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缺乏转化生长因子α的小鼠对硫酸葡聚糖诱导的结肠炎易感性增加。

Mice lacking transforming growth factor alpha have an increased susceptibility to dextran sulfate-induced colitis.

作者信息

Egger B, Procaccino F, Lakshmanan J, Reinshagen M, Hoffmann P, Patel A, Reuben W, Gnanakkan S, Liu L, Barajas L, Eysselein V E

机构信息

Inflammatory Bowel Disease Center, Harbor-UCLA Medical Center, Torrance, USA.

出版信息

Gastroenterology. 1997 Sep;113(3):825-32. doi: 10.1016/s0016-5085(97)70177-x.

Abstract

BACKGROUND & AIMS: There is indirect evidence that transforming growth factor alpha (TGF-alpha) is an important mediator of mucosal defense and repair. TGF-alpha knockout mice and TGF-alpha-deficient mice (wa-1) provide novel approaches to evaluate the role of TGF-alpha in preserving the integrity of the colon.

METHODS

Colitis was induced by oral administration of dextran sodium sulfate (DSS, 5 g/dL) to knockout mice, their genetic controls (GC), wa-1 mice, and BALB/c mice. TGF-alpha was also administered intraperitoneally to wa-1 mice to evaluate the effect of exogenous TGF-alpha in DSS colitis.

RESULTS

In response to DSS, nearly 60% of the entire colonic mucosa was destroyed in knockout and wa-1 mice, compared with 22% in GC mice and 16% in BALB/ c mice. Body weight loss was doubled in knockout (28%) and wa-1 mice (23%) compared with GC (11%) and Balb/c mice (12%). TGF-alpha application to wa-1 mice reduced the severity of mucosal injury by almost 70% compared with controls.

CONCLUSIONS

The marked susceptibility of TGF-alpha knockout and wa-1 mice to DSS and the obvious amelioration of the colonic injury by exogenous TGF-alpha application in wa-1 mice suggest that TGF-alpha is a mediator of protection and/or healing mechanisms in the colon.

摘要

背景与目的

有间接证据表明转化生长因子α(TGF-α)是黏膜防御和修复的重要介质。TGF-α基因敲除小鼠和TGF-α缺陷小鼠(wa-1)为评估TGF-α在维持结肠完整性中的作用提供了新方法。

方法

通过给基因敲除小鼠、其基因对照(GC)小鼠、wa-1小鼠和BALB/c小鼠口服葡聚糖硫酸钠(DSS,5 g/dL)诱导结肠炎。还对wa-1小鼠腹腔注射TGF-α,以评估外源性TGF-α在DSS诱导的结肠炎中的作用。

结果

对DSS的反应中,基因敲除小鼠和wa-1小鼠近60%的整个结肠黏膜被破坏,而GC小鼠为22%,BALB/c小鼠为16%。与GC小鼠(11%)和Balb/c小鼠(12%)相比,基因敲除小鼠(28%)和wa-1小鼠(23%)体重减轻增加了一倍。给wa-1小鼠应用TGF-α后,与对照组相比,黏膜损伤严重程度降低了近70%。

结论

TGF-α基因敲除小鼠和wa-1小鼠对DSS的显著易感性以及给wa-1小鼠应用外源性TGF-α后结肠损伤明显改善,表明TGF-α是结肠保护和/或愈合机制的介质。

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