Hop/STI1 modulates retinal proliferation and cell death independent of PrPC

Biochem Biophys Res Commun. 2007 Sep 21;361(2):474-80. doi: 10.1016/j.bbrc.2007.07.038. Epub 2007 Jul 18.

Abstract

Hop/STI1 is a co-chaperone adaptor protein for Hsp70/Hsp90 complexes. Hop/STI1 is found extracellularly and modulates cell death and differentiation through interaction with the prion protein (PrP(C)). Here, we investigated the expression of hop/STI1 and its role upon cell proliferation and cell death in the developing retina. Hop/STI1 is more expressed in developing rat retina than in the mature tissue. Hop/STI1 blocks retinal cell death in the neuroblastic layer (NBL) in a PrP(C) dependent manner, but failed to protect ganglion cells against axotomy-induced cell death. An antibody raised against hop/STI1 (alpha-STI1) blocked both ganglion cell and NBL cell death independent of PrP(C). cAMP/PKA, ERK, PI3K and PKC signaling pathways were not involved in these effects. Hop/STI1 treatment reduced proliferation, while alpha-STI1 increased proliferation in the developing retina, both independent of PrP(C). We conclude that hop/STI1 can modulate both proliferation and cell death in the developing retina independent of PrP(C).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Antibodies / pharmacology
  • Cell Death
  • Cell Proliferation / drug effects
  • Cytoprotection / drug effects
  • Gene Expression Regulation, Developmental / drug effects
  • Heat-Shock Proteins / genetics
  • Heat-Shock Proteins / metabolism*
  • Mice
  • PrPC Proteins / metabolism
  • Rats
  • Retina / cytology*
  • Retina / drug effects
  • Retina / embryology
  • Retinal Ganglion Cells / cytology
  • Retinal Ganglion Cells / drug effects

Substances

  • Antibodies
  • Heat-Shock Proteins
  • PrPC Proteins
  • Stip1 protein, mouse
  • Stip1 protein, rat