| Literature DB >> 28976809 |
Isadora F G Sena1, Isabella T Borges1, Luiza Lousado1, Patrick O Azevedo1, Julia P Andreotti1, Viviani M Almeida1, Ana E Paiva1, Gabryella S P Santos1, Daniel A P Guerra1, Pedro H D M Prazeres1, Luanny Souto1, Akiva Mintz2, Alexander Birbrair1,3,4.
Abstract
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.Entities:
Keywords: Gli1+ cells; LepR+ cells; differentiation; fibrosis; microenvironment; perivascular cells
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Year: 2017 PMID: 28976809 PMCID: PMC5731410 DOI: 10.1080/15384101.2017.1367072
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534