Department of Biochemistry, Kobe Pharmaceutical University, Kobe 658-8558, Japan.
J Biol Chem. 2011 Feb 11;286(6):4199-208. doi: 10.1074/jbc.M110.155093. Epub 2010 Dec 1.
During metazoan development, Wnt molecules are secreted from Wnt-producing cells, diffuse to target cells, and determine cell fates; therefore, Wnt secretion is tightly regulated. However, the molecular mechanisms controlling Wnt diffusion are not fully elucidated. The specific chondroitin sulfate (CS) structure synthesized by chondroitin-4-O-sulfotransferase-1 (C4ST-1) binds to Wnt-3a with high affinity (Nadanaka, S., Ishida, M., Ikegami, M., and Kitagawa, H. (2008) J. Biol. Chem. 283, 27333-27343). In this study we tested whether Wnt signaling regulates sulfation patterns of cell-associated CS chains by suppressing expression of C4ST-1 to trigger release of Wnt molecules from Wnt-producing cells. C4ST-1 expression was dramatically reduced in L cells that stably expressed Wnt-3a (L-Wnt-3a cells) and had CS with low affinity for Wnt-3a. Forced expression of C4ST-1 in L-Wnt-3a cells inhibited diffusion of Wnt-3a due to structural alterations in CS chains mediated by C4ST-1. Furthermore, sustained Wnt signaling negatively regulated C4ST-1 expression in a cell-autonomous and non-cell autonomous fashion. These results demonstrated that C4ST-1 is a key downstream target of Wnt signaling that regulates Wnt diffusion from Wnt-producing cells.
在后生动物发育过程中,Wnt 分子从 Wnt 产生细胞中分泌,扩散到靶细胞,并决定细胞命运;因此,Wnt 分泌受到严格调控。然而,控制 Wnt 扩散的分子机制尚未完全阐明。软骨素-4-O-硫酸转移酶-1(C4ST-1)合成的特定的软骨素硫酸盐(CS)结构与 Wnt-3a 具有高亲和力(Nadanaka,S.,Ishida,M.,Ikegami,M.,和 Kitagawa,H.(2008)J. Biol. Chem. 283,27333-27343)。在这项研究中,我们通过抑制 C4ST-1 的表达来触发 Wnt 分子从 Wnt 产生细胞中释放,从而测试 Wnt 信号是否通过调节细胞相关 CS 链的硫酸化模式来调节 Wnt 信号。稳定表达 Wnt-3a 的 L 细胞(L-Wnt-3a 细胞)中 C4ST-1 的表达显著降低,并且 CS 与 Wnt-3a 的亲和力较低。在 L-Wnt-3a 细胞中强制表达 C4ST-1 会由于 C4ST-1 介导的 CS 链结构改变而抑制 Wnt-3a 的扩散。此外,持续的 Wnt 信号以细胞自主和非细胞自主的方式负调控 C4ST-1 的表达。这些结果表明,C4ST-1 是 Wnt 信号的关键下游靶标,可调节 Wnt 从 Wnt 产生细胞中的扩散。