Xavier Alvarez, Zoey K Wallis, Cecily C Midkiff, Jaclyn Mallard, Pete J Didier, Kenneth C Williams
{"title":"Simian Immunodeficiency Virus-Infected Macrophage Traffic Out of the Central Nervous System.","authors":"Xavier Alvarez, Zoey K Wallis, Cecily C Midkiff, Jaclyn Mallard, Pete J Didier, Kenneth C Williams","doi":"10.21203/rs.3.rs-6435804/v1","DOIUrl":null,"url":null,"abstract":"<p><p>We use intracisternal (i.c.) injection of fluorescent-superparamagnetic iron oxide nanoparticles (SPION) in SIV-infected monkeys that labeled CNS CD68-CD163-CD206 perivascular, meningeal, and choroid plexus (CP) macrophages. SPION + CD163 + macrophages are also found in the optic nerves, nasal septum, and cribriform plate - potential sites-paths of macrophage exit. Outside the CNS CD163 + SPION + macrophages labeled in the CNS are in deep cervical lymph node (dCLN), spleen, dorsal root ganglia (DRG). CD163 + SPION + CNS macrophages are abundant 24 hours p.i. in normal animals and decrease over time without CNS inflammation, but accumulate with SIV infection and inflammation. Greater numbers of SPION + macrophages traffic out of the CNS in normal animals and decrease with infection. Productively infected, SPION + macrophages are found in the CNS and dCLN, spleen, and DRG of infected animals 7-14 days post i.c. injection. These data are consistent with SPION + macrophages, some of which are viral infected, trafficking out of the CNS.</p>","PeriodicalId":519972,"journal":{"name":"Research square","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12136738/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Research square","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21203/rs.3.rs-6435804/v1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
We use intracisternal (i.c.) injection of fluorescent-superparamagnetic iron oxide nanoparticles (SPION) in SIV-infected monkeys that labeled CNS CD68-CD163-CD206 perivascular, meningeal, and choroid plexus (CP) macrophages. SPION + CD163 + macrophages are also found in the optic nerves, nasal septum, and cribriform plate - potential sites-paths of macrophage exit. Outside the CNS CD163 + SPION + macrophages labeled in the CNS are in deep cervical lymph node (dCLN), spleen, dorsal root ganglia (DRG). CD163 + SPION + CNS macrophages are abundant 24 hours p.i. in normal animals and decrease over time without CNS inflammation, but accumulate with SIV infection and inflammation. Greater numbers of SPION + macrophages traffic out of the CNS in normal animals and decrease with infection. Productively infected, SPION + macrophages are found in the CNS and dCLN, spleen, and DRG of infected animals 7-14 days post i.c. injection. These data are consistent with SPION + macrophages, some of which are viral infected, trafficking out of the CNS.