Carregant...
Miniatura

Tipus de document

Article

Versió

Versió publicada

Data de publicació

Llicència de publicació

cc-by (c) Pannunzio, Bruno et al., 2022
Si us plau utilitzeu sempre aquest identificador per citar o enllaçar aquest document: https://hdl.handle.net/2445/187251

CD200R1 contributes to successful functional reinnervation after a sciatic nerve injury

Títol de la revista

Director/Tutor

ISSN de la revista

Títol del volum

Resum

Activating and inhibitory immune receptors play a critical role in regulating systemic and central nervous system (CNS) immune and inflammatory processes. The CD200R1 immunoreceptor induces a restraining signal modulating inflammation and phagocytosis in the CNS under different inflammatory conditions. However, it remains unknown whether CD200R1 has a role in modulating the inflammatory response after a peripheral nerve injury, an essential component of the successful regeneration. Expression of CD200R1 and its ligand CD200 was analyzed during homeostasis and after a sciatic nerve crush injury in C57Bl/6 mice. The role of CD200R1 inWallerian Degeneration (WD) and nerve regeneration was studied using a specific antibody against CD200R1 injected into the nerve at the time of injury. We found an upregulation of CD200R1 mRNA after injury whereas CD200 was downregulated acutely after nerve injury. Blockade of CD200R1 significantly reduced the acute entrance of both neutrophils and monocytes from blood after nerve injury. When long term regeneration and functional recovery were evaluated, we found that blockade of CD200R1 had a significant effect impairing the spontaneous functional recovery. Taken together, these results show that CD200R1 has a role in mounting a successful acute inflammatory reaction after injury, and contributes to an effective functional recovery.

Citació

Citació

PANNUNZIO, Bruno, AMO APARICIO, Jesús, JULIÁN, Camila, LÓPEZ VALES, Rubèn, PELUFFO, Hugo, LAGO, Natalia. CD200R1 contributes to successful functional reinnervation after a sciatic nerve injury. _Cells_. 2022. Vol. 11, núm. 1786. [consulta: 23 de gener de 2026]. ISSN: 2073-4409. [Disponible a: https://hdl.handle.net/2445/187251]

Exportar metadades

JSON - METS

Compartir registre