| Literature DB >> 33490647 |
Yuki Fujihara1, Koji Yamanegi2, Yasuyuki Nagasawa3, Ayu Yoshida4, Yukako Goto4, Shunsuke Kumanishi1, Hiroyuki Futani1, Shigeo Fukunishi1, Shinichi Yoshiya1, Hiroshi Nishiura2.
Abstract
Circulating lymphocytes infiltrate into local foci at the inflammatory phase of acute wound healing for activation of the immune system and express an immune checkpoint protein programmed cell death 1 (PD-1) at the resolution phase for inactivation of the immune system. Conversely, the PD-1 expression was still found even on circulating lymphocytes of the elder patients with chronic tonsillitis at the palliative stage. Recently, an adhesion G protein coupled receptor 56 (GPR56) was reported to at least work as a proliferation factor for infiltrated lymphocytes into local foci at the resolution phase of acute wound healing. To preliminary examine a similar role of PD-1 and GPR56 at local foci at chronic inflammation, palate tonsils were prepared from small amounts of patients with chronic tonsillitis and tonsillar hypertrophy. A positive relationship of RNA expression might be observed between PD-1 and GPR56 in the elder patients with chronic tonsillitis. In regard to immunohistopathological findings, there were huge and small amounts of PD-1 and GPR56 expression at the marginal zone of lymphoid follicles of palate tonsils with chronic tonsillitis. Moreover, the positive relationship of RNA expression between PD-1 and GPR56 confirmed in large numbers of the elder patients with chronic tonsillitis. Probably, GPR56 participates in a supplement of PD-1+ lymphocytes to circulating bloods of the elder patients with chronic tonsillitis through a lymphocyte cell maintenance system at the marginal zone of the lymphoid follicles of palate tonsils.Entities:
Keywords: C5a receptor, (C5aR); Chronic tonsillitis; G protein-coupled receptor, (GPCR); GPR56; Janus kinase 1, (JAK1); Lymphocytes; Marginal zone; PD-1; T cell receptor, (TCR); cytotoxic T lymphocyte-associated protein-4, (CTLA-4); programmed cell death 1, (PD-1); ribosomal protein S19, (RP S19); signal transducers and activator of transcription 1, (STAT1); type I interferons, (IFNα and IFNβ)
Year: 2021 PMID: 33490647 PMCID: PMC7809388 DOI: 10.1016/j.bbrep.2020.100898
Source DB: PubMed Journal: Biochem Biophys Rep ISSN: 2405-5808