p21^Cip1 modulates arterial wound repair through the stromal cell–derived factor-1/CXCR4 axis in mice
J. Clin. Invest. Michelle Olive, et al. 118:2050 doi:10.1172/JCI31244 [Go to this article.]

Figure 6
SDF-1 is localized to the arterial media, and SDF-1 tissue levels are increased in p21^–/– mice receiving p21^+/+ BM after arterial injury. (A) SDF-1 staining in uninjured arteries (left panels) and in arteries 3 days after injury (right panels) from p21^+/+ (upper panels) and p21^–/– (lower panels) mice. VSMCs were identified by smooth muscle α-actin (in green), endothelial cells by CD31 (in green), and inflammatory cells by CD45 (in green). SDF-1 staining is represented in red, and nuclei were counterstained by DAPI (blue). For uninjured and injured groups, left and middle columns represent individual staining; right columns are merged images. Scale bars: 40 μm. (B) Increased arterial tissue SDF-1 levels were observed in p21^–/– (blue bars) compared with p21^+/+ mice (yellow bars) 3 and 7 days after injury (n = 3; **P < 0.01 versus p21^+/+ at same time point). Increased SDF-1 levels were also observed in p21^+/+ mice 3 days after injury compared with uninjured p21^+/+ mice (n = 3; *P < 0.05). (C) Arterial SDF-1 levels measured 7 days after injury were increased in p21^–/– mice that received either p21^+/+ (orange bar) or p21^–/– (light blue bar) BM compared with p21^+/+ mice that received either p21^+/+ (yellow bar) or p21^–/– (dark blue bar) BM, respectively (n = 5; **P < 0.01).