Endogenous α-crystallin inhibits expression of caspase-3 induced by hypoxia in retinal neurons

Life Sci. 2014 Aug 28;111(1-2):42-6. doi: 10.1016/j.lfs.2014.07.008. Epub 2014 Jul 24.

Abstract

Aim: To investigate the expression of endogenous, hypoxic stress-induced α-crystallin and caspase-3 in rat retinal neurons in vitro.

Main methods: Retinal neurons were cultured from Long-Evans rats. The expression of endogenous α-crystallin was analyzed by immunohistochemistry and reverse transcriptase-polymerase chain reaction (RT-PCR). Furthermore, hypoxic exposure was performed in cultured cells, and the expression of endogenous α-crystallin and caspase-3 was assayed by Western blotting.

Key findings: Positive α-crystallin staining was observed in cultured retinal neurons, and expression of endogenous α-crystallin mRNA peaked 3-5d after inoculation (P<0.05). Moreover, endogenous, hypoxic stress-induced α-crystallin expression increased gradually, peaking 6h after hypoxia. The expression was more abundant compared to the control (P<0. 01) and was associated with a decrease in caspase-3 expression (P<0. 05).

Significance: The present study demonstrates that the expression of endogenous α-crystallin in retinal neurons, especially over-expression induced by hypoxic stress, results in the down regulation of caspase-3. The data suggest that endogenous α-crystallin may act as an endogenous neuroprotective factor in retinal neurons.

Keywords: Caspase-3; Endogenous α-crystallin; Hypoxia; Retinal neurons.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Caspase 3 / biosynthesis*
  • Cells, Cultured
  • Hypoxia / enzymology
  • Hypoxia / metabolism*
  • In Vitro Techniques
  • Rats
  • Rats, Long-Evans
  • Retina / enzymology
  • Retina / metabolism
  • Retinal Diseases / enzymology
  • Retinal Diseases / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • alpha-Crystallins / physiology*

Substances

  • alpha-Crystallins
  • Caspase 3