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Notch Intracellular Domain Plasmid Delivery via Poly(Lactic-Co-Glycolic Acid) Nanoparticles to Upregulate Notch Pathway Molecules
Notch signaling is a highly conserved signaling system that is required for embryonic development and regeneration of organs. When the signal is lost, maldevelopment occurs and leads to a lethal state. Delivering exogenous genetic materials encoding Notch into cells can reestablish downstream signal...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8507495/ https://www.ncbi.nlm.nih.gov/pubmed/34651022 http://dx.doi.org/10.3389/fcvm.2021.707897 |
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author | Messerschmidt, Victoria L. Chintapula, Uday Kuriakose, Aneetta E. Laboy, Samantha Truong, Thuy Thi Dang Kydd, LeNaiya A. Jaworski, Justyn Pan, Zui Sadek, Hesham Nguyen, Kytai T. Lee, Juhyun |
author_facet | Messerschmidt, Victoria L. Chintapula, Uday Kuriakose, Aneetta E. Laboy, Samantha Truong, Thuy Thi Dang Kydd, LeNaiya A. Jaworski, Justyn Pan, Zui Sadek, Hesham Nguyen, Kytai T. Lee, Juhyun |
author_sort | Messerschmidt, Victoria L. |
collection | PubMed |
description | Notch signaling is a highly conserved signaling system that is required for embryonic development and regeneration of organs. When the signal is lost, maldevelopment occurs and leads to a lethal state. Delivering exogenous genetic materials encoding Notch into cells can reestablish downstream signaling and rescue cellular functions. In this study, we utilized the negatively charged and FDA approved polymer poly(lactic-co-glycolic acid) to encapsulate Notch Intracellular Domain-containing plasmid in nanoparticles. We show that primary human umbilical vein endothelial cells (HUVECs) readily uptake the nanoparticles with and without specific antibody targets. We demonstrated that our nanoparticles are non-toxic, stable over time, and compatible with blood. We further demonstrated that HUVECs could be successfully transfected with these nanoparticles in static and dynamic environments. Lastly, we elucidated that these nanoparticles could upregulate the downstream genes of Notch signaling, indicating that the payload was viable and successfully altered the genetic downstream effects. |
format | Online Article Text |
id | pubmed-8507495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85074952021-10-13 Notch Intracellular Domain Plasmid Delivery via Poly(Lactic-Co-Glycolic Acid) Nanoparticles to Upregulate Notch Pathway Molecules Messerschmidt, Victoria L. Chintapula, Uday Kuriakose, Aneetta E. Laboy, Samantha Truong, Thuy Thi Dang Kydd, LeNaiya A. Jaworski, Justyn Pan, Zui Sadek, Hesham Nguyen, Kytai T. Lee, Juhyun Front Cardiovasc Med Cardiovascular Medicine Notch signaling is a highly conserved signaling system that is required for embryonic development and regeneration of organs. When the signal is lost, maldevelopment occurs and leads to a lethal state. Delivering exogenous genetic materials encoding Notch into cells can reestablish downstream signaling and rescue cellular functions. In this study, we utilized the negatively charged and FDA approved polymer poly(lactic-co-glycolic acid) to encapsulate Notch Intracellular Domain-containing plasmid in nanoparticles. We show that primary human umbilical vein endothelial cells (HUVECs) readily uptake the nanoparticles with and without specific antibody targets. We demonstrated that our nanoparticles are non-toxic, stable over time, and compatible with blood. We further demonstrated that HUVECs could be successfully transfected with these nanoparticles in static and dynamic environments. Lastly, we elucidated that these nanoparticles could upregulate the downstream genes of Notch signaling, indicating that the payload was viable and successfully altered the genetic downstream effects. Frontiers Media S.A. 2021-09-28 /pmc/articles/PMC8507495/ /pubmed/34651022 http://dx.doi.org/10.3389/fcvm.2021.707897 Text en Copyright © 2021 Messerschmidt, Chintapula, Kuriakose, Laboy, Truong, Kydd, Jaworski, Pan, Sadek, Nguyen and Lee. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cardiovascular Medicine Messerschmidt, Victoria L. Chintapula, Uday Kuriakose, Aneetta E. Laboy, Samantha Truong, Thuy Thi Dang Kydd, LeNaiya A. Jaworski, Justyn Pan, Zui Sadek, Hesham Nguyen, Kytai T. Lee, Juhyun Notch Intracellular Domain Plasmid Delivery via Poly(Lactic-Co-Glycolic Acid) Nanoparticles to Upregulate Notch Pathway Molecules |
title | Notch Intracellular Domain Plasmid Delivery via Poly(Lactic-Co-Glycolic Acid) Nanoparticles to Upregulate Notch Pathway Molecules |
title_full | Notch Intracellular Domain Plasmid Delivery via Poly(Lactic-Co-Glycolic Acid) Nanoparticles to Upregulate Notch Pathway Molecules |
title_fullStr | Notch Intracellular Domain Plasmid Delivery via Poly(Lactic-Co-Glycolic Acid) Nanoparticles to Upregulate Notch Pathway Molecules |
title_full_unstemmed | Notch Intracellular Domain Plasmid Delivery via Poly(Lactic-Co-Glycolic Acid) Nanoparticles to Upregulate Notch Pathway Molecules |
title_short | Notch Intracellular Domain Plasmid Delivery via Poly(Lactic-Co-Glycolic Acid) Nanoparticles to Upregulate Notch Pathway Molecules |
title_sort | notch intracellular domain plasmid delivery via poly(lactic-co-glycolic acid) nanoparticles to upregulate notch pathway molecules |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8507495/ https://www.ncbi.nlm.nih.gov/pubmed/34651022 http://dx.doi.org/10.3389/fcvm.2021.707897 |
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