Department of Biomedical Engineering, The Chinese University of Hong Kong, Hong Kong, China.
Department of Orthopaedic Surgery, The First Affiliated Hospital of Soochow University, Soochow University, Suzhou, Jiangsu, China; Orthopaedic Institute, Medical College, Soochow University, Suzhou, Jiangsu, China.
Biomaterials. 2018 Sep;178:681-696. doi: 10.1016/j.biomaterials.2018.03.007. Epub 2018 Apr 21.
Macrophages are multifunctional immune cells with diverse physiological functions such as fighting against infection, influencing progression of pathologies, maintaining homeostasis, and regenerating tissues. Macrophages can be induced to adopt distinct polarized phenotypes, such as classically activated pro-inflammatory (M1) phenotypes or alternatively activated anti-inflammatory and pro-healing (M2), to execute diverse and dynamic immune functions. However, unbalanced polarizations of macrophage can lead to various pathologies, such as atherosclerosis, obesity, tumor, and asthma. Thus, the capability to remotely control macrophage phenotypes is important to the success of treating many pathological conditions involving macrophages. In this study, we developed an upconversion nanoparticle (UCNP)-based photoresponsive nanocarrier for near-infrared (NIR) light-mediated control of intracellular calcium levels to regulate macrophage polarization. UCNP was coated with mesoporous silica (UCNP@mSiO), into which loaded calcium regulators that can either supply or deplete calcium ions. UCNP@mSiO was chemically modified through serial coupling of photocleavable linker and Arg-Gly-Asp (RGD) peptide-bearing molecular cap via cyclodextrin-adamantine host-guest complexation. The RGD-bearing cap functioned as the photolabile gating structure to control the release of calcium regulators and facilitated the cellular uptake of UCNP@mSiO nanocarrier. The upconverted UV light emission from the UCNP@mSiO under NIR light excitation triggered the cleavage of cap and intracellular release of calcium regulators, thereby allowing temporal regulation on the intracellular calcium levels. Application of NIR light through skin tissue promoted M1 or M2 polarization of macrophages, by elevating or depleting intracellular calcium levels, respectively. To the best of our knowledge, this is the first demonstration of NIR light-mediated remote control on macrophage polarization. This photoresponsive nanocarrier offers the potential to remotely manipulate in vivo immune functions, such as inflammation or tissue regeneration, via NIR light-controlled macrophage polarization.
巨噬细胞是具有多种生理功能的多功能免疫细胞,例如抵抗感染、影响疾病进展、维持内稳态和组织再生。巨噬细胞可以被诱导采用不同的极化表型,例如经典激活的促炎(M1)表型或替代激活的抗炎和促愈合(M2)表型,以执行多样化和动态的免疫功能。然而,巨噬细胞的极化失衡可导致各种病理状况,如动脉粥样硬化、肥胖、肿瘤和哮喘。因此,远程控制巨噬细胞表型的能力对于成功治疗涉及巨噬细胞的许多病理状况非常重要。在这项研究中,我们开发了一种基于上转换纳米粒子(UCNP)的光响应纳米载体,用于近红外(NIR)光介导的细胞内钙离子水平的控制,以调节巨噬细胞的极化。UCNP 被介孔二氧化硅(UCNP@mSiO)包覆,其中装载有可以供应或耗尽钙离子的钙调节剂。UCNP@mSiO 通过光裂解连接子和 Arg-Gly-Asp(RGD)肽承载分子帽的化学偶联,依次进行化学修饰。RGD 承载的帽作为光不稳定的门控结构,控制钙调节剂的释放,并促进 UCNP@mSiO 纳米载体的细胞摄取。在近红外光激发下,UCNP@mSiO 发出的上转换紫外光引发帽的裂解和细胞内钙调节剂的释放,从而允许对细胞内钙离子水平进行时间调节。通过皮肤组织应用近红外光可分别通过升高或降低细胞内钙离子水平来促进巨噬细胞的 M1 或 M2 极化。据我们所知,这是首次证明通过近红外光介导对巨噬细胞极化进行远程控制。这种光响应纳米载体为通过近红外光控制的巨噬细胞极化来远程操纵体内免疫功能(如炎症或组织再生)提供了潜力。