pH-Dependent migratory behaviors of neutrophil-like cells in a microfluidic device with controllability of dissolved gas concentrations

Inflammatory microenvironments often become acidic (pH < 7.4) due to tissue oxygen deprivation and lactate release in glycolysis by activated immune cells. Although neutrophils are known to accumulate in such microenvironments, the effects of pH on their migration are not fully understood. Here, we first investigated the pH control around cultured cells with a microfluidic device, which was equipped with two gas channels above three parallel media channels. By supplying gas mixtures with predefined carbon dioxide (CO<sub>2</sub>) concentrations to the gas channels, the gas exchange adjusted the dissolved CO<sub>2</sub> and affected the chemical equilibrium of sodium hydrogen carbonate in the cell culture medium. A pH gradient from 8.3 to 6.8 was generated along the media channels when gas mixtures containing 1% and 50% CO<sub>2</sub> were supplied to the left and right gas channels, respectively. Neutrophil-like differentiated human promyelocytic leukemia cells (HL-60) were then seeded to the fibronectin-coated media channels and their migratory behaviors were quantified while varying the pH. The cell migration became more active and faster under high pH than under low pH conditions. However, no directional migration along the pH gradient was detected during the three-hour observation. Thus, the microfluidic device is useful to elucidate pH-dependent cellular dynamics.

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Publication Details

Journal
Scientific Reports
Published
2024-11-20
DOI
https://doi.org/10.1038/s41598-024-79625-3
Citations
1
Primary Topic
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Type
article
Field-Weighted Citation Impact
0.24

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article

pH-Dependent migratory behaviors of neutrophil-like cells in a microfluidic device with controllability of dissolved gas concentrations

Masashi Tomita, Kenichi Funamoto, Satomi Hirose, Taishi Nakamura
1 citations
Scientific Reports
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
0.24
article

pH-Dependent migratory behaviors of neutrophil-like cells in a microfluidic device with controllability of dissolved gas concentrations

Masashi Tomita, Kenichi Funamoto, Satomi Hirose, Taishi Nakamura
article en
1 citations

Abstract

Inflammatory microenvironments often become acidic (pH < 7.4) due to tissue oxygen deprivation and lactate release in glycolysis by activated immune cells. Although neutrophils are known to accumulate in such microenvironments, the effects of pH on their migration are not fully understood. Here, we first investigated the pH control around cultured cells with a microfluidic device, which was equipped with two gas channels above three parallel media channels. By supplying gas mixtures with predefined carbon dioxide (CO<sub>2</sub>) concentrations to the gas channels, the gas exchange adjusted the dissolved CO<sub>2</sub> and affected the chemical equilibrium of sodium hydrogen carbonate in the cell culture medium. A pH gradient from 8.3 to 6.8 was generated along the media channels when gas mixtures containing 1% and 50% CO<sub>2</sub> were supplied to the left and right gas channels, respectively. Neutrophil-like differentiated human promyelocytic leukemia cells (HL-60) were then seeded to the fibronectin-coated media channels and their migratory behaviors were quantified while varying the pH. The cell migration became more active and faster under high pH than under low pH conditions. However, no directional migration along the pH gradient was detected during the three-hour observation. Thus, the microfluidic device is useful to elucidate pH-dependent cellular dynamics.

Scientific ReportsVol. 14(1)
Tohoku University (JP)
Japan Society for the Promotion of Science, Precursory Research for Embryonic Science and Technology
Openalex Percentile: Top 40%
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
0.24
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pH-Dependent migratory behaviors of neutrophil-like cells in a microfluidic device with controllability of dissolved gas concentrations — Masashi Tomita, Kenichi Funamoto, et al. · Scientific Reports (2024) | TGRS Research Map | TGRS