Impact of cell culture on the transcriptomic programs of primary and iPSC-derived human alveolar type 2 cells

The alveolar epithelial type 2 cell (AEC2) is the facultative progenitor of lung alveoli tasked to maintain distal lung homeostasis. AEC2 dysfunction has been implicated in the pathogenesis of a number of pulmonary diseases, including idiopathic pulmonary fibrosis (IPF), highlighting the importance of human in vitro models of the alveolar epithelium. However, AEC2-like cells captured in cell culture have yet to be directly compared to their in vivo counterparts at single cell resolution. Here, we apply single cell RNA sequencing to perform head-to-head comparisons between the global transcriptomes of freshly isolated primary (1°) adult human AEC2s, their isogenic cultured progeny, and human iPSC-derived AEC2s (iAEC2s) cultured in identical conditions. We find each population occupies a distinct transcriptomic space with both types of cultured AEC2s (1° and iAEC2s) exhibiting similarities to and differences from freshly purified 1° cells. Across each cell type, we find an inverse relationship between proliferative states and AEC2 maturation states, with uncultured 1° AEC2s being most quiescent and mature, their cultured progeny being more proliferative/less mature, and cultured iAEC2s being most proliferative/least mature. iAEC2s also express significantly lower levels of major histocompatibility complex (MHC) genes compared to 1° cells, suggesting immunological immaturity. Cultures of either type of human AEC2 (1° or iAEC2) do not generate detectable type 1 alveolar cells in these defined conditions; however, iAEC2s after co-culture with fibroblasts can give rise to a subset of cells expressing “transitional cell markers” recently described in fibrotic lung tissue of patients with pulmonary fibrosis or in mouse models of pulmonary fibrosis. Hence, we provide direct comparisons of the transcriptomic programs of 1° and engineered AEC2s, two in vitro model systems that can be harnessed for studies of human lung health and disease.

[1]  C. Yao,et al.  Cryobanking of human distal lung epithelial cells for preservation of their phenotypic and functional characteristics , 2021, bioRxiv.

[2]  Derek C. Liberti,et al.  Organoid models: assessing lung cell fate decisions and disease responses. , 2021, Trends in molecular medicine.

[3]  Derek C. Liberti,et al.  Age-dependent alveolar epithelial plasticity orchestrates lung homeostasis and regeneration. , 2021, Cell stem cell.

[4]  Yutaka Suzuki,et al.  Directed induction of alveolar type I cells derived from pluripotent stem cells via Wnt signaling inhibition , 2020, Stem cells.

[5]  Grace X. Y. Zheng,et al.  Progenitor identification and SARS-CoV-2 infection in human distal lung organoids , 2020, Nature.

[6]  Kyle J. Gaulton,et al.  Single-cell multiomic profiling of human lungs reveals cell-type-specific and age-dynamic control of SARS-CoV2 host genes , 2020, eLife.

[7]  Ho Min Kim,et al.  Three-Dimensional Human Alveolar Stem Cell Culture Models Reveal Infection Response to SARS-CoV-2 , 2020, Cell Stem Cell.

[8]  R. Baric,et al.  Human Lung Stem Cell-Based Alveolospheres Provide Insights into SARS-CoV-2-Mediated Interferon Responses and Pneumocyte Dysfunction , 2020, Cell Stem Cell.

[9]  B. Koo,et al.  Inflammatory Signals Induce AT2 Cell-Derived Damage-Associated Transient Progenitors that Mediate Alveolar Regeneration , 2020, Cell stem cell.

[10]  Fabian J. Theis,et al.  Alveolar regeneration through a Krt8+ transitional stem cell state that persists in human lung fibrosis , 2020, Nature Communications.

[11]  Jianhong Ou,et al.  Persistence of a regeneration-associated, transitional alveolar epithelial cell state in pulmonary fibrosis , 2020, Nature Cell Biology.

[12]  Jessie Huang,et al.  SARS-CoV-2 Infection of Pluripotent Stem Cell-derived Human Lung Alveolar Type 2 Cells Elicits a Rapid Epithelial-Intrinsic Inflammatory Response , 2020, bioRxiv.

[13]  C. Yao,et al.  SARS-CoV-2 infection of primary human lung epithelium for COVID-19 modeling and drug discovery , 2020, bioRxiv.

[14]  Taylor M. Matte,et al.  Human iPSC-derived alveolar and airway epithelial cells can be cultured at air-liquid interface and express SARS-CoV-2 host factors , 2020, bioRxiv.

[15]  K. Pandit,et al.  Genome-wide integration of microRNA and transcriptomic profiles of differentiating human alveolar epithelial cells. , 2020, American journal of physiology. Lung cellular and molecular physiology.

[16]  A. Emili,et al.  Patient-specific iPSCs carrying an SFTPC mutation reveal the intrinsic alveolar epithelial dysfunction at the inception of interstitial lung disease , 2020, bioRxiv.

[17]  Ignacio S. Caballero,et al.  Reconstructed Single-Cell Fate Trajectories Define Lineage Plasticity Windows during Differentiation of Human PSC-Derived Distal Lung Progenitors. , 2020, Cell stem cell.

[18]  Y. Kluger,et al.  Single-cell connectomic analysis of adult mammalian lungs , 2019, Science Advances.

[19]  Jonathan A. Kropski,et al.  Single-cell RNA-sequencing reveals profibrotic roles of distinct epithelial and mesenchymal lineages in pulmonary fibrosis , 2019, bioRxiv.

[20]  Naftali Kaminski,et al.  Single Cell RNA-seq reveals ectopic and aberrant lung resident cell populations in Idiopathic Pulmonary Fibrosis , 2019, bioRxiv.

[21]  Irving L. Weissman,et al.  A molecular cell atlas of the human lung from single cell RNA sequencing , 2019, Nature.

[22]  D. Kotton,et al.  Derivation of self-renewing lung alveolar epithelial type II cells from human pluripotent stem cells , 2019, Nature Protocols.

[23]  J. Kropski,et al.  Epithelial Injury and Dysfunction in the Pathogenesis of Idiopathic PulmonaryFibrosis. , 2019, The American journal of the medical sciences.

[24]  Alyssa J. Miller,et al.  Single cell RNA sequencing identifies TGFβ as a key regenerative cue following LPS-induced lung injury. , 2019, JCI insight.

[25]  E. Morrisey,et al.  Early lineage specification defines alveolar epithelial ontogeny in the murine lung , 2019, Proceedings of the National Academy of Sciences.

[26]  Joseph C. Wu,et al.  Strategies for Improving the Maturity of Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes. , 2018, Circulation research.

[27]  E. Morrisey,et al.  Regeneration of the lung alveolus by an evolutionarily conserved epithelial progenitor , 2018, Nature.

[28]  Ignacio S. Caballero,et al.  Pluripotent stem cell differentiation reveals distinct developmental pathways regulating lung- versus thyroid-lineage specification , 2017, Development.

[29]  E. Morrisey,et al.  Differentiation of Human Pluripotent Stem Cells into Functional Lung Alveolar Epithelial Cells. , 2017, Cell stem cell.

[30]  Yutaka Suzuki,et al.  Long-term expansion of alveolar stem cells derived from human iPS cells in organoids , 2017, Nature Methods.

[31]  Ahmad S. Khalil,et al.  Prospective isolation of NKX2-1–expressing human lung progenitors derived from pluripotent stem cells , 2017, The Journal of clinical investigation.

[32]  E. Tran,et al.  Cross‐Species Transcriptome Profiling Identifies New Alveolar Epithelial Type I Cell‐Specific Genes , 2017, American journal of respiratory cell and molecular biology.

[33]  Ravi S. Misra,et al.  Lung Gene Expression Analysis (LGEA): an integrative web portal for comprehensive gene expression data analysis in lung development , 2017, Thorax.

[34]  B. Stripp,et al.  Single-cell RNA sequencing identifies diverse roles of epithelial cells in idiopathic pulmonary fibrosis. , 2016, JCI insight.

[35]  M. Lu,et al.  Emergence of a Wave of Wnt Signaling that Regulates Lung Alveologenesis by Controlling Epithelial Self-Renewal and Differentiation. , 2016, Cell reports.

[36]  J. Epstein,et al.  Plasticity of Hopx+ Type I alveolar cells to regenerate Type II cells in the lung , 2015, Nature Communications.

[37]  C. Barkauskas,et al.  Cellular mechanisms of tissue fibrosis. 7. New insights into the cellular mechanisms of pulmonary fibrosis. , 2014, American Journal of Physiology - Cell Physiology.

[38]  M. Selman,et al.  Revealing the pathogenic and aging-related mechanisms of the enigmatic idiopathic pulmonary fibrosis. an integral model. , 2014, American journal of respiratory and critical care medicine.

[39]  H. Johansson,et al.  Whole-Genome Analysis of Temporal Gene Expression during Early Transdifferentiation of Human Lung Alveolar Epithelial Type 2 Cells In Vitro , 2014, PloS one.

[40]  B. Stripp,et al.  Lung Stem Cell Differentiation in Mice Directed by Endothelial Cells via a BMP4-NFATc1-Thrombospondin-1 Axis , 2014, Cell.

[41]  C. Guillemette,et al.  Three-dimensional culture and cAMP signaling promote the maturation of human pluripotent stem cell-derived hepatocytes , 2013, Development.

[42]  Michael J. Cronce,et al.  Type 2 alveolar cells are stem cells in adult lung. , 2013, The Journal of clinical investigation.

[43]  B. Brockway,et al.  Airway Epithelial Progenitors Are Region Specific and Show Differential Responses to Bleomycin‐Induced Lung Injury , 2012, Stem Cells.

[44]  Michael J. Cronce,et al.  Multiple stromal populations contribute to pulmonary fibrosis without evidence for epithelial to mesenchymal transition , 2011, Proceedings of the National Academy of Sciences.

[45]  P. Ballard,et al.  HTII-280, a Biomarker Specific to the Apical Plasma Membrane of Human Lung Alveolar Type II Cells , 2010, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[46]  Yongsheng Chang,et al.  Differentiated human alveolar epithelial cells and reversibility of their phenotype in vitro. , 2007, American journal of respiratory cell and molecular biology.

[47]  R. Mason,et al.  Ozone induces oxidative stress in rat alveolar type II and type I-like cells. , 2006, Free radical biology & medicine.

[48]  R. Mason,et al.  Alveolar epithelial cells secrete chemokines in response to IL-1beta and lipopolysaccharide but not to ozone. , 2006, American journal of respiratory cell and molecular biology.

[49]  A. Postle,et al.  Differentiation of human pulmonary type II cells in vitro by glucocorticoid plus cAMP. , 2002, American journal of physiology. Lung cellular and molecular physiology.

[50]  Y. Cao,et al.  Modulation of t1alpha expression with alveolar epithelial cell phenotype in vitro. , 1998, The American journal of physiology.

[51]  M. Williams,et al.  Monoclonal antibodies specific to apical surfaces of rat alveolar type I cells bind to surfaces of cultured, but not freshly isolated, type II cells. , 1988, Biochimica et biophysica acta.

[52]  A. Katzenstein Pathogenesis of "fibrosis" in interstitial pneumonia: an electron microscopic study. , 1985, Human pathology.

[53]  M. Williams,et al.  Changes in biochemical characteristics and pattern of lectin binding of alveolar type II cells with time in culture. , 1985, Biochimica et biophysica acta.

[54]  Ignacio S. Caballero,et al.  Heterogeneity in Human Induced Pluripotent Stem Cell – derived Alveolar Epithelial Type II Cells Revealed with ABCA3/SFTPC Reporters , 2021 .

[55]  Yee Hwa Yang,et al.  Freshly isolated rat alveolar type I cells, type II cells, and cultured type II cells have distinct molecular phenotypes. , 2005, American journal of physiology. Lung cellular and molecular physiology.