FIGURE

Fig 3

ID
ZDB-FIG-261014-381
Publication
Saurav et al., 2026 - IP3R2-mediated inter-organelle calcium signaling suppresses melanosome degradation
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Fig 3

IP3R2 silencing stabilize melanogenic proteins and triggers autophagy.
(A) Representative image of immunoblot showing expression of GP100 in B16 B16 cells transfected with siNT or siIP3R2 along with 10 µM MG132 treatment for 6 h. (B) Bar graph showing the densitometry of the GP100 band normalized to β-Tubulin (N = 3). (C) Representative image of immunoblot showing expression of DCT in B16 cells transfected with siNT or siIP3R2 along with 10 µM MG132 treatment for 6 h. (D) Bar graph showing the densitometry of the DCT band normalized to β-Tubulin (N = 3). (E) Representative image of immunoblot showing expression of IP3R2 in B16 cells transfected with siNT or siIP3R2 along with 10 µM MG132 treatment for 6 h. (F) Bar graph showing the densitometry of the IP3R2 band normalized to β-Tubulin (N = 3). (G) Representative image of immunoblot showing expression of Calnexin in B16 cells transfected with siNT or siIP3R2 along with 10 µM MG132 treatment for 6 h. (H) Bar graph showing the densitometry of the Calnexin band normalized to β-Tubulin (N = 4). (I) Representative image of immunoblot showing expression of LC3II and LC3I in B16 cells transfected with siNT or siIP3R2 along with 10 µM MG132 treatment for 6 h. (J) Bar graph showing the densitometric analysis of the LC3II/LC3I ratio (N = 4). (K) Representative image of immunoblot showing expression of LC3II and LC3I in B16 cells after siRNA silencing of IP3R2. (L) Bar graph showing the densitometric analysis of the LC3II/LC3I ratio (N = 3). (M) Representative images of confocal imaging in B16 cells after transfected with siNT or siIP3R2 along with pMRX-IP-GFP-LC3-RFP probe, scale bar, 10 µm. (N) Bar graph shows the quantification of the autolysosome intensity in the GFP:RFP ratio, where ‘N’ denotes the number of cells. (O) Representative image of immunoblot showing expression of LC3II in B16 cells after siRNA transfection including 6 h of treatment with 100 nM of the lysosomal inhibitor Bafilomycin A1. (P) Bar graph showing the densitometric analysis of the LC3II/LC3I ratio (N = 3). Data presented are mean ± SEM. For statistical analysis, one-sample t test was performed for panel L, an unpaired t test was performed for panel N, and Tukey’s multiple comparisons test was performed for panel B, D, F, H, J, P using GraphPad Prism software. Here, ‘ns’ means non-significant; * p < 0.05, ** p < 0.01, and **** p < 0.0001.

Expression Data

Expression Detail
Antibody Labeling
Phenotype Data

Phenotype Detail
Acknowledgments
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