Panicker Leelamma M, Miller Diana, Awad Ola, Bose Vivek, Lun Yu, Park Tea Soon, Zambidis Elias T, Sgambato Judi A, Feldman Ricardo A
Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Stem Cells. 2014 Sep;32(9):2338-49. doi: 10.1002/stem.1732.
Gaucher disease (GD) is an autosomal recessive disorder caused by mutations in the acid β-glucocerebrosidase (GCase; GBA) gene. The hallmark of GD is the presence of lipid-laden Gaucher macrophages, which infiltrate bone marrow and other organs. These pathological macrophages are believed to be the sources of elevated levels of inflammatory mediators present in the serum of GD patients. The alteration in the immune environment caused by GD is believed to play a role in the increased risk of developing multiple myeloma and other malignancies in GD patients. To determine directly whether Gaucher macrophages are abnormally activated and whether their functional defects can be reversed by pharmacological intervention, we generated GD macrophages by directed differentiation of human induced pluripotent stem cells (hiPSC) derived from patients with types 1, 2, and 3 GD. GD hiPSC-derived macrophages expressed higher levels of tumor necrosis factor α, IL-6, and IL-1β than control cells, and this phenotype was exacerbated by treatment with lipopolysaccharide. In addition, GD hiPSC macrophages exhibited a striking delay in clearance of phagocytosed red blood cells, recapitulating the presence of red blood cell remnants in Gaucher macrophages from bone marrow aspirates. Incubation of GD hiPSC macrophages with recombinant GCase, or with the chaperones isofagomine and ambroxol, corrected the abnormal phenotypes of GD macrophages to an extent that reflected their known clinical efficacies. We conclude that Gaucher macrophages are the likely source of the elevated levels of inflammatory mediators in the serum of GD patients and that GD hiPSC are valuable new tools for studying disease mechanisms and drug discovery.
戈谢病(GD)是一种常染色体隐性疾病,由酸性β-葡萄糖脑苷脂酶(GCase;GBA)基因突变引起。GD的标志是存在充满脂质的戈谢巨噬细胞,这些细胞浸润骨髓和其他器官。据信这些病理性巨噬细胞是GD患者血清中炎症介质水平升高的来源。GD引起的免疫环境改变被认为在GD患者发生多发性骨髓瘤和其他恶性肿瘤的风险增加中起作用。为了直接确定戈谢巨噬细胞是否被异常激活,以及它们的功能缺陷是否可以通过药物干预得到逆转,我们通过定向分化来自1型、2型和3型GD患者的人诱导多能干细胞(hiPSC)生成了GD巨噬细胞。与对照细胞相比,GD hiPSC衍生的巨噬细胞表达更高水平的肿瘤坏死因子α、IL-6和IL-1β,并且脂多糖处理会加剧这种表型。此外,GD hiPSC巨噬细胞在吞噬红细胞的清除方面表现出明显延迟,重现了骨髓穿刺物中戈谢巨噬细胞中红细胞残余物的存在。用重组GCase或伴侣异麦角胺和氨溴索孵育GD hiPSC巨噬细胞,在一定程度上纠正了GD巨噬细胞的异常表型,这反映了它们已知的临床疗效。我们得出结论,戈谢巨噬细胞可能是GD患者血清中炎症介质水平升高的来源,并且GD hiPSC是研究疾病机制和药物发现的有价值的新工具。