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.

Highlights

  • Prion diseases, which are caused by misfolded cellular prion proteins termed prions and denoted PrPSc, are a group of infectious and invariably fatal neurodegenerative diseases that can be acquired (

  • The gene expression signature of Sporadic Creutzfeldt–Jakob disease (sCJD) CB sample FFCJD_CB-20 suggested that it was an frontal cortex (FC) sample, and it was removed from further analyses

  • We generated data that provide an overview of differentially expressed genes, the most involved canonical pathways and upstream regulators, and their biological functions in sCJD patients as compared to controls; in FC compared to CB; and even the sub-clusters observed within each brain region

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Summary

Introduction

Prion diseases, which are caused by misfolded cellular prion proteins termed prions and denoted PrPSc , are a group of infectious and invariably fatal neurodegenerative diseases that can be acquired (

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