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The elephant in the lung: Integrating lineage-tracing,molecular markers,and single cell sequencing data to identify distinct fibroblast populations during lung development and regeneration
Affiliation:1. The Perinatal Institute and Section of Neonatology, Perinatal and Pulmonary Biology, Cincinnati Children''s Hospital Medical Center, Cincinnati, OH, United States;2. Molecular and Developmental Biology Graduate Program, Cincinnati Children''s Hospital Medical Center, Cincinnati, OH, United States;3. Department of Biomedical Informatics, Cincinnati Children''s Hospital Medical Center, Cincinnati, OH, United States;4. Department of Pediatrics, University of Cincinnati School of Medicine, Cincinnati, OH, United States;1. Cancer Biology, Fox Chase Cancer Center, Philadelphia PA 19111, United States;2. Molecular Therapeutics, Fox Chase Cancer Center, Philadelphia PA 19111, United States;3. Marvin and Concetta Greenberg Pancreatic Cancer Institute, Fox Chase Cancer Center, Philadelphia PA 19111, United States
Abstract:During lung development, the mesenchyme and epithelium are dependent on each other for instructive morphogenic cues that direct proliferation, cellular differentiation and organogenesis. Specification of epithelial and mesenchymal cell lineages occurs in parallel, forming cellular subtypes that guide the formation of both transitional developmental structures and the permanent architecture of the adult lung. While epithelial cell types and lineages have been relatively well-defined in recent years, the definition of mesenchymal cell types and lineage relationships has been more challenging. Transgenic mouse lines with permanent and inducible lineage tracers have been instrumental in identifying lineage relationships among epithelial progenitor cells and their differentiation into distinct airway and alveolar epithelial cells. Lineage tracing experiments with reporter mice used to identify fibroblast progenitors and their lineage trajectories have been limited by the number of cell specific genes and the developmental timepoint when the lineage trace was activated. In this review, we discuss major developmental mesenchymal lineages, focusing on time of origin, major cell type, and other lineage derivatives, as well as the transgenic tools used to find and define them. We describe lung fibroblasts using function, location, and molecular markers in order to compare and contrast cells with similar functions. The temporal and cell-type specific expression of fourteen “fibroblast lineage” genes were identified in single-cell RNA-sequencing data from LungMAP in the LGEA database. Using these lineage signature genes as guides, we clustered murine lung fibroblast populations from embryonic day 16.5 to postnatal day 28 (E16.5-PN28) and generated heatmaps to illustrate expression of transcription factors, signaling receptors and ligands in a temporal and population specific manner.
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