The bloodstream stage of Trypanosoma brucei, the causative agent of African trypanosomiasis, is characterized by its high rate of endocytosis, which is involved in remodeling of its surface coat. Here we present evidence that RNAi-mediated expression down-regulation of vacuolar protein sorting 41 (Vps41), a component of the homotypic fusion and vacuole protein sorting (HOPS) complex, leads to a strong inhibition of endocytosis, vesicle accumulation, enlargement of the flagellar pocket ("big eye" phenotype), and dramatic effect on cell growth. Unexpectedly, other functions described for Vps41 in mammalian cells and yeasts, such as delivery of proteins to lysosomes, and lysosome-related organelles (acidocalcisomes) were unaffected, indicating that in trypanosomes post-Golgi trafficking is distinct from that of mammalian cells and yeasts. The essentiality of TbVps41 suggests that it is a potential drug target.
TbVps41 regulates trafficking of endocytic but not biosynthetic cargo to lysosomes of bloodstream forms of Trypanosoma brucei.
TbVps41 调节布氏锥虫血液型内吞作用物质向溶酶体的运输,但不调节生物合成物质向溶酶体的运输
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作者:Ramakrishnan Srinivasan, Baptista Rodrigo P, Asady Beejan, Huang Guozhong, Docampo Roberto
| 期刊: | FASEB Journal | 影响因子: | 4.200 |
| 时间: | 2021 | 起止号: | 2021 Jun;35(6):e21641 |
| doi: | 10.1096/fj.202100487R | 研究方向: | 免疫/内分泌 |
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