Keenan Research Centre for Biomedical Science, St. Michael's Hospital, Unity Health Toronto, Toronto, Canada.
Keenan Research Centre for Biomedical Science, St. Michael's Hospital, Unity Health Toronto, Toronto, Canada; Faculty of Dentistry, University of Toronto, Toronto, Canada.
J Invest Dermatol. 2024 Sep;144(9):1923-1934. doi: 10.1016/j.jid.2024.05.033. Epub 2024 Jul 29.
During the physiological healing of skin wounds, fibroblasts recruited from the uninjured adjacent dermis and deeper subcutaneous fascia layers are transiently activated into myofibroblasts to first secrete and then contract collagen-rich extracellular matrix into a mechanically resistant scar. Scar tissue restores skin integrity after damage but comes at the expense of poor esthetics and loss of tissue function. Stiff scar matrix also mechanically activates various precursor cells into myofibroblasts in a positive feedback loop. Persistent myofibroblast activation results in pathologic accumulation of fibrous collagen and hypertrophic scarring, called fibrosis. Consequently, the mechanisms of fibroblast-to-myofibroblast activation and persistence are studied to develop antifibrotic and prohealing treatments. Mechanistic understanding often starts in a plastic cell culture dish. This can be problematic because contact of fibroblasts with tissue culture plastic or glass surfaces invariably generates myofibroblast phenotypes in standard culture. We describe a straight-forward method to produce soft cell culture surfaces for fibroblast isolation and continued culture and highlight key advantages and limitations of the approach. Adding a layer of elastic silicone polymer tunable to the softness of normal skin and the stiffness of pathologic scars allows to control mechanical fibroblast activation while preserving the simplicity of conventional 2-dimensional cell culture.
在皮肤伤口的生理愈合过程中,从未受伤的相邻真皮和更深的皮下筋膜层招募的成纤维细胞被短暂激活为肌成纤维细胞,首先分泌富含胶原蛋白的细胞外基质,然后收缩为具有机械抗性的瘢痕。瘢痕组织在损伤后恢复皮肤完整性,但代价是美观度差和组织功能丧失。僵硬的瘢痕基质还通过正反馈循环机械激活各种前体细胞成为肌成纤维细胞。持续的肌成纤维细胞激活导致纤维胶原的病理性积累和增生性瘢痕形成,称为纤维化。因此,研究成纤维细胞向肌成纤维细胞的激活和持续激活的机制,以开发抗纤维化和促进愈合的治疗方法。机制研究通常从塑料细胞培养皿开始。这可能会产生问题,因为成纤维细胞与组织培养塑料或玻璃表面的接触总是会在标准培养中产生肌成纤维细胞表型。我们描述了一种简单的方法来制备用于成纤维细胞分离和持续培养的软细胞培养表面,并强调了该方法的关键优点和局限性。添加一层弹性硅酮聚合物,其柔软度可调至正常皮肤的柔软度和病理瘢痕的硬度,可控制机械性成纤维细胞激活,同时保留传统二维细胞培养的简单性。