Abstract
Mitochondria are crucial to cellular physiology, and growing evidence highlights the significant impact of mitochondrial dysfunction in diabetes, aging, neurodegenerative disorders, and cancers. Therefore, mitochondrial transplantation shows great
potential for therapeutic use in treating these diseases. However, transplantation process is notably challenging due to very low efficiency and rapid loss of bioactivity post‐isolation, leading to poor reproducibility and reliability. In this study, we develop a novel strategy to form a nanometer‐thick protective shell around isolated mitochondria using Metal‐Organic Frameworks (MOFs) through biomineralization. Our findings demonstrate that this encapsulation method effectively maintains mito-
chondria bioactivity for at least 4 weeks at room temperature. Furthermore, the efficiency of intracellular delivery of mitochondria is significantly enhanced through the surface functionalization of MOFs with polyethyleneimine (PEI) and the cell‐
penetrating peptide Tat. The successful delivery of mitochondria isolated from non‐tumorigenic cells into cancer cells results in notable tumor‐suppressive effects. Taken together, our technology represents a significant advancement in mitochondria
research, particularly on understanding their role in cancer. It also lays the groundwork for utilizing mitochondria as therapeutic agents in cancer treatment.
potential for therapeutic use in treating these diseases. However, transplantation process is notably challenging due to very low efficiency and rapid loss of bioactivity post‐isolation, leading to poor reproducibility and reliability. In this study, we develop a novel strategy to form a nanometer‐thick protective shell around isolated mitochondria using Metal‐Organic Frameworks (MOFs) through biomineralization. Our findings demonstrate that this encapsulation method effectively maintains mito-
chondria bioactivity for at least 4 weeks at room temperature. Furthermore, the efficiency of intracellular delivery of mitochondria is significantly enhanced through the surface functionalization of MOFs with polyethyleneimine (PEI) and the cell‐
penetrating peptide Tat. The successful delivery of mitochondria isolated from non‐tumorigenic cells into cancer cells results in notable tumor‐suppressive effects. Taken together, our technology represents a significant advancement in mitochondria
research, particularly on understanding their role in cancer. It also lays the groundwork for utilizing mitochondria as therapeutic agents in cancer treatment.
| Original language | English |
|---|---|
| Article number | e134 |
| Pages (from-to) | 1-16 |
| Number of pages | 16 |
| Journal | Smart medicine |
| Volume | 4 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 2025 |
| Publication type | A1 Journal article-refereed |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- biomineralization
- cancer cells
- metal‐organic frameworks
- mitochondria
- mitochondria transplantation
Publication forum classification
- Publication forum level 1
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