JNK inhibitory kinase is up-regulated in retinal ganglion cells after axotomy and enhances BimEL expression level in neuronal cells.

Abstract

Optic nerve transection results in retinal ganglion cell (RGC) death in adult mammals, after the alteration of gene expression of RGCs. To elucidate the molecular mechanism by which axotomy induces RGC death, we isolated the molecules up-regulated after optic nerve transection. One of these, axotomy-related [corrected] gene (ARG)357, an 898-amino-acid [corrected] protein containing a complete serine-threonine kinase domain, was isolated from a subtraction library of the rat retina. The sequence showed that this gene was a rat homolog of human c-Jun N-terminal kinase (JNK) inhibitory kinase and so belonged to the germinal center kinase-VIII subfamily of Sterile20s protein kinase. We designated ARG357 as rat JNK inhibitory kinase (JIK). Rat JIK was expressed ubiquitously in various tissues and was highly expressed in the retina, with selective expression in RGCs. After axotomy, BimEL and Hrk, which are BH3-only proteins, and rat JIK were up-regulated in RGCs. Overexpression of rat JIK in neuronal cells up-regulated the expression of BimEL, but not that of Hrk. These results indicate that JIK may contribute to axotomy-induced RGC death by up-regulating the expression of BH3-only protein.

• Authors: Taketoshi Wakabayashi, Jun Kosaka, Tetsuro Oshika
• Journal: Journal of neurochemistry (J Neurochem) Vol. 95 Issue 2 Pg. 526-36 (Oct 2005) ISSN: 0022-3042 [Print] England
• PMID: 16092929 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Adaptor Proteins, Signal Transducing
• Apoptosis Regulatory Proteins
• BCL2L11 protein, human
• Bcl-2-Like Protein 11
• Bcl2l11 protein, rat
• DNA, Complementary
• Membrane Proteins
• Proto-Oncogene Proteins
• RNA, Messenger

Topics

• Adaptor Proteins, Signal Transducing (biosynthesis)
• Amino Acid Sequence
• Animals
• Apoptosis Regulatory Proteins
• Axotomy
• Bcl-2-Like Protein 11
• Blotting, Northern
• Cell Death (drug effects)
• DNA, Complementary (biosynthesis, genetics)
• Humans
• In Situ Hybridization
• Membrane Proteins
• Molecular Sequence Data
• Neurons (enzymology, metabolism)
• Optic Nerve (physiology)
• PC12 Cells
• Plasmids
• Proto-Oncogene Proteins
• RNA, Messenger (biosynthesis)
• Rats
• Retina (metabolism)
• Retinal Ganglion Cells (metabolism)
• Reverse Transcriptase Polymerase Chain Reaction
• Transcription, Genetic
• Up-Regulation (physiology)