Miner Kaitlyn, Murphy Ryan, Steiss Samantha, Burian McKenzie, Welp Hannah, Loperfito Alexandra, O'Malley Ashley, Misra Radhika, Frasier Kelly M
College of Medicine, Kansas City University, Kansas City, USA.
College of Osteopathic Medicine, Philadelphia College of Osteopathic Medicine, Philadelphia, USA.
Cureus. 2025 Apr 17;17(4):e82463. doi: 10.7759/cureus.82463. eCollection 2025 Apr.
Lipid dysregulation within sebaceous glands is a critical factor underlying the pathogenesis of sebaceous gland disorders, particularly acne vulgaris. Sebaceous glands synthesize and secrete a complex mixture of lipids, including triglycerides, wax esters, free fatty acids, and sphingolipids, which contribute to skin barrier function and microbial homeostasis. Dysregulated lipid production, characterized by increased sebum secretion and altered lipid composition, has been implicated in promoting proliferation, hyperkeratinization, and inflammation, key processes in acne pathogenesis. Recent research highlights the pivotal role of sphingolipid metabolism, particularly ceramides, in modulating sebaceous gland activity and skin inflammation. Ceramide deficiencies in acne-prone skin contribute to compromised barrier integrity, increased microbial colonization, and an exaggerated inflammatory response. Furthermore, sphingolipid intermediates such as sphingosine-1-phosphate (S1P) influence sebocyte differentiation, lipid synthesis, and cytokine release, linking sphingolipid metabolism to sebaceous gland homeostasis. Emerging therapeutic strategies targeting sphingolipid pathways offer new opportunities for managing sebaceous gland disorders. Topical and systemic therapies designed to restore ceramide levels and modulate S1P signaling have shown promise in preclinical studies, with potential to reduce sebum production, enhance barrier function, and attenuate inflammation. Additionally, sphingolipid-targeted formulations combined with established treatments, such as retinoids and antimicrobial agents, may enhance therapeutic outcomes while minimizing side effects. The dysregulation of sebaceous lipid metabolism, particularly sphingolipid pathways, plays a central role in acne pathogenesis, and emerging insights into these mechanisms are shaping innovative strategies for the treatment and prevention of sebaceous gland disorders.
皮脂腺内的脂质失调是皮脂腺疾病发病机制的关键因素,尤其是寻常痤疮。皮脂腺合成并分泌脂质的复杂混合物,包括甘油三酯、蜡酯、游离脂肪酸和鞘脂,这些脂质有助于皮肤屏障功能和微生物稳态。脂质生成失调,其特征是皮脂分泌增加和脂质组成改变,与促进增殖、过度角化和炎症有关,这些是痤疮发病机制中的关键过程。最近的研究强调了鞘脂代谢,尤其是神经酰胺,在调节皮脂腺活动和皮肤炎症中的关键作用。易长痤疮皮肤中的神经酰胺缺乏导致屏障完整性受损、微生物定植增加和炎症反应过度。此外,鞘脂中间体如1-磷酸鞘氨醇(S1P)影响皮脂细胞分化、脂质合成和细胞因子释放,将鞘脂代谢与皮脂腺稳态联系起来。针对鞘脂途径的新兴治疗策略为管理皮脂腺疾病提供了新机会。旨在恢复神经酰胺水平和调节S1P信号的局部和全身疗法在临床前研究中显示出前景,有可能减少皮脂分泌、增强屏障功能和减轻炎症。此外,靶向鞘脂的制剂与已有的治疗方法如维甲酸和抗菌剂联合使用,可能会提高治疗效果,同时将副作用降至最低。皮脂腺脂质代谢失调,尤其是鞘脂途径,在痤疮发病机制中起核心作用,对这些机制的新认识正在塑造治疗和预防皮脂腺疾病的创新策略。