Cantemir V, Cai D H, Reedy M V, Brauer P R
Department of Biomedical Science, Creighton University, Omaha, Nebraska 68178, USA.
Dev Dyn. 2004 Dec;231(4):709-19. doi: 10.1002/dvdy.20171.
Matrix metalloproteinases (MMPs) are important mediators of neural crest (NC) cell migration. Here, we examine the distribution of tissue inhibitor of metalloproteinase (TIMP) -2 and TIMP-3 and test whether manipulating TIMP levels alters chicken cardiac NC cell migration. TIMP-2 mRNA is expressed at stage 11 in the neural epithelium and only in migrating cardiac NC cells. TIMP-3 mRNA is expressed only in the notochord at stage 8 and later in the outflow tract myocardium. Exogenous TIMP-2 increases NC motility in vitro at low concentrations but has no effect when concentrations are increased. In vitro, NC cells express membrane type-1 matrix metalloproteinase (MT1-MMP) and TIMP-2 and they secrete and activate proMMP-2. Antisense TIMP-2 oligonucleotides block proMMP-2 activation, decrease NC cell migration from explants, and perturb NC morphogenesis in ovo. Because TIMP-2 is required for activation of proMMP-2 by MT1-MMP, this finding suggests TIMP-2 expression by cardiac NC cells initiates proMMP-2 activation important for their migration.
基质金属蛋白酶(MMPs)是神经嵴(NC)细胞迁移的重要介质。在此,我们研究金属蛋白酶组织抑制剂(TIMP)-2和TIMP-3的分布,并测试操纵TIMP水平是否会改变鸡心脏NC细胞的迁移。TIMP-2 mRNA在第11阶段的神经上皮中表达,且仅在迁移的心脏NC细胞中表达。TIMP-3 mRNA仅在第8阶段的脊索中表达,随后在流出道心肌中表达。低浓度的外源性TIMP-2可增加体外NC的运动性,但浓度增加时则无作用。在体外,NC细胞表达膜型-1基质金属蛋白酶(MT1-MMP)和TIMP-2,它们分泌并激活前MMP-2。反义TIMP-2寡核苷酸可阻断前MMP-2的激活,减少外植体中NC细胞的迁移,并扰乱鸡胚中的NC形态发生。由于TIMP-2是MT1-MMP激活前MMP-2所必需的,这一发现表明心脏NC细胞表达TIMP-2可启动对其迁移重要的前MMP-2激活。