Identification of multiple cellular uptake pathways of polystyrene nanoparticles and factors affecting the uptake: Relevance for drug delivery systems
The given type of polystyrene nanoparticles is taken up by bone marrow-derived macrophages via multiple distinct endocytic pathways simultaneously. Nanoparticles may address challenges by human diseases through improving diagnosis, vaccination and treatment. The uptake mechanism regulates the type o...
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Veröffentlicht in: | European journal of cell biology 2014-08, Vol.93 (8-9), p.323-337 |
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description | The given type of polystyrene nanoparticles is taken up by bone marrow-derived macrophages via multiple distinct endocytic pathways simultaneously.
Nanoparticles may address challenges by human diseases through improving diagnosis, vaccination and treatment. The uptake mechanism regulates the type of threat a particle poses on the host cells and how a cell responds to it. Hence, understanding the uptake mechanisms and cellular interactions of nanoparticles at the cellular and subcellular level is a prerequisite for their effective biomedical applications. The present study shows the uptake mechanisms of polystyrene nanoparticles and factors affecting their uptake in bone marrow-derived macrophages, 293T kidney epithelial cells and L929 fibroblasts. Labeling with the endocytic marker FM4-64 and transmission electron microscopy studies show that the nanoparticles were internalized rapidly via endocytosis and accumulated in intracellular vesicles. Soon after their internalizations, nanoparticles trafficked to organelles with acidic pH. Analysis of the ultrastructural morphology of the plasma membrane invaginations or extravasations provides clear evidence for the involvement of several uptake routes in parallel to internalize a given type of nanoparticles by mammalian cells, highlighting the complexity of the nanoparticle–cell interactions. Blocking the specific endocytic pathways by different pharmacological inhibitors shows similar outcomes. The potential to take up nanoparticles varies highly among different cell types in a particle sizes-, time- and energy-dependent manner. Furthermore, infection and the activation status of bone marrow-derived macrophages significantly affect the uptake potential of the cells, indicating the need to understand the diseases’ pathogenesis to establish effective and rational drug-delivery systems. This study enhances our understanding of the application of nanotechnology in biomedical sciences. |
doi_str_mv | 10.1016/j.ejcb.2014.08.001 |
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Nanoparticles may address challenges by human diseases through improving diagnosis, vaccination and treatment. The uptake mechanism regulates the type of threat a particle poses on the host cells and how a cell responds to it. Hence, understanding the uptake mechanisms and cellular interactions of nanoparticles at the cellular and subcellular level is a prerequisite for their effective biomedical applications. The present study shows the uptake mechanisms of polystyrene nanoparticles and factors affecting their uptake in bone marrow-derived macrophages, 293T kidney epithelial cells and L929 fibroblasts. Labeling with the endocytic marker FM4-64 and transmission electron microscopy studies show that the nanoparticles were internalized rapidly via endocytosis and accumulated in intracellular vesicles. Soon after their internalizations, nanoparticles trafficked to organelles with acidic pH. Analysis of the ultrastructural morphology of the plasma membrane invaginations or extravasations provides clear evidence for the involvement of several uptake routes in parallel to internalize a given type of nanoparticles by mammalian cells, highlighting the complexity of the nanoparticle–cell interactions. Blocking the specific endocytic pathways by different pharmacological inhibitors shows similar outcomes. The potential to take up nanoparticles varies highly among different cell types in a particle sizes-, time- and energy-dependent manner. Furthermore, infection and the activation status of bone marrow-derived macrophages significantly affect the uptake potential of the cells, indicating the need to understand the diseases’ pathogenesis to establish effective and rational drug-delivery systems. This study enhances our understanding of the application of nanotechnology in biomedical sciences.</description><identifier>ISSN: 0171-9335</identifier><identifier>EISSN: 1618-1298</identifier><identifier>DOI: 10.1016/j.ejcb.2014.08.001</identifier><identifier>PMID: 25224362</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><subject>Animals ; Cell Membrane - metabolism ; Cell Membrane - ultrastructure ; Cells, Cultured ; Drug Delivery Systems ; Endocytosis ; Endosomes - metabolism ; Endosomes - ultrastructure ; Epithelial Cells - metabolism ; Factor determining uptake ; Female ; Fibroblasts - metabolism ; Fluorescent Dyes - metabolism ; Hydrogen-Ion Concentration ; Kidney - cytology ; Kidney - metabolism ; Leishmania major ; Macrophages - metabolism ; Macrophages - parasitology ; Mice, Inbred BALB C ; Microscopy, Electron, Transmission ; Multiple uptake ; Nanoparticle ; Nanoparticles - metabolism ; Particle Size ; Polystyrenes - metabolism ; Pyridinium Compounds - metabolism ; Quaternary Ammonium Compounds - metabolism ; Time Factors ; Transcytosis ; Ultrastructure</subject><ispartof>European journal of cell biology, 2014-08, Vol.93 (8-9), p.323-337</ispartof><rights>2014 Elsevier GmbH</rights><rights>Copyright © 2014 Elsevier GmbH. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c459t-6995212e762a2d931b4d2fe829335394aa6f75c869a9ee676758fa2e76ff73d93</citedby><cites>FETCH-LOGICAL-c459t-6995212e762a2d931b4d2fe829335394aa6f75c869a9ee676758fa2e76ff73d93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ejcb.2014.08.001$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25224362$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Firdessa, Rebuma</creatorcontrib><creatorcontrib>Oelschlaeger, Tobias A.</creatorcontrib><creatorcontrib>Moll, Heidrun</creatorcontrib><title>Identification of multiple cellular uptake pathways of polystyrene nanoparticles and factors affecting the uptake: Relevance for drug delivery systems</title><title>European journal of cell biology</title><addtitle>Eur J Cell Biol</addtitle><description>The given type of polystyrene nanoparticles is taken up by bone marrow-derived macrophages via multiple distinct endocytic pathways simultaneously.
Nanoparticles may address challenges by human diseases through improving diagnosis, vaccination and treatment. The uptake mechanism regulates the type of threat a particle poses on the host cells and how a cell responds to it. Hence, understanding the uptake mechanisms and cellular interactions of nanoparticles at the cellular and subcellular level is a prerequisite for their effective biomedical applications. The present study shows the uptake mechanisms of polystyrene nanoparticles and factors affecting their uptake in bone marrow-derived macrophages, 293T kidney epithelial cells and L929 fibroblasts. Labeling with the endocytic marker FM4-64 and transmission electron microscopy studies show that the nanoparticles were internalized rapidly via endocytosis and accumulated in intracellular vesicles. Soon after their internalizations, nanoparticles trafficked to organelles with acidic pH. Analysis of the ultrastructural morphology of the plasma membrane invaginations or extravasations provides clear evidence for the involvement of several uptake routes in parallel to internalize a given type of nanoparticles by mammalian cells, highlighting the complexity of the nanoparticle–cell interactions. Blocking the specific endocytic pathways by different pharmacological inhibitors shows similar outcomes. The potential to take up nanoparticles varies highly among different cell types in a particle sizes-, time- and energy-dependent manner. Furthermore, infection and the activation status of bone marrow-derived macrophages significantly affect the uptake potential of the cells, indicating the need to understand the diseases’ pathogenesis to establish effective and rational drug-delivery systems. This study enhances our understanding of the application of nanotechnology in biomedical sciences.</description><subject>Animals</subject><subject>Cell Membrane - metabolism</subject><subject>Cell Membrane - ultrastructure</subject><subject>Cells, Cultured</subject><subject>Drug Delivery Systems</subject><subject>Endocytosis</subject><subject>Endosomes - metabolism</subject><subject>Endosomes - ultrastructure</subject><subject>Epithelial Cells - metabolism</subject><subject>Factor determining uptake</subject><subject>Female</subject><subject>Fibroblasts - metabolism</subject><subject>Fluorescent Dyes - metabolism</subject><subject>Hydrogen-Ion Concentration</subject><subject>Kidney - cytology</subject><subject>Kidney - metabolism</subject><subject>Leishmania major</subject><subject>Macrophages - metabolism</subject><subject>Macrophages - parasitology</subject><subject>Mice, Inbred BALB C</subject><subject>Microscopy, Electron, Transmission</subject><subject>Multiple uptake</subject><subject>Nanoparticle</subject><subject>Nanoparticles - metabolism</subject><subject>Particle Size</subject><subject>Polystyrenes - metabolism</subject><subject>Pyridinium Compounds - metabolism</subject><subject>Quaternary Ammonium Compounds - metabolism</subject><subject>Time Factors</subject><subject>Transcytosis</subject><subject>Ultrastructure</subject><issn>0171-9335</issn><issn>1618-1298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcGO1SAYhYnRONfRF3BhWLppBdpSMG7MRJ1JJjExuiZc-jPDlZYK9E76Ij6vNPc6S13B4jsn-c-H0GtKakoof3eo4WD2NSO0rYmoCaFP0I5yKirKpHiKdoT2tJJN012gFykdCtAJKZ-jC9Yx1jac7dDvmwGm7KwzOrsw4WDxuPjsZg_YgPeL1xEvc9Y_Ac863z_oNW3QHPya8hphAjzpKcw6Zmc8JKynAVttcojlby2Y7KY7nO_hXPMefwMPRz0ZwDZEPMTlDg_g3RHiilNphTG9RM-s9glend9L9OPzp-9X19Xt1y83Vx9vK9N2Mldcyo5RBj1nmg2yoft2YBYE245uZKs1t31nBJdaAvCe952weuOt7ZsSuERvT71zDL8WSFmNLm136wnCkhTtiaSia6n4P9pxLlgr-76g7ISaGFKKYNUc3ajjqihRmzp1UJs6talTRKhipoTenPuX_QjDY-SvqwJ8OAFQBjk6iCoZB2XGwcWyshqC-1f_H4sCrV8</recordid><startdate>20140801</startdate><enddate>20140801</enddate><creator>Firdessa, Rebuma</creator><creator>Oelschlaeger, Tobias A.</creator><creator>Moll, Heidrun</creator><general>Elsevier GmbH</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20140801</creationdate><title>Identification of multiple cellular uptake pathways of polystyrene nanoparticles and factors affecting the uptake: Relevance for drug delivery systems</title><author>Firdessa, Rebuma ; Oelschlaeger, Tobias A. ; Moll, Heidrun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c459t-6995212e762a2d931b4d2fe829335394aa6f75c869a9ee676758fa2e76ff73d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Cell Membrane - metabolism</topic><topic>Cell Membrane - ultrastructure</topic><topic>Cells, Cultured</topic><topic>Drug Delivery Systems</topic><topic>Endocytosis</topic><topic>Endosomes - metabolism</topic><topic>Endosomes - ultrastructure</topic><topic>Epithelial Cells - metabolism</topic><topic>Factor determining uptake</topic><topic>Female</topic><topic>Fibroblasts - metabolism</topic><topic>Fluorescent Dyes - metabolism</topic><topic>Hydrogen-Ion Concentration</topic><topic>Kidney - cytology</topic><topic>Kidney - metabolism</topic><topic>Leishmania major</topic><topic>Macrophages - metabolism</topic><topic>Macrophages - parasitology</topic><topic>Mice, Inbred BALB C</topic><topic>Microscopy, Electron, Transmission</topic><topic>Multiple uptake</topic><topic>Nanoparticle</topic><topic>Nanoparticles - metabolism</topic><topic>Particle Size</topic><topic>Polystyrenes - metabolism</topic><topic>Pyridinium Compounds - metabolism</topic><topic>Quaternary Ammonium Compounds - metabolism</topic><topic>Time Factors</topic><topic>Transcytosis</topic><topic>Ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Firdessa, Rebuma</creatorcontrib><creatorcontrib>Oelschlaeger, Tobias A.</creatorcontrib><creatorcontrib>Moll, Heidrun</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>European journal of cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Firdessa, Rebuma</au><au>Oelschlaeger, Tobias A.</au><au>Moll, Heidrun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of multiple cellular uptake pathways of polystyrene nanoparticles and factors affecting the uptake: Relevance for drug delivery systems</atitle><jtitle>European journal of cell biology</jtitle><addtitle>Eur J Cell Biol</addtitle><date>2014-08-01</date><risdate>2014</risdate><volume>93</volume><issue>8-9</issue><spage>323</spage><epage>337</epage><pages>323-337</pages><issn>0171-9335</issn><eissn>1618-1298</eissn><abstract>The given type of polystyrene nanoparticles is taken up by bone marrow-derived macrophages via multiple distinct endocytic pathways simultaneously.
Nanoparticles may address challenges by human diseases through improving diagnosis, vaccination and treatment. The uptake mechanism regulates the type of threat a particle poses on the host cells and how a cell responds to it. Hence, understanding the uptake mechanisms and cellular interactions of nanoparticles at the cellular and subcellular level is a prerequisite for their effective biomedical applications. The present study shows the uptake mechanisms of polystyrene nanoparticles and factors affecting their uptake in bone marrow-derived macrophages, 293T kidney epithelial cells and L929 fibroblasts. Labeling with the endocytic marker FM4-64 and transmission electron microscopy studies show that the nanoparticles were internalized rapidly via endocytosis and accumulated in intracellular vesicles. Soon after their internalizations, nanoparticles trafficked to organelles with acidic pH. Analysis of the ultrastructural morphology of the plasma membrane invaginations or extravasations provides clear evidence for the involvement of several uptake routes in parallel to internalize a given type of nanoparticles by mammalian cells, highlighting the complexity of the nanoparticle–cell interactions. Blocking the specific endocytic pathways by different pharmacological inhibitors shows similar outcomes. The potential to take up nanoparticles varies highly among different cell types in a particle sizes-, time- and energy-dependent manner. Furthermore, infection and the activation status of bone marrow-derived macrophages significantly affect the uptake potential of the cells, indicating the need to understand the diseases’ pathogenesis to establish effective and rational drug-delivery systems. This study enhances our understanding of the application of nanotechnology in biomedical sciences.</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>25224362</pmid><doi>10.1016/j.ejcb.2014.08.001</doi><tpages>15</tpages></addata></record> |
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subjects | Animals Cell Membrane - metabolism Cell Membrane - ultrastructure Cells, Cultured Drug Delivery Systems Endocytosis Endosomes - metabolism Endosomes - ultrastructure Epithelial Cells - metabolism Factor determining uptake Female Fibroblasts - metabolism Fluorescent Dyes - metabolism Hydrogen-Ion Concentration Kidney - cytology Kidney - metabolism Leishmania major Macrophages - metabolism Macrophages - parasitology Mice, Inbred BALB C Microscopy, Electron, Transmission Multiple uptake Nanoparticle Nanoparticles - metabolism Particle Size Polystyrenes - metabolism Pyridinium Compounds - metabolism Quaternary Ammonium Compounds - metabolism Time Factors Transcytosis Ultrastructure |
title | Identification of multiple cellular uptake pathways of polystyrene nanoparticles and factors affecting the uptake: Relevance for drug delivery systems |
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