Gow Deborah J, Sauter Kristin A, Pridans Clare, Moffat Lindsey, Sehgal Anuj, Stutchfield Ben M, Raza Sobia, Beard Philippa M, Tsai Yi Ting, Bainbridge Graeme, Boner Pamela L, Fici Greg, Garcia-Tapia David, Martin Roger A, Oliphant Theodore, Shelly John A, Tiwari Raksha, Wilson Thomas L, Smith Lee B, Mabbott Neil A, Hume David A
The Roslin Institute and Royal (Dick) School of Veterinary Studies, The University of Edinburgh, Easter Bush, Midlothian, UK.
The University of Edinburgh/MRC centre for Inflammation Research, The Queen's Medical Research Institute, Edinburgh, UK.
Mol Ther. 2014 Sep;22(9):1580-92. doi: 10.1038/mt.2014.112. Epub 2014 Jun 25.
We have produced an Fc conjugate of colony-stimulating factor (CSF) 1 with an improved circulating half-life. CSF1-Fc retained its macrophage growth-promoting activity, and did not induce proinflammatory cytokines in vitro. Treatment with CSF1-Fc did not produce adverse effects in mice or pigs. The impact of CSF1-Fc was examined using the Csf1r-enhanced green fluorescent protein (EGFP) reporter gene in MacGreen mice. Administration of CSF1-Fc to mice drove extensive infiltration of all tissues by Csf1r-EGFP positive macrophages. The main consequence was hepatosplenomegaly, associated with proliferation of hepatocytes. Expression profiles of the liver indicated that infiltrating macrophages produced candidate mediators of hepatocyte proliferation including urokinase, tumor necrosis factor, and interleukin 6. CSF1-Fc also promoted osteoclastogenesis and produced pleiotropic effects on other organ systems, notably the testis, where CSF1-dependent macrophages have been implicated in homeostasis. However, it did not affect other putative CSF1 targets, notably intestine, where Paneth cell numbers and villus architecture were unchanged. CSF1 has therapeutic potential in regenerative medicine in multiple organs. We suggest that the CSF1-Fc conjugate retains this potential, and may permit daily delivery by injection rather than continuous infusion required for the core molecule.
我们制备了一种集落刺激因子(CSF)1与Fc的偶联物,其循环半衰期有所延长。CSF1-Fc保留了其促进巨噬细胞生长的活性,且在体外不会诱导促炎细胞因子。用CSF1-Fc处理对小鼠或猪未产生不良影响。在MacGreen小鼠中使用Csf1r增强型绿色荧光蛋白(EGFP)报告基因研究了CSF1-Fc的作用。给小鼠注射CSF1-Fc促使Csf1r-EGFP阳性巨噬细胞广泛浸润所有组织。主要后果是肝脾肿大,与肝细胞增殖有关。肝脏的表达谱表明,浸润的巨噬细胞产生了包括尿激酶、肿瘤坏死因子和白细胞介素6在内的肝细胞增殖候选介质。CSF1-Fc还促进破骨细胞生成,并对其他器官系统产生多效性作用,尤其是睾丸,其中依赖CSF1的巨噬细胞与内环境稳定有关。然而,它不影响其他假定的CSF1靶标,尤其是肠道,其中潘氏细胞数量和绒毛结构未发生变化。CSF1在多个器官的再生医学中具有治疗潜力。我们认为CSF1-Fc偶联物保留了这种潜力,并且可能允许通过注射每日给药,而不是核心分子所需的持续输注。