间质细胞
骨髓
间充质干细胞
造血
干细胞
医学
造血干细胞
人口
地中海贫血
内科学
癌症研究
免疫学
生物
病理
细胞生物学
环境卫生
作者
Stefania Crippa,Valeria Rossella,Annamaria Aprile,Laura Silvestri,Silvia Rivis,Samantha Scaramuzza,Stefania Pirroni,Maria Antonietta Avanzini,Luca Basso‐Ricci,Raisa Jofra Hernández,Marco Zecca,Sarah Marktel,Fabio Ciceri,Alessandro Aiuti,Giuliana Ferrari,Maria Ester Bernardo
摘要
BACKGROUND. The human bone marrow (BM) niche contains a population of mesenchymal stromal cells (MSCs) that provide physical support and regulate hematopoietic stem cell (HSC) homeostasis. β-Thalassemia (BT) is a hereditary disorder characterized by altered hemoglobin beta-chain synthesis amenable to allogeneic HSC transplantation and HSC gene therapy. Iron overload (IO) is a common complication in BT patients affecting several organs. However, data on the BM stromal compartment are scarce.
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