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LIM-only protein 4 interacts directly with the repulsive guidance molecule A receptor Neogenin.
- Source :
-
Journal of neurochemistry [J Neurochem] 2008 Oct; Vol. 107 (2), pp. 418-31. Date of Electronic Publication: 2008 Aug 12. - Publication Year :
- 2008
-
Abstract
- Repulsive guidance molecule A (RGM A) was recently described as a potent inhibitor of neuroregeneration in a rat spinal cord injury model. The receptor mediating RGM A's repulsive activity was shown to be Neogenin, a member of the Deleted in Colorectal Cancer (DCC) family of netrin receptors. Binding of RGM A to Neogenin induces activation of the small GTPase RhoA and of its effector Rho-kinase by an unknown mechanism. Here we show, that the cytoplasmic tail of Neogenin interacts directly with the transcriptional coactivator LIM domain only 4 (LMO4) in human SH-SY5Y cells, human Ntera neurons, and in embryonic rat cortical neurons. RGM A binding to Neogenin but not binding of Netrin-1, induces release of LMO4 from Neogenin. Down-regulation of LMO4 neutralizes the repulsive activity of RGM A in neuronal cell lines and embryonic rat cortical neurons and prevents RhoA activation. These results show for the first time that an interaction of Neogenin with LMO4 is involved in the RGM A - Neogenin signal transduction pathway for RhoA activation.
- Subjects :
- Adaptor Proteins, Signal Transducing
Amides pharmacology
Analysis of Variance
Animals
Cells, Cultured
Cerebral Cortex cytology
Embryo, Mammalian
Enzyme Inhibitors pharmacology
GPI-Linked Proteins
Gene Expression drug effects
Green Fluorescent Proteins biosynthesis
Homeodomain Proteins biosynthesis
Humans
LIM Domain Proteins
Neurites drug effects
Neurites physiology
Neurons cytology
Neurons drug effects
Protein Structure, Tertiary
Pyridines pharmacology
RNA, Small Interfering pharmacology
Rats
Transcription Factors biosynthesis
Transfection methods
Tubulin pharmacology
Two-Hybrid System Techniques
rhoA GTP-Binding Protein genetics
rhoA GTP-Binding Protein metabolism
Homeodomain Proteins metabolism
Membrane Glycoproteins metabolism
Membrane Proteins metabolism
Nerve Tissue Proteins metabolism
Neurons physiology
Transcription Factors metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1471-4159
- Volume :
- 107
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Journal of neurochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 18702663
- Full Text :
- https://doi.org/10.1111/j.1471-4159.2008.05621.x