Burnett Sandra H, Beus Bo J, Avdiushko Rita, Qualls Joseph, Kaplan Alan M, Cohen Don A
Department of Microbiology and Molecular Biology, Brigham Young University, Provo, Utah 84602, USA.
J Surg Res. 2006 Apr;131(2):296-301. doi: 10.1016/j.jss.2005.08.026. Epub 2005 Nov 14.
We present a new mouse model for the study of peritoneal adhesions using macrophage Fas-induced apoptosis (Mafia) transgenic mice expressing a Fas-FKBP construct under control of the murine c-fms promoter. Mafia mice allow systemic macrophage depletion by dimerization of Fas with a synthetic dimerizer, AP20187. Results demonstrate that macrophage depletion in Mafia mice induces peritoneal adhesion formation when the peritoneal cavity is also exposed to an irritant. The Mafia mouse model presents a reproducible, non-surgical approach for research in adhesion formation and prevention.
Mafia mice were treated with AP20187 using an intravenous (i.v.) or intraperitoneal (i.p.) injection. Control groups included mock-treated Mafia mice and both AP20187 and mock-treated wild type mice. Seven days after treatment, mice were observed for the presence of adhesions.
After i.p. injection with AP20187, 76% of Mafia mice developed adhesions whereas none of the mock-treated Mafia or wild-type mice developed adhesions, and only one AP20187-treated wild-type mouse (5.8%) developed a mild adhesion. Mafia mice treated with AP20187 i.v. exhibited macrophage depletion not significantly different than i.p. treated mice, but did not develop adhesions. In contrast, Mafia mice treated with AP20187 i.v. developed adhesions when diluent was also injected into the peritoneal cavity, whereas i.p diluent alone had no effect.
Macrophage depletion, combined with a peritoneal irritant, results in peritoneal adhesion formation in transgenic Mafia mice. Macrophages appear to play a protective role in the development and/or repair of peritoneal adhesions.
我们提出了一种用于研究腹膜粘连的新型小鼠模型,该模型使用巨噬细胞Fas诱导凋亡(Mafia)转基因小鼠,其在鼠源c-fms启动子的控制下表达Fas-FKBP构建体。Mafia小鼠可通过Fas与合成二聚体AP20187的二聚化实现全身巨噬细胞耗竭。结果表明,当腹腔同时暴露于刺激物时,Mafia小鼠体内巨噬细胞耗竭会诱导腹膜粘连形成。Mafia小鼠模型为粘连形成和预防的研究提供了一种可重复的、非手术的方法。
通过静脉内(i.v.)或腹腔内(i.p.)注射,用AP20187处理Mafia小鼠。对照组包括未处理的Mafia小鼠以及接受AP20187处理和未处理的野生型小鼠。处理7天后,观察小鼠是否存在粘连。
腹腔注射AP20187后,76%的Mafia小鼠出现粘连,而未处理的Mafia小鼠或野生型小鼠均未出现粘连,仅一只接受AP20187处理的野生型小鼠(5.8%)出现轻度粘连。静脉注射AP20187处理的Mafia小鼠巨噬细胞耗竭情况与腹腔注射处理的小鼠无显著差异,但未出现粘连。相比之下,静脉注射AP20187处理的Mafia小鼠在向腹腔内注射稀释剂时会出现粘连,而单独腹腔注射稀释剂则无影响。
巨噬细胞耗竭与腹腔刺激物相结合,会导致转基因Mafia小鼠形成腹膜粘连。巨噬细胞似乎在腹膜粘连的发生和/或修复中发挥保护作用。