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急性免疫介导性肝炎转基因小鼠模型中肝血窦的显著变化。

Marked changes of the hepatic sinusoid in a transgenic mouse model of acute immune-mediated hepatitis.

作者信息

Warren Alessandra, Bertolino Patrick, Benseler Volker, Fraser Robin, McCaughan Geoffrey W, Le Couteur David G

机构信息

Centre for Education and Research on Ageing and the ANZAC Research Institute, Concord RG Hospital and University of Sydney, Sydney, Australia.

出版信息

J Hepatol. 2007 Feb;46(2):239-46. doi: 10.1016/j.jhep.2006.08.022. Epub 2006 Oct 23.

Abstract

BACKGROUND/AIMS: The liver sinusoidal endothelial cell (LSEC) is increasingly recognized as having an important role in hepatic immunity. However, the responses of LSECs and the hepatic sinusoid in immune-mediated hepatitis are poorly described.

METHODS

We studied a transgenic mouse model of acute immune-mediated hepatitis: Met-Kb mice injected with T cells from Des-TCR mice.

RESULTS

Hepatitis was characterized by lymphocyte infiltrates causing severe but transient liver damage. There were marked changes in the ultrastructure of the LSEC five days after injection of the T cells that coincided with the peak of the hepatitis. The porosity of fenestrations in the LSEC decreased and the endothelium became thickened. LSECs appeared to be markedly activated. These changes were associated with narrowing of the space of Disse, loss of hepatocellular microvilli and deposition of basal lamina. Lymphocytes were seen passing through fenestrations. Loss of fenestration in the LSEC prevented hepatitis induced by a second injection of lymphocytes on day 5.

CONCLUSIONS

Structural changes in the LSEC occur during the peak of a mouse model of immune-mediated hepatitis. These changes were associated with attenuation of subsequent liver damage, suggesting that they may influence immunological responses mediated by LSECs or the passage of lymphocytes through LSEC fenestrations.

摘要

背景/目的:肝窦内皮细胞(LSEC)在肝脏免疫中的重要作用日益受到认可。然而,在免疫介导性肝炎中LSEC和肝窦的反应鲜有描述。

方法

我们研究了急性免疫介导性肝炎的转基因小鼠模型:给Met-Kb小鼠注射来自Des-TCR小鼠的T细胞。

结果

肝炎的特征是淋巴细胞浸润导致严重但短暂的肝损伤。注射T细胞五天后,LSEC的超微结构出现明显变化,这与肝炎的高峰期一致。LSEC窗孔的孔隙率降低,内皮增厚。LSEC似乎被显著激活。这些变化与狄氏间隙变窄、肝细胞微绒毛丧失和基底膜沉积有关。可见淋巴细胞穿过窗孔。LSEC窗孔丧失可预防在第5天再次注射淋巴细胞诱导的肝炎。

结论

在免疫介导性肝炎小鼠模型的高峰期,LSEC会发生结构变化。这些变化与随后肝损伤的减轻有关,表明它们可能影响由LSEC介导的免疫反应或淋巴细胞通过LSEC窗孔的过程。

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