Coxon Fraser P, Taylor Adam
Bone & Musculoskeletal Programme, School of Medicine & Dentistry, Institute of Medical Sciences, University of Aberdeen, Foresterhill, UK.
Semin Cell Dev Biol. 2008 Oct;19(5):424-33. doi: 10.1016/j.semcdb.2008.08.004. Epub 2008 Aug 14.
Bone-resorbing osteoclasts are highly dependent on vesicular trafficking pathways that are regulated by Rab GTPases. In particular, polarised transport of acidic vesicles of the endocytic/lysosomal pathway is required for formation of the ruffled border, the resorptive organelle of the osteoclast. The breakdown products of resorption are then transported through the osteoclast by transcytosis, enabling their excretion. In this review, we summarise these trafficking routes, highlight the emerging evidence that the bone disease osteopetrosis results from defects in vesicular trafficking in osteoclasts, and outline the similarities between the endocytic/lysosomal compartment in osteoclasts and secretory lysosomes in other cell types.
骨吸收破骨细胞高度依赖于由Rab GTP酶调节的囊泡运输途径。特别是,内吞/溶酶体途径的酸性囊泡的极化运输是破骨细胞吸收性细胞器——皱褶缘形成所必需的。吸收的分解产物随后通过转胞吞作用穿过破骨细胞,实现其排泄。在这篇综述中,我们总结了这些运输途径,强调了骨疾病骨质石化是由破骨细胞囊泡运输缺陷导致的这一最新证据,并概述了破骨细胞内吞/溶酶体区室与其他细胞类型的分泌性溶酶体之间的相似之处。