Protein nanoparticle cellular fate and responses in murine macrophages
Nanoparticles (NPs), both organic and inorganic, have been identified as tools for diagnostic and therapeutic (theranostic) applications. Macrophages constitute the first line of defense in the human body following the introduction of foreign antigens, including nanoparticles. However, there is a li...
Saved in:
Main Authors: | , , , , , |
---|---|
Other Authors: | |
Format: | Article |
Language: | English |
Published: |
2023
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/168731 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
id |
sg-ntu-dr.10356-168731 |
---|---|
record_format |
dspace |
spelling |
sg-ntu-dr.10356-1687312023-06-16T15:31:43Z Protein nanoparticle cellular fate and responses in murine macrophages Ravishankar, Samyukta Nedumaran, Anu Maashaa Gautam, Archana Ng, Kee Woei Czarny, Bertrand Lim, Sierin School of Chemistry, Chemical Engineering and Biotechnology School of Materials Science and Engineering Engineering::Materials Cellulars Foreign Antigens Nanoparticles (NPs), both organic and inorganic, have been identified as tools for diagnostic and therapeutic (theranostic) applications. Macrophages constitute the first line of defense in the human body following the introduction of foreign antigens, including nanoparticles. However, there is a limited understanding of the cellular fate and trafficking of organic NPs in macrophages as well as the molecular responses that are triggered. This knowledge is crucial for the effective translation of these engineered molecules for theranostic applications. In this work, we performed an in-depth study on the intracellular fate and relevant immune responses of a model organic NP, Archaeoglobus fulgidus ferritin, in murine macrophage (RAW264.7) cells. Ferritin, a naturally occurring iron storage protein, has been reported to target tumors and atherosclerotic lesion sites. Herein, we demonstrate a concentration-dependent internalization mechanism and quantify the subcellular localization of ferritin NPs in various organelles. After NP exposure, export of the iron present in the ferritin core occurred over an extended period of time along with upregulation of iron-related gene mRNA expression. A study on the modulation of the intracellular localization of the NPs was conducted by incorporating peptides to mediate endosomal escape and examining their molecular effects using transcriptional analysis. To further investigate the physiological effects, we monitored the upregulation of immune-related markers (i.e., CCR2, IL1β, TNFα, VCAM-1) along with ROS generation in cells treated with ferritin under various conditions. The in-depth analyses of cellular uptake and responses to versatile protein NPs, such as ferritin, provide basic principles to design and engineer other protein NPs with similar properties for future biomedical applications. Ministry of Education (MOE) Nanyang Technological University Published version This work is supported in parts by Nanyang Technological University, Singapore Start-Up Grant through the School of Materials Science and Engineering and Institute for Digital Molecular Analytics and Science (IDMxS) at Nanyang Technological University, Singapore through Singapore Ministry of Education funding under the Research Centres of Excellence scheme. 2023-06-16T07:08:32Z 2023-06-16T07:08:32Z 2023 Journal Article Ravishankar, S., Nedumaran, A. M., Gautam, A., Ng, K. W., Czarny, B. & Lim, S. (2023). Protein nanoparticle cellular fate and responses in murine macrophages. NPG Asia Materials, 15(1), 1-. https://dx.doi.org/10.1038/s41427-022-00453-w 1884-4049 https://hdl.handle.net/10356/168731 10.1038/s41427-022-00453-w 2-s2.0-85146321956 1 15 1 en NPG Asia Materials © 2023 The Author(s). This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. application/pdf |
institution |
Nanyang Technological University |
building |
NTU Library |
continent |
Asia |
country |
Singapore Singapore |
content_provider |
NTU Library |
collection |
DR-NTU |
language |
English |
topic |
Engineering::Materials Cellulars Foreign Antigens |
spellingShingle |
Engineering::Materials Cellulars Foreign Antigens Ravishankar, Samyukta Nedumaran, Anu Maashaa Gautam, Archana Ng, Kee Woei Czarny, Bertrand Lim, Sierin Protein nanoparticle cellular fate and responses in murine macrophages |
description |
Nanoparticles (NPs), both organic and inorganic, have been identified as tools for diagnostic and therapeutic (theranostic) applications. Macrophages constitute the first line of defense in the human body following the introduction of foreign antigens, including nanoparticles. However, there is a limited understanding of the cellular fate and trafficking of organic NPs in macrophages as well as the molecular responses that are triggered. This knowledge is crucial for the effective translation of these engineered molecules for theranostic applications. In this work, we performed an in-depth study on the intracellular fate and relevant immune responses of a model organic NP, Archaeoglobus fulgidus ferritin, in murine macrophage (RAW264.7) cells. Ferritin, a naturally occurring iron storage protein, has been reported to target tumors and atherosclerotic lesion sites. Herein, we demonstrate a concentration-dependent internalization mechanism and quantify the subcellular localization of ferritin NPs in various organelles. After NP exposure, export of the iron present in the ferritin core occurred over an extended period of time along with upregulation of iron-related gene mRNA expression. A study on the modulation of the intracellular localization of the NPs was conducted by incorporating peptides to mediate endosomal escape and examining their molecular effects using transcriptional analysis. To further investigate the physiological effects, we monitored the upregulation of immune-related markers (i.e., CCR2, IL1β, TNFα, VCAM-1) along with ROS generation in cells treated with ferritin under various conditions. The in-depth analyses of cellular uptake and responses to versatile protein NPs, such as ferritin, provide basic principles to design and engineer other protein NPs with similar properties for future biomedical applications. |
author2 |
School of Chemistry, Chemical Engineering and Biotechnology |
author_facet |
School of Chemistry, Chemical Engineering and Biotechnology Ravishankar, Samyukta Nedumaran, Anu Maashaa Gautam, Archana Ng, Kee Woei Czarny, Bertrand Lim, Sierin |
format |
Article |
author |
Ravishankar, Samyukta Nedumaran, Anu Maashaa Gautam, Archana Ng, Kee Woei Czarny, Bertrand Lim, Sierin |
author_sort |
Ravishankar, Samyukta |
title |
Protein nanoparticle cellular fate and responses in murine macrophages |
title_short |
Protein nanoparticle cellular fate and responses in murine macrophages |
title_full |
Protein nanoparticle cellular fate and responses in murine macrophages |
title_fullStr |
Protein nanoparticle cellular fate and responses in murine macrophages |
title_full_unstemmed |
Protein nanoparticle cellular fate and responses in murine macrophages |
title_sort |
protein nanoparticle cellular fate and responses in murine macrophages |
publishDate |
2023 |
url |
https://hdl.handle.net/10356/168731 |
_version_ |
1772826080352141312 |