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Access to Follicular Dendritic Cells Is a Pivotal Step in Murine Chronic Lymphocytic Leukemia B-cell Activation and Proliferation

机译:滤泡树突状细胞的访问是小鼠慢性淋巴细胞性白血病B细胞活化和增殖的关键一步。

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摘要

In human chronic lymphocytic leukemia (CLL) pathogenesis, B-cell antigen receptor signaling seems important for leukemia B-cell ontogeny, whereas the microenvironment influences B-cell activation, tumor cell lodging, and provision of antigenic stimuli. Using the murine E mu-Tcl1 CLL model, we demonstrate that CXCR5-controlled access to follicular dendritic cells confers proliferative stimuli to leukemia B cells. Intravital imaging revealed a marginal zone B cell-like leukemia cell trafficking route. Murine and human CLL cells reciprocally stimulated resident mesenchymal stromal cells through lymphotoxin-beta-receptor activation, resulting in CXCL13 secretion and stromal compartment remodeling. Inhibition of lymphotoxin/lymphotoxin-beta-receptor signaling or of CXCR5 signaling retards leukemia progression. Thus, CXCR5 activity links tumor cell homing, shaping a survival niche, and access to localized proliferation stimuli.
机译:在人类慢性淋巴细胞性白血病(CLL)发病机理中,B细胞抗原受体信号转导对于白血病B细胞个体发育似乎很重要,而微环境影响B细胞活化,肿瘤细胞倒伏和抗原刺激的提供。使用鼠E mu-Tcl1 CLL模型,我们证明CXCR5控制访问的滤泡树突状细胞赋予白血病B细胞增殖性刺激。活体内成像显示边缘区B细胞样白血病细胞运输途径。鼠和人CLL细胞通过淋巴毒素β受体的激活相互刺激常驻间充质基质细胞,导致CXCL13分泌和基质区室重塑。淋巴毒素/淋巴毒素-β受体信号转导或CXCR5信号转导的抑制会延迟白血病的进展。因此,CXCR5活性链接肿瘤细胞归巢,塑造生存环境和访问局部增殖刺激。

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