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甲状旁腺素/甲状旁腺素相关蛋白和维生素 D 控制抗菌肽的表达和对皮肤细菌感染的易感性。

PTH/PTHrP and vitamin D control antimicrobial peptide expression and susceptibility to bacterial skin infection.

机构信息

Division of Dermatology, University of California, San Diego, La Jolla, CA 92093, USA.

出版信息

Sci Transl Med. 2012 May 23;4(135):135ra66. doi: 10.1126/scitranslmed.3003759.

Abstract

The production of antimicrobial peptides is essential for protection against a wide variety of microbial pathogens and plays an important role in the pathogenesis of several diseases. The mechanisms responsible for expression of antimicrobial peptides are incompletely understood, but a role for vitamin D as a transcriptional inducer of the antimicrobial peptide cathelicidin has been proposed. We show that 1,25-dihydroxyvitamin D(3) (1,25-D3) acts together with parathyroid hormone (PTH), or the shared amino-terminal domain of PTH-related peptide (PTHrP), to synergistically increase cathelicidin and immune defense. Administration of PTH to mouse skin decreased susceptibility to skin infection by group A Streptococcus. Mice on dietary vitamin D(3) restriction that responded with an elevation in PTH have an increased risk of infection if they lack 1,25-D3. These results identify PTH/PTHrP as a variable that serves to compensate for inadequate vitamin D during activation of antimicrobial peptide production.

摘要

抗菌肽的产生对于抵御各种微生物病原体至关重要,并且在几种疾病的发病机制中发挥着重要作用。负责抗菌肽表达的机制尚不完全清楚,但维生素 D 作为抗菌肽 cathelicidin 的转录诱导物的作用已被提出。我们表明,1,25-二羟基维生素 D(3)(1,25-D3)与甲状旁腺激素(PTH)或 PTH 相关肽(PTHrP)的共同氨基末端结构域一起协同增加 cathelicidin 和免疫防御。给予甲状旁腺激素(PTH)到小鼠皮肤会降低 A 组链球菌皮肤感染的易感性。饮食中维生素 D(3)限制的小鼠,如果缺乏 1,25-D3,则对 PTH 反应性升高的情况下,感染的风险增加。这些结果表明,PTH/PTHrP 是一种变量,可在激活抗菌肽产生时补偿维生素 D 不足。

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