Role of LTBP4 in alveolarization, angiogenesis, and fibrosis in lungs

Author:

Bultmann-Mellin Insa1,Dinger Katharina12,Debuschewitz Carolin1,Loewe Katharina M. A.1,Melcher Yvonne1,Plum Miro T. W.1,Appel Sarah2,Rappl Gunter34,Willenborg Sebastian5,Schauss Astrid C.6,Jüngst Christian6,Krüger Marcus378,Dressler Sven9,Nakamura Tomoyuki10,Wempe Frank11,Alejandre Alcázar Miguel A.2,Sterner-Kock Anja1

Affiliation:

1. Center for Experimental Medicine, Medical Faculty, University of Cologne, Cologne, Germany;

2. Department of Pediatrics and Adolescent Medicine, Medical Faculty, University of Cologne, Cologne, Germany;

3. Center for Molecular Medicine Cologne, University of Cologne, Cologne, Germany;

4. Department I of Internal Medicine, University Hospital Cologne, Cologne, Germany;

5. Department of Dermatology, University Hospital Cologne, Cologne, Germany;

6. Cluster of Excellence, Cellular Stress Response in Aging-Related Diseases, Core Facility Imaging, University of Cologne, Cologne, Germany;

7. Cluster of Excellence, Cellular Stress Response in Aging-Related Diseases, Core Facility Proteomics, University of Cologne, Cologne, Germany;

8. Institute for Genetics, University of Cologne, Cologne, Germany;

9. Institute of Medical Immunology, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany;

10. Department of Pharmacology, Kansai Medical University, Osaka, Japan; and

11. Department of Molecular Hematology, University of Frankfurt Medical School, Frankfurt am Main, Germany

Abstract

Deficiency of the extracellular matrix protein latent transforming growth factor-β (TGF-β)-binding protein-4 (LTBP4) results in lack of intact elastic fibers, which leads to disturbed pulmonary development and lack of normal alveolarization in humans and mice. Formation of alveoli and alveolar septation in pulmonary development requires the concerted interaction of extracellular matrix proteins, growth factors such as TGF-β, fibroblasts, and myofibroblasts to promote elastogenesis as well as vascular formation in the alveolar septae. To investigate the role of LTBP4 in this context, lungs of LTBP4-deficient ( Ltbp4−/−) mice were analyzed in close detail. We elucidate the role of LTBP4 in pulmonary alveolarization and show that three different, interacting mechanisms might contribute to alveolar septation defects in Ltbp4−/− lungs: 1) absence of an intact elastic fiber network, 2) reduced angiogenesis, and 3) upregulation of TGF-β activity resulting in profibrotic processes in the lung.

Funder

Hochhaus-Stiftung

Maria Pesch-Stiftung

Imhoff-Stiftung

United Nations Development Programme (UNDP)

Publisher

American Physiological Society

Subject

Cell Biology,Physiology (medical),Pulmonary and Respiratory Medicine,Physiology

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