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. 2022 Sep 4;11(17):2758. doi: 10.3390/cells11172758

Table 1.

Identification and application of existing lung organoids.

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]