A natural immunity-activating plant lectin, Viscum album agglutinin-I, induces apoptosis in human lymphocytes, monocytes, monocytic THP-1 cells and murine thymocytes.

Natural immunity Pub Date : 1996-01-01
K Hostanska, T Hajto, K Weber, J Fischer, H Lentzen, B Sütterlin, R Saller
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Abstract

A galactoside-specific plant lectin, Viscum album agglutinin-I (VAA-I) with protein synthesis-inhibiting properties, has been shown to be cytotoxic in various eukaryotic cells, in vitro above a 10 ng/ml concentration. Noncytotoxic concentrations of VAA-I induced mRNA expression and enhanced secretion of proinflammatory cytokines in cultures of human peripheral blood mononuclear cells. In an animal model VAA-I has been shown to stimulate natural killer cells and granulocytes. In this study, human peripheral blood lymphocytes (PBL), human peripheral blood monocytes (PBM), murine thymocytes and human monocytic THP-1 cells were incubated for 24 h in the presence of various concentrations of VAA-I. The apoptotic effect of VAA-I was analyzed by flow cytometry following staining of the apoptotic nuclei in the cells with PI in hypotonic buffer and quantitative detection of DNA breaks were analyzed by the terminal deoxynucleotidyl transferase-mediated dUTP-digoxigenin nick end-labeling (TUNEL) assay. In cultures of all types of investigated cells, a dose-dependent VAA-I concentrations above 10 ng/ml in PBL and at 1 ng/ml VAA-I concentration in PBM, thymocytes and THP-1 cells, a lectin-induced increase of the apoptotic nuclei was observed. In 24-hour cultures of PBL and thymocytes, the ratios between apoptotic and nonapoptotic cells were enhanced 10 times and 8 times, respectively, by 100 ng/ml VAA-I compared to the negative control. The concentration of 100 micrograms/ml VAA-I only caused necrosis. The isolated A chain of the VAA-I induced apoptosis in PBL and thymocytes. In the culture of PBL the isolated B chain of the VAA-I was not effective indicating that cytokine induction by VAA-I is probably not involved in its apoptotic effect. On CD4+8+ thymocytes, VAA-I resulted in a reduced expression of CD8+ molecules that could be related to a loss of volume and increase of density, both characteristic features of apoptosis.

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一种天然的免疫激活植物凝集素Viscum album agglutinin-I,可诱导人淋巴细胞、单核细胞、单核THP-1细胞和小鼠胸腺细胞凋亡。
半乳糖苷特异性植物凝集素Viscum album agglutinin-I (VAA-I)具有蛋白质合成抑制特性,在体外浓度超过10 ng/ml时,已被证明在多种真核细胞中具有细胞毒性。在培养的人外周血单核细胞中,无细胞毒性浓度的VAA-I诱导mRNA表达并增强促炎细胞因子的分泌。在动物模型中,VAA-I已被证明能刺激自然杀伤细胞和粒细胞。本研究将人外周血淋巴细胞(PBL)、人外周血单核细胞(PBM)、小鼠胸腺细胞和人单核THP-1细胞在不同浓度的VAA-I存在下孵育24 h。低渗缓冲液中PI染色细胞凋亡细胞核,流式细胞术分析VAA-I对细胞凋亡的影响;末端脱氧核苷酸转移酶介导dutp -地高igenin缺口末端标记法(TUNEL)定量检测DNA断裂。在所有类型细胞的培养中,在PBL中,VAA-I浓度高于10 ng/ml,在PBM,胸腺细胞和THP-1细胞中,VAA-I浓度为1 ng/ml时,观察到凝集素诱导的凋亡核增加。在PBL和胸腺细胞24小时培养中,与阴性对照相比,100 ng/ml VAA-I可使凋亡细胞和非凋亡细胞的比例分别提高10倍和8倍。100微克/毫升浓度的VAA-I仅引起坏死。分离的VAA-I A链诱导PBL和胸腺细胞凋亡。在PBL培养中,分离的VAA-I的B链不有效,这表明VAA-I的细胞因子诱导可能与其凋亡作用无关。在CD4+8+胸腺细胞上,VAA-I导致CD8+分子的表达减少,这可能与体积损失和密度增加有关,这两者都是细胞凋亡的特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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