Center for Neuroscience, University of California Davis, Davis, California, 95618.
Dev Neurobiol. 2017 Oct;77(10):1161-1174. doi: 10.1002/dneu.22503. Epub 2017 May 13.
The formation and stabilization of new dendritic spines is a key component of the experience-dependent neural circuit plasticity that supports learning, but the molecular maturation of nascent spines remains largely unexplored. The PSD95-family of membrane-associated guanylate kinases (PSD-MAGUKs), most notably PSD95, has a demonstrated role in promoting spine stability. However, nascent spines contain low levels of PSD95, suggesting that other members of the PSD-MAGUK family might act to stabilize nascent spines in the early stages of spiny synapse formation. Here, we used GFP-fusion constructs to quantitatively define the molecular composition of new spines, focusing on the PSD-MAGUK family. We found that PSD95 levels in new spines were as low as those previously associated with rapid subsequent spine elimination, and new spines did not achieve mature levels of PSD95 until between 12 and 20 h following new spine identification. Surprisingly, we found that the PSD-MAGUKs PSD93, SAP97, and SAP102 were also substantially less enriched in new spines. However, they accumulated in new spines more quickly than PSD95: SAP102 enriched to mature levels within 3 h, SAP97 and PSD93 enriched gradually over the course of 6 h. Intriguingly, when we restricted our analysis to only those new spines that persisted, SAP97 was the only PSD-MAGUK already present at mature levels in persistent new spines when first identified. Our findings uncover a key structural difference between nascent and mature spines, and suggest a mechanism for the stabilization of nascent spines through the sequential arrival of PSD-MAGUKs. © 2017 Wiley Periodicals, Inc. Develop Neurobiol 77: 1161-1174, 2017.
新树突棘的形成和稳定是支持学习的经验依赖性神经回路可塑性的关键组成部分,但新生棘突的分子成熟在很大程度上仍未得到探索。突触后密度蛋白 95 家族(PSD-MAGUKs)的膜相关鸟苷酸激酶(PSD-MAGUKs),尤其是 PSD95,已被证明在促进棘突稳定性方面具有作用。然而,新生棘突中 PSD95 的水平较低,这表明 PSD-MAGUK 家族的其他成员可能在棘突突触形成的早期阶段发挥作用,以稳定新生棘突。在这里,我们使用 GFP 融合构建体来定量定义新棘突的分子组成,重点是 PSD-MAGUK 家族。我们发现,新棘突中的 PSD95 水平低至先前与快速随后的棘突消除相关的水平,并且新棘突在新棘突鉴定后 12 至 20 小时之间才达到成熟的 PSD95 水平。令人惊讶的是,我们发现 PSD-MAGUKs PSD93、SAP97 和 SAP102 在新棘突中也明显含量较低。然而,它们在新棘突中更快地积累:SAP102 在 3 小时内富集到成熟水平,SAP97 和 PSD93 在 6 小时内逐渐富集。有趣的是,当我们将分析仅限于那些持续存在的新棘突时,当首次鉴定时,SAP97 是仅有的在持续存在的新棘突中已经存在成熟水平的 PSD-MAGUK。我们的研究结果揭示了新生和成熟棘突之间的关键结构差异,并提出了一种通过 PSD-MAGUK 的顺序到达来稳定新生棘突的机制。 © 2017 Wiley Periodicals, Inc. 发展神经生物学 77:1161-1174,2017 年。