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响应革兰氏阳性菌和革兰氏阴性菌控制粘蛋白产生的信号网络。

Signaling networks controlling mucin production in response to Gram-positive and Gram-negative bacteria.

作者信息

McNamara N, Basbaum C

机构信息

Biomedical Sciences Program, Cardiovascular Research Institute and Department of Anatomy, University of California, San Francisco, CA 94143, USA.

出版信息

Glycoconj J. 2001 Sep;18(9):715-22. doi: 10.1023/a:1020875423678.

Abstract

Human lung cells exposed to pathogenic bacteria upregulate the production of mucin, the major macromolecular component of mucus. Generally this upregulation is beneficial for the host, however, in the lungs of cystic fibrosis patients, overproduction of mucin can lead to the plugging of pulmonary airways. Mucus plugging impedes airflow and creates an environment that is highly compartmentalized: those bacteria within the mucus layer are shielded from high doses of antibiotics whereas those outside the mucus are exposed. These conditions augment mutation rate and the development of drug resistance in bacteria that colonize the lungs of cystic fibrosis patients. While therapeutic inhibition of mucin induction would improve airflow and reduce antibiotic resistance in these patients, the challenge is to develop drugs that block excessive mucin production while leaving beneficial aspects of the response intact. To do this, we must understand the molecular mechanisms underlying mucin production. Here we review the signal transduction pathways that control mucin production in response to Gram-positive and Gram-negative bacteria.

摘要

暴露于致病细菌的人肺细胞会上调粘蛋白的产生,粘蛋白是黏液的主要大分子成分。一般来说,这种上调对宿主有益,然而,在囊性纤维化患者的肺部,粘蛋白的过度产生会导致肺气道堵塞。黏液堵塞会阻碍气流,并创造一个高度分隔的环境:黏液层内的细菌受到高剂量抗生素的保护,而黏液层外的细菌则暴露在外。这些情况会提高细菌的突变率和耐药性,这些细菌会在囊性纤维化患者的肺部定植。虽然对粘蛋白诱导的治疗性抑制会改善这些患者的气流并降低抗生素耐药性,但挑战在于开发能够阻断过量粘蛋白产生同时保持反应有益方面不变的药物。要做到这一点,我们必须了解粘蛋白产生的分子机制。在这里,我们综述了响应革兰氏阳性菌和革兰氏阴性菌控制粘蛋白产生的信号转导途径。

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