Particle size affects the cellular response in macrophages.

Particle size affects the cellular response in macrophages.
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DOI:
10.1016/j.ejps.2010.09.006
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发表时间:
2010-12
期刊:
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences
影响因子:
--
通讯作者:
H. Yue;Wei Wei-Wei;Zhanguo Yue;Piping Lv;Lianyan Wang;G. Ma;Z. Su
H. Yue;Wei Wei-Wei;Zhanguo Yue;Piping Lv;Lianyan Wang;G. Ma;Z. Su
中科院分区:
其他
文献类型:
--
作者:
H. Yue;Wei Wei-Wei;Zhanguo Yue;Piping Lv;Lianyan Wang;G. Ma;Z. Su

文献摘要

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A deeper understanding of how the physical properties of particles regulate specific biological responses is becoming a crucial requirement for their successful biomedical application. To provide insights on their design and application, J774A.1 cells are exposed to particles with different diameters (430nm, 1.9μm and 4.8μm), and the size effects on a series of cellular responses in macrophages are evaluated. Cellular uptake study demonstrates that nanosized particles accumulate in the cells at a faster rate, and with a higher surface area. Once the data are converted into the expression of particle volume, the maximum value is found with 1.9μm particles instead of nanoparticles. Moreover, the uptake intermediates are also trapped, and the steps of particle internalization include filopodia sensing, skeleton rearrangement, and morphology change. Subsequent cellular trafficking reveals that only nanosized particles transport via lysosomal pathway, which is consistent with their uptake mechanisms. Furthermore, nanosized particles prefer to promote the secretion of Th1-specific molecule signals (e.g. IFN, IL-12) rather than immune suppressors. All these results, along with a couple of surprises, are discussed in the view of clinical practice. They are expected, in principle, to establish the basis of new design concepts for particle-based biomedical applications.