Identification of a myofibroblast differentiation program during neonatal lung development

Author:

Yin Yongjun1ORCID,Koenitzer Jeffrey R.2ORCID,Patra Debabrata1ORCID,Dietmann Sabine13ORCID,Bayguinov Peter4ORCID,Hagan Andrew S.1ORCID,Ornitz David M.1ORCID

Affiliation:

1. Washington University School of Medicine 1 Department of Developmental Biology , , St. Louis, MO 63110 , USA

2. Washington University School of Medicine 2 Department of Medicine , , St. Louis, MO 63110 , USA

3. Institute for Informatics, Data Science and Biostatistics, Washington University School of Medicine 3 , St. Louis, MO 63110 , USA

4. Washington University School of Medicine 4 Department of Neuroscience , , St. Louis, MO 63110 , USA

Abstract

ABSTRACT Alveologenesis is the final stage of lung development in which the internal surface area of the lung is increased to facilitate efficient gas exchange in the mature organism. The first phase of alveologenesis involves the formation of septal ridges (secondary septae) and the second phase involves thinning of the alveolar septa. Within secondary septa, mesenchymal cells include a transient population of alveolar myofibroblasts (MyoFBs) and a stable but poorly described population of lipid-rich cells that have been referred to as lipofibroblasts or matrix fibroblasts (MatFBs). Using a unique Fgf18CreER lineage trace mouse line, cell sorting, single-cell RNA sequencing and primary cell culture, we have identified multiple subtypes of mesenchymal cells in the neonatal lung, including an immature progenitor cell that gives rise to mature MyoFB. We also show that the endogenous and targeted ROSA26 locus serves as a sensitive reporter for MyoFB maturation. These studies identify a MyoFB differentiation program that is distinct from other mesenchymal cell types and increases the known repertoire of mesenchymal cell types in the neonatal lung.

Funder

National Institutes of Health

American Heart Association

National Cancer Institute

Publisher

The Company of Biologists

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