Table 1.
Organoid Model | Original Cells or Tissues | Differentiated Cell Types and Biomarker | Potential Application | Limitation | Ref. |
---|---|---|---|---|---|
Human lung organoids (HLOs) | hPSCs iPSCs |
Goblet cells (MUC5AC) Ciliated cells (FOXJ1, ACTTUB) Multi-ciliated cells (FOXJ1) Club cells (SCGB1A1) Basal cells (P63, NGFR, CK5) ATII cells (SFTPC, SFTPB) ATI cells (HOPX, PDPN) Distal progenitor (NMYC, ID2) Proximal lung (SOX2) Distal lung (SOX9) |
Lung development, Proximal and distal epithelium maturation, Epithelial–mesenchymal interactions, Airway remodeling after injury, Epithelial–mesenchymal crosstalk. |
No branching morphogenesis; Lack of immune cells, vasculature, innervation. |
[32] [37] [39] [40] |
Lung bud organoids (LBOs) | hPSCs hESCs |
Goblet cells (MUC5AC+, MUC5B) Ciliated cells (FOXJ1) Club cells (CC10) Basal cells (p63+) ATII cells (SFTPC, SFTPB, ABCA3, HT2-280) ATI cells (HT1-56, HOPX, PDPN, CAV1, SCNN1A, AKAP5, CLIC5) Neuroendocrine cells (SNY, CHGA) |
Lung development, Epithelial fate decisions, Pulmonary fibrosis. |
Terminal maturation, Branching appears random, Exact nature and patterning of the mechanism unclear, Biased toward distal lung. |
[17] [41] [39] |
Human proximal airway organoids (hAWOs) | hPSCs | Multi-ciliated cells (FOXJ1) Goblet cells (MUC5AC+) Basal cells (TP63+, KRT5+) Club cells (SCGB3A2+) |
Inherited airway diseases (cystic fibrosis, primary ciliary dyskinesia), Drug screening, Precision medicine. |
[35] [42] |
|
Human alveolar organoids (hALOs) | hPSCs lung epithelial stem lung progenitor cells |
ATII cells (SFTPC) ATI cells (PDPN) |
Respiratory diseases (idiopathic pulmonary fibrosis, tuberculosis infection, respiratory virus infection), Individualized medicine. |
Hard to model inflate and deflate during gas exchange; Lack of developed vasculature. |
[43] [42] |