Comprehensive RNA Expression Analysis Revealed Biological Functions of Key Gene Sets and Identified Disease-Associated Cell Types Involved in Rat Traumatic Brain Injury.
Qilin TangMengmeng SongRongrong ZhaoXiao HanLin DengHao XueWeiguo LiGang LiPublished in: Journal of clinical medicine (2022)
Traumatic brain injury (TBI) is a worldwide public health concern without major therapeutic breakthroughs over the past decades. Developing effective treatment options and improving the prognosis of TBI depends on a better understanding of the mechanisms underlying TBI. This study performed a comprehensive analysis of 15 RNA expression datasets of rat TBIs from the GEO database. By integrating the results from the various analyses, this study investigated the biological processes, pathways, and cell types associated with TBI and explored the activity of these cells during various TBI phases. The results showed the response to cytokine, inflammatory response, bacteria-associated response, metabolic and biosynthetic processes, and pathways of neurodegeneration to be involved in the pathogenesis of TBI. The cellular abundance of microglia, perivascular macrophages (PM), and neurons were found to differ after TBI and at different times postinjury. In conclusion, immune- and inflammation-related pathways, as well as pathways of neurodegeneration, are closely related to TBI. Microglia, PM, and neurons are thought to play roles in TBI with different activities that vary by phase of TBI.
Keyphrases
- traumatic brain injury
- severe traumatic brain injury
- inflammatory response
- public health
- oxidative stress
- mild traumatic brain injury
- single cell
- spinal cord
- particulate matter
- cell therapy
- emergency department
- gene expression
- stem cells
- mass spectrometry
- induced apoptosis
- toll like receptor
- heavy metals
- risk assessment
- lipopolysaccharide induced
- genome wide
- binding protein
- signaling pathway
- electronic health record
- polycyclic aromatic hydrocarbons