Gonthier Bertrand, Koncina Eric, Satkauskas Saulius, Perraut Martine, Roussel Guy, Aunis Dominique, Kapfhammer Josef P, Bagnard Dominique
INSERM U575, Physiopathologie du Système Nerveux, Strasbourg, France.
PLoS One. 2009;4(4):e5099. doi: 10.1371/journal.pone.0005099. Epub 2009 Apr 8.
There is increasing evidence for a crucial role of proteases and metalloproteinases during axon growth and guidance. In this context, we recently described a functional link between the chemoattractive Sema3C and Matrix metalloproteinase 3 (MMP3). Here, we provide data demonstrating the involvement of MMP-2 to trigger the growth-promoting effect of Sema3A in cortical dendrites. The in situ analysis of MMP-2 expression and activity is consistent with a functional growth assay demonstrating in vitro that the pharmacological inhibition of MMP-2 reduces the growth of cortical dendrites in response to Sema3A. Hence, our results suggest that the selective recruitment and activation of MMP-2 in response to Sema3A requires a PKC alpha dependent mechanism. Altogether, we provide a second set of data supporting MMPs as effectors of the growth-promoting effects of semaphorins, and we identify the potential signalling pathway involved.
越来越多的证据表明蛋白酶和金属蛋白酶在轴突生长和导向过程中起关键作用。在此背景下,我们最近描述了趋化性信号分子3C(Sema3C)与基质金属蛋白酶3(MMP3)之间的功能联系。在此,我们提供数据证明MMP-2参与触发信号分子3A(Sema3A)对皮质树突的促生长作用。MMP-2表达和活性的原位分析与功能性生长试验一致,体外试验表明对MMP-2的药理抑制会降低皮质树突对Sema3A的反应性生长。因此,我们的结果表明,响应Sema3A时MMP-2的选择性募集和激活需要蛋白激酶Cα(PKCα)依赖性机制。总之,我们提供了第二组数据支持金属蛋白酶作为信号分子促生长作用的效应器,并确定了其中涉及的潜在信号通路。