PCLAF induces bone marrow adipocyte senescence and contributes to skeletal aging.
Lingqi XieYalun ChengBiao HuXin ChenYuze AnZhuying XiaGuangping CaiChang-Jun LiHui PengPublished in: Bone research (2024)
Bone marrow adipocytes (BMAds) affect bone homeostasis, but the mechanism remains unclear. Here, we showed that exercise inhibited PCNA clamp-associated factor (PCLAF) secretion from the bone marrow macrophages to inhibit BMAds senescence and thus alleviated skeletal aging. The genetic deletion of PCLAF in macrophages inhibited BMAds senescence and delayed skeletal aging. In contrast, the transplantation of PCLAF-mediated senescent BMAds into the bone marrow of healthy mice suppressed bone turnover. Mechanistically, PCLAF bound to the ADGRL2 receptor to inhibit AKT/mTOR signaling that triggered BMAds senescence and subsequently spread senescence among osteogenic and osteoclastic cells. Of note, we developed a PCLAF-neutralizing antibody and showed its therapeutic effects on skeletal health in old mice. Together, these findings identify PCLAF as an inducer of BMAds senescence and provide a promising way to treat age-related osteoporosis.
Keyphrases
- bone marrow
- dna damage
- mesenchymal stem cells
- endothelial cells
- bone mineral density
- stress induced
- adipose tissue
- healthcare
- high fat diet induced
- cell proliferation
- postmenopausal women
- public health
- insulin resistance
- mental health
- induced apoptosis
- oxidative stress
- gene expression
- soft tissue
- body composition
- cell death
- bone loss
- dna methylation
- resistance training
- binding protein
- human health
- pi k akt