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Shrimp miR-965 transfers tumoricidal mitochondria
BACKGROUND: Micro RNA of Marsupenaeus japonicas has been known to promote apoptosis of tumor cells. However, the detailed mechanisms are not well understood. RESULTS: Using tomographic microscope, which can detect the internal structure of cells, we observed breast tumor cells following treatment of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9598032/ https://www.ncbi.nlm.nih.gov/pubmed/36289539 http://dx.doi.org/10.1186/s12575-022-00178-8 |
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author | Kim, Hyueyun Choi, Ji Ha Moon, Chang Mo Kang, Jihee Lee Woo, Minna Kim, Minsuk |
author_facet | Kim, Hyueyun Choi, Ji Ha Moon, Chang Mo Kang, Jihee Lee Woo, Minna Kim, Minsuk |
author_sort | Kim, Hyueyun |
collection | PubMed |
description | BACKGROUND: Micro RNA of Marsupenaeus japonicas has been known to promote apoptosis of tumor cells. However, the detailed mechanisms are not well understood. RESULTS: Using tomographic microscope, which can detect the internal structure of cells, we observed breast tumor cells following treatment of the miRNA. Intriguingly, we found that mitochondria migrate to an adjacent tumor cells through a tunneling nanotube. To recapitulate this process, we engineered a microfluidic device through which mitochondria were transferred. We show that this mitochondrial transfer process released endonuclease G (Endo G) into tumor cells, which we referred to herein as unsealed mitochondria. Importantly, Endo G depleted mitochondria alone did not have tumoricidal effects. Moreover, unsealed mitochondria had synergistic apoptotic effects with subtoxic dose of doxorubicin thereby mitigating cardiotoxicity. CONCLUSIONS: Together, we show that the mitochondrial transfer through microfluidics can provide potential novel strategies towards tumor cell death. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12575-022-00178-8. |
format | Online Article Text |
id | pubmed-9598032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95980322022-10-27 Shrimp miR-965 transfers tumoricidal mitochondria Kim, Hyueyun Choi, Ji Ha Moon, Chang Mo Kang, Jihee Lee Woo, Minna Kim, Minsuk Biol Proced Online Methodology BACKGROUND: Micro RNA of Marsupenaeus japonicas has been known to promote apoptosis of tumor cells. However, the detailed mechanisms are not well understood. RESULTS: Using tomographic microscope, which can detect the internal structure of cells, we observed breast tumor cells following treatment of the miRNA. Intriguingly, we found that mitochondria migrate to an adjacent tumor cells through a tunneling nanotube. To recapitulate this process, we engineered a microfluidic device through which mitochondria were transferred. We show that this mitochondrial transfer process released endonuclease G (Endo G) into tumor cells, which we referred to herein as unsealed mitochondria. Importantly, Endo G depleted mitochondria alone did not have tumoricidal effects. Moreover, unsealed mitochondria had synergistic apoptotic effects with subtoxic dose of doxorubicin thereby mitigating cardiotoxicity. CONCLUSIONS: Together, we show that the mitochondrial transfer through microfluidics can provide potential novel strategies towards tumor cell death. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12575-022-00178-8. BioMed Central 2022-10-26 /pmc/articles/PMC9598032/ /pubmed/36289539 http://dx.doi.org/10.1186/s12575-022-00178-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Methodology Kim, Hyueyun Choi, Ji Ha Moon, Chang Mo Kang, Jihee Lee Woo, Minna Kim, Minsuk Shrimp miR-965 transfers tumoricidal mitochondria |
title | Shrimp miR-965 transfers tumoricidal mitochondria |
title_full | Shrimp miR-965 transfers tumoricidal mitochondria |
title_fullStr | Shrimp miR-965 transfers tumoricidal mitochondria |
title_full_unstemmed | Shrimp miR-965 transfers tumoricidal mitochondria |
title_short | Shrimp miR-965 transfers tumoricidal mitochondria |
title_sort | shrimp mir-965 transfers tumoricidal mitochondria |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9598032/ https://www.ncbi.nlm.nih.gov/pubmed/36289539 http://dx.doi.org/10.1186/s12575-022-00178-8 |
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