Department of Neuroscience, Brown University, Providence, United States.
The Scripps Research Institute, La Jolla, United States.
Elife. 2021 Jul 20;10:e62147. doi: 10.7554/eLife.62147.
Matrix metalloproteinase-9 (MMP-9) is a secreted endopeptidase targeting extracellular matrix proteins, creating permissive environments for neuronal development and plasticity. Developmental dysregulation of MMP-9 may also lead to neurodevelopmental disorders (ND). Here, we test the hypothesis that chronically elevated MMP-9 activity during early neurodevelopment is responsible for neural circuit hyperconnectivity observed in tadpoles after early exposure to valproic acid (VPA), a known teratogen associated with ND in humans. In tadpoles, VPA exposure results in excess local synaptic connectivity, disrupted social behavior and increased seizure susceptibility. We found that overexpressing MMP-9 in the brain copies effects of VPA on synaptic connectivity, and blocking MMP-9 activity pharmacologically or genetically reverses effects of VPA on physiology and behavior. We further show that during normal neurodevelopment MMP-9 levels are tightly regulated by neuronal activity and required for structural plasticity. These studies show a critical role for MMP-9 in both normal and abnormal development.
基质金属蛋白酶-9(MMP-9)是一种分泌型内肽酶,可靶向细胞外基质蛋白,为神经元发育和可塑性创造许可环境。MMP-9 的发育失调也可能导致神经发育障碍(ND)。在这里,我们假设在早期神经发育过程中 MMP-9 活性的慢性升高是导致早期暴露于丙戊酸(VPA)的蝌蚪中观察到的神经回路过度连接的原因,VPA 是一种与人类 ND 相关的已知致畸剂。在蝌蚪中,VPA 暴露会导致局部突触连接过度,破坏社交行为并增加癫痫易感性。我们发现,在大脑中过表达 MMP-9 会复制 VPA 对突触连接的影响,并且通过药理学或遗传学阻断 MMP-9 活性可逆转 VPA 对生理和行为的影响。我们进一步表明,在正常神经发育过程中,MMP-9 的水平受到神经元活动的严格调节,并且是结构可塑性所必需的。这些研究表明 MMP-9 在正常和异常发育中都起着关键作用。