| First Author | Jun JI | Year | 2015 |
| Journal | Nat Commun | Volume | 6 |
| Pages | 7386 | PubMed ID | 26077348 |
| Mgi Jnum | J:223027 | Mgi Id | MGI:5646344 |
| Doi | 10.1038/ncomms8386 | Citation | Jun JI, et al. (2015) The matricellular protein CCN1 mediates neutrophil efferocytosis in cutaneous wound healing. Nat Commun 6:7386 |
| abstractText | Neutrophil infiltration constitutes the first step in wound healing, although their timely clearance by macrophage engulfment, or efferocytosis, is critical for efficient tissue repair. However, the specific mechanism for neutrophil clearance in wound healing remains undefined. Here we uncover a key role for CCN1 in neutrophil efferocytosis by acting as a bridging molecule that binds phosphatidylserine, the 'eat-me' signal on apoptotic cells and integrins alphavbeta3/alphavbeta5 in macrophages to trigger efferocytosis. Both knockin mice expressing a mutant CCN1 that is unable to bind alphavbeta3/alphavbeta5 and mice with Ccn1 knockdown are defective in neutrophil efferocytosis, resulting in exuberant neutrophil accumulation and delayed healing. Treatment of wounds with CCN1 accelerates neutrophil clearance in both Ccn1 knockin mice and diabetic Lepr(db/db) mice, which suffer from neutrophil persistence and impaired healing. These findings establish CCN1 as a critical opsonin in skin injury and suggest a therapeutic potential for CCN1 in certain types of non-healing wounds. |
