Inflammation and wound repair

被引:52
作者
LeBert, Danny C. [1 ]
Huttenlocher, Anna [2 ,3 ]
机构
[1] Univ Wisconsin, Cellular & Mol Pathol Grad Program, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Pediat, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Med Microbiol & Immunol, Madison, WI 53706 USA
关键词
Inflammation; Chronic wounds; Wound repair; Regeneration; MYELOID-SPECIFIC EXPRESSION; ZEBRAFISH HEART; ADULT ZEBRAFISH; PAPA SYNDROME; IN-VIVO; REGENERATIVE CAPACITY; PYODERMA-GANGRENOSUM; NEUTROPHIL MOTILITY; TISSUE REGENERATION; GENE-EXPRESSION;
D O I
10.1016/j.smim.2014.04.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Wound repair requires the integration of complex cellular networks to restore tissue homeostasis. Defects in wound repair are associated with human disease including pyoderma gangrenosum, a heterogeneous disorder that is characterized by unhealed wounds and chronic inflammation of unclear etiology. Despite its clinical importance, there remain significant gaps in understanding how different types of cells communicate to integrate inflammation and wound repair. Recent progress in wound and regenerative biology has been gained by studying genetically tractable model organisms, like zebrafish, that retain the ability to regenerate. The optical transparency and ease of genetic manipulation make zebrafish an ideal model system to dissect multi-cellular and tissue level interactions during wound repair. The focus of this review is on recent advances in understanding how inflammation and wound repair are orchestrated and integrated to achieve wound resolution and tissue regeneration using zebrafish. (C) 2014 Published by Elsevier Ltd.
引用
收藏
页码:315 / 320
页数:6
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