Ten-eleven translocation methylcytosine dioxygenase 3-loaded microspheres penetrate neurons in vitro causing active demethylation and neurite outgrowth.
Katarzyna NawrotekKarolina RudnickaJustyna GatkowskaSylwia MichlewskaBrandon L PearsonPrzemysław PłocińskiMarek WieczorekPublished in: Journal of tissue engineering and regenerative medicine (2021)
Epigenetic processes, such as DNA methylation and other chromatin modifications, are believed to be largely responsible for establishing a reduced capacity for growth in the mature nervous system. Ten-eleven translocation methylcytosine dioxygenase 3 (Tet3)-, a member of the Tet gene family, plays a crucial role in promoting injury-induced DNA demethylation and expression of regeneration-associated genes in the peripheral nervous system. Here, we encapsulate Tet3 protein within a clinically tolerated poly(lactide-co-glycolide) microsphere system. Next, we show that Tet3-loaded microspheres are internalized into mHippoE-18 embryonic hippocampal cells. We compare the outgrowth potential of Tet3 microspheres with that of commonly used nerve growth factor (NGF)-loaded microspheres in an in vitro injury model. Tet3-containing microspheres increased levels of nuclear 5-hydroxymethylcytosine indicating active demethylation and outperformed NGF-containing microspheres in measures of neurite outgrowth. Our results suggest that encapsulated demethylases may represent a novel avenue to treat nerve injuries.
Keyphrases
- growth factor
- dna methylation
- molecularly imprinted
- drug delivery
- gene expression
- genome wide
- wound healing
- induced apoptosis
- stem cells
- cancer therapy
- poor prognosis
- transcription factor
- dna damage
- endoplasmic reticulum stress
- long non coding rna
- risk assessment
- endothelial cells
- small molecule
- solid phase extraction
- cell cycle arrest
- subarachnoid hemorrhage
- cell free
- diabetic rats
- liquid chromatography
- protein protein