Rennert Knut, Nitschke Mirko, Wallert Maria, Keune Natalie, Raasch Martin, Lorkowski Stefan, Mosig Alexander S
Center for Sepsis Control and Care, Jena University Hospital, Jena, Germany.
Institute of Biochemistry II, Jena University Hospital, Germany.
J Tissue Eng. 2017 Aug 25;8:2041731417726428. doi: 10.1177/2041731417726428. eCollection 2017 Jan-Dec.
Harvesting cultivated macrophages for tissue engineering purposes by enzymatic digestion of cell adhesion molecules can potentially result in unintended activation, altered function, or behavior of these cells. Thermo-responsive polymer is a promising tool that allows for gentle macrophage detachment without artificial activation prior to subculture within engineered tissue constructs. We therefore characterized different species of thermo-responsive polymers for their suitability as cell substrate and to mediate gentle macrophage detachment by temperature shift. Primary human monocyte- and THP-1-derived macrophages were cultured on thermo-responsive polymers and characterized for phagocytosis and cytokine secretion in response to lipopolysaccharide stimulation. We found that both cell types differentially respond in dependence of culture and stimulation on thermo-responsive polymers. In contrast to THP-1 macrophages, primary monocyte-derived macrophages showed no signs of impaired viability, artificial activation, or altered functionality due to culture on thermo-responsive polymers compared to conventional cell culture. Our study demonstrates that along with commercially available UpCell carriers, two other thermo-responsive polymers based on poly(vinyl methyl ether) blends are attractive candidates for differentiation and gentle detachment of primary monocyte-derived macrophages. In summary, we observed similar functionality and viability of primary monocyte-derived macrophages cultured on thermo-responsive polymers compared to standard cell culture surfaces. While this first generation of custom-made thermo-responsive polymers does not yet outperform standard culture approaches, our results are very promising and provide the basis for exploiting the unique advantages offered by custom-made thermo-responsive polymers to further improve macrophage culture and recovery in the future, including the covalent binding of signaling molecules and the reduction of centrifugation and washing steps. Optimizing these and other benefits of thermo-responsive polymers could greatly improve the culture of macrophages for tissue engineering applications.
通过酶解细胞粘附分子来获取用于组织工程目的的培养巨噬细胞,可能会导致这些细胞意外激活、功能改变或行为异常。热响应聚合物是一种很有前景的工具,它能在工程组织构建物中继代培养之前,温和地使巨噬细胞脱离,而无需人工激活。因此,我们对不同种类的热响应聚合物进行了表征,以确定它们作为细胞底物的适用性以及通过温度变化介导巨噬细胞温和脱离的能力。将原代人单核细胞和THP-1来源的巨噬细胞培养在热响应聚合物上,并对其在脂多糖刺激下的吞噬作用和细胞因子分泌进行表征。我们发现,这两种细胞类型在热响应聚合物上的培养和刺激反应存在差异。与THP-1巨噬细胞不同,与传统细胞培养相比,原代单核细胞来源的巨噬细胞在热响应聚合物上培养时,没有显示出活力受损、人工激活或功能改变的迹象。我们的研究表明,除了市售的UpCell载体外,另外两种基于聚(乙烯基甲醚)共混物的热响应聚合物是原代单核细胞来源巨噬细胞分化和温和脱离的有吸引力的候选材料。总之,我们观察到与标准细胞培养表面相比,在热响应聚合物上培养的原代单核细胞来源巨噬细胞具有相似的功能和活力。虽然第一代定制的热响应聚合物尚未超越标准培养方法,但我们的结果非常有前景,并为利用定制热响应聚合物提供的独特优势进一步改善未来巨噬细胞培养和回收奠定了基础,包括信号分子的共价结合以及离心和洗涤步骤的减少。优化热响应聚合物的这些及其他优势可以极大地改善用于组织工程应用的巨噬细胞培养。