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Osteoblast-Osteoclast Communication and Bone Homeostasis

Cells · 2020 · Vol. 9(9) · pp. 2073–2073
Jung‐Min KimChujiao LinZheni StavreMatthew B. GreenblattJae‐Hyuck Shim

Abstract

Bone remodeling is tightly regulated by a cross-talk between bone-forming osteoblasts and bone-resorbing osteoclasts. Osteoblasts and osteoclasts communicate with each other to regulate cellular behavior, survival and differentiation through direct cell-to-cell contact or through secretory proteins. A direct interaction between osteoblasts and osteoclasts allows bidirectional transduction of activation signals through EFNB2-EPHB4, FASL-FAS or SEMA3A-NRP1, regulating differentiation and survival of osteoblasts or osteoclasts. Alternatively, osteoblasts produce a range of different secretory molecules, including M-CSF, RANKL/OPG, WNT5A, and WNT16, that promote or suppress osteoclast differentiation and development. Osteoclasts also influence osteoblast formation and differentiation through secretion of soluble factors, including S1P, SEMA4D, CTHRC1 and C3. Here we review the current knowledge regarding membrane bound- and soluble factors governing cross-talk between osteoblasts and osteoclasts.

Bone Metabolism and DiseasesBone health and treatmentsBone and Dental Protein StudiesOsteoclastRANKLOsteoblastCell biologyChemistryBone remodelingCellular differentiationSignal transductionEndocrinologyBiology

MeSH terms

Bone and BonesCell CommunicationCell DifferentiationHomeostasisHumansOsteoblastsOsteoclastsSignal TransductionBone Remodeling

Funding

  • National Institutes of Health
  • National Institute of Arthritis and Musculoskeletal and Skin Diseases
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