Holl Myriam, Rasch Marie-Lena, Becker Lucas, Keller Anna-Lena, Schultze-Rhonhof Laura, Ruoff Felix, Templin Markus, Keller Silke, Neis Felix, Keßler Franziska, Andress Jürgen, Bachmann Cornelia, Krämer Bernhard, Schenke-Layland Katja, Brucker Sara Y, Marzi Julia, Weiss Martin
Department of Women's Health Tübingen, Eberhard Karls University Tübingen, 72076 Tübingen, Germany.
NMI Natural and Medical Sciences Institute, University Tübingen, 72770 Reutlingen, Germany.
Biomedicines. 2022 Apr 18;10(4):927. doi: 10.3390/biomedicines10040927.
Postoperative abdominal adhesions are responsible for serious clinical disorders. Administration of plasma-activated media (PAM) to cell type-specific modulated proliferation and protein biosynthesis is a promising therapeutic strategy to prevent pathological cell responses in the context of wound healing disorders. We analyzed PAM as a therapeutic option based on cell type-specific anti-adhesive responses. Primary human peritoneal fibroblasts and mesothelial cells were isolated, characterized and exposed to different PAM dosages. Cell type-specific PAM effects on different cell components were identified by contact- and marker-independent Raman imaging, followed by thorough validation by specific molecular biological methods. The investigation revealed cell type-specific molecular responses after PAM treatment, including significant cell growth retardation in peritoneal fibroblasts due to transient DNA damage, cell cycle arrest and apoptosis. We identified a therapeutic dose window wherein specifically pro-adhesive peritoneal fibroblasts were targeted, whereas peritoneal mesothelial cells retained their anti-adhesive potential of epithelial wound closure. Finally, we demonstrate that PAM treatment of peritoneal fibroblasts reduced the expression and secretion of pro-adhesive cytokines and extracellular matrix proteins. Altogether, we provide insights into biochemical PAM mechanisms which lead to cell type-specific pro-therapeutic cell responses. This may open the door for the prevention of pro-adhesive clinical disorders.
术后腹部粘连会引发严重的临床疾病。给予血浆激活介质(PAM)以调节特定细胞类型的增殖和蛋白质生物合成,是一种在伤口愈合紊乱情况下预防病理性细胞反应的有前景的治疗策略。我们基于特定细胞类型的抗粘连反应分析了PAM作为一种治疗选择。分离、鉴定了原代人腹膜成纤维细胞和间皮细胞,并使其暴露于不同剂量的PAM中。通过非接触和非标记的拉曼成像确定了PAM对不同细胞成分的特定细胞类型效应,随后通过特定分子生物学方法进行了全面验证。研究揭示了PAM处理后特定细胞类型的分子反应,包括腹膜成纤维细胞因短暂DNA损伤、细胞周期停滞和凋亡而出现显著的细胞生长迟缓。我们确定了一个治疗剂量窗口,其中特定的促粘连腹膜成纤维细胞成为靶点,而腹膜间皮细胞保留了其上皮伤口闭合的抗粘连潜力。最后,我们证明对腹膜成纤维细胞进行PAM处理可降低促粘连细胞因子和细胞外基质蛋白的表达与分泌。总之,我们深入了解了导致特定细胞类型治疗性细胞反应的PAM生化机制。这可能为预防促粘连临床疾病打开大门。