骨髓
骨髓纤维化
生物
造血
间质细胞
间充质干细胞
祖细胞
干细胞
癌症研究
免疫学
细胞生物学
作者
Christophe Martinaud,Christophe Desterke,Johanna Konopacki,Alessandro M. Vannucchi,Lisa Pieri,Paola Guglielmelli,Brigitte Dupriez,Jean‐Christophe Ianotto,Laetitia Boutin,Jean‐Jacques Lataillade,Marie‐Caroline Le Bousse‐Kerdilès
标识
DOI:10.1016/j.gdata.2015.04.017
摘要
Primary myelofibrosis (PMF) is a clonal myeloproliferative neoplasm whose severity and treatment complexity are attributed to the presence of bone marrow (BM) fibrosis and alterations of stroma impairing the production of normal blood cells. Despite the recently discovered mutations including the JAK2V617F mutation in about half of patients, the primitive event responsible for the clonal proliferation is still unknown. In the highly inflammatory context of PMF, the presence of fibrosis associated with a neoangiogenesis and an osteosclerosis concomitant to the myeloproliferation and to the increase number of circulating hematopoietic progenitors suggests that the crosstalk between hematopoietic and stromal cells is deregulated in the PMF BM microenvironmental niches. Within these niches, mesenchymal stromal cells (BM-MSC) play a hematopoietic supportive role in the production of growth factors and extracellular matrix which regulate the proliferation, differentiation, adhesion and migration of hematopoietic stem/progenitor cells. A transcriptome analysis of BM-MSC in PMF patients will help to characterize their molecular alterations and to understand their involvement in the hematopoietic stem/progenitor cell deregulation that features PMF.
科研通智能强力驱动
Strongly Powered by AbleSci AI