Luker J N, Vigiola Cruz M, Carney B C, Day A, Moffatt L T, Johnson L S, Shupp J W
Firefighters' Burn and Surgical Research Laboratory, MedStar Health Research Institute, Washington, USA.
The Burn Center, Department of Surgery, MedStar Washington Hospital Center, Washington, USA.
Ann Burns Fire Disasters. 2018 Mar 31;31(1):17-22.
Limited information exists regarding endothelial dysfunction following burn injury. This project aims to evaluate whether thermal injury results in shedding of the endothelial glycocalyx in a manner quantitatively proportional to injury severity, and whether theloss of intact glycocalyx is measurable in end organs. C57BL/6 mice were grouped as uninjured controls, 10% or 25% Total Body Surface Area (TBSA) scald burns. Blood and tissue sampling was performed over a specific time course. Plasma levels of shed syndecan-1, a marker of glycocalyx damage, were quantified by ELISA. Lung and spleen sections were stained with immunofluorescent anti-syndecan-1 antibodies to evaluate intact glycocalyx. Plasma syndecan-1 levels were higher in injured versus uninjured animals. Normalized levels of syndecan-1 in burned mice were significantly increased compared to hour 0 (p<0.05) at hours 4 and 8 post-injury in the 10% TBSA, and at hour 4 in the 25% TBSA group. Levels in the 10% and 25% TBSA groups peaked at hour 4 with fold change of 2.3 and 2.4 respectively. There was less pulmonary syndecan-1 immunostaining in burned animals compared to controls, and the levels inversely correlated with systemic shed syndecan- 1, beginning at hour 4 in the 10% TBSA injury group and at all time points in the 25% TBSA injury group, (0.27±0.06 and 0.14±0.04 respectively for hour 4). Similarly, there was less spleen syndecan-1 immunostaining in burned animals compared to controls at all time points. Burn injury causes shedding of syndecan-1 in a murine model, with levels correlated to injury severity and loss of the glycocalyx in lung and spleen. This work provides further insight into quantification and temporality of glycocalyx damage and systemic response to burn.
关于烧伤后内皮功能障碍的信息有限。本项目旨在评估热损伤是否会导致内皮糖萼脱落,且脱落程度与损伤严重程度呈定量比例关系,以及在终末器官中是否可检测到完整糖萼的丢失。将C57BL/6小鼠分为未受伤对照组、10%或25%体表面积(TBSA)烫伤组。在特定时间进程内进行血液和组织采样。通过酶联免疫吸附测定(ELISA)对血浆中糖萼损伤标志物脱落 syndecan-1的水平进行定量。用免疫荧光抗syndecan-1抗体对肺和脾切片进行染色,以评估完整糖萼情况。与未受伤动物相比,受伤动物的血浆syndecan-1水平更高。在10%TBSA组中,受伤小鼠的syndecan-1标准化水平在伤后4小时和8小时显著高于伤后0小时(p<0.05),在25%TBSA组中在伤后4小时显著升高。10%和25%TBSA组的水平在伤后4小时达到峰值,倍数变化分别为2.3和2.4。与对照组相比,烧伤动物肺组织中syndecan-1免疫染色较少,且在10%TBSA损伤组伤后4小时及25%TBSA损伤组所有时间点,肺组织中syndecan-1水平与全身脱落的syndecan-1呈负相关(伤后4小时分别为0.27±0.06和0.14±0.04)。同样,在所有时间点,与对照组相比,烧伤动物脾组织中syndecan-1免疫染色较少。烧伤会导致小鼠模型中syndecan-1脱落,其水平与损伤严重程度以及肺和脾中糖萼丢失相关。这项工作进一步深入了解了糖萼损伤的定量和时间性以及对烧伤的全身反应。