Stamenkovic Ivan, Yu Qin
Experimental Pathology Division, Institut Universitaire de Pathologie CHUV, Faculty of Biology and Medicine, University of Lausanne, Lausanne, Switzerland.
J Invest Dermatol. 2009 Jun;129(6):1321-4. doi: 10.1038/jid.2009.13.
CD44 is the major cell-surface receptor for hyaluronan, which is implicated in cell-cell and cell-matrix adhesion, cell migration, and signaling. Studies have shown that CD44-dependent migration requires CD44 to be shed from the cell surface and that matrix metalloproteinase-mediated cleavage may provide an underlying mechanism. However, the full spectrum of proteases that may participate in CD44 shedding has yet to be defined. In this issue, Anderegg et al. demonstrate that ADAM10, but not ADAM17 or MMP14, mediates constitutive shedding of CD44 in human melanoma cells and that knockdown of ADAM10 blocks the antiproliferative activity of the soluble proteolytic cleavage product of CD44.
CD44是透明质酸的主要细胞表面受体,与细胞间和细胞与基质的黏附、细胞迁移及信号传导有关。研究表明,依赖CD44的迁移需要CD44从细胞表面脱落,基质金属蛋白酶介导的裂解可能是其潜在机制。然而,可能参与CD44脱落的蛋白酶的完整谱尚未明确。在本期杂志中,安德雷格等人证明,在人黑色素瘤细胞中,是ADAM10而非ADAM17或MMP14介导CD44的组成型脱落,并且敲低ADAM10可阻断CD44可溶性蛋白水解裂解产物的抗增殖活性。