An angiogenic role for the human peptide antibiotic LL-37/hCAP-18
J. Clin. Invest. Rembert Koczulla, et al. 111:1665
doi:10.1172/JCI17545 [Go to this article.]

Figure 3
Mice with disrupted Cnlp gene show decreased wound revascularization. (a and b) Vascular structures are identified in microsections by CD31 immunostaining at the wound edge 3 days after full-thickness aseptic injury. An asterisk denotes the wound site and location of crust. Wild-type 129/SvJ mice show multiple vascular structures in granulation tissue at the margin of the repairing wound (a). Mice with homozygous deletion of Cnlp, therefore lacking CRAMP, have fewer vessels at an identical location relative to the wound (b). The bar = 12.5 μm in both micrographs. (c) Numbers of vessels in the skin near the site of injury are significantly decreased in Cnlp–/– compared with wild-type mice, but are similar distal to the wound in each group (*P < 0.05; n = 3/group, three sections per animal).