The Role of MEF2 Transcription Factor Family in Neuronal Survival and Degeneration.
Malwina LisekOskar PrzybyszewskiLudmila ZylinskaFeng GuoTomasz BoczekPublished in: International journal of molecular sciences (2023)
The family of myocyte enhancer factor 2 (MEF2) transcription factors comprises four highly conserved members that play an important role in the nervous system. They appear in precisely defined time frames in the developing brain to turn on and turn off genes affecting growth, pruning and survival of neurons. MEF2s are known to dictate neuronal development, synaptic plasticity and restrict the number of synapses in the hippocampus, thus affecting learning and memory formation. In primary neurons, negative regulation of MEF2 activity by external stimuli or stress conditions is known to induce apoptosis, albeit the pro or antiapoptotic action of MEF2 depends on the neuronal maturation stage. By contrast, enhancement of MEF2 transcriptional activity protects neurons from apoptotic death both in vitro and in preclinical models of neurodegenerative diseases. A growing body of evidence places this transcription factor in the center of many neuropathologies associated with age-dependent neuronal dysfunctions or gradual but irreversible neuron loss. In this work, we discuss how the altered function of MEF2s during development and in adulthood affecting neuronal survival may be linked to neuropsychiatric disorders.
Keyphrases
- transcription factor
- cerebral ischemia
- genome wide identification
- dna binding
- spinal cord
- cell death
- subarachnoid hemorrhage
- oxidative stress
- depressive symptoms
- free survival
- gene expression
- stem cells
- blood brain barrier
- cell cycle arrest
- endoplasmic reticulum stress
- computed tomography
- magnetic resonance imaging
- spinal cord injury
- living cells
- multiple sclerosis
- cell therapy
- contrast enhanced
- bone marrow
- cell proliferation
- quantum dots
- heat stress
- heat shock protein
- heat shock