The effect of adoptive transferring myeloid-derived suppressor cells in ventilator-induced lung injury mice

被引:1
|
作者
Shan, Fangzhen [1 ,2 ]
Tang, Fenglian [1 ]
Liu, Yuan [3 ]
Han, Xiao [1 ]
Wu, Wei [1 ]
Tang, Yanhua [1 ]
Zhan, Qingyuan [4 ]
Zhang, Nannan [1 ,4 ,5 ,6 ]
机构
[1] Jining Med Univ, Dept Pulm & Crit Care Med, Affiliated Hosp, Jining, Shandong, Peoples R China
[2] Jining Med Univ, Med Res Ctr, Affiliated Hosp, Jining, Shandong, Peoples R China
[3] Jining Med Univ, Dept Intens Care Unit 3, Affiliated Hosp, Jining, Shandong, Peoples R China
[4] China Japan Friendship Hosp, Dept Pulm & Crit Care Med, Beijing, Peoples R China
[5] Jining Med Univ, Dept Pulm & Crit Care Med, Affiliated Hosp, Jining 272029, Shandong, Peoples R China
[6] 89 Guhuai Rd, Jining 272029, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Ventilator -induced lung injury; Myeloid -derived suppressor cells; Inflammation; T cells; MECHANICAL VENTILATION; INFLAMMATION; ACTIVATION; SURVIVAL; SEPSIS;
D O I
10.1016/j.heliyon.2024.e25595
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The effects of adoptive transferring myeloid-derived suppressor cells (MDSCs) to mice with ventilator-induced lung injury (VILI) are unclear. Our objective was to investigate the effects of adoptively transferring MDSCs in VILI. The mouse model was created by introducing mechanical ventilation through a high tidal volume of 20 ml/kg for 4 h. Inflammation-induced MDSCs (iMDSCs) were collected from the bone marrow of mice with cecal ligation and puncture. iMDSCs were administrated through retrobulbar angular vein 1 h before the mechanical ventilation. The control group was anesthetized and maintained spontaneous respiration. After the termination of mechanical ventilation, bronchoalveolar lavage fluid (BALF) and lung samples 6 h were collected. The concentrations of BALF protein, levels of inflammatory mediators, and white blood cells were all significantly decreased in mice treated with iMDSCs. Histological examinations indicated reduced lung damage after iMDSCs treatment. Moreover, adoptive transfer of iMDSCs could reduce CD4+ T-cell counts and inhibit its inflammatory cytokine secretion. iMDSCs treatment was found to had no immunostimulatory effects or cause secondary infections in mice. In conclusion, MDSCs might be a potential targeted therapy for alleviating the inflammatory response of VILI mice in a T-cell dependent manner.
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页数:15
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