4.6 Article

Probing Dynamic Features of Phagosome Maturation in Macrophage using Au@MnOx@SiO2 Nanoparticles as pH-Sensitive Plasmonic Nanoprobes

期刊

CHEMISTRY-AN ASIAN JOURNAL
卷 16, 期 9, 页码 1150-1156

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/asia.202100031

关键词

plasmonic nanoprobes; single particle imaging; nanosensor; phagosome acidification; macrophage

资金

  1. National Natural Science Foundation of China [21874039, 21977027, 21890744, 21521063]
  2. National Key R&D Program of China [2019YFA0210100]
  3. MOE Key Lab of Bioorganic Phosphorus Chemistry & Chemical Biology at Tsinghua University
  4. Fundamental Research Funds for the Central Universities at Hunan University

向作者/读者索取更多资源

The multilayered Au@MnOx@SiO2 nanoparticle was developed as a robust pH-sensitive plasmonic nanosensor for real-time monitoring of dynamic acidification features during phagosome maturation process in macrophages. The color changes of nanoprobes indicated a slow-to-fast acidification translation over time, which was related to V-ATPase activation. This nanosensor shows promise for studying phagosome dysfunctions and related disease pathogenesis.
Phagosome maturation in macrophage is essential to the clearance of pathogenic materials in host defence but the dynamic features remain difficult to be measured in real time. Herein, we reported the multilayered Au@MnOx@SiO2 nanoparticle as a robust pH-sensitive plasmonic nanosensor for monitoring the dynamic acidification features over the phagosome maturation process in macrophage under darkfield microscopy. For this multilayered nanosensor, the gold nanoparticle core plays a role of signal reporter, the MnOx shell and the outmost SiO2 act as the sensing layer and the protecting layer, respectively. After subject to the acidic buffer solution, the MnOx layer in the multilayered nanoprobe could be decomposed rapidly, resulting in a remarkable spectral shift and color change under darkfield microscopy. We demonstrated this nanosensor for the investigation of single phagosome acidification dynamics by monitoring the color changes of nanoprobes after phagocytosis over time. The nanoprobes after phagocytosized in macrophage displayed a slight color change within the first hour and then cost several minutes to change from red to green in the next stage, indicating the phagosome undergoes a slow first and then fast acidification feature as well as a slow-to-fast acidification translation over the phagosome maturation process. Moreover, we validated that the slow-to-fast acidification translation was dependent on the activation of V-ATPase from the ATP depletion assay. We believed that this nanosensor is promising for studying the dynamic acidification features as well as disorders in phagosome maturation in phagocytic cells, which might provide valuable information for understanding the disease pathogenesis related to phagosome dysfunctions.

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