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Dynamic changes in the cell membrane on three dimensional low coherent quantitative phase microscopy (3D LC-QPM) after treatment with the near infrared photoimmunotherapy

Near infrared photoimmunotherapy (NIR-PIT) is a newly developed cancer therapy that relies on the binding of a near-infrared antibody photoabsorber conjugate (APC) to a cancer cell. Subsequent exposure to NIR light selectively induces rapid necrotic cell death on target-expressing cells with minimal...

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Autores principales: Ogata, Fusa, Nagaya, Tadanobu, Okuyama, Shuhei, Maruoka, Yasuhiro, Choyke, Peter L., Yamauchi, Toyohiko, Kobayashi, Hisataka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732807/
https://www.ncbi.nlm.nih.gov/pubmed/29262641
http://dx.doi.org/10.18632/oncotarget.22223
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author Ogata, Fusa
Nagaya, Tadanobu
Okuyama, Shuhei
Maruoka, Yasuhiro
Choyke, Peter L.
Yamauchi, Toyohiko
Kobayashi, Hisataka
author_facet Ogata, Fusa
Nagaya, Tadanobu
Okuyama, Shuhei
Maruoka, Yasuhiro
Choyke, Peter L.
Yamauchi, Toyohiko
Kobayashi, Hisataka
author_sort Ogata, Fusa
collection PubMed
description Near infrared photoimmunotherapy (NIR-PIT) is a newly developed cancer therapy that relies on the binding of a near-infrared antibody photoabsorber conjugate (APC) to a cancer cell. Subsequent exposure to NIR light selectively induces rapid necrotic cell death on target-expressing cells with minimal off-target effects. When treated with NIR-PIT, targeted cells become swollen, develop blebs and burst within minutes of light exposure. Detailed spatial and temporal morphological changes of the cellular membrane of targeted cells treated with NIR-PIT have not been fully explored with state-of-the-art microscopic methods. In this study, we investigated the morphologic and kinetic effects of PIT on two types of cells, a spindle-shaped 3T3/Her cell and a spheric-shaped MDA-MB468 cell, after NIR-PIT using three-dimensional low-coherent quantitative phase microscopy (3D LC-QPM). Adhesive cells treated with NIR-PIT demonstrated region-specific cell membrane rupture occurring first on the distal free edge of the cell near the site of adhesion, in a process that was independent of cell shape. The results show that the peripheral portions of the cell membrane near the site of adhesion are particularly vulnerable to the effects of NIR-PIT, likely because these sites exhibit higher baseline surface tension.
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spelling pubmed-57328072017-12-19 Dynamic changes in the cell membrane on three dimensional low coherent quantitative phase microscopy (3D LC-QPM) after treatment with the near infrared photoimmunotherapy Ogata, Fusa Nagaya, Tadanobu Okuyama, Shuhei Maruoka, Yasuhiro Choyke, Peter L. Yamauchi, Toyohiko Kobayashi, Hisataka Oncotarget Research Paper Near infrared photoimmunotherapy (NIR-PIT) is a newly developed cancer therapy that relies on the binding of a near-infrared antibody photoabsorber conjugate (APC) to a cancer cell. Subsequent exposure to NIR light selectively induces rapid necrotic cell death on target-expressing cells with minimal off-target effects. When treated with NIR-PIT, targeted cells become swollen, develop blebs and burst within minutes of light exposure. Detailed spatial and temporal morphological changes of the cellular membrane of targeted cells treated with NIR-PIT have not been fully explored with state-of-the-art microscopic methods. In this study, we investigated the morphologic and kinetic effects of PIT on two types of cells, a spindle-shaped 3T3/Her cell and a spheric-shaped MDA-MB468 cell, after NIR-PIT using three-dimensional low-coherent quantitative phase microscopy (3D LC-QPM). Adhesive cells treated with NIR-PIT demonstrated region-specific cell membrane rupture occurring first on the distal free edge of the cell near the site of adhesion, in a process that was independent of cell shape. The results show that the peripheral portions of the cell membrane near the site of adhesion are particularly vulnerable to the effects of NIR-PIT, likely because these sites exhibit higher baseline surface tension. Impact Journals LLC 2017-11-01 /pmc/articles/PMC5732807/ /pubmed/29262641 http://dx.doi.org/10.18632/oncotarget.22223 Text en Copyright: © 2017 Ogata et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Ogata, Fusa
Nagaya, Tadanobu
Okuyama, Shuhei
Maruoka, Yasuhiro
Choyke, Peter L.
Yamauchi, Toyohiko
Kobayashi, Hisataka
Dynamic changes in the cell membrane on three dimensional low coherent quantitative phase microscopy (3D LC-QPM) after treatment with the near infrared photoimmunotherapy
title Dynamic changes in the cell membrane on three dimensional low coherent quantitative phase microscopy (3D LC-QPM) after treatment with the near infrared photoimmunotherapy
title_full Dynamic changes in the cell membrane on three dimensional low coherent quantitative phase microscopy (3D LC-QPM) after treatment with the near infrared photoimmunotherapy
title_fullStr Dynamic changes in the cell membrane on three dimensional low coherent quantitative phase microscopy (3D LC-QPM) after treatment with the near infrared photoimmunotherapy
title_full_unstemmed Dynamic changes in the cell membrane on three dimensional low coherent quantitative phase microscopy (3D LC-QPM) after treatment with the near infrared photoimmunotherapy
title_short Dynamic changes in the cell membrane on three dimensional low coherent quantitative phase microscopy (3D LC-QPM) after treatment with the near infrared photoimmunotherapy
title_sort dynamic changes in the cell membrane on three dimensional low coherent quantitative phase microscopy (3d lc-qpm) after treatment with the near infrared photoimmunotherapy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732807/
https://www.ncbi.nlm.nih.gov/pubmed/29262641
http://dx.doi.org/10.18632/oncotarget.22223
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