Multi-layered regulation of intestinal antimicrobial defense

被引:106
作者
Mukherjee, S. [1 ]
Vaishnava, S. [1 ]
Hooper, L. V. [1 ,2 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Immunol, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Microbiol, Dallas, TX 75390 USA
关键词
paneth cell; defensin; cathelicidin; C-type lectin; inflammatory bowel disease;
D O I
10.1007/s00018-008-8182-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The gastrointestinal tract of mammals is heavily colonized with a complex and dynamic microbial community. To cope with this complex microbial challenge, multiple epithelial lineages, such as enterocytes and Paneth cells, elaborate a diverse repertoire of protein antibiotics. The gut antimicrobial arsenal encompasses multiple protein families, including defensins, cathelicidins, and C-type lectins. These antimicrobial peptides and proteins play a key role in protecting the host against pathogen challenge, and likely also function to limit invasion of indigenous microbes. It is becoming increasingly apparent that expression of mucosal antimicrobial defenses is tightly controlled. This occurs at multiple levels, including transcriptional regulation in response to bacterial cues, post-translational proteolytic processing, and bacterial regulation of Paneth cell degranulation. Impaired antimicrobial peptide expression has also been implicated in inflammatory bowel disease, underscoring the essential role of antimicrobial defenses in maintaining intestinal homeostasis.
引用
收藏
页码:3019 / 3027
页数:9
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