Neuroscience and Cognitive Sciences Program, Department of Biology, University of Maryland, Maryland, United States.
Elife. 2017 Sep 6;6:e27345. doi: 10.7554/eLife.27345.
The sensitivity of ocular dominance to regulation by monocular deprivation is the canonical model of plasticity confined to a critical period. However, we have previously shown that visual deprivation through dark exposure (DE) reactivates critical period plasticity in adults. Previous work assumed that the elimination of visual input was sufficient to enhance plasticity in the adult mouse visual cortex. In contrast, here we show that light reintroduction (LRx) after DE is responsible for the reactivation of plasticity. LRx triggers degradation of the ECM, which is blocked by pharmacological inhibition or genetic ablation of matrix metalloproteinase-9 (MMP-9). LRx induces an increase in MMP-9 activity that is perisynaptic and enriched at thalamo-cortical synapses. The reactivation of plasticity by LRx is absent in mice, and is rescued by hyaluronidase, an enzyme that degrades core ECM components. Thus, the LRx-induced increase in MMP-9 removes constraints on structural and functional plasticity in the mature cortex.
光剥夺(DE)通过暗暴露重新激活成年小鼠视觉皮层的关键期可塑性。先前的工作假设消除视觉输入足以增强成年小鼠视觉皮层的可塑性。相比之下,我们在这里表明,DE 后的光再引入(LRx)负责重新激活可塑性。LRx 引发细胞外基质(ECM)的降解,而细胞外基质金属蛋白酶-9(MMP-9)的药理学抑制或基因消融可阻断这种降解。LRx 诱导 MMP-9 活性增加,这种增加位于突触旁,在丘脑皮质突触处富集。LRx 诱导的可塑性重新激活在 缺乏 MMP-9 的情况下不存在,并且可以通过透明质酸酶(一种降解核心 ECM 成分的酶)来挽救。因此,LRx 诱导的 MMP-9 增加消除了成熟皮层结构和功能可塑性的限制。