Institute of Pharmaceutical Sciences (IPW), Swiss Federal Institute of Technology (ETH) Zürich, Zürich, Switzerland.
Institute of Pharmaceutical Sciences (IPW), Swiss Federal Institute of Technology (ETH) Zürich, Zürich, Switzerland; Department of Biosciences, University of Milan, Milan, Italy.
J Invest Dermatol. 2022 Dec;142(12):3313-3326.e13. doi: 10.1016/j.jid.2022.05.1089. Epub 2022 Jun 28.
Psoriasis is a chronic inflammatory skin disease characterized by epidermal hyperplasia and hyperkeratosis, immune cell infiltration and vascular remodeling. Despite the emerging recognition of vascular normalization as a potential strategy for managing psoriasis, an in-depth delineation of the remodeled dermal vasculature has been missing. In this study, we exploited 5' single-cell RNA sequencing to investigate the transcriptomic alterations in different subpopulations of blood vascular and lymphatic endothelial cells directly isolated from psoriatic and healthy human skin. Individual subtypes of endothelial cells underwent specific molecular repatterning associated with cell adhesion and extracellular matrix organization. Blood capillaries, in particular, showed upregulation of the melanoma cell adhesion molecule as well as its binding partners and adopted postcapillary venule‒like characteristics during chronic inflammation that are more permissive to leukocyte transmigration. We also identified psoriasis-specific interactions between cis-regulatory enhancers and promoters for each endothelial cell subtype, revealing the dysregulated gene regulatory networks in psoriasis. Together, our results provide more insights into the specific transcriptional responses and epigenetic signatures of endothelial cells lining different vessel compartments in chronic skin inflammation.
银屑病是一种慢性炎症性皮肤病,其特征为表皮过度增生和角化、免疫细胞浸润和血管重塑。尽管血管正常化作为治疗银屑病的一种潜在策略已逐渐被人们所认识,但对重塑的真皮血管系统的深入描述仍存在缺失。在这项研究中,我们利用 5' 单细胞 RNA 测序技术,直接从银屑病和健康人的皮肤中分离出的血管和淋巴管内皮细胞的不同亚群,研究其转录组的改变。内皮细胞的各个亚型经历了与细胞黏附和细胞外基质组织相关的特定分子重编程。特别是,在慢性炎症中,毛细血管表现出黑色素瘤细胞黏附分子及其结合伴侣的上调,并呈现出类似于后微静脉的特征,从而更有利于白细胞的迁移。我们还鉴定了银屑病中每个内皮细胞亚型的顺式调控增强子和启动子之间的特异性相互作用,揭示了银屑病中基因调控网络的失调。总之,我们的研究结果提供了更多关于慢性皮肤炎症中不同血管腔内皮细胞的特定转录反应和表观遗传特征的见解。