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Single-Cell Biophysics: Measurement, Modulation, and Modeling

Poster Abstracts

138 

80-POS

Board 40

Heterogeneous Response of Lymphocytic Cells to Mitomycin-C Revealed by Microfluidic

Single-Cell Time-Lapse Microscopy

Akihisa Seita

1

, Yuichi Wakamoto

1,2

.

1

University of Tokyo, Bunkyo-ku, Tokyo, Japan,

2

University of Tokyo, Bunkyo-ku, Tokyo,

Japan.

Over the past years, single-cell analysis has revealed that cellular phenotypes are heterogeneous

even for genetically identical cells. It has been also shown that at least some types of phenotypic

heterogeneity contribute to adaptation of cellular population without apparent genetic mutations

from bacterial cells to cancer cells. However, understanding which single-cell phenotypic states

are related to growth and death of individual cells is generally difficult due to time-course

fluctuation of cellular phenotypes and transitions of environmental conditions caused by the

proliferation of cells. Microfluidic single-cell time-lapse microscopy is a promising technique to

achieve the reliable measurements on time-course fluctuations of cellular phenotype and tight

control of environmental conditions, yet such methods have been still limited to the

measurements for bacterial cells.

Here, we have created a microfluidics device for mammalian cells based on the “Mother

machine” scheme, that have allowed the long-term tracking of single bacterial cells in controlled

environments. With this device, we observed the response of single lymphocytic cells (L1210) to

Mitomycin-C for five days prior to drug treatment and six days under the continuous exposure to

the drug. The result showed that the cell lineages that divided more frequently before the drug

exposure had lower chances of survival after the exposure, which indicates that pre-exposure

growth states are correlated with the survival fates of individual cell lineages against Mitomycin-

C. In addition, pre-exposure interdivision times were positively correlated between the

neighboring generations (~0.6), suggesting some epigenetic factors affecting the growth

characteristics of cell lineages.