Induction of morphological changes in death-induced cancer cells monitored by holographic microscopy.
(2015) In Journal of Structural Biology 189(3). p.207-212- Abstract
- We are using the label-free technique of holographic microscopy to analyze cellular parameters including cell number, confluence, cellular volume and area directly in the cell culture environment. We show that death-induced cells can be distinguished from untreated counterparts by the use of holographic microscopy, and we demonstrate its capability for cell death assessment. Morphological analysis of two representative cell lines (L929 and DU145) was performed in the culture flasks without any prior cell detachment. The two cell lines were treated with the anti-tumour agent etoposide for 1-3days. Measurements by holographic microscopy showed significant differences in average cell number, confluence, volume and area when comparing... (More)
- We are using the label-free technique of holographic microscopy to analyze cellular parameters including cell number, confluence, cellular volume and area directly in the cell culture environment. We show that death-induced cells can be distinguished from untreated counterparts by the use of holographic microscopy, and we demonstrate its capability for cell death assessment. Morphological analysis of two representative cell lines (L929 and DU145) was performed in the culture flasks without any prior cell detachment. The two cell lines were treated with the anti-tumour agent etoposide for 1-3days. Measurements by holographic microscopy showed significant differences in average cell number, confluence, volume and area when comparing etoposide-treated with untreated cells. The cell volume of the treated cell lines was initially increased at early time-points. By time, cells decreased in volume, especially when treated with high doses of etoposide. In conclusion, we have shown that holographic microscopy allows label-free and completely non-invasive morphological measurements of cell growth, viability and death. Future applications could include real-time monitoring of these holographic microscopy parameters in cells in response to clinically relevant compounds. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/5145873
- author
- El-Schish, Zahra LU ; Mölder, Anna ; Tassidis, Helena LU ; Härkönen, Pirkko LU ; Falck Miniotis, Maria LU and Gjörloff Wingren, Anette LU
- organization
- publishing date
- 2015
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Journal of Structural Biology
- volume
- 189
- issue
- 3
- pages
- 207 - 212
- publisher
- Elsevier
- external identifiers
-
- pmid:25637284
- wos:000351249500005
- scopus:84923275881
- pmid:25637284
- ISSN
- 1095-8657
- DOI
- 10.1016/j.jsb.2015.01.010
- language
- English
- LU publication?
- yes
- additional info
- Department affilation moved from v1000588 (Tumour Biology, Malmö) to v1000562 (Department of Translational Medicine) on 2016-01-18 14:39:28.
- id
- 403a0305-fe3f-495a-86f7-cd1b608f513d (old id 5145873)
- alternative location
- http://www.ncbi.nlm.nih.gov/pubmed/25637284?dopt=Abstract
- date added to LUP
- 2016-04-01 10:50:45
- date last changed
- 2022-04-20 06:47:33
@article{403a0305-fe3f-495a-86f7-cd1b608f513d,
abstract = {{We are using the label-free technique of holographic microscopy to analyze cellular parameters including cell number, confluence, cellular volume and area directly in the cell culture environment. We show that death-induced cells can be distinguished from untreated counterparts by the use of holographic microscopy, and we demonstrate its capability for cell death assessment. Morphological analysis of two representative cell lines (L929 and DU145) was performed in the culture flasks without any prior cell detachment. The two cell lines were treated with the anti-tumour agent etoposide for 1-3days. Measurements by holographic microscopy showed significant differences in average cell number, confluence, volume and area when comparing etoposide-treated with untreated cells. The cell volume of the treated cell lines was initially increased at early time-points. By time, cells decreased in volume, especially when treated with high doses of etoposide. In conclusion, we have shown that holographic microscopy allows label-free and completely non-invasive morphological measurements of cell growth, viability and death. Future applications could include real-time monitoring of these holographic microscopy parameters in cells in response to clinically relevant compounds.}},
author = {{El-Schish, Zahra and Mölder, Anna and Tassidis, Helena and Härkönen, Pirkko and Falck Miniotis, Maria and Gjörloff Wingren, Anette}},
issn = {{1095-8657}},
language = {{eng}},
number = {{3}},
pages = {{207--212}},
publisher = {{Elsevier}},
series = {{Journal of Structural Biology}},
title = {{Induction of morphological changes in death-induced cancer cells monitored by holographic microscopy.}},
url = {{http://dx.doi.org/10.1016/j.jsb.2015.01.010}},
doi = {{10.1016/j.jsb.2015.01.010}},
volume = {{189}},
year = {{2015}},
}