a Department of Pathology , Federal University of Minas Gerais , Belo Horizonte , MG , Brazil.
b Department of Radiology , Columbia University Medical Center , New York , NY , USA.
Cell Cycle. 2017;16(21):2018-2022. doi: 10.1080/15384101.2017.1367072. Epub 2017 Oct 4.
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.
骨髓纤维化是一种反应性过程,也是原发性骨髓纤维化的中心病理特征。揭示骨髓中纤维母细胞的起源至关重要,因为这些细胞被认为是抗纤维化治疗的理想和必要靶点。在最近的两项研究中,Decker 等人(2017 年)和 Schneider 等人(2017 年)采用包括体内谱系追踪在内的最先进技术,提供了证据表明瘦素受体(LepR)表达细胞和 Gli1 表达细胞负责骨髓纤维化组织的沉积。然而,这两种骨髓细胞群之间的关系是什么,它们对骨髓纤维化的相对贡献是什么,目前尚不清楚。从药物开发的角度来看,这些研究为骨髓纤维化带来了新的细胞靶点。