Bcl-2 overexpression in type II epithelial cells does not prevent hyperoxia-induced acute lung injury in mice

作者
Isabelle Ruchonnet-Métrailler,Alessandra Pagano,Stéphanie Carnésecchi,Karim Khatib,Pedro Luis Herrera,Yves R. A. Donati,Camille Bron,Constance Barazzone‐Argiroffo
出处
期刊:American Journal of Physiology-lung Cellular and Molecular Physiology [American Physical Society]
卷期号:299 (3): L312-L322 被引量:16
标识
DOI:10.1152/ajplung.00212.2009
摘要

Bcl-2 is an anti-apoptotic molecule preventing oxidative stress damage and cell death. We have previously shown that Bcl-2 is able to prevent hyperoxia-induced cell death when overexpressed in a murine fibrosarcoma cell line L929. We hypothesized that its specific overexpression in pulmonary epithelial type II cells could prevent hyperoxia-induced lung injury by protecting the epithelial side of the alveolo-capillary barrier. In the present work, we first showed that in vitro Bcl-2 can rescue murine pulmonary epithelial cells (MLE12) from oxygen-induced cell apoptosis, as shown by analysis of LDH release, annexin V/propidium staining, and caspase-3 activity. We then generated transgenic mice overexpressing specifically Bcl-2 in lung epithelial type II cells under surfactant protein C (SP-C) promoter (Tg-Bcl-2) and exposed them to hyperoxia. Bcl-2 did not hinder hyperoxia-induced mitochondria and DNA oxidative damage of type II cell in vivo. Accordingly, lung damage was identical in both Tg-Bcl-2 and littermate mice strains, as measured by lung weight, bronchoalveolar lavage, and protein content. Nevertheless, we observed a significant lower number of TUNEL-positive cells in type II cells isolated from Tg-Bcl-2 mice exposed to hyperoxia compared with cells isolated from littermate mice. In summary, these results show that although Bcl-2 overexpression is able to prevent hyperoxia-induced cell death at single cell level in vitro and ex vivo, it is not sufficient to prevent cell death of parenchymal cells and to protect the lung from acute damage in mice.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
研友_LMBPXn完成签到,获得积分10
刚刚
1秒前
落寞妙松完成签到,获得积分10
2秒前
科研通AI6.4的应助被Rita采纳,获得10
5秒前
5秒前
5秒前
汉堡包的应助被mltyyds采纳,获得10
7秒前
HelloFM发布了新的文献求助10
8秒前
白风笙发布了新的文献求助10
9秒前
伊莎贝拉发布了新的文献求助10
9秒前
丰富鞋子完成签到,获得积分10
10秒前
13秒前
阿水的应助被汤圆软软软采纳,获得10
15秒前
Warma的应助被汤圆软软软采纳,获得10
15秒前
111zzzzzz的应助被丰富鞋子采纳,获得10
15秒前
Warma的应助被汤圆软软软采纳,获得10
15秒前
搜集达人的应助被汤圆软软软采纳,获得10
15秒前
研友_VZG7GZ的应助被汤圆软软软采纳,获得10
16秒前
Hello的应助被汤圆软软软采纳,获得10
16秒前
SciGPT的应助被汤圆软软软采纳,获得10
16秒前
清爽老九的应助被汤圆软软软采纳,获得30
16秒前
思源的应助被汤圆软软软采纳,获得10
16秒前
香蕉觅云的应助被汤圆软软软采纳,获得10
17秒前
nnn发布了新的文献求助10
17秒前
忧郁小刺猬完成签到,获得积分10
22秒前
小毛竹完成签到 ,获得积分10
23秒前
24秒前
zzsr完成签到,获得积分20
24秒前
Tomqiu完成签到 ,获得积分10
26秒前
酷波er的应助被澳bobo采纳,获得10
26秒前
可爱的函函的应助被HelloFM采纳,获得10
27秒前
27秒前
xiaoyuan发布了新的文献求助10
27秒前
白风笙完成签到,获得积分20
28秒前
30秒前
zzsr发布了新的文献求助10
30秒前
31秒前
逆袭者发布了新的文献求助10
32秒前
34秒前
澳bobo发布了新的文献求助10
35秒前
高分求助中
(应助此贴封号)通过应助OA文献获取积分 10000
Rosenblum, Global Change Biology 800
Computational Chemical Reaction Engineering: Modeling, Simulation, and Design with MATLAB 600
Organizational Behavior 510
Management and the Arts 510
A Will for the Machine: Computerization, Automation, and the Arts in South Africa 400
Decentring Leadership 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 计算机科学 工程类 纳米技术 内科学 物理 有机化学 化学工程 生物化学 复合材料 光电子学 细胞生物学 心理学 量子力学 催化作用 物理化学 电极
热门帖子
关注 科研通微信公众号,转发送积分 7809249
求助须知:如何正确求助?哪些是违规求助? 9341509
关于积分的说明 20507275
捐赠科研通 7401778
什么是DOI,文献DOI怎么找? 3329050
关于科研通互助平台的介绍 2475843
邀请新用户注册赠送积分活动 2347610