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小鼠β-防御素1(Defb1)突变小鼠模型的特征分析。

Characterization of the mouse beta defensin 1, Defb1, mutant mouse model.

作者信息

Morrison Gillian, Kilanowski Fiona, Davidson Donald, Dorin Julia

机构信息

MRC Human Genetics Unit, Western General Hospital, Edinburgh, EH4 2XU, Scotland.

出版信息

Infect Immun. 2002 Jun;70(6):3053-60. doi: 10.1128/IAI.70.6.3053-3060.2002.

Abstract

Beta defensins are small cationic antimicrobial peptides present in the respiratory system which have been proposed to be dysfunctional in the environment of the cystic fibrosis lung. Defb1, a murine homologue to the human beta defensins, has also been found to be expressed in the respiratory system and, in order to examine the function of beta defensins in vivo, gene targeting was used to generate Defb1-deficient (Defb1(tm1Hgu)/Defb1(tm1Hgu) [Defb1(-/-)]) mice. The Defb1 synthetic peptide was shown to have a salt-sensitive antimicrobial activity that was stronger against Staphylococcus aureus than against Escherichia coli or Pseudomonas aeruginosa. Defb1(-/-) mice were found, however, to be effective in the clearance of the cystic fibrosis relevant pathogen S. aureus from the airways after nebulization. Although no overt deleterious phenotype was evident in the Defb1(-/-) mice, the number of mutant mice found to harbor bacteria of the Staphylococcus species in the bladder was significantly higher (P = 0.008) than that of controls, suggesting a role for these peptides in resistance to urinary tract infection.

摘要

β-防御素是存在于呼吸系统中的小阳离子抗菌肽,有人提出在囊性纤维化肺部环境中其功能会失调。Defb1是人类β-防御素的小鼠同源物,也已发现在呼吸系统中表达。为了研究β-防御素在体内的功能,采用基因打靶技术培育出Defb1基因缺陷型(Defb1(tm1Hgu)/Defb1(tm1Hgu) [Defb1(-/-)])小鼠。Defb1合成肽显示出对盐敏感的抗菌活性,对金黄色葡萄球菌的抗菌活性比对大肠杆菌或铜绿假单胞菌更强。然而,发现Defb1(-/-)小鼠在雾化后能有效清除气道中与囊性纤维化相关的病原体金黄色葡萄球菌。虽然Defb1(-/-)小鼠没有明显的有害表型,但发现膀胱中携带葡萄球菌属细菌的突变小鼠数量显著高于对照组(P = 0.008),表明这些肽在抵抗尿路感染中发挥作用。

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