The Lymphatic Endothelial Cell Secretome Inhibits Osteoblast Differentiation and Bone Formation

Author:

Solorzano Ernesto123,Alejo Andrew L.1ORCID,Ball Hope C.123ORCID,Robinson Gabrielle T.123,Solorzano Andrea L.1,Safadi Rama4,Douglas Jacob2,Kelly Michael35,Safadi Fayez F.1236

Affiliation:

1. Department of Anatomy and Neurobiology, Northeast Ohio Medical University (NEOMED), Rootstown, OH 44272, USA

2. Musculoskeletal Research Group, NEOMED, Rootstown, OH 44272, USA

3. Basic and Translational Biomedicine (BTB) Graduate Program, College of Graduate Studies, NEOMED, Rootstown, OH 44272, USA

4. College of Arts and Sciences, Kent State University, Kent, OH 44243, USA

5. Department of Pediatric Hematology Oncology and Blood, Cleveland Clinic, Cleveland, OH 44195, USA

6. Rebecca D. Considine Research Institute, Akron Children’s Hospital, Akron, OH 44308, USA

Abstract

Complex lymphatic anomalies (CLAs) are a set of rare diseases with unique osteopathic profiles. Recent efforts have identified how lymphatic-specific somatic activating mutations can induce abnormal lymphatic formations that are capable of invading bone and inducing bone resorption. The abnormal bone resorption in CLA patients has been linked to overactive osteoclasts in areas with lymphatic invasions. Despite these findings, the mechanism associated with progressive bone loss in CLAs remains to be elucidated. In order to determine the role of osteoblasts in CLAs, we sought to assess osteoblast differentiation and bone formation when exposed to the lymphatic endothelial cell secretome. When treated with lymphatic endothelial cell conditioned medium (L-CM), osteoblasts exhibited a significant decrease in proliferation, differentiation, and function. Additionally, L-CM treatment also inhibited bone formation through a neonatal calvaria explant culture. These findings are the first to reveal how osteoblasts may be actively suppressed during bone lymphatic invasion in CLAs.

Funder

Lymphatic Malformation Institute

Basic and Translational Biomedicine (BTB) NEOMED PhD Program

Publisher

MDPI AG

Subject

General Medicine

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