Key result
Antisense TIMP-2 blocks proMMP-2 activation and impairs neural crest cell migration and morphogenesis.
Why the study?
The role of TIMP-2 expression in cardiac neural crest cell migration and proMMP-2 activation was not fully understood.
TIMP-2 expression by cardiac neural crest cells initiates proMMP-2 activation, which is essential for their migration and morphogenesis.
Answers are grounded in this paper and cite their sources.
Exogenous TIMP-2 alters chick cardiac NC migration; leaves open conservation in human outflow tract defects.
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.
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Cantemir et al. (2004) studied Cardiac neural crest cell migration. Antisense TIMP-2 oligonucleotides was evaluated on Neural crest cell migration and proMMP-2 activation. Antisense TIMP-2 oligonucleotides blocked proMMP-2 activation, decreased neural crest cell migration from explants, and perturbed neural crest morphogenesis in ovo.
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