GDNF secreted by pre-osteoclasts induces migration of bone marrow mesenchymal stem cells and stimulates osteogenesis

• Published in: BMB reports Vol. 53; no. 12; pp. 646 - 651
• Main Authors: Yi, Sol, Kim, Jihee, Lee, Soo Young
• Format: Journal Article
• Language: Korean
• Published: 생화학분자생물학회 31-12-2020
• Subjects: Bone homeostasis; Bone marrow mesenchymal stem cell; Cell migration; Glial cell-derived neurotrophic factor; Osteogenesis; Glial cell-derived neurotrophic factor; Bone homeostasis; Bone marrow mesenchymal stem cell; Cell migration; Osteogenesis
• ISSN: 1976-6696; 1976-670X

Bone resorption is linked to bone formation via temporal and spatial coupling within the remodeling cycle. Several lines of evidence point to the critical role of coupling factors derived from pre-osteoclasts (POCs) during the regulation of bone marrowderived mesenchymal stem cells (BMMSCs). However, the role of glial cell-derived neurotrophic factor (GDNF) in BMMSCs is not completely understood. Herein, we demonstrate the role of POC-derived GDNF in regulating the migration and osteogenic differentiation of BMMSCs. RNA sequencing revealed GDNF upregulation in POCs compared with monocytes/macrophages. Specifically, BMMSC migration was inhibited by a neutralizing antibody against GDNF in pre-osteoclast-conditioned medium (POC-CM), whereas treatment with a recombinant GDNF enhanced migration and osteogenic differentiation. In addition, POC-CM derived from GDNF knock-downed bone marrow macrophages suppressed BMMSC migration and osteogenic differentiation. SPP86, a small molecule inhibitor, inhibits BMMSC migration and osteogenic differentiation by targeting the receptor tyrosine kinase RET, which is recruited by GDNF into the GFRa1 complex. Overall, this study highlights the role of POC-derived GDNF in BMMSC migration and osteogenic differentiation, suggesting that GDNF regulates bone metabolism. [BMB Reports 2020; 53(12): 646-651]