Autophagy maturation associated with CD38-mediated regulation of lysosome function in mouse glomerular podocytes

Jing Xiong, Min Xia, Ming Xu, Yang Zhang, Justine M. Abais, Guangbi Li, Christopher R. Riebling, Joseph K. Ritter, Krishna M. Boini, Pin Lan Li

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

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.

Original languageEnglish (US)
Pages (from-to)1598-1607
Number of pages10
JournalJournal of Cellular and Molecular Medicine
Volume17
Issue number12
DOIs
StatePublished - Dec 2013

Keywords

  • ADP-ribosylcyclase
  • Autophagic flux
  • CD38
  • Glomeruli
  • Lysosome trafficking

ASJC Scopus subject areas

  • Molecular Medicine
  • Cell Biology

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