controlled degradation in vivo provides a promising alternative to these nondegradable synthetic grafts. [4] Soon after implantation, the grafts will induce inflammation. As inflammation resolves and scaffold degrades, autogenous vascular cells are recruited, and neo-tissues grow in. After full degradation of graft scaffolds, artery-like tissues could then form in situ. Central to this transformation is how inflammation changes over time and how host populates the porous grafts with vascular endothelial and smooth muscle cells (SMCs). Macrophages play an important role during this process. [5] Our data reveal that not only is macrophage essential to the inflammation, but they also directly participate in the "vitalization" of the graft, that is, turning the acellular graft into a living vascular conduit. Macrophages exhibit continuum phenotypes with two extremes: M1, the classically activated one, which is pro-inflammatory; and M2, the alternatively activated one, which is anti-inflammatory and generally promotes regeneration. Transition of macrophages into M2 phenotype has been shown to promote vascular graft remodeling. [4,6] In addition to switching between M1/M2 states, there is evidence that monocytes/macrophages in peripheral blood can transdifferentiate into endothelial cells (ECs) or endothelial progenitor cells. [7] A recent study shows that circulating monocytes participate in endothelialization of vascular grafts by trans-differentiation into ECs. [8] Meanwhile, macrophages have been reported to express myofibroblast markers and deposit collagens. [9] The plasticity of monocytes/macrophages endow them the potential to transdifferentiate into ECs, SMCs, and fibroblast cells to regenerate blood vessels in situ. However, there remains little evidence that monocytes/macrophages could contribute to vascular graft remodeling in vivo via trans-differentiation into vascular cells. Porous poly(glycerol sebacate) (PGS) conduits sheathed with electrospun polycaprolactone (PCL) have good performances in arterial circulation in abdominal aortas [10] and carotid arteries in rats. [10c,11] In addition, the composite grafts show a near complete host remodeling with minimal graft materials left after 3 months in vivo. [12] However, a major issue associated with graft remodeling in vivo is limited neo-tissue formation inside PCL layers. The possible reason for this is small pores of PCL sheaths that inhibit cell infiltration and migration. Similar phenomena have Vasculopathy and the consequential ischemia are major medical challenges. Grafting is an effective treatment to vascular occlusion. However, autologous grafting, despite scarcity, is the only choice for small diameter blood vessels. Synthetic grafts can fill the gap if they can work satisfactorily in arterial circulation. Electrospun polycaprolactone (PCL) sheathed porous poly(glycerol sebacate) (PGS) vascular grafts have good performances in arterial circulation in abdominal aortas and carotid arteries in rats. However, a major issue associated with the graft r...