Critical role of FPR1 in splenocyte migration into brain to worsen inflammation and ischemic brain injury in mice

• Published in: Theranostics Vol. 12; no. 7; pp. 3024 - 3044
• Main Authors: Li, Jun, Chordia, Mahendra D, Zhang, Yi, Zong, Hui, Pan, Dongfeng, Zuo, Zhiyi
• Format: Journal Article
• Language: English
• Published: Australia Ivyspring International Publisher Pty Ltd 01.01.2022; Ivyspring International Publisher
• Subjects: Animals; Brain - metabolism; Brain Injuries; Brain Ischemia; Carotid arteries; Cytokines; Inflammation; Ischemia; Ischemic Stroke; Laboratory animals; Mice; Mice, Inbred C57BL; Neutrophils; Peptides; Receptors, Formyl Peptide - metabolism; Research Paper; Spleen; Spleen - metabolism; Stroke; Sutures; Traumatic brain injury; Veins & arteries; Beijing China; China; formyl peptide receptor 1; Brain imaging; brain ischemia; splenocyte migration; neuroinflammation; neuroprotection
• ISSN: 1838-7640; 1838-7640
• DOI: 10.7150/thno.57218

Splenocyte contribution to ischemic brain injury has been suggested. It is not known whether this effect is due to systemic action or direct influence in ischemic brain tissues. It is also not known how splenocytes migrate into the brain and worsen neurological outcome after brain ischemia. We determined the role of formyl peptide receptor 1 (FPR1), a receptor expressed in monocytes, in the migration of splenocytes into ischemic brain tissues and the contribution of these splenocytes to ischemic brain injury. Mice with or without knockout were subjected to transient focal brain ischemia. The migration of splenocytes was assessed under and conditions. cFLFLF, a FPR1 antagonist, inhibited splenocyte migration into the brain and neuroinflammation after ischemic stroke. cFLFLF improved neurological outcome assessed 24 hours or 28 days after stroke. cFLFLF did not alter blood-brain barrier permeability in the ischemic brain. mice had an attenuated peripheral monocyte and neutrophil infiltration into the brain, a reduced proinflammatory cytokine level and an improved neurological outcome compared with wild-type mice after brain ischemia. cFLFLF did not affect the proinflammatory cytokine levels in the spleen and brain of mice after ischemic stroke. These results suggest that FPR1 facilitates splenocyte migration into the brain and proinflammatory cytokine production to worsen neurological outcome after brain ischemia, indicating a direct effect of splenocytes on ischemic brain tissues. Our results support the notion that cFLFLF via blocking FPR1 signaling inhibits those pathological processes and is a potential agent for neuroprotection.