Transforming Growth Factor-β1 Induces Concurrent Periostin and SLUG Expression in Normal Human Dermal Fibroblasts: Potential Implications for Extracellular Matrix Remodeling.

IF 4.5 3区 工程技术 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Patrycja Sputa-Grzegrzolka, Anna Socha-Banasiak, Natalia Glatzel-Plucinska, Mateusz Olbromski, Katarzyna Ratajczak-Wielgomas, Tomasz Gornicki, Elzbieta Czkwianianc, Piotr Dziegiel, Bartosz Kempisty
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Abstract

Background: Transforming growth factor beta 1 (TGF-β1) is a master regulator of fibrogenesis and extracellular matrix (ECM) remodeling. Among molecules involved in profibrotic signaling, periostin (POSTN) and the Snail family transcriptional repressor 2 (SLUG, SNAI2) have emerged as potential regulators of tissue remodeling and fibroblast activation. However, the temporal relationship between TGF-β1-induced expression of SLUG and periostin in human dermal fibroblasts remains poorly understood. Objectives: This study aimed to evaluate the effect of TGF-β1 stimulation on SNAI2/SLUG and POSTN/periostin expression dynamics in normal human dermal fibroblasts (NHDFs) and characterize their association with profibrotic responses. Methods: NHDFs were stimulated with recombinant human TGF-β1 (20 ng/mL) for 24, 48, and 72 h. SNAI2 and POSTN mRNA expression was quantified by RT-qPCR, intracellular SLUG protein levels were assessed by Western blotting, and periostin accumulation in the culture medium was measured by enzyme-linked immunosorbent assay (ELISA). The RT-qPCR and ELISA data were analyzed using two-way ANOVA with Bonferroni correction; because of the small number of replicates (n = 2), the Western blot data are presented descriptively. Results: TGF-β1 significantly increased POSTN mRNA expression after 24 and 48 h (both p < 0.001); at 72 h, POSTN mRNA levels remained numerically elevated relative to the control, although this difference did not reach statistical significance. Periostin accumulation in the culture medium increased progressively and was significantly higher than in the control group after 48 and 72 h (p < 0.001). In contrast, SNAI2/SLUG exhibited transient expression kinetics, with increased SNAI2 mRNA at 48 h (p < 0.05) and the highest SLUG protein levels also observed after 48 h of stimulation, followed by a decline at 72 h. Conclusions: TGF-β1 induced time-dependent changes in SNAI2/SLUG and POSTN/periostin expression in human dermal fibroblasts. As fibroblast activation and ECM remodeling were not directly assessed, the present conclusions are restricted to the expression changes in the two investigated molecules, whose concurrent yet temporally distinct regulation may indicate potential relevance in the fibroblast response to profibrotic signaling. Further studies are required to determine whether they participate in common regulatory mechanisms or independently contribute to fibrotic processes.

转化生长因子-β1诱导正常人真皮成纤维细胞同时表达骨膜蛋白和SLUG:细胞外基质重塑的潜在意义
背景:转化生长因子β1 (TGF-β1)是纤维形成和细胞外基质(ECM)重塑的主要调节因子。在参与纤维化信号传导的分子中,骨膜蛋白(POSTN)和蜗牛家族转录抑制因子2 (SLUG, SNAI2)已成为组织重塑和成纤维细胞激活的潜在调节因子。然而,TGF-β1诱导的SLUG和骨膜蛋白在人真皮成纤维细胞中的表达之间的时间关系尚不清楚。目的:本研究旨在评估TGF-β1刺激对正常人真皮成纤维细胞(NHDFs)中SNAI2/SLUG和POSTN/periostin表达动态的影响,并表征其与纤维化反应的关系。方法:重组人TGF-β1 (20 ng/mL)刺激NHDFs 24、48、72 h, RT-qPCR检测SNAI2和POSTN mRNA表达,Western blotting检测细胞内SLUG蛋白水平,ELISA检测培养基中骨膜素积累。RT-qPCR和ELISA数据采用Bonferroni校正的双因素方差分析;由于重复次数少(n = 2), Western blot数据以描述性方式呈现。结果:TGF-β1显著提高24、48 h后POSTN mRNA表达量(p < 0.001);72h时,与对照组相比,POSTN mRNA水平仍在数值上升高,但这种差异没有达到统计学意义。48 h和72 h后,培养液中的骨膜素积累逐渐增加,显著高于对照组(p < 0.001)。相反,SNAI2/SLUG表现出瞬时表达动力学,在刺激48 h时SNAI2 mRNA升高(p < 0.05),并且在刺激48 h时SLUG蛋白水平最高,随后在72 h时下降。结论:TGF-β1诱导了人真皮成纤维细胞SNAI2/SLUG和POSTN/periostin表达的时间依赖性变化。由于未直接评估成纤维细胞活化和ECM重塑,因此目前的结论仅限于所研究的两种分子的表达变化,它们同时存在但在时间上不同的调节可能表明成纤维细胞对纤维化信号的反应具有潜在的相关性。需要进一步的研究来确定它们是否参与共同的调节机制或独立地参与纤维化过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biomedicines
Biomedicines Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
5.20
自引率
8.50%
发文量
2823
审稿时长
8 weeks
期刊介绍: Biomedicines (ISSN 2227-9059; CODEN: BIOMID) is an international, scientific, open access journal on biomedicines published quarterly online by MDPI.
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