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Versatile workflow for cell type–resolved transcriptional and epigenetic profiles from cryopreserved human lung
Maria Llamazares-Prada, Elisa Espinet, Vedrana Mijošek, Uwe Schwartz, Pavlo Lutsik, Raluca Tamas, Mandy Richter, Annika Behrendt, Stephanie T. Pohl, Naja P. Benz, Thomas Muley, Arne Warth, Claus Peter Heußel, Hauke Winter, Jonathan J. M. Landry, Felix J.F. Herth, Tinne C.J. Mertens, Harry Karmouty-Quintana, Ina Koch, Vladimir Benes, Jan O. Korbel, Sebastian M. Waszak, Andreas Trumpp, David M. Wyatt, Heiko F. Stahl, Christoph Plass, Renata Z. Jurkowska
Maria Llamazares-Prada, Elisa Espinet, Vedrana Mijošek, Uwe Schwartz, Pavlo Lutsik, Raluca Tamas, Mandy Richter, Annika Behrendt, Stephanie T. Pohl, Naja P. Benz, Thomas Muley, Arne Warth, Claus Peter Heußel, Hauke Winter, Jonathan J. M. Landry, Felix J.F. Herth, Tinne C.J. Mertens, Harry Karmouty-Quintana, Ina Koch, Vladimir Benes, Jan O. Korbel, Sebastian M. Waszak, Andreas Trumpp, David M. Wyatt, Heiko F. Stahl, Christoph Plass, Renata Z. Jurkowska
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Resource and Technical Advance Pulmonology

Versatile workflow for cell type–resolved transcriptional and epigenetic profiles from cryopreserved human lung

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Abstract

Complexity of lung microenvironment and changes in cellular composition during disease make it exceptionally hard to understand molecular mechanisms driving development of chronic lung diseases. Although recent advances in cell type–resolved approaches hold great promise for studying complex diseases, their implementation relies on local access to fresh tissue, as traditional tissue storage methods do not allow viable cell isolation. To overcome these hurdles, we developed a versatile workflow that allows storage of lung tissue with high viability, permits thorough sample quality check before cell isolation, and befits sequencing-based profiling. We demonstrate that cryopreservation enables isolation of multiple cell types from both healthy and diseased lungs. Basal cells from cryopreserved airways retain their differentiation ability, indicating that cellular identity is not altered by cryopreservation. Importantly, using RNA sequencing and EPIC Array, we show that gene expression and DNA methylation signatures are preserved upon cryopreservation, emphasizing the suitability of our workflow for omics profiling of lung cells. Moreover, we obtained high-quality single-cell RNA-sequencing data of cells from cryopreserved human lungs, demonstrating that cryopreservation empowers single-cell approaches. Overall, thanks to its simplicity, our workflow is well suited for prospective tissue collection by academic collaborators and biobanks, opening worldwide access to viable human tissue.

Authors

Maria Llamazares-Prada, Elisa Espinet, Vedrana Mijošek, Uwe Schwartz, Pavlo Lutsik, Raluca Tamas, Mandy Richter, Annika Behrendt, Stephanie T. Pohl, Naja P. Benz, Thomas Muley, Arne Warth, Claus Peter Heußel, Hauke Winter, Jonathan J. M. Landry, Felix J.F. Herth, Tinne C.J. Mertens, Harry Karmouty-Quintana, Ina Koch, Vladimir Benes, Jan O. Korbel, Sebastian M. Waszak, Andreas Trumpp, David M. Wyatt, Heiko F. Stahl, Christoph Plass, Renata Z. Jurkowska

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Figure 3

Cell viability and function are maintained in cryopreserved lung samples.

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Cell viability and function are maintained in cryopreserved lung samples...
(A) FACS quantification of viable cells from dissociated lung tissues using SyTOX blue as a viability dye. Comparison between fresh and cryopreserved lung parenchyma (left) and lung tumor (middle) from 4 donors showing overall viability values above 80% (NS, nonsignificant, P value= 0.125, n = 4, Wilcoxon’s matched pairs signed-rank test). Right, the viability of single-cell suspensions obtained from cryopreserved tissue of healthy control donors (n = 6) and COPD (n = 13) samples (NS, P value = 0.865, Mann-Whitney test). (B) Immunofluorescence images of fibroblasts derived from cryopreserved lung parenchyma (left) and small airway (right), demonstrating expression of a mesenchymal marker (vimentin, green). Discrete fibroblasts expressing α–smooth muscle actin (red) are also present. (C) Immunofluorescence images of different epithelial cells isolated from cryopreserved material including basal cells from large (top left panel) and small airways (top right panel), distal epithelial cells from parenchyma (bottom left), and tumor epithelial cells derived from lung SCC showing expression of the epithelial marker EPCAM (red). (D) Basal cell–derived spheres show that basal cells (TP63+, red; KRT5+ green, as indicated on the panels) derived from cryopreserved airways are functional and can differentiate into goblet (MUC5AC+, green) and ciliated cells (FOXJ1+, red). (B–D) All the nuclei were counterstained with DAPI (blue); scale bars: 50 μm.

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