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Bafilomycin

Manufactured by Abcam
Sourced in United Kingdom

Bafilomycin is a macrolide antibiotic that acts as a specific inhibitor of vacuolar-type H+-ATPase. It is commonly used as a tool compound in cell biology research.

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2 protocols using bafilomycin

1

Lysosomal Activity Assay in Macrophages

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Seventy-two hours after IP injection of 4 mL of 4% thioglycollate broth (Brewer thioglycollate medium, Fluka, Sigma Aldrich, St. Louis, MO), macrophages were harvested from the peritoneum of euthanized EKO mice with ice-cold PBS, centrifuged, and suspended in DMEM (Dulbecco’s modified Eagle’s medium) medium (Lonza, Basel, Switzerland) supplemented with penicillin/streptomycin (100 U/mL each; Gibco, Rodano, Milan, Italy) and plated. After one hour, plates were washed, and adherent cells were left for 16 hours in DMEM containing 10% fetal calf serum, then treated with DMEM containing 0.2% BSA (Sigma Aldrich, St. Louis, MO) and either Bafilomycin 1×, acetylated LDL 50 μg/mL (ThermoFisher, Milan, Italy; Catalog No. L35354), or acetylated LDL 50 μg/mL supplemented with increasing concentrations of HDL (100, 250, and 500 μg/mL; Merck, Darmstadt, Germany; Catalog No. LP3-5MG), for 48 hours. Lysosomal activity was measured with a self-quenched substrate, with Bafilomycin 1× as control, following manufacturer’s instructions (Lysosomal Intracellular Activity Assay kit, Abcam, Cambridge, United Kingdom; Catalog No. ab234622). Cells were fixed and counterstained with DAPI, then the signal was quantified for each treatment by fluorescence microscopy in 6 randomly chosen 63× fields among biological replicates from 3 independent experiments per group with ImageJ.49 (link)
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2

TDP-43 Degradation Kinetics in N2a Cells

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TDP-43 degradation was analyzed in N2a cells plated in 6-well plates (30,000 cells/well density) at 0 min, 30 min, 1 h, 2 h, 3 h, 15 h, and 24 h after transfection. In a set of experiments, the cells were pre-treated with 100 nM epoxomicin (Abcam, Cambridge, UK), a potent proteasome inhibitor [53 (link)], or with 400 nM bafilomycin (Abcam, Cambridge, UK), which inhibits autophagic flux by preventing the acidification of endosomes and lysosomes [54 (link)]. Then, the cells were washed with PBS, fixed in 2% (w/v) buffered paraformaldehyde for 10 min at room temperature (20 °C), and permeabilized with a 0.5% (v/v) Triton X-100 solution for 5 min. Then, the cells were incubated for 60 min at 37 °C with 1:500 mouse monoclonal anti-TDP-43 antibodies (Novus Biologicals, Littleton, CO, USA) or with 1:500 rabbit polyclonal anti-murine TDP-43 antibodies (LSBio, Seattle, WA, USA), which only recognize the murine protein, and for 90 min with 1:1000 diluted Alexa Fluor 488-conjugated anti-mouse or 594-conjugated anti-rabbit secondary antibodies, respectively, and then analyzed by confocal microscopy, as described above.
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