ENGRAILED-1 transcription factor has a paracrine neurotrophic activity on adult spinal α-motoneurons.
Mélanie LebœufStephanie E Vargas-AbonceEugénie Pezé-HedsieckEdmond DupontLucia Jimenez-AlonsoKenneth L MoyaAlain ProchiantzPublished in: EMBO reports (2023)
Several homeoprotein transcription factors transfer between cells and regulate gene expression, protein translation, and chromatin organization in recipient cells. ENGRAILED-1 is one such homeoprotein expressed in spinal V1 interneurons that synapse on α-motoneurons. Neutralizing extracellular ENGRAILED-1 by expressing a secreted single-chain antibody blocks its capture by spinal motoneurons resulting in α-motoneuron loss and limb weakness. A similar but stronger phenotype is observed in the Engrailed-1 heterozygote mouse, confirming that ENGRAILED-1 exerts a paracrine neurotrophic activity on spinal cord α-motoneurons. Intrathecal injection of ENGRAILED-1 leads to its specific internalization by spinal motoneurons and has long-lasting protective effects against neurodegeneration and weakness. Midbrain dopaminergic neurons express Engrailed-1 and, similarly to spinal cord α-motoneurons, degenerate in the heterozygote. We identify genes expressed in spinal cord motoneurons whose expression changes in mouse Engrailed-1 heterozygote midbrain neurons. Among these, p62/SQSTM1 shows increased expression during aging in spinal cord motoneurons in the Engrailed-1 heterozygote and upon extracellular ENGRAILED-1 neutralization. We conclude that ENGRAILED-1 might regulate motoneuron aging and has non-cell-autonomous neurotrophic activity.
Keyphrases
- spinal cord
- transcription factor
- neuropathic pain
- spinal cord injury
- gene expression
- induced apoptosis
- poor prognosis
- binding protein
- cell cycle arrest
- signaling pathway
- dna methylation
- stem cells
- small molecule
- single cell
- long non coding rna
- mesenchymal stem cells
- dna damage
- endoplasmic reticulum stress
- cell therapy
- young adults
- ultrasound guided