Selig Mischa, Walz Kathrin, Lauer Jasmin C, Rolauffs Bernd, Hart Melanie L
G.E.R.N. Center for Tissue Replacement, Regeneration & Neogenesis, Department of Orthopedics and Trauma Surgery, Faculty of Medicine, Albert-Ludwigs-University of Freiburg, Engesserstraße 4, 79108 Freiburg, Germany.
Faculty of Biology, University of Freiburg, Schaenzlestrasse 1, 79104 Freiburg, Germany.
Polymers (Basel). 2023 Jul 14;15(14):3041. doi: 10.3390/polym15143041.
Despite lignin's global abundance and its use in biomedical studies, our understanding of how lignin regulates disease through modulation of cell morphology and associated phenotype of human cells is unknown. We combined an automated high-throughput image cell segmentation technique for quantitatively measuring a panel of cell shape descriptors, droplet digital Polymerase Chain Reaction for absolute quantification of gene expression and multivariate data analyses to determine whether lignin could therapeutically modulate the cell morphology and phenotype of inflamed, degenerating diseased human cells (osteoarthritic (OA) chondrocytes) towards a healthier cell morphology and phenotype. Lignin dose-dependently modified all aspects of cell morphology and ameliorated the diseased shape of OA chondrocytes by inducing a less fibroblastic healthier cell shape, which correlated with the downregulation of collagen 1A2 (COL1A2, a major fibrosis-inducing gene), upregulation of collagen 2A1 (COL2A1, a healthy extracellular matrix-inducing gene) and downregulation of interleukin-6 (IL-6, a chronic inflammatory cytokine). This is the first study to show that lignin can therapeutically target cell morphology and change a diseased cells' function towards a healthier cell shape and phenotype. This opens up novel opportunities for exploiting lignin in modulation of disease, tissue degeneration, fibrosis, inflammation and regenerative medical implants for therapeutically targeting cell function and outcome.
尽管木质素在全球范围内储量丰富且已用于生物医学研究,但我们对木质素如何通过调节人类细胞的形态及相关表型来调控疾病仍不清楚。我们结合了一种用于定量测量一组细胞形状描述符的自动化高通量图像细胞分割技术、用于基因表达绝对定量的液滴数字聚合酶链反应以及多变量数据分析,以确定木质素是否能够治疗性地调节发炎、退化的患病人类细胞(骨关节炎(OA)软骨细胞)的细胞形态和表型,使其朝着更健康的细胞形态和表型转变。木质素以剂量依赖的方式改变细胞形态的各个方面,并通过诱导形成纤维样较少的更健康细胞形状来改善OA软骨细胞的病变形状,这与1型胶原α2(COL1A2,一种主要的纤维化诱导基因)的下调、2型胶原α1(COL2A1,一种健康的细胞外基质诱导基因)的上调以及白细胞介素-6(IL-6,一种慢性炎症细胞因子)的下调相关。这是第一项表明木质素可以治疗性地靶向细胞形态并将患病细胞的功能转变为更健康的细胞形状和表型的研究。这为在疾病调节、组织退化、纤维化、炎症以及再生医疗植入物中利用木质素来治疗性地靶向细胞功能和结果开辟了新的机会。