MicroRNA-138-5p Targets Pro-Apoptotic Factors and Favors Neural Cell Survival: Analysis in the Injured Spinal Cord.
Rodrigo M MazaMaría Asunción Barreda-MansoDavid ReigadaÁgata SilvánTeresa Muñoz-GaldeanoAltea SotoÁngela Del ÁguilaManuel Nieto-DíazPublished in: Biomedicines (2022)
The central nervous system microRNA miR-138-5p has attracted much attention in cancer research because it inhibits pro-apoptotic genes including CASP3. We hypothesize that miR-138-5p downregulation after SCI leads to overexpression of pro-apoptotic genes, sensitizing neural cells to noxious stimuli. This study aimed to identify miR-138-5p targets among pro-apoptotic genes overexpressed following SCI and to confirm that miR-138-5p modulates cell death in neural cells. Gene expression and histological analyses revealed that the drop in miR-138-5p expression after SCI is due to the massive loss of neurons and oligodendrocytes and its downregulation in neurons. Computational analyses identified 176 potential targets of miR-138-5p becoming dysregulated after SCI, including apoptotic proteins CASP-3 and CASP-7, and BAK. Reporter, RT-qPCR, and immunoblot assays in neural cell cultures confirmed that miR-138-5p targets their 3'UTRs, reduces their expression and the enzymatic activity of CASP-3 and CASP-7, and protects cells from apoptotic stimuli. Subsequent RT-qPCR and histological analyses in a rat model of SCI revealed that miR-138-5p downregulation correlates with the overexpression of its pro-apoptotic targets. Our results suggest that the downregulation of miR-138-5p after SCI may have deleterious effects on neural cells, particularly on spinal neurons.
Keyphrases
- cell death
- cell cycle arrest
- anti inflammatory
- spinal cord injury
- spinal cord
- induced apoptosis
- cell proliferation
- gene expression
- signaling pathway
- neuropathic pain
- genome wide
- poor prognosis
- single cell
- dna methylation
- oxidative stress
- endoplasmic reticulum stress
- stem cells
- transcription factor
- papillary thyroid
- hydrogen peroxide
- lymph node metastasis
- genome wide identification