Yinghua Xu
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Engineered exosome MDC@Ex-γ3-CeO₂@PDA for multi-target therapy of sepsis-induced acute lung injury
Abstract Sepsis-induced acute lung injury (ALI), with a complex pathogenesis, currently lacks clinically effective multi-target therapeutic strategies. Musca domestica cecropin (MDC), a promising antimicrobial, anti-inflammatory, and endothelial-repairing peptide, is limited by its high molecular weight and poor selectivity. Here, we developed an engineered exosome-based drug delivery system, MDC@Ex-γ3-CeO₂@PDA, for targeted treatment of sepsis-induced ALI.
An Electrochemical Oxidative Two-Fold C─C Bond Formation of Indolizines With Xanthenes
Conflicts of Interest The authors declare no conflicts of interest. Data Availability Statement The data supporting this article have been included as part of the Supplementary Information.
Correction to: Autocrine activation of JAK2 by IL-11 promotes platinum drug resistance
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Correction to: Oncogene https://doi.org/10.1038/s41388-018-0238-8, published online 17 April 2018 Following the publication of this article, the authors noted two inadvertent errors in Figure 5c, which occurred during figure assembly. The JAK2 immunoblot was mistakenly used in place of the STAT5 immunoblot, and the GAPDH loading control was inadvertently taken from a different blot generated from the same cell lysates. The corrected Figure 5c is provided below.
By Wei Zhou, Wei Sun, Sheng Dai, Yihua Cai, Chi-Wei Chen, Yunxiao Meng, Jennifer Lee, John Braisted, Yinghua Xu, Noel Southall, Paul Shinn, Xuefeng Huang, Zhangfa Song, Xiulei Chen, Yan Kai, Xin Cai, Qiang Hao, Stephanie Liu Verified, Stephanie Barak, Jing Hao, Zhijun Dai, Weiqun Peng, Huadong Pei, Zhiyong Han, David Chan, Wei Zheng, Wenge Zhu, Mingo M. H. Yung, Zongzhu Li, Annie N. Y. Cheung, Hextan Y. S. Ngan, Alexandros Tzatsos
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Nature
Verified
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