Williams Michael R, Cauvi David M, Rivera Isabel, Hawisher Dennis, De Maio Antonio
Initiative for Maximizing Student Development, University of California San Diego, La Jolla, CA, USA.
Department of Surgery, University of California San Diego, La Jolla, CA, USA.
Innate Immun. 2016 Apr;22(3):141-51. doi: 10.1177/1753425916633886. Epub 2016 Mar 7.
Macrophages (Mφs) play a critical role in the defense against pathogens, orchestrating the inflammatory response during injury and maintaining tissue homeostasis. During these processes, macrophages encounter a variety of environmental conditions that are likely to change their gene expression pattern, which modulates their function. In this study, we found that murine Mφs displayed two different subpopulations characterized by differences in morphologies, expression of surface markers and phagocytic capacity under non-stimulated conditions. These two subpopulations could be recapitulated by changes in the culture conditions. Thus, Mφs grown in suspension in the presence of serum were highly phagocytic, whereas subtraction of serum resulted in rapid attachment and reduced phagocytic activity. The difference in phagocytosis between these subpopulations was correlated with the expression levels of FcγR. These two cell subpopulations also differed in their responses to LPS and the expression of surface markers, including CD14, CD86, scavenger receptor A1, TLR4 and low-density lipoprotein receptor. Moreover, we found that the lipid/cholesterol content in the culture medium mediated the differences between these two cell subpopulations. Thus, we described a mechanism that modulates Mφ function depending on the exposure to lipids within their surrounding microenvironment.
巨噬细胞(Mφs)在抵御病原体、协调损伤期间的炎症反应以及维持组织稳态方面发挥着关键作用。在这些过程中,巨噬细胞会遇到各种可能改变其基因表达模式的环境条件,而基因表达模式的改变又会调节其功能。在本研究中,我们发现小鼠巨噬细胞在非刺激条件下表现出两种不同的亚群,其特征在于形态、表面标志物表达和吞噬能力的差异。这两种亚群可以通过培养条件的变化得以重现。因此,在血清存在下悬浮培养的巨噬细胞具有高度吞噬能力,而去除血清则导致细胞快速贴壁并降低吞噬活性。这些亚群之间吞噬作用的差异与FcγR的表达水平相关。这两种细胞亚群对脂多糖(LPS)的反应以及包括CD14、CD86、清道夫受体A1、Toll样受体4(TLR4)和低密度脂蛋白受体在内的表面标志物的表达也有所不同。此外,我们发现培养基中的脂质/胆固醇含量介导了这两种细胞亚群之间的差异。因此,我们描述了一种根据巨噬细胞周围微环境中脂质暴露情况来调节其功能的机制。