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Model & assay dataModel characterization

Normal lung organoids: identity and LPS injury

ATII and SCGB1A1/KRT5 profiling, serial morphology, and AT1/AT2 changes after LPS exposure together guide pulmonary-injury model selection, observation timing and endpoint design.

STUDY EVIDENCE

From lung phenotypes to an LPS injury study

ATII, SCGB1A1 (CC10) and KRT5 profiling establishes the alveolar and airway context. Serial morphology and AT1/AT2 readouts under LPS conditions help define observation windows and endpoints for pulmonary-injury studies.

01Alveolar
Alveolar organoid morphology and ATII-associated LysoTracker signal

Alveolar organoid morphology and ATII-associated LysoTracker signal

Bright-field, DAPI, LysoTracker and merged views show alveolar organoid structure and ATII-associated acidic-organelle signal.

Supports selection of alveolar-associated phenotype and injury endpoints
02Airway
SCGB1A1 (CC10), KRT5 and merged signals

SCGB1A1 (CC10), KRT5 and merged signals

Immunofluorescence adds club-cell and basal-cell profiling to distinguish airway- and alveolar-focused questions.

Supports selection of airway-focused assays
03LPS injury | serial morphology
Control and LPS observations on days 1, 5 and 7

Control and LPS observations on days 1, 5 and 7

Serial bright-field views guide post-treatment timing and the transition into quantitative assays.

Supports selection of the injury-study window and sampling points
04LPS injury | alveolar readouts
AT1/AT2 profiling under normal and LPS conditions

AT1/AT2 profiling under normal and LPS conditions

Bright-field, AT1, AT2, DAPI and merged views provide alveolar-cell context under the injury condition.

Supports interpretation of morphology alongside alveolar-cell endpoints

The normal-lung organoid study covers model identity, serial morphology and alveolar readouts under LPS conditions. Candidate safety studies can add program-specific dosing and exposure conditions, appropriate controls and replication, and organ-specific quantitative endpoints.

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