| First Author | Møller-Kristensen M | Year | 2007 |
| Journal | J Invest Dermatol | Volume | 127 |
| Issue | 6 | Pages | 1524-31 |
| PubMed ID | 17363917 | Mgi Jnum | J:121549 |
| Mgi Id | MGI:3710447 | Doi | 10.1038/sj.jid.5700748 |
| Citation | Moller-Kristensen M, et al. (2007) Burn injury reveals altered phenotype in mannan-binding lectin-deficient mice. J Invest Dermatol 127(6):1524-31 |
| abstractText | Burn injury destroys skin, the second largest innate immune organ in the body, and triggers chaotic immune and inflammatory responses. The pattern recognition molecule, mannan-binding lectin (MBL), plays an important role in the first-line host defense against infectious agents. MBL initiates the lectin complement pathway and acts as an opsonin. Recent studies suggest that MBL also modulates inflammatory responses. We report that local responses after burn in MBL null mice differ from those found in wild-type (WT) mice in the following important biological markers: spontaneous eschar separation, thinned epidermis and dermis, upregulation of soluble factors including cytokines, chemokines, cell adhesion molecules, a growth factor-binding protein, and matrix metalloproteinases. Mice lacking C1q, C4, or C3 did not show the lack of eschar separation seen in MBL null-burn phenotype. These findings implicate MBL as an important molecule in the maintenance of the homeostatic balance. |
