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首页> 外文期刊>Infection and immunity >Neurotrophin Receptor TrkC Is an Entry Receptor for Trypanosoma cruzi in Neural, Glial, and Epithelial Cells
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Neurotrophin Receptor TrkC Is an Entry Receptor for Trypanosoma cruzi in Neural, Glial, and Epithelial Cells

机译:Neurotrophin受体TrkC是神经,神经胶质和上皮细胞中的克鲁氏锥虫的进入受体

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摘要

Trypanosoma cruzi, the agent of Chagas' disease, infects a variety of mammalian cells in a process that includes multiple cycles of intracellular division and differentiation starting with host receptor recognition by a parasite ligand(s). Earlier work in our laboratory showed that the neurotrophin-3 (NT-3) receptor TrkC is activated by T. cruzi surface trans-sialidase, also known as parasite-derived neurotrophic factor (PDNF). However, it has remained unclear whether TrkC is used by T. cruzi to enter host cells. Here, we show that a neuronal cell line (PC12-NNR5) relatively resistant to T. cruzi became highly susceptible to infection when overexpressing human TrkC but not human TrkB. Furthermore, trkC transfection conferred an ~3.0-fold intracellular growth advantage. Sialylation-deficient Chinese hamster ovarian (CHO) epithelial cell lines Lec1 and Lec2 also became much more permissive to T. cruzi after transfection with the trkC gene. Additionally, NT-3 specifically blocked T. cruzi infection of the TrkC-NNR5 transfectants and of naturally permissive TrkC-bearing Schwann cells and astrocytes, as did recombinant PDNF. Two specific inhibitors of Trk autophosphorylation (K252a and AG879) and inhibitors of Trk-induced MAPK/Erk (U0126) and Akt kinase (LY294002) signaling, but not an inhibitor of insulin-like growth factor 1 receptor, abrogated TrkC-mediated cell invasion. Antibody to TrkC blocked T. cruzi infection of the TrkC-NNR5 transfectants and of cells that naturally express TrkC. The TrkC antibody also significantly and specifically reduced cutaneous infection in a mouse model of acute Chagas' disease. TrkC is ubiquitously expressed in the peripheral and central nervous systems, and in nonneural cells infected by T. cruzi, including cardiac and gastrointestinal muscle cells. Thus, TrkC is implicated as a functional PDNF receptor in cell entry, independently of sialic acid recognition, mediating broad T. cruzi infection both in vitro and in vivo.
机译:恰加斯氏锥虫(Trypanosoma cruzi)是恰加斯氏病的病原体,在一个过程中感染了多种哺乳动物细胞,该过程包括多个细胞内分裂和分化周期,这些过程始于宿主受体被寄生虫配体识别。在我们实验室的早期工作中,神经营养蛋白3(NT-3)受体TrkC被克鲁维氏锥虫表面转唾液酸酶激活,也称为寄生虫衍生的神经营养因子(PDNF)。然而,尚不清楚克鲁维球菌是否使用TrkC进入宿主细胞。在这里,我们显示了相对抗克鲁斯氏菌的神经元细胞系(PC12-NNR5)在过度表达人TrkC而不是人TrkB时变得极易感染。此外,trkC转染可提供约3.0倍的细胞内生长优势。唾液酸化缺陷的中国仓鼠卵巢(CHO)上皮细胞系Lec1和Lec2在用trkC基因转染后也变得对克鲁斯氏锥虫更宽容。另外,与重组PDNF一样,NT-3特异性阻断TrkC-NNR5转染子以及天然允许携带TrkC的雪旺氏细胞和星形胶质细胞的克鲁氏杆菌感染。两种特异性的Trk自磷酸化抑制剂(K252a和AG879)和Trk诱导的MAPK / Erk(U0126)和Akt激酶(LY294002)信号抑制剂,但不是胰岛素样生长因子1受体抑制剂,废除了TrkC介导的细胞侵袭。 。 TrkC抗体阻断了TrkC-NNR5转染子和天然表达TrkC的细胞的克鲁氏杆菌感染。在急性恰加斯氏病小鼠模型中,TrkC抗体还可以显着并特异性地减少皮肤感染。 TrkC在周围和中枢神经系统中以及在被克鲁氏杆菌感染的非神经细胞中广泛表达,包括心脏和胃肠道肌肉细胞。因此,TrkC被认为是功能性PDNF受体进入细胞,独立于唾液酸识别,在体内和体外介导广泛的克鲁氏锥虫感染。

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