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. 2019 Feb 14;9:2096. doi: 10.1038/s41598-018-38312-w

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© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Cationic liposome mediated gene transfer of BiP/GRP78-DN dampens LPS-induced lung injury. WT C57BL/6 mice were injected i.v. with empty vector (EV)/liposome or dominant negative mutant BiP/GRP78 (BiP/GRP78-DN)/liposome complex. After 72 h, mice were aerosolized with 6 ml of saline alone or saline containing E.Coli LPS (0.5 mg/ml) for 30 min. Sixteen hours later, lung homogenates were analyzed for expression of BiP/GRP78-DN (A). BAL fluids were analyzed for ICAM-1 (B) and MCP-1 (C) levels. Lung homogenates were analyzed for MPO activity (D).