Osteolectin increases bone elongation and body length by promoting growth plate chondrocyte proliferation

Author:

Zhang Jingzhu1ORCID,Du Liming1,Davis Bethany1,Gu Zhimin1,Lyu Junhua1,Zhao Zhiyu1,Xu Jian1ORCID,Morrison Sean J.123ORCID

Affiliation:

1. Children’s Research Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390

2. Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX 75390

3. HHMI, University of Texas Southwestern Medical Center, Dallas, TX 75390

Abstract

Osteolectin is a recently identified osteogenic growth factor that binds to Integrin α11 (encoded byItga11), promoting Wnt pathway activation and osteogenic differentiation by bone marrow stromal cells. WhileOsteolectinandItga11are not required for the formation of the skeleton during fetal development, they are required for the maintenance of adult bone mass. Genome-wide association studies in humans reported a single-nucleotide variant (rs182722517) 16 kb downstream ofOsteolectinassociated with reduced height and plasma Osteolectin levels. In this study, we tested whether Osteolectin promotes bone elongation and found thatOsteolectin-deficient mice have shorter bones than those of sex-matched littermate controls. Integrin α11 deficiency in limb mesenchymal progenitors or chondrocytes reduced growth plate chondrocyte proliferation and bone elongation. Recombinant Osteolectin injections increased femur length in juvenile mice. Human bone marrow stromal cells edited to contain the rs182722517 variant produced less Osteolectin and underwent less osteogenic differentiation than that of control cells. These studies identify Osteolectin/Integrin α11 as a regulator of bone elongation and body length in mice and humans.

Funder

Howard Hughes Medical Institute

Josephine Hughes Sterling Foundation

HHS | National Institutes of Health

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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