Molecular Signature of Neuroinflammation Induced in Cytokine-Stimulated Human Cortical Spheroids.
Kim M A De KleijnKirsten R StraasheijmWieteke A ZuureGerard J M MartensPublished in: Biomedicines (2022)
Crucial in the pathogenesis of neurodegenerative diseases is the process of neuroinflammation that is often linked to the pro-inflammatory cytokines Tumor necrosis factor alpha (TNFα) and Interleukin-1beta (IL-1β). Human cortical spheroids (hCSs) constitute a valuable tool to study the molecular mechanisms underlying neurological diseases in a complex three-dimensional context. We recently designed a protocol to generate hCSs comprising all major brain cell types. Here we stimulate these hCSs for three time periods with TNFα and with IL-1β. Transcriptomic analysis reveals that the main process induced in the TNFα- as well as in the IL-1β-stimulated hCSs is neuroinflammation. Central in the neuroinflammatory response are endothelial cells, microglia and astrocytes, and dysregulated genes encoding cytokines, chemokines and their receptors, and downstream NFκB- and STAT-pathway components. Furthermore, we observe sets of neuroinflammation-related genes that are specifically modulated in the TNFα-stimulated and in the IL-1β-stimulated hCSs. Together, our results help to molecularly understand human neuroinflammation and thus a key mechanism of neurodegeneration.
Keyphrases
- endothelial cells
- high glucose
- lps induced
- rheumatoid arthritis
- lipopolysaccharide induced
- traumatic brain injury
- cerebral ischemia
- inflammatory response
- cognitive impairment
- induced pluripotent stem cells
- pluripotent stem cells
- randomized controlled trial
- diabetic rats
- single cell
- oxidative stress
- gene expression
- spinal cord injury
- immune response
- vascular endothelial growth factor
- white matter
- rna seq
- resting state
- functional connectivity
- nuclear factor
- bone marrow
- transcription factor
- bioinformatics analysis