CIBER de enfermedades respiratorias, Health Institute Carlos III, Valencia, Spain.
Department of Pharmacology, Faculty of Medicine, University of Valencia, Avenida Blasco Ibáñez, 15, Valencia, 46010, Spain.
Mol Med. 2024 Sep 2;30(1):134. doi: 10.1186/s10020-024-00906-8.
Epidermal remodeling and hypertrophy are hallmarks of skin fibrotic disorders, and keratinocyte to mesenchymal (EMT)-like transformations drive epidermis alteration in skin fibrosis such as keloids and hypertrophic scars (HTS). While phosphodiesterase 4 (PDE4) inhibitors have shown effectiveness in various fibrotic disorders, their role in skin fibrosis is not fully understood. This study aimed to explore the specific role of PDE4B in epidermal remodeling and hypertrophy seen in skin fibrosis.
In vitro experiments examined the effects of inhibiting PDE4A-D (with Roflumilast) or PDE4B (with siRNA) on TGFβ1-induced EMT differentiation and dedifferentiation in human 3D epidermis. In vivo studies investigated the impact of PDE4 inhibition on HOCl-induced skin fibrosis and epidermal hypertrophy in mice, employing both preventive and therapeutic approaches.
The study found increased levels of PDE4B (mRNA, protein) in keloids > HTS compared to healthy epidermis, as well as in TGFβ-stimulated 3D epidermis. Keloids and HTS epidermis exhibited elevated levels of collagen Iα1, fibronectin, αSMA, N-cadherin, and NOX4 mRNA, along with decreased levels of E-cadherin and ZO-1, confirming an EMT process. Inhibition of both PDE4A-D and PDE4B prevented TGFβ1-induced Smad3 and ERK1/2 phosphorylation and mesenchymal differentiation in vitro. PDE4A-D inhibition also promoted mesenchymal dedifferentiation and reduced TGFβ1-induced ROS and keratinocyte senescence by rescuing PPM1A, a Smad3 phosphatase. In vivo, PDE4 inhibition mitigated HOCl-induced epidermal hypertrophy in mice in both preventive and therapeutic settings.
Overall, the study supports the potential of PDE4 inhibitors, particularly PDE4B, in treating skin fibrosis, including keloids and HTS, shedding light on their functional role in this condition.
表皮重塑和肥大是皮肤纤维化疾病的标志,角质形成细胞向间质(EMT)样转化驱动皮肤纤维化中的表皮改变,如瘢痕疙瘩和肥厚性瘢痕(HTS)。虽然磷酸二酯酶 4(PDE4)抑制剂在各种纤维化疾病中已显示出有效性,但它们在皮肤纤维化中的作用尚未完全了解。本研究旨在探讨 PDE4B 在皮肤纤维化中所见的表皮重塑和肥大中的特定作用。
体外实验研究了抑制 PDE4A-D(罗氟司特)或 PDE4B(siRNA)对 TGFβ1 诱导的人 3D 表皮 EMT 分化和去分化的影响。体内研究采用预防和治疗两种方法,研究了 PDE4 抑制对 HOCl 诱导的皮肤纤维化和表皮肥大的影响。
研究发现,与健康表皮相比,瘢痕疙瘩 > HTS 中的 PDE4B(mRNA、蛋白)水平升高,TGFβ 刺激的 3D 表皮也是如此。瘢痕疙瘩和 HTS 表皮的胶原 Iα1、纤维连接蛋白、αSMA、N-钙粘蛋白和 NOX4mRNA 水平升高,E-钙粘蛋白和 ZO-1 水平降低,证实存在 EMT 过程。抑制 PDE4A-D 和 PDE4B 均可预防 TGFβ1 诱导的 Smad3 和 ERK1/2 磷酸化和间质分化。PDE4A-D 抑制还通过恢复 Smad3 磷酸酶 PPM1A 促进间质去分化,并减少 TGFβ1 诱导的 ROS 和角质形成细胞衰老,从而促进间质去分化。在体内,PDE4 抑制在预防和治疗两种情况下均减轻了 HOCl 诱导的小鼠表皮肥大。
总之,该研究支持 PDE4 抑制剂,特别是 PDE4B,在治疗皮肤纤维化,包括瘢痕疙瘩和 HTS 中的潜力,揭示了它们在这种疾病中的功能作用。