生物基、可生物降解但非生物中性:关于聚乳酸纳米颗粒对巨噬细胞的影响

Véronique Collin-Faure, Marianne Vitipon, Hélène Diemer, Sarah Cianférani, Elisabeth Darrouzet, Thierry Rabilloud
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引用次数: 0

摘要

塑料是一种持久性污染物,因为它们降解缓慢,这表明它们可能会随着时间的推移逐渐积累,从而导致累积性和/或延迟性的不利影响。人类活动产生的大塑料被释放到环境中,降解为微塑料和纳米塑料,很容易被包括人类在内的各种生物吸收。微塑料和纳米塑料都是微粒,在人体内会被巨噬细胞(或其进化对应物)等特化细胞处理,从而引起各种反应。缓解生物持久性问题的一个解决方案是使用可生物降解塑料,例如在生命周期中的累积。聚乳酸是新兴的生物降解塑料之一,我们决定采用非靶向蛋白质组学和靶向验证实验相结合的方法,测试巨噬细胞对聚乳酸纳米粒子的反应。蛋白质组学显示,在暴露于聚乳酸纳米粒子后,蛋白质组发生了重要的适应性变化。这些变化不仅影响了线粒体、细胞骨架和溶酶体蛋白,还影响了与免疫功能或氧化还原平衡有关的蛋白。验证实验表明,其中许多变化是平衡的,没有诱发氧化应激,也没有严重扰乱线粒体功能。然而,聚乳酸颗粒改变了免疫功能,如吞噬能力(-20%)或细胞因子的产生(TNF 的产生增加了 2 倍),这可能会导致巨噬细胞应对细菌感染的能力下降。此外,聚乳酸微粒还与一些醌类物质(如菲醌)产生中度交叉毒性,菲醌是一种燃烧副产品,被怀疑是一种致癌物质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biobased, Biodegradable but not bio-neutral: about the effects of polylactic acid nanoparticles on macrophages
Plastics are persistent pollutants, because of their slow degradation, which suggests that they may lead to cumulative and/or delayed adverse effects due to their progressive accumulation over time. Macroplastics produced by human activity are released in the environment, where they degrade into micro and nanoplastics that are very easily uptaken by a wide variety of organisms, including humans. Microplastics and nanoplastics being particulates, they are handled in the body by specialized cells such as macrophages (or their evolutionary counterparts), where they can elicit a variety of responses. One solution to alleviate the problems due to biopersistence, such as accumulation over life, would be to use biodegradable plastics. One of the emerging biodegradable plastics being polylactide, we decided to test the responses of macrophages to polylactide nanoparticles, using a combination of untargeted proteomics and targeted validation experiments. Proteomics showed important adaptive changes in the proteome in response to exposure to polylactide nanoparticles. These changes affected for example mitochondrial, cytoskeletal and lysosomal proteins, but also proteins implicated in immune functions or redox homeostasis. Validation experiments showed that many of these changes were homeostatic, with no induced oxidative stress and no gross perturbation of the mitochondrial function. However, polylactide particles altered the immune functions such as phagocytosis (−20%) or cytokine production (2-fold increase for TNF production), which may translate into a decreased ability to macrophages to respond to bacterial infections. Furthermore, polylactide particles also induced moderate cross-toxicity with some quinones such as phenanthrene quinone, a combustion by-product that is a suspected carcinogen.
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