Fas-deficient mice have impaired alveolar neutrophil recruitment and decreased expression of anti-KC autoantibody:KC complexes in a model of acute lung injury.
Fas-deficient mice have impaired alveolar neutrophil recruitment and decreased expression of anti-KC autoantibody:KC complexes in a model of acute lung injury.
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缺乏FAS的小鼠在急性肺损伤模型中损害了肺泡嗜中性粒细胞的募集和抗KC自身抗体的表达降低。
DOI:
10.1186/1465-9921-13-91
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发表时间:
2012-10-09
影响因子:
5.8
通讯作者:
Matute-Bello G
中科院分区:
文献类型:
--
作者:
Gil S;Farnand AW;Altemeier WA;Gill SE;Kurdowska A;Krupa A;Florence JM;Matute-Bello G
Exposure to mechanical ventilation enhances lung injury in response to various stimuli, such as bacterial endotoxin (LPS). The Fas/FasL system is a receptor ligand system that has dual pro-apoptotic and pro-inflammatory functions and has been implicated in the pathogenesis of lung injury. In this study we test the hypothesis that a functioning Fas/FasL system is required for the development of lung injury in mechanically ventilated mice. C57BL/6 (B6) and Fas-deficient lpr mice were exposed to either intra-tracheal PBS followed by spontaneous breathing or intra-tracheal LPS followed by four hours mechanical ventilation with tidal volumes of 10 mL/kg, respiratory rate of 150 breaths per minute, inspired oxygen 0.21 and positive end expiratory pressure (PEEP) of 3 cm of water. Compared with the B6 mice, the lpr mice showed attenuation of the neutrophilic response as measured by decreased numbers of BAL neutrophils and lung myeloperoxidase activity. Interestingly, the B6 and lpr mice had similar concentrations of pro-inflammatory cytokines, including CXCL1 (KC), and similar measurements of permeability and apoptosis. However, the B6 mice showed greater deposition of anti-KC:KC immune complexes in the lungs, as compared with the lpr mice. We conclude that a functioning Fas/FasL system is required for full neutrophilic response to LPS in mechanically ventilated mice.
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DOI:
10.1042/cs20090422
发表时间:
2010-01-26
期刊:
Clinical science (London, England : 1979)
影响因子:
--
作者:
Fudala R;Krupa A;Stankowska D;Allen TC;Kurdowska AK
通讯作者:
Kurdowska AK
DOI:
10.1165/rcmb.2006-0395oc
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2007-11-01
影响因子:
6.4
作者:
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通讯作者:
Kurdowska, Anna K.
DOI:
10.1186/cc5050
发表时间:
2006
期刊:
Critical care (London, England)
影响因子:
--
作者:
O'Mahony DS;Liles WC;Altemeier WA;Dhanireddy S;Frevert CW;Liggitt D;Martin TR;Matute-Bello G
通讯作者:
Matute-Bello G
影响因子:
5.5
作者:
Boxio, R;Bossenmeyer-Pourié, C;Nüsse, O
通讯作者:
Nüsse, O
DOI:
10.1164/rccm.200509-1473oc
发表时间:
2006-03-15
影响因子:
24.7
作者:
Gharib, SA;Liles, WC;Altemeier, WA
通讯作者:
Altemeier, WA