Literature DB >> 28762188

A comparative study of U937 cell size changes during apoptosis initiation by flow cytometry, light scattering, water assay and electronic sizing.

Valentina Yurinskaya1, Nikolay Aksenov1, Alexey Moshkov1, Michael Model2, Tatyana Goryachaya1, Alexey Vereninov3.   

Abstract

A decrease in flow cytometric forward light scatter (FSC) is commonly interpreted as a sign of apoptotic cell volume decrease (AVD). However, the intensity of light scattering depends not only on the cell size but also on its other characteristics, such as hydration, which may affect the scattering in the opposite way. That makes estimation of AVD by FSC problematic. Here, we aimed to clarify the relationship between light scattering, cell hydration (assayed by buoyant density) and cell size by the Coulter technique. We used human lymphoid cells U937 exposed to staurosporine, etoposide or hypertonic stress as an apoptotic model. An initial increase in FSC was found to occur in apoptotic cells treated with staurosporine and hypertonic solutions; it is accompanied by cell dehydration and is absent in apoptosis caused by etoposide that is consistent with the lack of dehydration in this case. Thus, the effect of dehydration on the scattering signal outweighs the effect of reduction in cell size. The subsequent FSC decrease, which occurred in parallel to accumulation of annexin-positive cells, was similar in apoptosis caused by all three types of inducers. We conclude that an increase, but not a decrease in light scattering, indicates the initial cell volume decrease associated with apoptotic cell dehydration.

Entities:  

Keywords:  Apoptosis; Apoptotic volume decrease; Cell volume assay; Cell water; Flow cytometer light scattering

Mesh:

Substances:

Year:  2017        PMID: 28762188     DOI: 10.1007/s10495-017-1406-y

Source DB:  PubMed          Journal:  Apoptosis        ISSN: 1360-8185            Impact factor:   4.677


  5 in total

1.  Simple and Efficient Microsolid-Phase Extraction Tip-Based Sample Preparation Workflow to Enable Sensitive Proteomic Profiling of Limited Samples (200 to 10,000 Cells).

Authors:  James C Kostas; Michal Greguš; Jan Schejbal; Somak Ray; Alexander R Ivanov
Journal:  J Proteome Res       Date:  2021-02-24       Impact factor: 4.466

2.  Flow fluorometry quantification of anion channel VRAC subunit LRRC8A at the membrane of living U937 cells.

Authors:  Valentina Yurinskaya; Nikolay Aksenov; Alexey Moshkov; Tatyana Goryachaya; Ashley Shemery; Alexey Vereninov
Journal:  Channels (Austin)       Date:  2020-12       Impact factor: 2.581

3.  Daphnoretin induces reactive oxygen species-mediated apoptosis in melanoma cells.

Authors:  Hui Wang; Xue Hu; Minjing Li; Zhaohai Pan; Defang Li; Qiusheng Zheng
Journal:  Oncol Lett       Date:  2021-04-08       Impact factor: 2.967

4.  Cation-Chloride Cotransporters, Na/K Pump, and Channels in Cell Water/Ionic Balance Regulation Under Hyperosmolar Conditions: In Silico and Experimental Studies of Opposite RVI and AVD Responses of U937 Cells to Hyperosmolar Media.

Authors:  Valentina E Yurinskaya; Alexey A Vereninov
Journal:  Front Cell Dev Biol       Date:  2022-01-24

5.  A Tool for Computation of Changes in Na+, K+, Cl- Channels and Transporters Due to Apoptosis by Data on Cell Ion and Water Content Alteration.

Authors:  Valentina E Yurinskaya; Igor A Vereninov; Alexey A Vereninov
Journal:  Front Cell Dev Biol       Date:  2019-04-17
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.