Direct Transfer of Mesoporous Silica Nanoparticles between Macrophages and Cancer Cells
Macrophages line the walls of microvasculature, extending processes into the blood flow to capture foreign invaders, including nano-scale materials. Using mesoporous silica nanoparticles (MSNs) as a model nano-scale system, we show the interplay between macrophages and MSNs from initial uptake to in...
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2020-10-01
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doaj-132da8c4982f49978c639aa4eea84ac22020-11-25T03:55:51ZengMDPI AGCancers2072-66942020-10-01122892289210.3390/cancers12102892Direct Transfer of Mesoporous Silica Nanoparticles between Macrophages and Cancer CellsStefan Franco0Achraf Noureddine1Jimin Guo2Jane Keth3Michael L. Paffett4C. Jeffrey Brinker5Rita E. Serda6Internal Medicine, University of New Mexico Health Science Center, Albuquerque, NM 87131, USADepartment of Chemical and Biological Engineering, University of New Mexico, Albuquerque, NM 87131, USAInternal Medicine, University of New Mexico Health Science Center, Albuquerque, NM 87131, USAInternal Medicine, University of New Mexico Health Science Center, Albuquerque, NM 87131, USAFluorescence Microscopy Shared Resource, University of New Mexico Comprehensive Cancer Center, Albuquerque, NM 87131, USADepartment of Chemical and Biological Engineering, University of New Mexico, Albuquerque, NM 87131, USAInternal Medicine, University of New Mexico Health Science Center, Albuquerque, NM 87131, USAMacrophages line the walls of microvasculature, extending processes into the blood flow to capture foreign invaders, including nano-scale materials. Using mesoporous silica nanoparticles (MSNs) as a model nano-scale system, we show the interplay between macrophages and MSNs from initial uptake to intercellular trafficking to neighboring cells along microtubules. The nature of cytoplasmic bridges between cells and their role in the cell-to-cell transfer of nano-scale materials is examined, as is the ability of macrophages to function as carriers of nanomaterials to cancer cells. Both direct administration of nanoparticles and adoptive transfer of nanoparticle-loaded splenocytes in mice resulted in abundant localization of nanomaterials within macrophages 24 h post-injection, predominately in the liver. While heterotypic, trans-species nanomaterial transfer from murine macrophages to human HeLa cervical cancer cells or A549 lung cancer cells was robust, transfer to syngeneic 4T1 breast cancer cells was not detected in vitro or in vivo. Cellular connections and nanomaterial transfer in vivo were rich among immune cells, facilitating coordinated immune responses.https://www.mdpi.com/2072-6694/12/10/2892macrophagemesoporous silica nanoparticledoxorubicincancerintercellular transporttunneling nanotubes |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Stefan Franco Achraf Noureddine Jimin Guo Jane Keth Michael L. Paffett C. Jeffrey Brinker Rita E. Serda |
spellingShingle |
Stefan Franco Achraf Noureddine Jimin Guo Jane Keth Michael L. Paffett C. Jeffrey Brinker Rita E. Serda Direct Transfer of Mesoporous Silica Nanoparticles between Macrophages and Cancer Cells Cancers macrophage mesoporous silica nanoparticle doxorubicin cancer intercellular transport tunneling nanotubes |
author_facet |
Stefan Franco Achraf Noureddine Jimin Guo Jane Keth Michael L. Paffett C. Jeffrey Brinker Rita E. Serda |
author_sort |
Stefan Franco |
title |
Direct Transfer of Mesoporous Silica Nanoparticles between Macrophages and Cancer Cells |
title_short |
Direct Transfer of Mesoporous Silica Nanoparticles between Macrophages and Cancer Cells |
title_full |
Direct Transfer of Mesoporous Silica Nanoparticles between Macrophages and Cancer Cells |
title_fullStr |
Direct Transfer of Mesoporous Silica Nanoparticles between Macrophages and Cancer Cells |
title_full_unstemmed |
Direct Transfer of Mesoporous Silica Nanoparticles between Macrophages and Cancer Cells |
title_sort |
direct transfer of mesoporous silica nanoparticles between macrophages and cancer cells |
publisher |
MDPI AG |
series |
Cancers |
issn |
2072-6694 |
publishDate |
2020-10-01 |
description |
Macrophages line the walls of microvasculature, extending processes into the blood flow to capture foreign invaders, including nano-scale materials. Using mesoporous silica nanoparticles (MSNs) as a model nano-scale system, we show the interplay between macrophages and MSNs from initial uptake to intercellular trafficking to neighboring cells along microtubules. The nature of cytoplasmic bridges between cells and their role in the cell-to-cell transfer of nano-scale materials is examined, as is the ability of macrophages to function as carriers of nanomaterials to cancer cells. Both direct administration of nanoparticles and adoptive transfer of nanoparticle-loaded splenocytes in mice resulted in abundant localization of nanomaterials within macrophages 24 h post-injection, predominately in the liver. While heterotypic, trans-species nanomaterial transfer from murine macrophages to human HeLa cervical cancer cells or A549 lung cancer cells was robust, transfer to syngeneic 4T1 breast cancer cells was not detected in vitro or in vivo. Cellular connections and nanomaterial transfer in vivo were rich among immune cells, facilitating coordinated immune responses. |
topic |
macrophage mesoporous silica nanoparticle doxorubicin cancer intercellular transport tunneling nanotubes |
url |
https://www.mdpi.com/2072-6694/12/10/2892 |
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