Malovitski Kiril, Feller Yarden, Giladi Moshe, Janagond Ajit B, Shivaraj Namratha, Kadakol Gurushantappa S, Khair Lubna, Assaf Sari, Mohamad Janan, Ishtewy Rawaa, Ildardashty Alexander, Samuelov Liat, Sarig Ofer, Inamadar Arun C, Sprecher Eli
Division of Dermatology, Tel Aviv Medical Center, Tel Aviv, Israel.
Grey Faculty of Medicine and Health Sciences, Tel Aviv, Israel.
Br J Dermatol. 2025 Aug 18;193(3):532-543. doi: 10.1093/bjd/ljaf181.
Dual specificity phosphatase 1 (DUSP1) has recently been shown to regulate keratinocyte (KC) proliferation through extracellular regulated kinase (ERK) signalling.
To delineate the genetic basis underlying inherited palmoplantar keratoderma (PPK) in two families.
We used whole-exome and direct sequencing, quantitative real-time polymerase chain reaction, protein modelling, immunofluorescence confocal microscopy, immunoblotting, three-dimensional skin equivalents and the dispase-based KC dissociation assay.
Whole-exome sequencing revealed two variants in DUSP1 (c.809T>G, p.Leu270Arg and c.251T>A, p.Val84Glu), encoding DUSP1, in four individuals with PPK belonging to two unrelated families affected by a semidominant form of PPK. Bioinformatics and protein modelling predicted the variants to be pathogenic. Primary human KCs transfected with constructs expressing the PPK-causing pathogenic variants in DUSP1 showed decreased DUSP1 expression and concomitant increased expression of phosphorylated (p-)ERK1/2, as well as reduced desmoglein 1 (DSG1) expression. Accordingly, primary human KCs downregulated for DUSP1 displayed disrupted cell-cell adhesion, increased p-ERK1/2 and reduced DSG1 expression. Three-dimensional organotypic skin equivalents downregulated for DUSP1 demonstrated reduced DSG1 expression and increased epidermal thickness, reminiscent of the human phenotype. ERK1/2 inhibition rescued this abnormal phenotype.
This study attributes to DUSP1 a hitherto unrecognized role in epidermal differentiation and expands the spectrum of genetic defects known to cause inherited PPK.
双特异性磷酸酶1(DUSP1)最近被证明可通过细胞外调节激酶(ERK)信号传导来调节角质形成细胞(KC)的增殖。
阐明两个家族中遗传性掌跖角化病(PPK)的遗传基础。
我们使用了全外显子测序和直接测序、定量实时聚合酶链反应、蛋白质建模、免疫荧光共聚焦显微镜、免疫印迹、三维皮肤等效物和基于dispase的KC解离试验。
全外显子测序在4名患有PPK的个体中发现了DUSP1的两个变体(c.809T>G,p.Leu270Arg和c.251T>A,p.Val84Glu),这4名个体来自两个受半显性PPK形式影响的无关家族。生物信息学和蛋白质建模预测这些变体具有致病性。用表达导致PPK的DUSP1致病性变体的构建体转染的原代人KC显示DUSP1表达降低,同时磷酸化(p-)ERK1/2表达增加,以及桥粒芯糖蛋白1(DSG1)表达降低。因此,DUSP1下调的原代人KC显示细胞间粘附破坏,p-ERK1/2增加,DSG1表达降低。DUSP1下调的三维器官型皮肤等效物显示DSG1表达降低,表皮厚度增加,类似于人类表型。ERK1/2抑制挽救了这种异常表型。
本研究揭示了DUSP1在表皮分化中迄今未被认识的作用,并扩展了已知导致遗传性PPK的遗传缺陷谱。