Enzymatic Dissociation Induces Transcriptional and Proteotype Bias in Brain Cell Populations.
Daniele MatteiAndranik IvanovMarc van OostrumStanislav PantelyushinJuliet RichettoFlavia MuellerMichal BeffingerLinda SchellhammerJohannes Vom BergBernd WollscheidDieter BeuleRosa Chiara PaolicelliUrs MeyerPublished in: International journal of molecular sciences (2020)
Different cell isolation techniques exist for transcriptomic and proteotype profiling of brain cells. Here, we provide a systematic investigation of the influence of different cell isolation protocols on transcriptional and proteotype profiles in mouse brain tissue by taking into account single-cell transcriptomics of brain cells, proteotypes of microglia and astrocytes, and flow cytometric analysis of microglia. We show that standard enzymatic digestion of brain tissue at 37 °C induces profound and consistent alterations in the transcriptome and proteotype of neuronal and glial cells, as compared to an optimized mechanical dissociation protocol at 4 °C. These findings emphasize the risk of introducing technical biases and biological artifacts when implementing enzymatic digestion-based isolation methods for brain cell analyses.
Keyphrases
- single cell
- rna seq
- induced apoptosis
- white matter
- resting state
- high throughput
- cell therapy
- cell cycle arrest
- hydrogen peroxide
- inflammatory response
- cerebral ischemia
- functional connectivity
- gene expression
- stem cells
- transcription factor
- multiple sclerosis
- magnetic resonance imaging
- computed tomography
- bone marrow
- magnetic resonance
- nitric oxide
- mesenchymal stem cells
- pi k akt
- anaerobic digestion