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在表达基于Fas的自杀基因的转基因小鼠中进行条件性巨噬细胞消融。

Conditional macrophage ablation in transgenic mice expressing a Fas-based suicide gene.

作者信息

Burnett Sandra H, Kershen Edward J, Zhang Jiayou, Zeng Li, Straley Susan C, Kaplan Alan M, Cohen Donald A

机构信息

Department of Microbiology, University of Kentucky College of Medicine, Lexington, Kentucky 40536-0084, USA.

出版信息

J Leukoc Biol. 2004 Apr;75(4):612-23. doi: 10.1189/jlb.0903442. Epub 2004 Jan 14.

Abstract

Transgenic mice expressing an inducible suicide gene, which allows systemic and reversible elimination of macrophages, were developed. A macrophage-specific c-fms promoter was used to express enhanced green fluorescent protein and a drug-inducible suicide gene that leads to Fas-mediated apoptosis in resting and cycling cells of the macrophage lineage. Transgenic mice were fertile, of normal weight, and showed no abnormal phenotype before drug exposure. The transgene was expressed constitutively in macrophages and dendritic cells (DC) but not significantly in T cells or B cells. Induction of the suicide gene led to depletion of 70-95% of macrophages and DC in nearly all tissues examined. Depletion reduced the ability to clear bacteria from the blood and led to increased bacterial growth in the liver. Depleted mice displayed several abnormalities, including splenomegaly, lymphadenopathy, thymic atrophy, extramedullary hematopoiesis, and development of peritoneal adhesions. This new, transgenic line will be useful in investigating the role of macrophages and DC.

摘要

构建了表达可诱导自杀基因的转基因小鼠,该基因可实现巨噬细胞的全身性可逆清除。使用巨噬细胞特异性c-fms启动子来表达增强型绿色荧光蛋白和药物诱导型自杀基因,该自杀基因可导致巨噬细胞谱系的静止和循环细胞发生Fas介导的凋亡。转基因小鼠可育,体重正常,在药物暴露前未表现出异常表型。转基因在巨噬细胞和树突状细胞(DC)中组成性表达,但在T细胞或B细胞中表达不明显。自杀基因的诱导导致几乎所有检测组织中70-95%的巨噬细胞和DC耗竭。巨噬细胞耗竭降低了从血液中清除细菌的能力,并导致肝脏中细菌生长增加。耗竭的小鼠表现出多种异常,包括脾肿大、淋巴结病、胸腺萎缩、髓外造血和腹膜粘连的形成。这种新的转基因品系将有助于研究巨噬细胞和DC的作用。

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