Author
Listed:
- Carlos Boto
(CNC-Center for Neurosciences and Cell Biology, University of Coimbra
3Is—Institute for Interdisciplinary Research, University of Coimbra)
- Emanuel Quartin
(CNC-Center for Neurosciences and Cell Biology, University of Coimbra
3Is—Institute for Interdisciplinary Research, University of Coimbra)
- Yijun Cai
(Key Laboratory of Cell Differentiation and Apoptosis of National Ministry of Education, Shanghai Jiao Tong University School of Medicine)
- Alberto Martín-Lorenzo
(Experimental Therapeutics and Translational Oncology Program, Instituto de Biologia Molecular y Celular del Cancer (IBMCC), CSIC/University of Salamanca
Institute of Biomedical Research of Salamanca (IBSAL))
- María Begoña García Cenador
(Institute of Biomedical Research of Salamanca (IBSAL)
University of Salamanca)
- Sandra Pinto
(CNC-Center for Neurosciences and Cell Biology, University of Coimbra
3Is—Institute for Interdisciplinary Research, University of Coimbra)
- Rajeev Gupta
(UCL Cancer Institute, University College London)
- Tariq Enver
(UCL Cancer Institute, University College London)
- Isidro Sánchez-García
(Experimental Therapeutics and Translational Oncology Program, Instituto de Biologia Molecular y Celular del Cancer (IBMCC), CSIC/University of Salamanca
Institute of Biomedical Research of Salamanca (IBSAL))
- Dengli Hong
(Key Laboratory of Cell Differentiation and Apoptosis of National Ministry of Education, Shanghai Jiao Tong University School of Medicine)
- Ricardo Pires das Neves
(CNC-Center for Neurosciences and Cell Biology, University of Coimbra
3Is—Institute for Interdisciplinary Research, University of Coimbra)
- Lino Ferreira
(CNC-Center for Neurosciences and Cell Biology, University of Coimbra
Faculty of Medicine, University of Coimbra)
Abstract
Leukaemia cells that are resistant to conventional therapies are thought to reside in protective niches. Here, we describe light-inducible polymeric retinoic acid (RA)-containing nanoparticles (NPs) with the capacity to accumulate in the cytoplasm of leukaemia cells for several days and release their RA payloads within a few minutes upon exposure to blue/UV light. Compared to NPs that are not activated by light exposure, these NPs more efficiently reduce the clonogenicity of bone marrow cancer cells from patients with acute myeloid leukaemia (AML) and induce the differentiation of RA-low sensitive leukaemia cells. Importantly, we show that leukaemia cells transfected with light-inducible NPs containing RA can engraft into bone marrow in vivo in the proximity of other leukaemic cells, differentiate upon exposure to blue light and release paracrine factors that modulate nearby cells. The NPs described here offer a promising strategy for controlling distant cell populations and remotely modulating leukaemic niches.
Suggested Citation
Carlos Boto & Emanuel Quartin & Yijun Cai & Alberto Martín-Lorenzo & María Begoña García Cenador & Sandra Pinto & Rajeev Gupta & Tariq Enver & Isidro Sánchez-García & Dengli Hong & Ricardo Pires das N, 2017.
"Prolonged intracellular accumulation of light-inducible nanoparticles in leukemia cells allows their remote activation,"
Nature Communications, Nature, vol. 8(1), pages 1-13, August.
Handle:
RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms15204
DOI: 10.1038/ncomms15204
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms15204. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.