Literature DB >> 32314275

IP10, KC and M-CSF Are Remarkably Increased in the Brains from the Various Strains of Experimental Mice Infected with Different Scrapie Agents.

Jia Chen1,2, Cao Chen3,4,5, Chao Hu2,6, Lian Liu2,7, Ying Xia2,7, Lin Wang2,7, Wei Yang2,7, Hai-Yan Wu1, Wei Zhou2,6, Kang Xiao2,6, Qi Shi2,6, Yuezhang Wu2, Zhi-Bao Chen8, Xiao-Ping Dong9,10,11,12,13.   

Abstract

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.

Entities:  

Keywords:  Cytokines; Interferon gamma-induced protein 10 (IP10); Keratinocyte chemoattractant (KC); Macrophage colony stimulating factor (M-CSF); Prion

Year:  2020        PMID: 32314275      PMCID: PMC7736440          DOI: 10.1007/s12250-020-00216-3

Source DB:  PubMed          Journal:  Virol Sin        ISSN: 1995-820X            Impact factor:   4.327


  43 in total

1.  Molecular biology of prion diseases.

Authors:  C Weissmann
Journal:  Trends Cell Biol       Date:  1994-01       Impact factor: 20.808

2.  Multiplication of scrapie agent in mouse spleen.

Authors:  M C Clarke; D A Haig
Journal:  Res Vet Sci       Date:  1971-03       Impact factor: 2.534

3.  C-reactive protein and IL-6: new marker proteins for the diagnosis of CJD in plasma?

Authors:  D Völkel; K Zimmermann; I Zerr; T Lindner; M Bodemer; S Poser; H P Schwarz
Journal:  Transfusion       Date:  2001-12       Impact factor: 3.157

4.  Alzheimer's disease amyloid beta and prion protein amyloidogenic peptides promote macrophage survival, DNA synthesis and enhanced proliferative response to CSF-1 (M-CSF).

Authors:  John A Hamilton; Genevieve Whitty; Anthony R White; Michael F Jobling; Andrew Thompson; Colin J Barrow; Roberto Cappai; Konrad Beyreuther; Colin L Masters
Journal:  Brain Res       Date:  2002-06-14       Impact factor: 3.252

5.  Inducible cytokine gene expression in the brain in the ME7/CV mouse model of scrapie is highly restricted, is at a strikingly low level relative to the degree of gliosis and occurs only late in disease.

Authors:  Alan R Brown; Jeanette Webb; Selma Rebus; Robert Walker; Alun Williams; John K Fazakerley
Journal:  J Gen Virol       Date:  2003-09       Impact factor: 3.891

6.  Neurons and astrocytes respond to prion infection by inducing microglia recruitment.

Authors:  Mathieu Marella; Joëlle Chabry
Journal:  J Neurosci       Date:  2004-01-21       Impact factor: 6.167

Review 7.  Prions.

Authors:  S B Prusiner
Journal:  Proc Natl Acad Sci U S A       Date:  1998-11-10       Impact factor: 11.205

8.  Activation of cerebral cytokine gene expression and its correlation with onset of reactive astrocyte and acute-phase response gene expression in scrapie.

Authors:  I L Campbell; M Eddleston; P Kemper; M B Oldstone; M V Hobbs
Journal:  J Virol       Date:  1994-04       Impact factor: 5.103

9.  TAZ sensitizes EGFR wild-type non-small-cell lung cancer to gefitinib by promoting amphiregulin transcription.

Authors:  Weiwei Yuan; Wei Xu; Yan Li; Wei Jiang; Yue Li; Qiqing Huang; Bo Chen; Shuangshuang Wu; Yu Wang; Weiwei Song; Weihong Zhao; Jianqing Wu
Journal:  Cell Death Dis       Date:  2019-03-25       Impact factor: 8.469

10.  Re-infection of the prion from the scrapie‑infected cell line SMB-S15 in three strains of mice, CD1, C57BL/6 and Balb/c.

Authors:  Kang Xiao; Bao-Yun Zhang; Xiao-Mei Zhang; Jing Wang; Cao Chen; Li-Na Chen; Yan Lv; Qi Shi; Xiao-Ping Dong
Journal:  Int J Mol Med       Date:  2016-01-25       Impact factor: 4.101

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  2 in total

Review 1.  Colony stimulating factors in the nervous system.

Authors:  Violeta Chitu; Fabrizio Biundo; E Richard Stanley
Journal:  Semin Immunol       Date:  2021-11-04       Impact factor: 11.130

2.  Enhanced M-CSF/CSF1R Signaling Closely Associates with PrPSc Accumulation in the Scrapie-Infected Cell Line and the Brains of Scrapie-Infected Experimental Rodents.

Authors:  Ying Xia; Cao Chen; Jia Chen; Chao Hu; Wei Yang; Lin Wang; Lian Liu; Li-Ping Gao; Yue-Zhang Wu; Dong-Dong Chen; Qi Shi; Zhi-Bao Chen; Xiao-Ping Dong
Journal:  Mol Neurobiol       Date:  2022-08-15       Impact factor: 5.682

  2 in total

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