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液泡型三磷酸腺苷酶耗竭导致布氏锥虫血液体形式的内吞作用失调。

Vacuolar ATPase depletion contributes to dysregulation of endocytosis in bloodstream forms of Trypanosoma brucei.

机构信息

Center for Parasitic Organisms, State Key Laboratory of Biocontrol, School of Life Sciences, and Key Laboratory of Tropical Disease Control (Sun Yat-Sen University), Ministry of Education, Sun Yat-Sen University, Guangzhou, 510275, The People's Republic of China.

Department of Biological Sciences, National University of Singapore, Singapore, 11754, Singapore.

出版信息

Parasit Vectors. 2020 Apr 25;13(1):214. doi: 10.1186/s13071-020-04068-4.

Abstract

BACKGROUND

Vacuolar H-ATPase (V-ATPase) is a highly conserved protein complex which hydrolyzes ATP and pumps protons to acidify vacuolar vesicles. Beyond its role in pH maintenance, the involvement of V-ATPase in endocytosis is well documented in mammals and plants but is less clear in Trypanosoma brucei.

METHODS

In this study, the subcellular localization of V-ATPase subunit B (TbVAB) of T. brucei was assessed via in situ N-terminal YFP-tagging and immunofluorescence assays. Transgenic bloodstream forms (BSF) of T. brucei were generated which comprised either a V-ATPase subunit B (TbVAB) conditional knockout or a V-ATPase subunit A (TbVAA) knockdown. Acridine orange and BCECF-AM were employed to assess the roles of V-ATPase in the pH regulation of BSF T. brucei. The endocytic activities of three markers were also characterized by flow cytometry analyses. Furthermore, trypanosomes were counted from trypanolysis treatment groups (either containing 1% or 5% NHS) and endocytosed trypanosome lytic factor (TLF) was also analyzed by an immunoblotting assay.

RESULTS

TbVAB was found to localize to acidocalcisomes, lysosomes and probably also to endosomes of BSF of T. brucei and was demonstrated to be essential for cell growth. TbVAB depletion neutralized acidic organelles at 24 hours post-tetracycline depletion (hpd), meanwhile the steady state intracellular pH increased from 7.016 ± 0.013 to 7.422 ± 0.058. Trypanosomes with TbVAB depletion at 24 hpd were found to take up more transferrin (2.068 ± 0.277 fold) but less tomato lectin (49.31 ± 22.57%) by endocytosis, while no significant change was detected in dextran uptake. Similar endocytic dysregulated phenotypes were also observed in TbVAA knockdown cells. In addition, TbVAB depleted trypanosomes showed a low uptake of TLF and exhibited less sensitive to lysis in both 1% and 5% NHS treatments.

CONCLUSIONS

TbVAB is a key component of V-ATPase and was found to play a key function in endocytosis as well as exhibiting different effects in a receptor/cargo dependent manner in BSF of T. brucei. Besides vacuolar alkalinization, the dysregulation of endocytosis in TbVAB depleted T. brucei is considered to contribute to the reduced sensitivity to lysis by normal human serum.

摘要

背景

液泡型 H+-ATP 酶(V-ATPase)是一种高度保守的蛋白复合物,可水解 ATP 并泵出质子,使液泡囊泡酸化。除了在 pH 值维持中的作用外,V-ATPase 参与内吞作用在哺乳动物和植物中已有很好的记录,但在布氏锥虫中则不太清楚。

方法

在这项研究中,通过原位 N 端 YFP 标记和免疫荧光测定评估了布氏锥虫 V-ATPase 亚基 B(TbVAB)的亚细胞定位。生成了包含 V-ATPase 亚基 B(TbVAB)条件性缺失或 V-ATPase 亚基 A(TbVAA)敲低的布氏锥虫血流形式(BSF)的转基因生物。使用吖啶橙和 BCECF-AM 评估 V-ATPase 在 BSF 布氏锥虫 pH 值调节中的作用。还通过流式细胞术分析了三种标记物的内吞作用。此外,从含有 1%或 5%NHS 的锥虫溶解处理组中计数锥虫,并通过免疫印迹分析也分析了内吞的锥虫溶细胞因子(TLF)。

结果

发现 TbVAB 定位于 BSF 的液泡钙调蛋白、溶酶体,可能还有内体,并被证明对细胞生长至关重要。TbVAB 耗尽在四环素耗尽后 24 小时(hpd)使酸性细胞器中和,同时细胞内 pH 值从 7.016±0.013 增加到 7.422±0.058。在 24 hpd 时 TbVAB 耗尽的锥虫被发现通过内吞作用摄取更多转铁蛋白(2.068±0.277 倍),但摄取的番茄凝集素较少(49.31±22.57%),而葡聚糖摄取没有明显变化。在 TbVAA 敲低细胞中也观察到类似的内吞作用失调表型。此外,耗尽 TbVAB 的锥虫对 TLF 的摄取减少,并且在 1%和 5%NHS 处理中对裂解的敏感性降低。

结论

TbVAB 是 V-ATPase 的关键组成部分,在布氏锥虫 BSF 中被发现在内吞作用中发挥关键作用,并以受体/ cargo 依赖的方式表现出不同的作用。除了液泡碱化外,耗尽 TbVAB 的锥虫内吞作用失调被认为导致对正常人血清裂解的敏感性降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0522/7183646/1709bc680314/13071_2020_4068_Fig1_HTML.jpg

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