Ultrastructural Alteration of Pulmonary Capillary Endothelial Glycocalyx During Endotoxemia

被引:91
作者
Inagawa, Risa [1 ]
Okada, Hideshi [1 ]
Takemura, Genzou [2 ]
Suzuki, Kodai [1 ]
Takada, Chihiro [1 ]
Yano, Hirohisa [1 ]
Ando, Yoshiaki [1 ]
Usui, Takahiro [1 ]
Hotta, Yasuaki [3 ]
Miyazaki, Nagisa [2 ]
Tsujimoto, Akiko [2 ]
Zaikokuji, Ryogen [4 ]
Matsumoto, Atsumu [1 ]
Kawaguchi, Tomonori [1 ]
Doi, Tomoaki [1 ]
Yoshida, Takahiro [1 ]
Yoshida, Shozo [1 ]
Kumada, Keisuke [1 ]
Ushikoshi, Hiroaki [1 ]
Toyoda, Izumi [1 ]
Ogura, Shinji [1 ]
机构
[1] Gifu Univ, Grad Sch Med, Dept Emergency & Disaster Med, 1-1 Yanagido, Gifu 5011194, Japan
[2] Asahi Univ, Sch Dent, Dept Internal Med, Mizuho, Japan
[3] Asahi Univ, Sch Dent, Res Inst Biotechnol, Mizuho, Japan
[4] Gifu Pharmaceut Univ, Dept Biofunct Anal, Lab Mol Biol, Gifu, Japan
关键词
acute lung injury; pathology; sepsis; vasculitis; FLUID SHEAR-STRESS; SEPTIC SHOCK; SEPSIS; CELLS; MODEL; LAYER; PERMEABILITY; HYALURONAN;
D O I
10.1016/j.chest.2018.03.003
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
BACKGROUND: The most recent diagnostic criteria for sepsis include organ failure. Microvascular endothelial injury is believed to lead to the multiple organ failure seen in sepsis, although the precisemechanismis still controversial. ARDS is the primary complication during the sequential development of multiple organ dysfunction in sepsis, and endothelial injury is deeply involved. Sugar-protein glycocalyx coats all healthy vascular endothelium, and its disruption is one factor believed to contribute to microvascular endothelial dysfunction during sepsis. The goal of this study was to observe the three-dimensional ultrastructural alterations in the pulmonary capillary endothelium, including the glycocalyx, during sepsis-induced pulmonary vasculitis. METHODS: This study investigated the three-dimensional ultrastructure of pulmonary vascular endothelial glycocalyx in a mouse lipopolysaccharide-induced endotoxemia model. Lungs were fixed with lanthanum-containing alkaline fixative to preserve the glycocalyx. RESULTS: On both scanning and transmission electron microscopic imaging, the capillary endothelial glycocalyx appeared as a moss-like structure entirely covering the endothelial cell surface in normal mice. In the septic lung following liposaccharide injection, however, this structure was severely disrupted; it appeared to be peeling away and coagulated. In addition, syndecan-1 levels were significantly reduced in the septic lung, and numerous spherical structures containing glycocalyx were observed on the endothelial surface. CONCLUSIONS: It appears that endothelial glycocalyx in the lung is markedly disrupted under experimental endotoxemia conditions. This finding supports the notion that disruption of the glycocalyx is causally related to the microvascular endothelial dysfunction that is characteristic of sepsis-induced ARDS.
引用
收藏
页码:317 / 325
页数:9
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