le Viseur Christoph, Hotfilder Marc, Bomken Simon, Wilson Kerrie, Röttgers Silja, Schrauder André, Rosemann Annegret, Irving Julie, Stam Ronald W, Shultz Leonard D, Harbott Jochen, Jürgens Heribert, Schrappe Martin, Pieters Rob, Vormoor Josef
Department of Pediatric Hematology and Oncology, University Children's Hospital Münster, 48129 Münster, Germany.
Cancer Cell. 2008 Jul 8;14(1):47-58. doi: 10.1016/j.ccr.2008.05.015.
We examined the leukemic stem cell potential of blasts at different stages of maturation in childhood acute lymphoblastic leukemia (ALL). Human leukemic bone marrow was transplanted intrafemorally into NOD/scid mice. Cells sorted using the B precursor differentiation markers CD19, CD20, and CD34 were isolated from patient samples and engrafted mice before serial transplantation into primary or subsequent (up to quaternary) recipients. Surprisingly, blasts representative of all of the different maturational stages were able to reconstitute and reestablish the complete leukemic phenotype in vivo. Sorted blast populations mirrored normal B precursor cells with transcription of a number of stage-appropriate genes. These observations inform a model for leukemia-propagating stem cells in childhood ALL.
我们研究了儿童急性淋巴细胞白血病(ALL)不同成熟阶段原始细胞的白血病干细胞潜能。将人白血病骨髓经股骨内移植到NOD/scid小鼠体内。使用B前体分化标志物CD19、CD20和CD34分选的细胞从患者样本中分离出来,并在连续移植到原代或后续(直至第四代)受体小鼠之前植入小鼠体内。令人惊讶的是,代表所有不同成熟阶段的原始细胞能够在体内重建并重新建立完整的白血病表型。分选的原始细胞群体反映了正常B前体细胞,具有许多阶段特异性基因的转录。这些观察结果为儿童ALL中白血病增殖干细胞的模型提供了依据。