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๐Ÿ‡ฐ๐Ÿ‡ท South Korea /Culture & Society

Seoul National University of Science and Technology team develops 3D cell tissue assembly using magnetic RNA building blocks

From Hankyoreh · () Korean

Translated from Korean and summarized by DistantNews. Read the original for the full story.

At a glance

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  • Researchers at Seoul National University of Science and Technology have developed a novel RNA-based platform for creating 3D cell cultures called spheroids.
  • The platform uses magnetic RNA building blocks and cell building blocks, allowing for precise control of cell structure assembly via external magnetic fields.
  • This technology shows promise for applications in tissue engineering, disease modeling, and drug screening, including improved tumor model formation in animal studies.

A research team at Seoul National University of Science and Technology has pioneered a new method for constructing 3D cell tissues, offering enhanced precision and reproducibility in creating spheroids. These spheroids are vital for applications in tissue engineering, disease modeling, and drug screening.

The breakthrough, led by Professor Lee Jong-beom and detailed in the journal 'Biomaterials', introduces a novel platform that combines magnetic RNA building blocks (RBBs) with cell building blocks (CBBs). This modular assembly strategy allows researchers to precisely control the position and arrangement of 3D cell structures using external magnetic fields. The RBBs are designed with magnetic properties and can selectively bind to cell surfaces through a bioorthogonal click chemistry reaction.

This innovative approach overcomes limitations of existing spheroid production methods, which often struggle with uniformity in size and shape, structural control, and biocompatibility. The RBB-driven platform has demonstrated its ability to produce spheroids with uniform 3D structures and high cell viability across various cell lines, including those from cervical cancer, liver cancer, and melanoma. Furthermore, spheroids created with RBBs exhibit superior structural stability and mechanical strength compared to those made with conventional techniques.

This study expands RNA from a simple carrier of genetic information to a functional biomaterial that can directly bind to cells, be controlled by magnetic fields, and be degraded when necessary.

โ€” Jong-beom LeeProfessor Lee Jong-beom, the research lead, described the significance of the study.

The technology extends beyond simple cell aggregation, enabling the spatial arrangement of different cell types to create heterogeneous modular spheroids. The external magnetic field can guide spheroid movement and pattern their arrangement into specific structures, such as rings. The RBBs are also biodegradable, breaking down in physiological conditions after assembly, which allows for the removal of residual magnetic scaffolds.

In vivo studies have further validated the platform's potential. An animal model comparing dispersed cells, conventional spheroids, and modular spheroids showed that the modular spheroids offered greater structural stability and engraftment, leading to higher efficiency in forming tumor models. Professor Lee Jong-beom highlighted the significance of the research, stating, "This study expands RNA from a simple carrier of genetic information to a functional biomaterial that can directly bind to cells, be controlled by magnetic fields, and be degraded when necessary." He anticipates it will become a key platform for creating precise 3D cell structures in fields like cancer modeling, drug screening, tissue engineering, and regenerative medicine.

It will develop into a key platform for creating precise 3D cell structures in fields like cancer modeling, drug screening, tissue engineering, and regenerative medicine.

โ€” Jong-beom LeeProfessor Lee Jong-beom, the research lead, discussed the future potential of the technology.
About this summary

Originally published by Hankyoreh in Korean. Translated, summarized, and contextualized automatically by DistantNews, with a note on how the source frames the story. Not individually reviewed before publishing. How this works.