Notch Intracellular Domain Plasmid Delivery via Poly(Lactic-Co-Glycolic Acid) Nanoparticles to Upregulate Notch Pathway Molecules.

Notch signaling PLGA gene delivery nanoparticles non-viral transfection

Journal

Frontiers in cardiovascular medicine
ISSN: 2297-055X
Titre abrégé: Front Cardiovasc Med
Pays: Switzerland
ID NLM: 101653388

Informations de publication

Date de publication:
2021
Historique:
received: 10 05 2021
accepted: 20 08 2021
entrez: 15 10 2021
pubmed: 16 10 2021
medline: 16 10 2021
Statut: epublish

Résumé

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.

Identifiants

pubmed: 34651022
doi: 10.3389/fcvm.2021.707897
pmc: PMC8507495
doi:

Types de publication

Journal Article

Langues

eng

Pagination

707897

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2021 Messerschmidt, Chintapula, Kuriakose, Laboy, Truong, Kydd, Jaworski, Pan, Sadek, Nguyen and Lee.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Victoria L Messerschmidt (VL)

Department of Bioengineering, University of Texas at Arlington, Arlington, TX, United States.
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, United States.

Uday Chintapula (U)

Department of Bioengineering, University of Texas at Arlington, Arlington, TX, United States.
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, United States.

Aneetta E Kuriakose (AE)

Department of Bioengineering, University of Texas at Arlington, Arlington, TX, United States.
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, United States.

Samantha Laboy (S)

Department of Bioengineering, University of Texas at Arlington, Arlington, TX, United States.

Thuy Thi Dang Truong (TTD)

Department of Bioengineering, University of Texas at Arlington, Arlington, TX, United States.

LeNaiya A Kydd (LA)

Department of Bioengineering, University of Texas at Arlington, Arlington, TX, United States.

Justyn Jaworski (J)

Department of Bioengineering, University of Texas at Arlington, Arlington, TX, United States.

Zui Pan (Z)

College of Nursing and Health Innovation, University of Texas at Arlington, Arlington, TX, United States.

Hashem Sadek (H)

Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, United States.

Kytai T Nguyen (KT)

Department of Bioengineering, University of Texas at Arlington, Arlington, TX, United States.
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, United States.

Juhyun Lee (J)

Department of Bioengineering, University of Texas at Arlington, Arlington, TX, United States.
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, United States.

Classifications MeSH