通过合成气味剂管理人类毛囊微生物组。

IF 4.6
Janin Edelkamp , Marta B. Lousada , Daniela Pinto , Jérémy Chéret , Francesco Maria Calabrese , Francisco Jiménez , Hanieh Erdmann , Julia Wessel , Bodo Phillip , Maria De Angelis , Fabio Rinaldi , Marta Bertolini , Ralf Paus
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引用次数: 1

摘要

背景:人类头皮毛囊(HFs)参与嗅觉受体(OR)依赖性化学补偿。合成的檀香类气味剂Sandalore®对嗅觉受体家族2 AT成员4亚家族(OR2AT4)的激活上调了皮霉素(DCD)的HF抗菌肽表达,此前人们认为皮霉素仅由汗液和皮脂腺产生。目的:了解一种常用的化妆品气味剂是否可以刺激毛囊内DCD的产生,从而以临床有益的方式改变人类HF微生物组的组成。方法:比较新鲜冷冻头皮活检与显微切割的全长头皮HFs、在存在/不存在OR2AT4激动剂Sandalore®和/或抗生素和/或竞争性OR2AT4拮抗剂Phenirat®的情况下培养的器官之间的DCD表达。进行了基于扩增子的测序和微生物生长测定,以评估这种治疗如何影响HF微生物组。结果:合成气味剂处理上调了人HFs离体上皮DCD的表达并发挥了抗菌活性。在离体微生态失调事件中,抗生素和气味剂的联合治疗可以防止HF组织损伤,并有利于更具生理学意义的微生物组组成。Sandalore®条件培养基含有更高的DCD含量,与金黄色葡萄球菌和球形葡萄球菌相比,有利于表皮葡萄球菌和限制性马拉色菌,同时对痤疮杆菌表现出抗菌活性。Phenirat®联合给药可逆转这些影响。结论:我们首次证明了化妆品气味剂通过以嗅觉受体依赖的方式上调抗菌肽的产生来影响人类HF微生物组的原理。具体而言,合成檀香类气味剂可能通过OR2AT4刺激卵泡内DCD的产生,从而控制微生物过度生长。因此,作为毛囊炎和微生态失调相关毛发疾病的辅助治疗原则,值得进一步探索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Management of the human hair follicle microbiome by a synthetic odorant

Background

Human scalp hair follicles (HFs) engage in olfactory receptor (OR)-dependent chemosensation. Activation of olfactory receptor family 2 subfamily AT member 4 (OR2AT4) by the synthetic, sandalwood-like odorant Sandalore® up-regulated HF antimicrobial peptide expression of dermcidin (DCD), which had previously been thought to be produced exclusively by sweat and sebaceous glands.

Objectives

To understand if intrafollicular DCD production can be stimulated by a commonly used cosmetic odorant, thus altering human HF microbiome composition in a clinically beneficial manner.

Methods

DCD expression was compared between fresh-frozen scalp biopsies and microdissected, full-length scalp HFs, organ-cultured in the presence/absence of the OR2AT4 agonist, Sandalore® and/or antibiotics and/or the competitive OR2AT4 antagonist, Phenirat®. Amplicon-based sequencing and microbial growth assays were performed to assess how this treatment affected the HF microbiome.

Results

Synthetic odorant treatment upregulated epithelial DCD expression and exerted antimicrobial activity in human HFs ex vivo. Combined antibiotic and odorant treatment, during an ex vivo dysbiosis event, prevented HF tissue damage and favoured a more physiological microbiome composition. Sandalore®-conditioned medium, containing higher DCD content, favoured Staphylococcus epidermidis and Malassezia restricta over S. aureus and M. globosa, while exhibiting antimicrobial activity against Cutibacterium acnes. These effects were reversed by co-administration of Phenirat®.

Conclusions

We provide the first proof-of-principle that a cosmetic odorant impacts the human HF microbiome by up-regulating antimicrobial peptide production in an olfactory receptor-dependent manner. Specifically, a synthetic sandalwood-like odorant stimulates intrafollicular DCD production, likely via OR2AT4, and thereby controls microbial overgrowth. Thus, deserving further exploration as an adjuvant therapeutic principle in the management of folliculitis and dysbiosis-associated hair diseases.

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