Bone marrow fibrosis is a reactive process, and a central pathological feature of primary myelofibrosis. Revealing the origin of fibroblastic cells in the bone marrow is crucial, as these cells are considered an ideal, and essential target for anti-fibrotic therapy. In 2 recent studies, Decker et al. (2017) and Schneider et al. (2017), by using state-of-the-art techniques including in vivo lineage-tracing, provide evidence that leptin receptor (LepR)-expressing and Gli1-expressing cells are responsible for fibrotic tissue deposition in the bone marrow. However, what is the relationship between these 2 bone marrow cell populations, and what are their relative contributions to bone marrow fibrosis remain unclear. From a drug development perspective, these works bring new cellular targets for bone marrow fibrosis.
CITATION STYLE
Sena, I. F. G., Borges, I. T., Lousado, L., Azevedo, P. O., Andreotti, J. P., Almeida, V. M., … Birbrair, A. (2017). LepR+ cells dispute hegemony with Gli1+ cells in bone marrow fibrosis. Cell Cycle, 16(21), 2018–2022. https://doi.org/10.1080/15384101.2017.1367072
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