Fig 1: Endogenous p62 and CSL Proteins Directly Interact in HDFs(A and B) Proximity ligation assays (PLAs) for in situ detection of CSL and p62 association in HDFs. Assays were carried out in the presence or absence of primary antibodies (A) or with HDFs plus/minus siRNA-mediated CSL gene silencing (B) as controls of specificity. Confocal microscopy was used to examine red fluorescence PLA puncta with concomitant DAPI staining of nuclei (blue). The white frames indicate the enlarged areas to better show PLA red puncta. Shown are representative images and quantification of the average number of puncta per cell, counting at least 30 cells in four fields per conditions. p = 0.05, two-tailed unpaired t test. Scale bars, 10 and 1 µm for enlargements. Additional PLA images of p62 and CSL interaction are provided in Figures S1A and S1B.(C) Endogenous p62 and CSL proteins interact. Immunoprecipitates from HDFs (strain SAN4) with anti-CSL antibodies and non-immune immunoglobulin Gs (IgGs) were analyzed, together with total inputs by sequential immunoblotting with antip62 and CSL antibodies. IgG light chains (LCs) are indicated. A similar immunoprecipitation in another HDF strain (SAN3) is shown in Figure S1C.(D) p62 and CSL proteins directly interact. Recombinant CSL and p62 proteins were admixed and incubated for 2 hr before immunoprecipitation with either anti-CSL or anti-p62 antibodies or nonimmune IgGs, followed by immunoblot analysis with anti-p62 antibodies (green) and anti-CSL antibodies (red). IgG heavy chains (HCs) are indicated.(E) p62 interaction with CSL requires p62 C-terminal region. Immunoblot analysis showed HEK293 transfected for 48 hr with expression vectors for CSL-FLAG, GFP-p62, and a combination of CSLFLAG and GFP-p62 wild-type (WT) or GFP-p62 constructs with deletions of the N-terminal PB1 region, LIR, and C-terminal UBA region (as indicated in the scheme) (Bjørkøy et al., 2005). Total lysates were immunoprecipitated with anti-FLAG antibodies, and blots were probed sequentially with anti-GFP and anti-FLAG antibodies. The input totals were analyzed by parallel immunoblotting as control for the level of expression.
Fig 2: CSL Protein Down-Modulation Requires Autophagy(A) Pharmacologic inhibition of autophagy blocks CSL down-modulation. Immunoblot analysis was performed for two HDF strains treated as indicated in Figure 1A for 24 hr and further incubated with 5 mM 3-methyladenine (3MA) for 8 hr to inhibit autophagy, in parallel with vehicle alone (DMEM). The blot was sequentially probed with antibodies against CSL, p62, and ß-ACTIN.(B and C) Targeting of autophagy-essential gene ATG5 blocks CSL down-modulation. Immunoblot analysis was performed for two HDFs plus/minus shRNA-mediated ATG5 gene silencing (B) or for mouse embryo fibroblasts (MEFs) plus/minus Atg5 gene disruption (+/+ and /) (Kuma et al., 2004) (C) that were either left untreated (untr.) or treated with various pro-autophagic stimuli as in Figure 1A. Blots were sequentially probed with antibodies against CSL, ATG5, and ACTIN as equal loading.
Fig 3: Autophagy Down-Modulates CSL Protein through a p62-Dependent Mechanism(A and B) Immunoblot analysis of two HDF strains (A) or MEFs (B) plus/minus p62 silencing by siRNA-mediated (A) or shRNA-mediated (B) RNA interference, either left untreated (untr.) or treated with various pro-autophagic stimuli as in Figure 1A. Blots were sequentially probed with antibodies against p62, CSL, and ACTIN antibodies.(C) Immunoblot analysis with antibodies against p62, CSL, and ACTIN antibodies of MEFs plus/minus p62 gene disruption (-/- and +/+) (Komatsu et al., 2006). Cells were either left untreated (untr.) or treated with various pro-autophagic stimuli as in Figure 1A.Immunofluorescence analysis with CSL antibodies and DAPI of p62 +/+ and p62 -/- MEFs treated as in Figure 1A.
Fig 4: CSL Down-Modulation Is Linked to Higher Autophagy in CAFs(A) p62 and CSL levels are concomitantly downmodulated in CAFs. Left: immunoblot with anti-p62, anti-CSL, and anti-ACTIN antibodies in nonmatched HDF and CAF strains. Right: immunoblot quantifications, n (HDF) = 2, n (CAF) = 4; *p < 0.05, two-tailed unpaired t test. Each derived HDF strain was marked by an operator identifier and progressive numbers (SAN1 and SAN2). CAF strains were marked only by a progressive number (CAF1–CAF4) (Goruppi et al., 2017).(B) CSL overexpression stabilizes p62 protein. Immunoblot analysis showed HDFs (SAN3) stably infected with a lentivirus for doxycycline-inducible CSL expression (Procopio et al., 2015), plus/minus doxycycline (200 ng/mL) for 3 days, under basal conditions and after autophagy activation by serum starvation (24 hr). Bafilomycin A1 was added for 2 hr to monitor autophagic flux (Klionsky et al., 2016). The arrow indicates the stabilized high-molecular p62 band upon CSL induction. The blots were sequentially probed with antibodies against p62, LC3, CSL, and ACTIN.(C) CSL overexpression inhibits autophagy geneexpression. RT-qPCR analysis with the indicated genes, normalized to ß-actin, in two HDF strains stably infected with an inducible CSL-expressing lentivirus, plus/minus CSL induction as in (B).(D) CSL overexpression stabilizes p62 in CAFs. Immunoblot analysis showed antibodies against p62, CSL, and GAPDH of two patient-derived CAF strains (CAF1 and CAF16) expressing a doxycycline-inducible CSL and plus/minus (200 ng/mL) for 2 days.Numbers refer to densitometry quantification of p62 in CSL-overexpressing versus noninduced control CAFs (folds of induction).
Fig 5: Autophagy Down-Modulates CSL Protein(A) CSL is down-regulated by autophagy. Immunoblot analysis was performed for four HDF strains that were untreated (untr.), serum starved (s.f.), or treated with the KU0063794 mTOR inhibitor (mTOR-i; 10 µM) or a mitochondria-uncoupling agent (CCCP; 5 µM) for 24 hr to induce autophagy. Blots were sequentially probed with antibodies against CSL, LC3- to monitor autophagic processing, and with anti ?-Tubulin (TUBULIN) or ß-Actin (ACTIN), as equal loading. The identifier of the operator and a progressive number classify each primary HDF strain (e.g., SAN3), and a list of all the cells used is provided in Key Resources Table.(B) Immunofluorescence analysis with anti-CSL antibodies (green), phalloidin (red), and DAPI (blue) of two HDF strains treated as in (A). Phalloidin and DAPI counterstained the cytoskeleton and the nuclei, respectively. Scale bar, 40 µm.(C) Autophagy down-modulates CSL protein independently of its RNA levels. RT-qPCR analysis of CSL expression, normalized to ß-actin, of two HDF strains (SAN4 and SAN5) treated as in (A).(D) CSL down-modulation results in the upregulation of CAF effector genes. RT-qPCR analysis of the indicated CAF effector gene expression, normalized to ß-actin, of two HDF (SAN2 and SAN3) treated as in (A).Mean ± SEM; n (experiments) = 3; NS, not significant; *p = 0.05, two-tailed unpaired t test.
Supplier Page from OriGene Technologies for RBPJK (RBPJ) (NM_005349) Human Recombinant Protein