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Autophagy maturation associated with CD38-mediated regulation of lysosome function in mouse glomerular podocytes.
- Source :
-
Journal of cellular and molecular medicine [J Cell Mol Med] 2013 Dec; Vol. 17 (12), pp. 1598-607. Date of Electronic Publication: 2013 Nov 17. - Publication Year :
- 2013
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Abstract
- Podocytes are highly differentiated glomerular epithelial cells that contribute to the glomerular barrier function of kidney. A role for autophagy has been proposed in maintenance of their cellular integrity, but the mechanisms controlling autophagy in podocytes are not clear. The present study tested whether CD38-mediated regulation of lysosome function contributes to autophagic flux or autophagy maturation in podocytes. Podocytes were found to exhibit a high constitutive level of LC3-II, a robust marker of autophagosomes (APs), suggesting a high basal level of autophagic activity. Treatment with the mTOR inhibitor, rapamycin, increased LC3-II and the content of both APs detected by Cyto-ID Green staining and autophagolysosomes (APLs) measured by acridine orange staining and colocalization of LC3 and Lamp1. Lysosome function inhibitor bafilomycin A1 increased APs, but decreased APLs content under both basal and rapamycin-induced conditions. Inhibition of CD38 activity by nicotinamide or silencing of CD38 gene produced the similar effects to that bafilomycin A1 did in podocytes. To explore the possibility that CD38 may control podocyte autophagy through its regulation of lysosome function, the fusion of APs with lysosomes in living podocytes was observed by co-transfection of GFP-LC3B and RFP-Lamp1 expression vectors. A colocalization of GFP-LC3B and RFP-Lamp1 upon stimulation of rapamycin became obvious in transfected podocytes, which could be substantially blocked by nicotinamide, CD38 shRNA, and bafilomycin. Moreover, blockade of the CD38-mediated regulation by PPADS completely abolished rapamycin-induced fusion of APs with lysosomes. These results indicate that CD38 importantly control lysosomal function and influence autophagy at the maturation step in podocytes.<br /> (© 2013 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.)
- Subjects :
- Adenosine Diphosphate Ribose metabolism
Animals
Calcium Signaling drug effects
Gene Silencing drug effects
Lysosomes drug effects
Membrane Fusion drug effects
Mice
NADP analogs & derivatives
NADP metabolism
Phagosomes drug effects
Phagosomes metabolism
Podocytes drug effects
Protein Transport drug effects
Proteolysis drug effects
Sirolimus pharmacology
Transcription Factor TFIIH
Transcription Factors metabolism
Ubiquitinated Proteins metabolism
ADP-ribosyl Cyclase 1 metabolism
Autophagy drug effects
Kidney Glomerulus cytology
Lysosomes metabolism
Podocytes cytology
Podocytes metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1582-4934
- Volume :
- 17
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Journal of cellular and molecular medicine
- Publication Type :
- Academic Journal
- Accession number :
- 24238063
- Full Text :
- https://doi.org/10.1111/jcmm.12173