# In silico modeling of anterior foregut endoderm differentiation towards lung epithelial progenitors

## TL;DR

This paper uses mathematical modeling to improve the process of turning stem cells into lung cells, which could help in understanding lung development and regenerative medicine.

## Contribution

The paper introduces the first mathematical model for the population dynamics of differentiating anterior foregut endoderm into lung progenitors.

## Key findings

- Daily media change nearly doubles lung progenitor yields compared to cultures without media replenishment.
- Higher split ratios on day 10 increase differentiation efficiency by 26%.

## Abstract

Directed differentiation of human induced pluripotent stem cells (iPSCs) into anterior foregut endoderm (AFE) and lung progenitors (LPs) has wide-ranging implications for lung developmental biology, disease modeling, and regenerative medicine. We expand on a previously developed mathematical modeling framework and apply it to the directed differentiation of AFE into LPs. A model-based approach guides experimental design, followed by a multistage model inference process: maximum likelihood estimation based on in vitro data and identifiability analyses to eliminate unidentifiable candidates, thereby guiding model selection. To the authors’ knowledge, this is the first mathematical model of the population dynamics of directed differentiation of AFE into LPs. The model suggests that the overall dynamics are primarily driven by AFE proliferation and differentiation into LPs. In silico experiments predict that daily media change nearly doubles LP yields compared to cultures without media replenishment. Moreover, the model suggests that higher split ratios on day 10 enhance yield per input cell, a measure of differentiation efficiency, by 26%. This work provides a blueprint for refining iPSC-based lung lineage differentiation protocols by combining empirical data and mathematical modeling.