| Literature DB >> 30880103 |
Sanae Hosomi1, Yoshihisa Koyama2, Tadashi Watabe3, Mitsuo Ohnishi4, Hiroshi Ogura5, Toshihide Yamashita6, Takeshi Shimazu7.
Abstract
Myeloid-derived suppressor cells (MDSCs) have strong immunosuppressive characteristics, which allow them to limit inflammation and facilitate wound healing and recovery. Although MDSCs are a newly-determined cell type that is gaining attention in the immunology field, their neuroimmunological characteristics remain unstudied. In this study, we explored the suppressive role of MDSCs in cerebral inflammatory reactions after focal traumatic brain injury (TBI) using in vivo imaging. Through morphological, functional, and phenotypic analyses we determined that CD11b+/Gr-1+ cells infiltrating the contusion area are MDSCs. MDSCs are among the first responders to tissue injury, responding even prior to microglial activation. Positron emission tomography imaging of translocator protein results suggest that infiltrating MDSCs suppress neuronal inflammation and interact with resident immune cells, like microglia, following focal TBI.Entities:
Keywords: blood–brain barrier; inflammation; microglia; myeloid-derived suppressor cells; traumatic brain injury
Year: 2019 PMID: 30880103 DOI: 10.1016/j.neuroscience.2019.03.015
Source DB: PubMed Journal: Neuroscience ISSN: 0306-4522 Impact factor: 3.590