Involvement of NINJ2 Protein in Inflammation and Blood-Brain Barrier Transmigration of Monocytes in Multiple Sclerosis.
Melissa SorosinaSilvia PeroniElisabetta MasciaSilvia SantoroAna Maria OsiceanuLaura FerrèFerdinando ClarelliAntonino GiordanoMiryam CannizzaroFilippo Giovanni Martinelli BoneschiMassimo FilippiFederica EspositoPublished in: Genes (2022)
Multiple sclerosis (MS) is an inflammatory neurodegenerative disorder of the central nervous system (CNS). The migration of immune cells into the CNS is essential for its development, and plasma membrane molecules play an important role in triggering and maintaining the inflammation. We previously identified ninjurin2, a plasma membrane protein encoded by NINJ2 gene, as involved in the occurrence of relapse under Interferon-β treatment in MS patients. The aim of the present study was to investigate the involvement of NINJ2 in inflammatory conditions and in the migration of monocytes through the blood-brain barrier (BBB). We observed that NINJ2 is downregulated in monocytes and in THP-1 cells after stimulation with the pro-inflammatory cytokine LPS, while in hCMEC/D3 cells, which represent a surrogate of the BBB, LPS stimulation increases its expression. We set up a transmigration assay using an hCMEC/D3 transwell-based model, finding a higher transmigration rate of monocytes from MS subjects compared to healthy controls (HCs) in the case of an activated hCMEC/D3 monolayer. Moreover, a positive correlation between NINJ2 expression in monocytes and monocyte migration rate was observed. Overall, our results suggest that ninjurin2 could be involved in the transmigration of immune cells into the CNS in pro-inflammatory conditions. Further experiments are needed to elucidate the exact molecular mechanisms.
Keyphrases
- blood brain barrier
- multiple sclerosis
- dendritic cells
- oxidative stress
- induced apoptosis
- peripheral blood
- poor prognosis
- cerebral ischemia
- mass spectrometry
- end stage renal disease
- cell cycle arrest
- ms ms
- chronic kidney disease
- inflammatory response
- white matter
- ejection fraction
- binding protein
- immune response
- gene expression
- signaling pathway
- high throughput
- copy number
- endothelial cells
- cell proliferation
- amino acid
- anti inflammatory
- long non coding rna
- density functional theory
- cerebrospinal fluid
- small molecule
- protein protein
- dna methylation
- subarachnoid hemorrhage
- patient reported outcomes
- replacement therapy
- smoking cessation