Division of Dermatology, University of California, San Diego, La Jolla, CA 92093, USA.
Sci Transl Med. 2012 May 23;4(135):135ra66. doi: 10.1126/scitranslmed.3003759.
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.
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。