Department of Pharmacology, Vanderbilt University School of Medicine, Nashville, TN, USA; These authors contributed equally to this work.
Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, TN, USA; These authors contributed equally to this work.
Trends Pharmacol Sci. 2018 Jun;39(6):536-546. doi: 10.1016/j.tips.2018.03.001. Epub 2018 Apr 5.
Macrophages are cells of the innate immune system that are resident in all tissues, including metabolic organs such as the liver and adipose tissue (AT). Because of their phenotypic flexibility, they play beneficial roles in tissue homeostasis, but they also contribute to the progression of metabolic disease. Thus, they are ideal therapeutic targets for diseases such as insulin resistance (IR), nonalcoholic fatty liver disease (NAFLD), and atherosclerosis. Recently, discoveries in the area of drug delivery have facilitated phenotype-specific targeting of macrophages. In this review we discuss advances in potential therapeutics for metabolic diseases via macrophage-specific delivery. We highlight micro- and nanoparticles, liposomes, and oligopeptide complexes, and how they can be used to alter macrophage phenotype for a more metabolically favorable tissue environment.
巨噬细胞是先天免疫系统的细胞,存在于所有组织中,包括代谢器官如肝脏和脂肪组织 (AT)。由于其表型的灵活性,它们在组织稳态中发挥有益作用,但也有助于代谢疾病的进展。因此,它们是胰岛素抵抗 (IR)、非酒精性脂肪肝 (NAFLD) 和动脉粥样硬化等疾病的理想治疗靶点。最近,药物输送领域的发现促进了巨噬细胞的表型特异性靶向。在这篇综述中,我们讨论了通过巨噬细胞特异性递送来治疗代谢疾病的潜在疗法的进展。我们强调了微纳米粒子、脂质体和寡肽复合物,以及它们如何用于改变巨噬细胞表型,以获得更有利于代谢的组织环境。