IP10, KC and M-CSF Are Remarkably Increased in the Brains from the Various Strains of Experimental Mice Infected with Different Scrapie Agents.
Jia ChenCao ChenChao HuLian LiuYing XiaLin WangWei YangHai-Yan WuWei ZhouKang XiaoQi ShiYuezhang WuZhi-Bao ChenXiao-Ping DongPublished in: Virologica Sinica (2020)
Activation of inflammatory cells and upregulations of a number of cytokines in the central nervous system (CNS) of patients with prion diseases are frequently observed. To evaluate the potential changes of some brain cytokines that were rarely addressed during prion infection, the levels of 17 different cytokines in the brain homogenates of mice infected with different scrapie mouse-adapted agents were firstly screened with Luminex assay. Significant upregulations of interferon gamma-induced protein 10 (IP10), keratinocyte chemoattractant (KC) and macrophage colony stimulating factor (M-CSF) were frequently detected in the brain lysates of many strains of scrapie infected mice. The upregulations of those three cytokines in the brains of scrapie infected mice were further validated by the individual specific ELISA and immunohistochemical assay. Increased specific mRNAs of IP10, M-CSF and KC in the brains of scrapie infected mice were also detected by the individual specific qRT-PCRs and IP10-specific digital PCR. Dynamic analyses of the brain samples collected at different time points post infection revealed the time-dependent increases of those three cytokines, particularly IP10 during the incubation period of scrapie infection. In addition, we also found that the levels of IP10 in cerebral spinal fluid (CSF) of 45 sporadic Creutzfeldt-Jakob disease (sCJD) patients were slightly but significantly higher than those of the cases who were excluded the diagnosis of prion diseases. These data give us a better understanding of inflammatory reaction during prion infection and progression of prion disease.
Keyphrases
- high fat diet induced
- resting state
- white matter
- escherichia coli
- cerebral ischemia
- wild type
- functional connectivity
- oxidative stress
- cerebrospinal fluid
- spinal cord
- spinal cord injury
- adipose tissue
- insulin resistance
- induced apoptosis
- subarachnoid hemorrhage
- machine learning
- multiple sclerosis
- newly diagnosed
- blood brain barrier
- high glucose
- immune response
- prognostic factors
- metabolic syndrome
- amyotrophic lateral sclerosis
- brain injury
- climate change
- cell cycle arrest
- patient reported outcomes
- protein protein
- cell proliferation
- endoplasmic reticulum stress
- data analysis
- real time pcr