Laboratory for Biointerfaces, Empa - Swiss Federal Laboratories for Materials Science and Technology, St. Gallen, Switzerland.
Department Tissue Engineering & Regenerative Medicine, University Hospital Würzburg, Würzburg, Germany.
Sci Rep. 2021 Mar 29;11(1):7070. doi: 10.1038/s41598-021-86486-7.
The replacement of animal models for investigation of inflammation and wound healing has been advancing by means of in vitro skin equivalents with increasing levels of complexity. However, the current in vitro skin models still have a limited pre-clinical relevance due to their lack of immune cells. So far, few steps have been made towards the incorporation of immune cells into in vitro skin and the requirements for immunocompetent co-cultures remain unexplored. To establish suitable conditions for incorporating macrophages into skin models, we evaluated the effects of different media on primary keratinocytes, fibroblasts and macrophages. Skin maturation was affected by culture in macrophage medium, while macrophages showed reduced viability, altered cell morphology and decreased response to pro- and anti-inflammatory stimuli in skin differentiation media, both in 2D and 3D. The results indicate that immunocompetent skin models have specific, complex requirements for supporting an accurate detection of immune responses, which point at the identification of a suitable culture medium as a crucial pre-requisite for the development of physiologically relevant models.
通过具有不同复杂程度的体外皮肤等效物,用于研究炎症和伤口愈合的动物模型的替代已经在不断发展。然而,由于缺乏免疫细胞,目前的体外皮肤模型仍然具有有限的临床前相关性。到目前为止,将免疫细胞纳入体外皮肤的步骤很少,免疫活性共培养的要求也尚未得到探索。为了将巨噬细胞纳入皮肤模型建立合适的条件,我们评估了不同培养基对原代角质形成细胞、成纤维细胞和巨噬细胞的影响。巨噬细胞培养基培养会影响皮肤成熟,而在皮肤分化培养基中,无论是在 2D 还是 3D 培养中,巨噬细胞的活力降低,细胞形态改变,对促炎和抗炎刺激的反应减弱。结果表明,免疫活性皮肤模型对支持准确检测免疫反应具有特定的、复杂的要求,这表明鉴定合适的培养基是开发具有生理相关性模型的关键前提。