# Cutting-Edge HEK293T Protein-Integrated Lipid Nanostructures: Boosting Biocompatibility and Efficacy

**Authors:** Jung-Hyun Park, Cheng-Zhe Bai, Jeong-Hun Kwak, Ho-Joong Choi, Dosang Lee, Ha-Eun Hong, Ok-Hee Kim, Say-June Kim

PMC · DOI: 10.3390/ijms25063294 · International Journal of Molecular Sciences · 2024-03-14

## TL;DR

This study creates artificial exosomes with HEK293T cell proteins to improve cancer treatment by boosting drug delivery and targeting.

## Contribution

The novel approach integrates HEK293T-derived membrane proteins into liposomes to enhance biocompatibility and tumor targeting.

## Key findings

- MPLCs showed superior membrane fusion and higher cellular uptake in cancer cell lines.
- MPLCs maintained better morphology and stability in serum compared to conventional liposomes.
- MPLCs accumulated more in tumor tissues in mouse models, indicating improved targeting.

## Abstract

Recently, artificial exosomes have been developed to overcome the challenges of natural exosomes, such as production scalability and stability. In the production of artificial exosomes, the incorporation of membrane proteins into lipid nanostructures is emerging as a notable approach for enhancing biocompatibility and treatment efficacy. This study focuses on incorporating HEK293T cell-derived membrane proteins into liposomes to create membrane-protein-bound liposomes (MPLCs), with the goal of improving their effectiveness as anticancer therapeutics. MPLCs were generated by combining two key elements: lipid components that are identical to those in conventional liposomes (CLs) and membrane protein components uniquely derived from HEK293T cells. An extensive comparison of CLs and MPLCs was conducted across multiple in vitro and in vivo cancer models, employing advanced techniques such as cryo-TEM (tramsmission electron microscopy) imaging and FT-IR (fourier transform infrared spectroscopy). MPLCs displayed superior membrane fusion capabilities in cancer cell lines, with significantly higher cellular uptake. Additionally, MPLCs maintained their morphology and size better than CLs when exposed to FBS (fetal bovine serum), suggesting enhanced serum stability. In a xenograft mouse model using HeLa and ASPC cancer cells, intravenous administration of MPLCs MPLCs accumulated more in tumor tissues, highlighting their potential for targeted cancer therapy. Overall, these results indicate that MPLCs have superior tumor-targeting properties, possibly attributable to their membrane protein composition, offering promising prospects for enhancing drug delivery efficiency in cancer treatments. This research could offer new clinical application opportunities, as it uses MPLCs with membrane proteins from HEK293T cells, which are known for their efficient production and compatibility with GMP (good manufacturing practice) standards.

## Linked entities

- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Diseases:** cancer (MESH:D009369)
- **Chemicals:** Lipid (MESH:D008055)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** ASPC — Homo sapiens (Human), Pancreatic ductal adenocarcinoma, Cancer cell line (CVCL_0152), HeLa — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_0030), HEK293T — Homo sapiens (Human), Transformed cell line (CVCL_0063)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10970359/full.md

## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC10970359/full.md

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Source: https://tomesphere.com/paper/PMC10970359