Multi‐organ phenotypes in mice lacking latent TGFβ binding protein 2 (LTBP2)

Author:

Bodmer Nicholas K.12ORCID,Knutsen Russell H.2,Roth Robyn A.2,Castile Ryan M.3,Brodt Michael D.4,Gierasch Carrie M.5,Broekelmann Thomas J.2,Gibson Mark A.6,Haspel Jeffrey A.5,Lake Spencer P.3,Koenitzer Jeffrey R.5,Brody Steven L.5,Silva Matthew J.4,Mecham Robert P.2,Ornitz David M.1ORCID

Affiliation:

1. Department of Developmental Biology Washington University School of Medicine St Louis Missouri USA

2. Department of Cell Biology and Physiology Washington University School of Medicine St Louis Missouri USA

3. Department of Mechanical Engineering and Materials Science Washington University School of Engineering St Louis Missouri USA

4. Department of Orthopedic Surgery Washington University School of Medicine St Louis Missouri USA

5. Division of Pulmonary & Critical Care Medicine, Department of Medicine Washington University School of Medicine St Louis Missouri USA

6. Discipline of Anatomy and Pathology, School of Medicine University of Adelaide Adelaide South Australia Australia

Abstract

AbstractBackgroundLatent TGFβ binding protein‐2 (LTBP2) is a fibrillin 1 binding component of the microfibril. LTBP2 is the only LTBP protein that does not bind any isoforms of TGFβ, although it may interfere with the function of other LTBPs or interact with other signaling pathways.ResultsHere, we investigate mice lacking Ltbp2 (Ltbp2−/−) and identify multiple phenotypes that impact bodyweight and fat mass, and affect bone and skin development. The alterations in skin and bone development are particularly noteworthy since the strength of these tissues is differentially affected by loss of Ltbp2. Interestingly, some tissues that express high levels of Ltbp2, such as the aorta and lung, do not have a developmental or homeostatic phenotype.ConclusionsAnalysis of these mice show that LTBP2 has complex effects on development through direct effects on the extracellular matrix (ECM) or on signaling pathways that are known to regulate the ECM.

Funder

National Center for Advancing Translational Sciences

National Institute of Allergy and Infectious Diseases

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Publisher

Wiley

Subject

Developmental Biology

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