A nature-inspired nanodelivery platform for gene silencing in hematopoietic stem and progenitor cells

Author:

Meel Roy van der1ORCID,Hofstraat Stijn2ORCID,Anbergen Tom3,Zwolsman Robby1,Deckers Jeroen3,Elsas Yuri van3,Trines Mirre1,Versteeg Iris3,Priem Bram3,Darwish Youssef4ORCID,Kleuskens Teun1,Borges Francisca3,Maas Rianne3ORCID,Verhalle Lars1,Tielemans Willem3,Vader Pieter5ORCID,de Jong Olivier6ORCID,Teunissen Abraham7,Brechbühl Eliane8ORCID,Janssen Henk9,Fransen Michel9,de Dreu Anne1,Schrijver David1ORCID,Toner Yohana C.3,Beldman Thijs3,Netea Mihai10ORCID,Mulder Willem3,Kluza Ewelina1ORCID

Affiliation:

1. Eindhoven University of Technology

2. Laboratory of Chemical Biology, Department of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, The Netherlands

3. Radboud University Medical Center

4. The Technical University of Eindhoven

5. University Medical Center Utrecht

6. Utrecht University

7. Icahn School of Medicine at Mount Sinai

8. Icahn Medical School at Mount Sinai

9. SyMO-Chem B.V.

10. Radboud University Nijmegen Medical Centre

Abstract

Abstract Nucleic acid therapeutics harbor great potential for silencing, expressing, or editing genes. Here, we introduce a nanodelivery platform based on natural lipoproteins, which prevents premature degradation of small interfering RNA (siRNA), ensuring its targeted and intracellular delivery to hematopoietic stem and progenitor cells (HSPCs) in the bone marrow. After establishing a prototype apolipoprotein lipid nanoparticle (aNP) that stably incorporates siRNA in its core, we built a comprehensive library of which we thoroughly characterized the individual aNPs’ physicochemical properties. Following the in vitro screening of all formulations, we selected eight siRNA-aNPs that are representative of the library’s diversity, and determined their capacity to silence lysosomal-associated membrane protein 1 (LAMP1) in immune cell subsets in mice, using an intravenous administration regimen. Our data show that using different aNPs, we can achieve functional gene silencing in immune cell subsets and their bone marrow progenitors. Beyond gene silencing, the aNP platform’s inherent capacity to engage immune cells provides it with considerable potential to deliver other types of nucleic acid therapeutics to HSPCs.

Publisher

Research Square Platform LLC

Reference42 articles.

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