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T/Tn特异性凝集素可诱导T/Tn抗原阴性的淋巴瘤细胞发生细胞死亡。

The T/Tn-Specific Lectin Induces Cell Death in Lymphoma Cells Negative for T/Tn Antigens.

作者信息

Simplicien Mathias, Barre Annick, Benkerrou Yamina, Van Damme Els J M, Rougé Pierre, Benoist Hervé

机构信息

UMR 152 PharmaDev, Institut de Recherche et Développement, Faculté de Pharmacie, Université Paul, Sabatier, F-31062 Toulouse, France.

Department of Biotechnology, Faculty of Bioscience Engineering, Ghent University, B-9000 Ghent, Belgium.

出版信息

Cancers (Basel). 2021 Aug 28;13(17):4356. doi: 10.3390/cancers13174356.

Abstract

Morniga G is a T/Tn-specific lectin, inducing cell death in Tn-positive leukemias but not in healthy lymphocytes. lectin (HPA) is another T/Tn-specific lectin, currently used as tool for cancer diagnostics. The HPA-mediated tumor cell death was evaluated on human leukemia and mouse lymphoma cells, and compared to the effect of Morniga G. Both lectins induced an equivalent percentage of cell death in Tn-positive Jurkat human leukemia. In contrast, EL4 mouse lymphoma resisted Morniga G-mediated cytotoxicity but were killed by HPA at concentrations of 2.5 μg/mL (0.032 nM) and higher. In both malignant cells, HPA-mediated cell death showed features compatible with apoptosis (annexin-externalization, caspase-activation, mitochondrial membrane depolarization, and ROS production). Cytometry analysis indicated that EL4 cells are T/Tn-negative. Because previous results showed a high amount of -acetylgalactosamine (GalNAc, sugar present in Tn antigen) on EL4 cell surface, this GalNAc could be involved in the formation of truncated -glycans other than the T/Tn residues. When compared to Morniga G, bioinformatic analysis suggested that HPA benefits from an extended carbohydrate-binding site, better adapted than Morniga G to the accommodation of more complex branched and truncated -glycans (such as core 2). Finally, HPA killed EL4 cells but not healthy lymphocytes in a mixture of lymphoma cells + lymphocytes, suggesting that HPA selectively triggers tumor cell death.

摘要

Morniga G是一种特异性识别T/Tn的凝集素,可诱导Tn阳性白血病细胞死亡,但对健康淋巴细胞无此作用。血凝素(HPA)是另一种特异性识别T/Tn的凝集素,目前用作癌症诊断工具。对人白血病细胞和小鼠淋巴瘤细胞评估了HPA介导的肿瘤细胞死亡,并与Morniga G的作用进行比较。两种凝集素在Tn阳性的Jurkat人白血病细胞中诱导的细胞死亡百分比相当。相比之下,EL4小鼠淋巴瘤对Morniga G介导的细胞毒性具有抗性,但在浓度为2.5μg/mL(0.032 nM)及更高时可被HPA杀死。在两种恶性细胞中,HPA介导的细胞死亡均表现出与凋亡相符的特征(膜联蛋白外化、半胱天冬酶激活、线粒体膜去极化和活性氧生成)。细胞计数分析表明EL4细胞为T/Tn阴性。由于先前的结果显示EL4细胞表面存在大量的N-乙酰半乳糖胺(GalNAc,Tn抗原中的糖类),这种GalNAc可能参与了除T/Tn残基之外的截短型O-聚糖的形成。与Morniga G相比,生物信息学分析表明HPA受益于一个扩展的碳水化合物结合位点,比Morniga G更能适应容纳更复杂的分支型和截短型O-聚糖(如核心2)。最后,在淋巴瘤细胞+淋巴细胞的混合物中,HPA可杀死EL4细胞但不杀死健康淋巴细胞,这表明HPA可选择性地触发肿瘤细胞死亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f15/8431231/a3044ad847d7/cancers-13-04356-g001.jpg

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