3'-Sialyllactose alleviates bone loss by regulating bone homeostasis.
Ahreum BaekDawoon BaekYoonhee ChoSeongmoon JoJinyoung KimYoontaik HongSeunghee ChoSung-Hoon KimSung Rae ChoPublished in: Communications biology (2024)
Osteoporosis is a common skeletal disease that results in an increased risk of fractures. However, there is no definitive cure, warranting the development of potential therapeutic agents. 3'-Sialyllactose (3'-SL) in human milk regulates many biological functions. However, its effect on bone metabolism remains unknown. This study aimed to investigate the molecular mechanisms underlying the effect of 3'-SL on bone homeostasis. Treatment of human bone marrow stromal cells (hBMSCs) with 3'-SL enhanced osteogenic differentiation and inhibited adipogenic differentiation of hBMSCs. RNA sequencing showed that 3'-SL enhanced laminin subunit gamma-2 expression and promoted osteogenic differentiation via the phosphatidylinositol 3‑kinase/protein kinase B signaling pathway. Furthermore, 3'-SL inhibited the receptor activator of nuclear factor κB ligand-induced osteoclast differentiation of bone marrow-derived macrophages through the nuclear factor κB and mitogen‑activated protein kinase signaling pathway, ameliorated osteoporosis in ovariectomized mice, and positively regulated bone remodeling. Our findings suggest 3'-SL as a potential drug for osteoporosis.
Keyphrases
- bone loss
- nuclear factor
- bone mineral density
- protein kinase
- bone marrow
- toll like receptor
- mesenchymal stem cells
- postmenopausal women
- signaling pathway
- human milk
- body composition
- pi k akt
- endothelial cells
- soft tissue
- epithelial mesenchymal transition
- low birth weight
- inflammatory response
- metabolic syndrome
- poor prognosis
- single cell
- drug induced
- diabetic rats
- transcription factor
- preterm infants
- squamous cell carcinoma
- emergency department
- cell proliferation
- rectal cancer
- preterm birth
- long non coding rna