Hurley-Novatny Amelia C, Allbritton-King Jules D, Jha Smita, Cowen Edward W, Colbert Robert A, Navid Fatemeh, Bhattacharyya Timothy
Clinical and Investigative Orthopedics Surgery Unit, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland, USA; Medical Scientist Training Program, University of Iowa Carver College of Medicine, Iowa City, Iowa, USA.
Clinical and Investigative Orthopedics Surgery Unit, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland, USA.
J Invest Dermatol. 2022 Sep;142(9):2406-2414.e5. doi: 10.1016/j.jid.2022.02.006. Epub 2022 Feb 19.
Melorheostosis is a rare sclerosing bone disease with associated vascular abnormalities in skin and bone, which is caused by somatic mosaic single nucleotide variations in the MAP2K1 gene, which encodes MAPK/extracellular signal‒regulated kinase (ERK) kinase 1. However, disease pathogenesis is poorly understood. Using patient-derived cells, we found that affected skin fibroblasts carrying the single nucleotide variations have increased activation of ERK1/2, which results in increased expression and secretion of proangiogenic factors, including VEGF. VEGF secretion was strongly reduced in affected cells after treatment with MAPK/ERK kinase 1 inhibitor trametinib. Treatment of healthy endothelial cells on matrigel with conditioned medium from affected fibroblasts induces the adoption of a proangiogenic phenotype. Direct coculture of fibroblasts and endothelial cells further shows that both secreted factors and extracellular matrix are capable of inducing a proangiogenic phenotype in healthy endothelial cells. Blocking VEGF with bevacizumab reduces the proangiogenic effect of affected fibroblasts in both the matrigel and direct coculture angiogenesis models, indicating that elevated VEGF secretion is a key mediator of increased angiogenesis in melorheostosis tissue. In conclusion, this work identifies the role of several important molecular mediators in the pathogenesis of melorheostosis, including MAPK/ERK kinase 1, phosphorylated ERK1/2, and VEGF, all of which have clinically available pharmacologic inhibitors, which could be further explored as therapeutic targets.
肢骨纹状肥大是一种罕见的硬化性骨病,伴有皮肤和骨骼相关的血管异常,由编码丝裂原活化蛋白激酶/细胞外信号调节激酶(ERK)激酶1的MAP2K1基因的体细胞镶嵌单核苷酸变异引起。然而,疾病的发病机制尚不清楚。利用患者来源的细胞,我们发现携带单核苷酸变异的受累皮肤成纤维细胞中ERK1/2的激活增加,这导致包括血管内皮生长因子(VEGF)在内的促血管生成因子的表达和分泌增加。用MAPK/ERK激酶1抑制剂曲美替尼处理后,受累细胞中的VEGF分泌显著减少。用受累成纤维细胞的条件培养基处理基质胶上的健康内皮细胞可诱导其呈现促血管生成表型。成纤维细胞与内皮细胞的直接共培养进一步表明,分泌因子和细胞外基质都能够在健康内皮细胞中诱导促血管生成表型。在基质胶和直接共培养血管生成模型中,用贝伐单抗阻断VEGF可降低受累成纤维细胞的促血管生成作用,表明VEGF分泌增加是肢骨纹状肥大组织中血管生成增加的关键介质。总之,这项研究确定了几种重要分子介质在肢骨纹状肥大发病机制中的作用,包括MAPK/ERK激酶1、磷酸化ERK1/2和VEGF,所有这些都有临床可用的药理抑制剂,可作为治疗靶点进一步探索。