Vascular endothelium plays a key role in directing pulmonary epithelial cell differentiation

Author:

Yao Jiayi1,Guihard Pierre J.1ORCID,Wu Xiuju1,Blazquez-Medela Ana M.1,Spencer Melissa J.2ORCID,Jumabay Medet1ORCID,Tontonoz Peter345,Fogelman Alan M.6,Boström Kristina I.15,Yao Yucheng17ORCID

Affiliation:

1. Division of Cardiology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA

2. Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA

3. Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA

4. Department of Pathology and Laboratory Medicine, Howard Hughes Medical Institute, University of California, Los Angeles, Los Angeles, CA

5. Molecular Biology Institute, University of California, Los Angeles, Los Angeles, CA

6. Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA

7. Jonsson Comprehensive Cancer Center, University of California, Los Angeles, Los Angeles, CA

Abstract

The vascular endothelium is critical for induction of appropriate lineage differentiation in organogenesis. In this study, we report that dysfunctional pulmonary endothelium, resulting from the loss of matrix Gla protein (MGP), causes ectopic hepatic differentiation in the pulmonary epithelium. We demonstrate uncontrolled induction of the hepatic growth factor (HGF) caused by dysregulated cross talk between pulmonary endothelium and epithelium in Mgp-null lungs. Elevated HGF induced hepatocyte nuclear factor 4 α (Hnf4a), which competed with NK2 homeobox 1 (Nkx2.1) for binding to forkhead box A2 (Foxa2) to drive hepatic differentiation in Mgp-null airway progenitor cells. Limiting endothelial HGF reduced Hnf4a, abolished interference of Hnf4a with Foxa2, and reduced hepatic differentiation in Mgp-null lungs. Together, our results suggest that endothelial–epithelial interactions, maintained by MGP, are essential in pulmonary cell differentiation.

Funder

National Institutes of Health

American Heart Association

Publisher

Rockefeller University Press

Subject

Cell Biology

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