The melanoma-associated transmembrane glycoprotein Gpnmb controls trafficking of cellular debris for degradation and is essential for tissue repair

Article

关键词: EPITHELIAL-CELLS;    APOPTOTIC CELLS;    KIDNEY INJURY;    DICTYOSTELIUM-DISCOIDEUM;    PHAGOSOME MATURATION;    THERAPEUTIC TARGET;    IN-VIVO;    MACROPHAGES;    AUTOPHAGY;    PATHWAY;   

DOI  :  10.1096/fj.10-154757

来源: SCIE

【 摘 要 】

Kidney damage due to injury rarely resolves completely, and there are currently no therapies capable of promoting repair. In addition to understanding mechanisms by which tissues are damaged, illuminating mechanisms of repair and regeneration is also of great importance. Here we show that the melanoma-associated, transmembrane glycoprotein, Gpnmb, is up-regulated 15-fold following ischemic damage in kidney tissue and by more than 10-fold in macrophages and 3-fold in surviving epithelial cells. Gpnmb-expressing macrophages and epithelial cells were found to contain apoptotic bodies at 3 times the rate of non-expressing cells. Either mutation of Gpnmb or ablation of inflammatory macrophages prevents normal repair of the kidney. Significantly, the kidneys from postischemic Gpnmb mutant mice exhibited a 5-fold increase in apoptotic cellular debris compared to wild-type mice. These mice also experienced an 85% increase in mortality following bilateral ischemic kidney. Finally, we demonstrate that Gpnmb is a phagocytic protein that is necessary for recruitment of the autophagy protein LC3 to the phagosome where these proteins are colocalized and for lysosomal fusion with the phagosome and hence bulk degradation of their content. Therefore, Gpnmb is a novel prorepair gene that is necessary for crosstalk between the macroautophagic degradation pathway and phagocytosis.-Li, B., Castano, A. P., Hudson, T. E., Nowlin, B. T., Lin, S.-L., Bonventre, J. V., Swanson, K. D., Duffield, J. S. The melanoma-associated transmembrane glycoprotein Gpnmb controls trafficking of cellular debris for degradation and is essential for tissue repair. FASEB J. 24, 4767-4781 (2010). www.fasebj.org

【 授权许可】

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