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声镊细胞术用于巨噬细胞的机械表型分析和机械药物细胞破碎。

Acoustic tweezing cytometry for mechanical phenotyping of macrophages and mechanopharmaceutical cytotripsy.

机构信息

Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.

Department of Pharmaceutical Sciences, University of Michigan, Ann Arbor, MI, 48109, USA.

出版信息

Sci Rep. 2019 Apr 5;9(1):5702. doi: 10.1038/s41598-019-42180-3.

Abstract

Macrophages are immune cells responsible for tissue debridement and fighting infection. Clofazimine, an FDA-approved antibiotic, accumulates and precipitates as rod-shaped, crystal-like drug inclusions within macrophage lysosomes. Drug treatment as well as pathophysiological states could induce changes in macrophage mechanical property which in turn impact their phenotype and function. Here we report the use of acoustic tweezing cytometry as a new approach for in situ mechanical phenotyping of macrophages and for targeted macrophage cytotripsy. Acoustic tweezing cytometry applies ultrasound pulses to exert controlled forces to individual cells via integrin-bound microbubbles, enabling a creep test for measuring cellular mechanical property or inducing irreversible changes to the cells. Our results revealed that macrophages with crystal-like drug inclusions became significantly softer with higher cell compliance, and behaved more elastic with faster creep and recovery time constants. On the contrary, phagocytosis of solid polyethylene microbeads or treatment with soluble clofazimine rendered macrophages stiffer. Most notably, application of ultrasound pulses of longer duration and higher amplitude in ATC actuated the integrin-bound microbubbles to mobilize the crystal-like drug inclusions inside macrophages, turning the rod-shaped drug inclusions into intracellular microblender that effectively destructed the cells. This phenomenon of acoustic mechanopharmaceutical cytotripsy may be exploited for ultrasound activated, macrophage-directed drug release and delivery.

摘要

巨噬细胞是负责组织清创和抗感染的免疫细胞。氯法齐明是一种获得 FDA 批准的抗生素,在巨噬细胞溶酶体中积累并沉淀为棒状、类似晶体的药物包涵体。药物治疗以及病理生理状态可能会导致巨噬细胞力学特性发生变化,进而影响其表型和功能。在这里,我们报告了使用声镊细胞术作为一种新的方法,用于原位机械表型分析巨噬细胞,并用于靶向巨噬细胞细胞破碎。声镊细胞术通过整合素结合的微泡应用超声脉冲对单个细胞施加可控的力,从而能够进行蠕变测试以测量细胞的力学特性,或对细胞产生不可逆的变化。我们的结果表明,含有类似晶体的药物包涵体的巨噬细胞变得明显柔软,细胞顺应性更高,表现出更快的蠕变和恢复时间常数,具有更高的弹性。相反,吞噬固体聚乙烯微球或用可溶性氯法齐明处理会使巨噬细胞变硬。值得注意的是,在 ATC 驱动下应用更长持续时间和更高幅度的超声脉冲会使整合素结合的微泡发生运动,从而将巨噬细胞内的类似晶体药物包涵体转化为细胞内的微搅拌器,有效地破坏细胞。这种声力药物细胞破碎的现象可用于超声激活、巨噬细胞定向药物释放和递送。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f894/6450871/a7613d6a00d6/41598_2019_42180_Fig1_HTML.jpg

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