14-3-3 epsilon modulates the stimulated secretion of endopeptidase 24.15

Flávia R. Carreño, Camila N. Goñi, Leandro M. Castro, Emer S. Ferro

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

Abstract

Endopeptidase 24.15 (ep24.15: EC3.4.24.15), a secreted protein involved in peptide metabolism, is unusual in that it does not contain a signal peptide sequence. In this work, we describe the physical interaction between ep24.15 and 14-3-3 epsilon, one isoform of a family of ubiquitous phosphoserine/threonine- scaffold proteins that organizes cell signaling and is involved in exocytosis. The interaction between ep24.15 and 14-3-3 epsilon increased following phosphorylation of ep24.15 at Ser644 by protein kinase A (PKA). The co-localization of ep24.15 and 14-3-3 epsilon was increased by exposure of HEK293 cells (human embryonic kidney cells) to forskolin (10 μM). Overexpression of 14-3-3 epsilon in HEK293 cells almost doubled the secretion of ep24.15 stimulated by A23187 (7.5 μM) from 10% [1.4 ± 0.24 AFU/(min 106 cells)] to 19% [2.54 ± 0.24 AFU/(min 106 cells)] (p < 0.001) of the total intracellular enzyme activity. Treatment with forskolin had a synergistic effect on the A23187-stimulated secretion of ep24.15 that was totally blocked by the PKA inhibitor KT5720. The ep24.15 point mutation S644A reduced the co-localization of ep24.15 and 14-3-3 in stably transfected HEK293 cells. Indeed, secretion of the ep24.15 S644A mutant from these cells was only slightly stimulated by A23187 and insensitive to forskolin, in contrast to that of the wild type enzyme. Together, these data suggest that prior interaction with 14-3-3 is an important step in the unconventional stimulated secretion of ep24.15.

Original languageEnglish (US)
Pages (from-to)10-25
Number of pages16
JournalJournal of neurochemistry
Volume93
Issue number1
DOIs
StatePublished - Apr 2005
Externally publishedYes

Keywords

  • 14-3-3 epsilon
  • Peptidase
  • Phosphorylation
  • Protein-protein interaction
  • Thimet-oligopeptidase
  • Unconventional secretion

ASJC Scopus subject areas

  • Biochemistry
  • Cellular and Molecular Neuroscience

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