Irradiation-induced secretion of BMP4 by marrow cells causes marrow adipogenesis post-myelosuppression

- Marrow tissue responds to irradiation with de novo expression and secretion of BMP4.
- BMP4 irreversibly commits marrow MSCs to adipogenic lineage.
- Simvastatin prevents BMP4-induced BM adipogenesis by inhibiting Ppar-γ expression.
- Simvastatin does not interfere with irradiation-induced BMP4 secretion.

Pre-transplant myeloablation is associated with marrow adipogenesis, resulting in delayed engraftment of hematopoietic stem cells (HSCs). This is strongly undesirable, especially when the donor HSCs are fewer in numbers or have compromised functionality. The molecular mechanisms behind irradiation-induced marrow adipogenesis have not been extensively investigated. Here we show that bone marrow (BM) cells, especially T-cells and stromal cells, express and secrete copious amounts of BMP4 in response to irradiation, which causes the bone marrow stromal cells to commit to adipocyte lineage, thereby contributing to an increase in bone marrow adipogenesis. We further demonstrate that Simvastatin inhibits the BMP4-mediated adipogenic commitment of marrow stromal cells by inhibiting Ppar-γ expression. Importantly, Simvastatin does not prevent BMP4 secretion by the BM cells, and thus does not interfere with its salutary role in post-transplant hematopoietic regeneration. Our data identify previously unknown mechanisms operative in marrow adipogenesis post-myeloablation. They also reveal the molecular mechanisms behind the advantage of using Simvastatin as a niche-targeting agent to improve HSC engraftment.

Irradiation-induced BMP4 secretion by T cells and stromal cells causes marrow adipogenesis post-myeloablation. Simvastatin inhibits the.BMP4-mediated adipogenic commitment of marrow stromal cells by inhibiting.Ppar-γ expression, but does not prevent BMP4 secretion. Our data suggest that Simvastatin could potentially serve as a good niche-targeting agent in clinical transplantations to minimize post-irradiation adipogenesis and increase the efficiency of HSC engraftment.142