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Flagellar membrane fusion and protein exchange in trypanosomes; a new form of cell-cell communication?

机译:锥虫的鞭毛膜融合和蛋白质交换;一种新的单元间通信形式?

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摘要

Diverse structures facilitate direct exchange of proteins between cells, including plasmadesmata in plants and tunnelling nanotubes in bacteria and higher eukaryotes.  Here we describe a new mechanism of protein transfer, flagellar membrane fusion, in the unicellular parasite Trypanosoma brucei. When fluorescently tagged trypanosomes were co-cultured, a small proportion of double-positive cells were observed. The formation of double-positive cells was dependent on the presence of extracellular calcium and was enhanced by placing cells in medium supplemented with fresh bovine serum. Time-lapse microscopy revealed that double-positive cells arose by bidirectional protein exchange in the absence of nuclear transfer.  Furthermore, super-resolution microscopy showed that this process occurred in ≤1 minute, the limit of temporal resolution in these experiments. Both cytoplasmic and membrane proteins could be transferred provided they gained access to the flagellum. Intriguingly, a component of the RNAi machinery (Argonaute) was able to move between cells, raising the possibility that small interfering RNAs are transported as cargo. Transmission electron microscopy showed that shared flagella contained two axonemes and two paraflagellar rods bounded by a single membrane. In some cases flagellar fusion was partial and interactions between cells were transient. In other cases fusion occurred along the entire length of the flagellum, was stable for several hours and might be irreversible. Fusion did not appear to be deleterious for cell function: paired cells were motile and could give rise to progeny while fused. The motile flagella of unicellular organisms are related to the sensory cilia of higher eukaryotes, raising the possibility that protein transfer between cells via cilia or flagella occurs more widely in nature.
机译:多样的结构促进了细胞之间蛋白质的直接交换,包括植物中的血浆等,以及细菌和高级真核生物中隧穿的纳米管。在这里,我们描述了在单细胞寄生虫布鲁氏锥虫中蛋白质转移的新机制,鞭毛膜融合。当荧光标记的锥虫共培养时,观察到小部分的双阳性细胞。双阳性细胞的形成取决于细胞外钙的存在,并且通过将细胞置于补充有新鲜牛血清的培养基中来增强。延时显微镜显示,在没有核转移的情况下,双向蛋白质交换产生了双阳性细胞。此外,超分辨率显微镜显示该过程发生在≤1分钟内,这是这些实验中时间分辨率的极限。只要能够进入鞭毛,细胞质和膜蛋白都可以被转移。有趣的是,RNAi机制(Argonaute)的一个组件能够在细胞之间移动,从而增加了小的干扰RNA作为货物运输的可能性。透射电子显微镜显示,共享鞭毛包含两个轴突和两个鞭毛杆,并由单个膜包围。在某些情况下,鞭毛融合是部分的,细胞之间的相互作用是瞬时的。在其他情况下,融合会沿着鞭毛的整个长度发生,稳定数小时,并且可能是不可逆的。融合似乎对细胞功能无害:成对的细胞是能动的,融合后会产生后代。单细胞生物的运动鞭毛与高等真核生物的感觉纤毛有关,从而增加了通过纤毛或鞭毛在细胞之间进行蛋白质转移的可能性在自然界中更为广泛。

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