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Involvement of NINJ2 Protein in Inflammation and Blood-Brain Barrier Transmigration of Monocytes in Multiple Sclerosis. | LitMetric

AI Article Synopsis

  • Multiple sclerosis (MS) is an inflammatory disease affecting the central nervous system, where immune cell migration plays a key role in its progression.
  • The study focused on ninjurin2 (NINJ2), a plasma membrane protein linked to MS relapse under certain treatments, and examined its role in inflammation and monocyte movement through the blood-brain barrier (BBB).
  • Results showed that NINJ2 levels changed in response to inflammation; it was lower in monocytes but higher in brain endothelial cells after stimulation, and there was a higher rate of monocyte migration from MS patients compared to healthy individuals, suggesting NINJ2 is significant for immune cell transmigration during inflammation.

Article Abstract

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 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 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9690398PMC
http://dx.doi.org/10.3390/genes13111946DOI Listing

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