Suppr超能文献

恶性疟原虫溶血磷脂酰基转移酶1在细胞周期进程和胞口内化中的关键作用。

Pivotal roles of Plasmodium falciparum lysophospholipid acyltransferase 1 in cell cycle progression and cytostome internalization.

作者信息

Fukumoto Junpei, Yoshida Minako, Tokuoka Suzumi M, H Hayakawa Eri Saki, Miyazaki Shinya, Sakura Takaya, Inaoka Daniel Ken, Kita Kiyoshi, Usukura Jiro, Shindou Hideo, Tokumasu Fuyuki

机构信息

Department of Cellular Architecture Studies, Division of Shionogi Global Infectious Diseases Division, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan.

Research Fellow of Japan Society for the Promotion of Science, Nagasaki, Japan.

出版信息

Commun Biol. 2025 Jan 29;8(1):142. doi: 10.1038/s42003-025-07564-4.

Abstract

The rapid intraerythrocytic replication of Plasmodium falciparum, a deadly species of malaria parasite, requires a quick but constant supply of phospholipids to support marked cell membrane expansion. In the malarial parasite, many enzymes functioning in phospholipid synthesis pathway have not been identified or characterized. Here, we identify P. falciparum lysophospholipid acyltransferase 1 (PfLPLAT1) and show that PfLPLAT1 is vital for asexual parasite cell cycle progression and cytostome internalization. Deficiency in PfLPLAT1 results in decreased parasitemia and prevents transition to the schizont stage. Parasites lacking PfLPLAT1 also exhibit distinctive omega-shaped vacuoles, indicating disrupted cytostome function. Transcriptomic analyses suggest that this deficiency impacts DNA replication and cell cycle regulation. Mass spectrometry-based enzyme assay and lipidomic analysis demonstrate that recombinant PfLPLAT1 exhibits lysophospholipid acyltransferase activity with a preference for unsaturated fatty acids as its acyl donors and lysophosphatidic acids as an acceptor, with its conditional knockout leading to abnormal lipid composition and marked morphological and developmental changes including stage arrest. These findings highlight PfLPLAT1 as a potential target for antimalarial therapy, particularly due to its unique role and divergence from human orthologs.

摘要

恶性疟原虫是一种致命的疟原虫,其在红细胞内的快速复制需要快速且持续地供应磷脂,以支持显著的细胞膜扩张。在疟原虫中,许多参与磷脂合成途径的酶尚未被鉴定或表征。在此,我们鉴定了恶性疟原虫溶血磷脂酰转移酶1(PfLPLAT1),并表明PfLPLAT1对无性疟原虫细胞周期进程和胞口内化至关重要。PfLPLAT1的缺陷导致疟原虫血症降低,并阻止向裂殖体阶段的转变。缺乏PfLPLAT1的疟原虫还表现出独特的ω形液泡,表明胞口功能受到破坏。转录组分析表明,这种缺陷影响DNA复制和细胞周期调控。基于质谱的酶活性测定和脂质组分析表明,重组PfLPLAT1表现出溶血磷脂酰转移酶活性,偏好不饱和脂肪酸作为其酰基供体,溶血磷脂酸作为受体,其条件性敲除导致脂质组成异常以及包括阶段停滞在内的显著形态和发育变化。这些发现突出了PfLPLAT1作为抗疟治疗潜在靶点的地位,特别是由于其独特的作用以及与人类同源物的差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/813b/11779973/048c52fc6085/42003_2025_7564_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验