isolation-nuclei-from-flash-frozen-liver-tissue-for-single-cell

Isolation of Nuclei from Flash-Frozen Liver Tissue for Single-Cell Multiomics

The liver is a complex and heterogenous tissue responsible for carrying out many critical physiological functions, such as the maintenance of energy ...

Helmholtz Munich

Technical University of Munich

Cellular heterogeneity is revolutionizing the way to study, monitor and dissect complex diseases. This has been possible with the technological and computational advances associated to single-cell genomics and epigenomics. Deeper understanding of cell-to-cell variation and its impact on tissue function will open new avenues for early disease detection, accurate diagnosis and personalized treatments, all together leading to the next generation of health care. This review focuses on the recent discoveries that single-cell genomics and epigenomics have facilitated in the context of human health. It highlights the potential of single-cell omics to further advance the development of personalized treatments and precision medicine in cancer, diabetes and chronic age-related diseases. The promise of single-cell technologies to generate new insights about the differences in function between individual cells is just emerging, and it is paving the way for identifying biomarkers and novel therapeutic targets to tackle age, complex diseases and understand the effect of life style interventions and environmental factors.

Advances of single-cell genomics and epigenomics in human disease: where are we now?

Single-cell RNA-seq reveals the role of pathogenic cell populations in development and progression of chronic diseases. In order to expand our knowledge on cellular heterogeneity, we have developed a single-nucleus RNA-seq2 method tailored for the comprehensive analysis of the nuclear transcriptome from frozen tissues, allowing the dissection of all cell types present in the liver, regardless of cell size or cellular fragility. We use this approach to characterize the transcriptional profile of individual hepatocytes with different levels of ploidy, and have discovered that ploidy states are associated with different metabolic potential, and gene expression in tetraploid mononucleated hepatocytes is conditioned by their position within the hepatic lobule. Our work reveals a remarkable crosstalk between gene dosage and spatial distribution of hepatocytes.

Celia P. Martinez-Jimenez

Helmholtz Pioneer Campus (HPC)

Helmholtz Munich

Isolation of Nuclei from Flash-Frozen Liver Tissue for Single-Cell Multiomics

Celia P. Martinez-Jimenez

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Helmholtz Pioneer Campus (HPC)

Helmholtz Munich

Isolation of Nuclei from Flash-Frozen Liver Tissue for Single-Cell Multiomics

Helmholtz Pioneer Campus (HPC)