Departamento de Bioingeniera e Ingeniera Aeroespacial, Universidad Carlos III de Madrid (UC3M), Madrid, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), ISCIII, Madrid, Spain; IIS-FJD, Madrid, Spain; División de Biomedicina Epitelial, Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT), Madrid, Spain.
Departamento de Bioingeniera e Ingeniera Aeroespacial, Universidad Carlos III de Madrid (UC3M), Madrid, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), ISCIII, Madrid, Spain; IIS-FJD, Madrid, Spain.
Matrix Biol. 2022 Aug;111:189-206. doi: 10.1016/j.matbio.2022.06.007. Epub 2022 Jun 30.
Recessive dystrophic epidermolysis bullosa (RDEB) is a genetic extracellular matrix disease caused by deficiency in type VII collagen (Col VII). The disease manifests with devastating mucocutaneous fragility leading to progressive fibrosis and metastatic squamous cell carcinomas. Although Col VII abundance is considered the main predictor of symptom course, previous studies have revealed the existence of mutation-independent mechanisms that control disease progression. Here, to investigate and validate new molecular modifiers of wound healing and fibrosis in a natural human setting, and toward development of disease-modulating treatment of RDEB, we performed gene expression profiling of primary fibroblast from RDEB siblings with marked phenotypic variations, despite having equal COL7A1 genotype. Gene enrichment analysis suggested that severe RDEB was associated with enhanced response to TGF-β stimulus, oxidoreductase activity, and cell contraction. Consistently, we found an increased response to TGF-β, higher levels of basal and induced reactive oxygen species (ROS), and greater contractile ability in collagen lattices in RDEB fibroblasts (RDEBFs) from donors with severe RDEB vs mild RDEB. Treatment with antioxidants allowed a reduction of the pro-fibrotic and contractile phenotype. Importantly, our analyses revealed higher expression and deposition in skin of the relatively uncharacterized small leucine-rich extracellular proteoglycan PRELP/prolargin associated with milder RDEB manifestations. Mechanistic investigations showed that PRELP effectively attenuated fibroblasts' response to TGF-β1 stimulus and cell contractile capacity. Moreover, PRELP overexpression in RDEBFs enhanced RDEB keratinocyte attachment to fibroblast-derived extracellular matrix in the absence of Col VII. Our results highlight the clinical relevance of pro-oxidant status and hyper-responsiveness to TGF-β in RDEB severity and progression. Of note, our study also reveals PRELP as a novel and natural TGF-β antagonist with a likely dermo-epidermal pro-adhesive capacity.
隐性营养不良型大疱性表皮松解症(RDEB)是一种遗传性细胞外基质疾病,由 VII 型胶原(Col VII)缺乏引起。该疾病表现为严重的黏膜皮肤脆弱性,导致进行性纤维化和转移性鳞状细胞癌。尽管 Col VII 的丰度被认为是症状进程的主要预测因素,但先前的研究已经揭示了存在控制疾病进展的突变非依赖性机制。在这里,为了在自然人类环境中研究和验证伤口愈合和纤维化的新分子调节剂,并开发 RDEB 的疾病调节治疗方法,我们对 RDEB 兄弟姐妹的原代成纤维细胞进行了基因表达谱分析,尽管他们具有相同的 COL7A1 基因型,但表现出明显的表型差异。基因富集分析表明,严重的 RDEB 与增强对 TGF-β刺激的反应、氧化还原酶活性和细胞收缩有关。一致地,我们发现严重 RDEB 供体的成纤维细胞对 TGF-β的反应增强,基础和诱导的活性氧(ROS)水平更高,以及在胶原基质中的收缩能力更强。抗氧化剂治疗可减少促纤维化和收缩表型。重要的是,我们的分析显示,与 RDEB 表现较轻相关的相对未表征的富含亮氨酸的小细胞外蛋白多糖 PRELP/prolargin 在皮肤中的表达和沉积更高。机制研究表明,PRELP 可有效减弱成纤维细胞对 TGF-β1刺激的反应和细胞收缩能力。此外,在 RDEBFs 中过表达 PRELP 可增强 RDEB 角质形成细胞在没有 Col VII 的情况下附着在成纤维细胞衍生的细胞外基质上。我们的结果强调了促氧化剂状态和对 TGF-β的高反应性在 RDEB 严重程度和进展中的临床相关性。值得注意的是,我们的研究还揭示了 PRELP 作为一种新型天然 TGF-β拮抗剂,具有潜在的皮肤表皮粘附能力。