Electrotaxis of alveolar epithelial cells in direct-current electric fields.
10.1016/j.cjtee.2023.03.003
- Author:
Chao-Yue YANG
1
;
Jian-Hui SUN
2
;
Kan ZHU
2
;
Juan DU
2
;
Ying ZHANG
1
;
Cong-Hua LU
1
;
Wen-Yi LIU
2
;
Ke-Jun ZHANG
3
;
An-Qiang ZHANG
2
;
Ling ZENG
2
;
Jian-Xin JIANG
2
;
Li LI
4
,
5
Author Information
1. Department of Respiratory Medicine, Daping Hospital, Third Military Medical University (Army Medical University), Chongqing, 400042, China.
2. State Key Laboratory of Trauma, Burns, and Combined Injury, Department of Trauma Medical Center, Daping Hospital, Third Military Medical University (Army Medical University), Chongqing, 400042, China.
3. Department of Outpatients, Daping Hospital, Third Military Medical University (Army Medical University), Chongqing, 400042, China.
4. Department of Respiratory Medicine, Daping Hospital, Third Military Medical University (Army Medical University), Chongqing, 400042, China
5. State Key Laboratory of Trauma, Burns, and Combined Injury, Department of Trauma Medical Center, Daping Hospital, Third Military Medical University (Army Medical University), Chongqing, 400042, China. Electronic address: dpyyhxlili@tmmu.edu.cn.
- Publication Type:Journal Article
- Keywords:
Acute lung injury;
Alveolar epithelial cells;
Electric fields;
Electrotaxis;
Migration
- MeSH:
Humans;
Rats;
Animals;
Alveolar Epithelial Cells;
Lung;
Lung Injury;
Cell Movement/physiology*
- From:
Chinese Journal of Traumatology
2023;26(3):155-161
- CountryChina
- Language:English
-
Abstract:
PURPOSE:This study aims to elucidate the electrotaxis response of alveolar epithelial cells (AECs) in direct-current electric fields (EFs), explore the impact of EFs on the cell fate of AECs, and lay the foundation for future exploitation of EFs for the treatment of acute lung injury.
METHODS:AECs were extracted from rat lung tissues using magnetic-activated cell sorting. To elucidate the electrotaxis responses of AECs, different voltages of EFs (0, 50, 100, and 200 mV/mm) were applied to two types of AECs, respectively. Cell migrations were recorded and trajectories were pooled to better demonstrate cellular activities through graphs. Cell directionality was calculated as the cosine value of the angle formed by the EF vector and cell migration. To further demonstrate the impact of EFs on the pulmonary tissue, the human bronchial epithelial cells transformed with Ad12-SV40 2B (BEAS-2B cells) were obtained and experimented under the same conditions as AECs. To determine the influence on cell fate, cells underwent electric stimulation were collected to perform Western blot analysis.
RESULTS:The successful separation and culturing of AECs were confirmed through immunofluorescence staining. Compared with the control, AECs in EFs demonstrated a significant directionality in a voltage-dependent way. In general, type Ⅰ alveolar epithelial cells migrated faster than type Ⅱ alveolar epithelial cells, and under EFs, these two types of cells exhibited different response threshold. For type Ⅱ alveolar epithelial cells, only EFs at 200 mV/mm resulted a significant difference to the velocity, whereas for, EFs at both 100 mV/mm and 200 mV/mm gave rise to a significant difference. Western blotting suggested that EFs led to an increased expression of a AKT and myeloid leukemia 1 and a decreased expression of Bcl-2-associated X protein and Bcl-2-like protein 11.
CONCLUSION:EFs could guide and accelerate the directional migration of AECs and exert antiapoptotic effects, which indicated that EFs are important biophysical signals in the re-epithelialization of alveolar epithelium in lung injury.
