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Regional Differences in Neuroinflammation-Associated Gene Expression in the Brain of Sporadic Creutzfeldt–Jakob Disease Patients
Authors:Au&#x;rin&#x; Are&#x;kevi i t&#x;  Thomas Litman  Helle Broholm  Linea C Melchior  Pia R Nielsen  Alison Green  Jens O Eriksen  Colin Smith  Eva L Lund
Affiliation:1.Department of Pathology, Danish Reference Center for Prion Diseases, Copenhagen University Hospital, 2100 Copenhagen, Denmark; (H.B.); (L.C.M.); (E.L.L.);2.Department of Immunology and Microbiology, University of Copenhagen, 2200 Copenhagen, Denmark;3.Department of Surgical Pathology, Zealand University Hospital, 4000 Roskilde, Denmark; (P.R.N.); (J.O.E.);4.National Creutzfeldt–Jakob Disease Research and Surveillance Unit, University of Edinburgh, Edinburgh EH8 9AB, UK; (A.G.); (C.S.)
Abstract:Neuroinflammation is an essential part of neurodegeneration. Yet, the current understanding of neuroinflammation-associated molecular events in distinct brain regions of prion disease patients is insufficient to lay the ground for effective treatment strategies targeting this complex neuropathological process. To address this problem, we analyzed the expression of 800 neuroinflammation-associated genes to create a profile of biological processes taking place in the frontal cortex and cerebellum of patients who suffered from sporadic Creutzfeldt–Jakob disease. The analysis was performed using NanoString nCounter technology with human neuroinflammation panel+. The observed gene expression patterns were regionally and sub-regionally distinct, suggesting a variable neuroinflammatory response. Interestingly, the observed differences could not be explained by the molecular subtypes of sporadic Creutzfeldt–Jakob disease. Furthermore, analyses of canonical pathways and upstream regulators based on differentially expressed genes indicated an overlap between biological processes taking place in different brain regions. This suggests that even smaller-scale spatial data reflecting subtle changes in brain cells’ functional heterogeneity and their immediate pathologic microenvironments are needed to explain the observed differential gene expression in a greater detail.
Keywords:prion disease  Creutzfeldt–  Jakob disease  neuroinflammation  microglia  immune response  gene expression analysis  brain microenvironment  regional pathogenesis  biomarkers
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