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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 2

Importance of thorough tissue quality control before cell isolation and profiling.

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Importance of thorough tissue quality control before cell isolation and ...
(A) Table showing spirometry values (forced expiratory volume in 1 s/forced vital capacity ratio [FEV1/FVC] and FEV1) of 6 normal donors. (B–G) Representative H&E images of lung parenchyma from each of the donors listed in the table (A). (B and C) Examples of donors with healthy lungs. (D–G) H&E images showing slight to moderate fibrosis with mild (G) and moderate (D–F) chronic inflammation and desquamative reaction (E). Donor D also presents anthracotic pigment deposits along the bronchovascular bundles. (H) Table summarizing the characteristics of 2 exemplary COPD donors. (I and J) corresponding H&E images showing mild to moderate emphysema (donor I) and moderate fibrosis with thickening of the alveolar walls and chronic inflammation (donor J). (K) Table indicating tumor type and presence/absence of healthy epithelium. (L and M) Exemplary images of 2 lung squamous cell carcinoma (SCC) samples. Tumor L represents a sample with very high tumor purity, whereas tumor M shows the invasion front of a non–small cell lung cancer specimen with intra-alveolar tumor spread (STAS; left side) and a significant amount of healthy lung parenchyma with mild emphysema on the right. Scale bars: 0.2 mm. –, absent; +, present.

Copyright © 2026 American Society for Clinical Investigation
ISSN 2379-3708

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