Osteocyte Cell-Cell Communication Within and Beyond Bone.
Bakker AD., van Santen VJB.
Narrative Review on Systemic / IV, published in Curr Osteoporos Rep (2026) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.
- Study type
- Narrative Review
- Journal
- Curr Osteoporos Rep (2026)
- Country
- United States
- Reported sample size
- —
- Source database
- PubMed
- PMID
- 41961340
- DOI
- 10.1007/s11914-026-00964-3
Abstract (original English)
PURPOSE OF REVIEW: Osteocytes form an extensive cellular network and communicate both with neighboring bone cells and with distant organs. Here, we review evidence on which tissues osteocytes communicate with, and the molecular “language” they use. RECENT FINDINGS: Recent work has expanded osteocyte communication beyond the classical triad of receptor activator of nuclear factor κB ligand, sclerostin, and fibroblast growth factor 23. Within bone, osteocytes coordinate remodeling through direct cell-cell contacts and rapidly released mediators, acting on timescales relevant to mechanotransduction. Beyond bone, osteocytes signal to adipose tissue, muscle, kidney, cartilage, and vasculature. Extracellular vesicles are increasingly implicated as messengers, as their cargo (RNAs and proteins) can influence stem cell lineage allocation and bone–cartilage interactions. Osteocytes may also support vascular function via mitochondria transfer. Osteocytes integrate mechanical and metabolic cues and transmit information through a broader repertoire of signaling molecules than traditionally appreciated. Recognizing the diversity of target cells and mediators will refine concepts of osteocyte-bone and osteocyte-organ crosstalk and highlight mechanisms that could be targeted to reduce skeletal fragility.
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is a narrative review: it collects no new patient data and does not systematically appraise evidence quality.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
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