 (1:750, goat, Cat# AF1197; R&D Systems) P2RY12 (1:200, rat, Cat# S16007D; Biolegend).

Techniques: Immunofluorescence, Binding Assay, Immunostaining

Journal: Neuroprotection

Article Title: Environmental enrichment modulates chronic poststroke inflammation and links white matter TREM2‐positive microglia in recovery in mice

doi: 10.1002/nep3.70028

Figure Lengend Snippet: Quantification of peri‐infarct myelin debris, white matter myelin loss, and their correlations with microglial markers. (A) Representative myelin staining in a standard environment mouse (at ×20 magnification). (B) Enlarged views of infarct contralateral cortical (green square) and peri‐infarct (red square) myelin in a standard environment (SE) mouse. (C) Representative myelin staining in an enriched environment mouse (at ×20 magnification). (D) Enlarged views of infarct contralateral cortical (green square) and peri‐infarct (red square) myelin in an enriched environment (EE) mouse. (E) Myelin debris coverage quantification measured as the percentage of peri‐infarct image covered by Black Gold Myelin dark debris area (%area). (F) Correlation of infarct area with myelin debris coverage. (G) Myelin loss quantification measured as the percentage of myelin lost at corpus callosum in ipsilateral versus contralateral infarct. (H) Correlation of infarct area with myelin loss. (I) Correlations of myelin debris with ionized calcium binding adaptor molecule 1 (Iba1), galectin‐3 (Gal3), purinergic receptor P2Y12 (P2RY12), cluster of differentiation 68 (CD68), and triggering receptor expressed on myeloid cells 2 (TREM2) coverages at peri‐infarct. (J) Correlations of myelin loss with Iba1, Gal3, P2RY12, CD68, and TREM2 coverages at white matter. In (E, G) values are expressed as individual experimental replicates with mean ± SEM. In (F, H, I, J), values are expressed as individual experimental replicates with simple linear regression lines; Pearson correlation's r value with p ‐value are also shown. In (E, G) unpaired t‐test was performed. n = 6 mice in SE and n = 7 mice in EE. p ‐Values and r values are expressed with 3 decimals. p ‐Values were not corrected for multiple comparisons.

Article Snippet: They were then incubated at 4°C overnight with one of the following antibodies: Iba1 (1:500, rabbit, Cat# 016‐26721; Wako), Gal3 (1:750, goat, Cat# AF1197; R&D Systems) P2RY12 (1:200, rat, Cat# S16007D; Biolegend).

Techniques: Staining, Binding Assay

Journal: Food Science & Nutrition

Article Title: Pinellia pedatisecta Schott‐Derived Exosome‐Like Nanovesicles Promote Apoptosis in Colorectal Cancer by Regulating the Lysosome‐Mediated Mitophagy Pathway

doi: 10.1002/fsn3.71500

Figure Lengend Snippet: Lysosome inhibitor suppressed mitophagy in PPS‐ELNs‐treated HCT116 cells. (A) The levels of ROS, SOD, and MDA were detected by commercial kits. (B) Autophagosomes in HCT116 cells were observed by TEM. Scale bar = 1 μm. (C) Lysosomes in HCT116 cells were detected by LysoTracker Red staining. Scale bar = 100 μm. (D) The co‐localization of LC3 and mitochondrial protein TOM20 was detected by immunofluorescence. Scale bar = 100 μm. (E) The expression of p62, PINK1, Parkin, Gal3, TOM20, and LC3‐II/I was detected by Western blot. ** p < 0.01 vs. Control group. # p < 0.05, ## p < 0.01 vs. PPS‐ELNs group. CQ, chloroquine.

Article Snippet: Subsequently, sections were incubated with primary antibodies including Ki67 (1:300, Affinity, AF0198) and Gal3 (1:100, CST, 87985) at 4°C overnight.

Techniques: Staining, Immunofluorescence, Expressing, Western Blot, Control

Journal: Food Science & Nutrition

Article Title: Pinellia pedatisecta Schott‐Derived Exosome‐Like Nanovesicles Promote Apoptosis in Colorectal Cancer by Regulating the Lysosome‐Mediated Mitophagy Pathway

doi: 10.1002/fsn3.71500

Figure Lengend Snippet: PPS‐ELNs regulated lysosome‐mediated mitophagy pathway in CRC mice. (A) The expression of Gal3 in tumors was detected by immunohistochemistry. Scale bar = 20 μm. (B) Autophagosomes in tumor tissues were observed by TEM. Scale bar = 1 μm. (C) The expression of p62, TOM20, LC3‐II/I, PINK1, and Parkin was detected by Western blot. * p < 0.05, ** p < 0.01 vs. Control group.

Article Snippet: Subsequently, sections were incubated with primary antibodies including Ki67 (1:300, Affinity, AF0198) and Gal3 (1:100, CST, 87985) at 4°C overnight.

Techniques: Expressing, Immunohistochemistry, Western Blot, Control