The Biphasic Activity of Auricularia Auricula-Judae Extract on Bone Homeostasis through Inhibition of Osteoclastogenesis and Modulation of Osteogenic Activity

J Microbiol Biotechnol. 2024 Dec 28;34(12):2576-2585. doi: 10.4014/jmb.2408.08055. Epub 2024 Oct 28.

Abstract

Osteoporosis arises from the disturbance of bone homeostasis, a process regulated by osteoblasts and osteoclasts. The treatment and prevention of bone metabolic disorders resulting from an imbalance in bone homeostasis require the use of agents that effectively promote both bone formation and anti-resorptive effects. Therefore, an investigation was carried out to determine the potential of the edible mushroom Auricularia auricula-judae in modulating bone remodeling by inhibiting RANKL-induced osteoclastogenesis and enhancing BMP-2-stimulated osteoblast differentiation. Moreover, this study assessed the mode of action of the Auricularia auricula-judae extracts. The staining of tartrate-resistant acid phosphatase (TRAP), a marker for osteoclast activity, demonstrated that Auricularia auricula-judae water extract (AAJWE) inhibited the formation of multinucleated osteoclasts while exhibiting no cytotoxic effects. The study demonstrated that AAJWE reduced RANKL-induced osteoclast differentiation by inhibiting c-Fos/NFATc1 through the inhibition of ERK and JNK phosphorylation during the RANKL-induced osteoclast differentiation. Moreover, AAJWE exhibited a dose-dependent induction of ALP expression in the presence of BMP-2 during osteoblast differentiation. The AAJWE strengthened BMP-2-induced osteogenesis through the activation of Runx2 and Smad phosphorylation. Therefore, AAJWE emerges as a promising candidate for both prevention and therapy owing to its biphasic effect, which aids in the preservation of bone homeostasis.

Keywords: Auricularia auricula-jadae; bone hemostasis; osteoblasts; osteoclasts; osteoporosis.

MeSH terms

  • Animals
  • Basidiomycota / chemistry
  • Bone Morphogenetic Protein 2* / metabolism
  • Bone and Bones / drug effects
  • Bone and Bones / metabolism
  • Cell Differentiation* / drug effects
  • Core Binding Factor Alpha 1 Subunit / genetics
  • Core Binding Factor Alpha 1 Subunit / metabolism
  • Homeostasis* / drug effects
  • Mice
  • NFATC Transcription Factors / metabolism
  • Osteoblasts* / drug effects
  • Osteoblasts* / metabolism
  • Osteoclasts* / drug effects
  • Osteoclasts* / metabolism
  • Osteogenesis* / drug effects
  • Phosphorylation / drug effects
  • Proto-Oncogene Proteins c-fos / metabolism
  • RANK Ligand* / metabolism
  • RAW 264.7 Cells
  • Tartrate-Resistant Acid Phosphatase / metabolism

Substances

  • Bone Morphogenetic Protein 2
  • RANK Ligand
  • NFATC Transcription Factors
  • Tartrate-Resistant Acid Phosphatase
  • Core Binding Factor Alpha 1 Subunit
  • Tnfsf11 protein, mouse
  • Bmp2 protein, mouse
  • Nfatc1 protein, mouse
  • Proto-Oncogene Proteins c-fos