Affiliation:
1. Wellcome – MRC Cambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre University of Cambridge, Cambridge, UK
2. Department of Physiology, Development and Neuroscience University of Cambridge, Cambridge, UK
Abstract
Abstract
Diseases such as idiopathic pulmonary fibrosis, chronic obstructive pulmonary disease, and bronchopulmonary dysplasia injure the gas-exchanging alveoli of the human lung. Animal studies have indicated that dysregulation of alveolar cells, including alveolar type II stem/progenitor cells, is implicated in disease pathogenesis. Due to mouse-human differences, there has been a desperate need to develop human-relevant lung models that can more closely recapitulate the human lung during homeostasis, injury repair, and disease. Here we discuss how current single-cell RNA sequencing studies have increased knowledge of the cellular and molecular composition of human lung alveoli, including the identification of molecular heterogeneity, cellular diversity, and previously unknown cell types, some of which arise specifically during disease. For functional analysis of alveolar cells, in vitro human alveolar organoids established from human pluripotent stem cells, embryonic progenitors, and adult tissue from both healthy and diseased lungs have modeled aspects of the cellular and molecular features of alveolar epithelium. Drawbacks of such systems are highlighted, along with possible solutions. Organoid-on-a-chip and ex vivo systems including precision-cut lung slices can complement organoid studies by providing further cellular and structural complexity of lung tissues, and have been shown to be invaluable models of human lung disease, while the production of acellular and synthetic scaffolds hold promise in lung transplant efforts. Further improvements to such systems will increase understanding of the underlying biology of human alveolar stem/progenitor cells, and could lead to future therapeutic or pharmacological intervention in patients suffering from end-stage lung diseases.
Significance statement Over the last decade, stem cell-derived culture model systems of human lungs have garnered renewed interest, as they recapitulate human lung tissues in a dish. This study summarizes the current concepts and advances in the field of human distal lung alveoli, which is the most critical region for the respiratory function and disease, and thereby has been moving forward so rapidly. Specifically, this study compares the differences in cellular compositions of distal lungs between mouse and human and discusses the current model systems to study maintenance, regeneration, and disease of human lung alveoli, which is difficult to model in animal studies.
Funder
Biotechnology and Biological Sciences Research Council
European Research Council
Royal Society
Wellcome
Wellcome Trust
Publisher
Oxford University Press (OUP)
Subject
Cell Biology,Developmental Biology,General Medicine
Cited by
70 articles.
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