Martin-Vilchez Samuel, Whitmore Leanna, Asmussen Hannelore, Zareno Jessica, Horwitz Rick, Newell-Litwa Karen
Department of Cell Biology, University of Virginia School of Medicine, Charlottesville, VA, United States of America.
Department of Anatomy and Cell Biology, Brody School of Medicine, East Carolina University, Greenville, NC, United States of America.
PLoS One. 2017 Jan 23;12(1):e0170464. doi: 10.1371/journal.pone.0170464. eCollection 2017.
Small RhoGTPases regulate changes in post-synaptic spine morphology and density that support learning and memory. They are also major targets of synaptic disorders, including Autism. Here we sought to determine whether upstream RhoGTPase regulators, including GEFs, GAPs, and GDIs, sculpt specific stages of synaptic development. The majority of examined molecules uniquely regulate either early spine precursor formation or later maturation. Specifically, an activator of actin polymerization, the Rac1 GEF β-PIX, drives spine precursor formation, whereas both FRABIN, a Cdc42 GEF, and OLIGOPHRENIN-1, a RhoA GAP, regulate spine precursor elongation. However, in later development, a novel Rac1 GAP, ARHGAP23, and RhoGDIs inactivate actomyosin dynamics to stabilize mature synapses. Our observations demonstrate that specific combinations of RhoGTPase regulatory proteins temporally balance RhoGTPase activity during post-synaptic spine development.
小RhoGTP酶调节突触后棘突形态和密度的变化,这些变化支持学习和记忆。它们也是包括自闭症在内的突触疾病的主要靶点。在这里,我们试图确定上游RhoGTP酶调节因子,包括鸟嘌呤核苷酸交换因子(GEFs)、GTP酶激活蛋白(GAPs)和鸟嘌呤核苷酸解离抑制因子(GDIs),是否塑造突触发育的特定阶段。大多数被检测的分子独特地调节早期棘突前体形成或后期成熟。具体而言,肌动蛋白聚合激活剂Rac1鸟嘌呤核苷酸交换因子β-PIX驱动棘突前体形成,而Cdc42鸟嘌呤核苷酸交换因子FRABIN和RhoA GAP寡突蛋白-1均调节棘突前体伸长。然而,在后期发育中,一种新型Rac1 GAP,即ARHGAP23,和RhoGDIs使肌动球蛋白动力学失活,以稳定成熟突触。我们的观察结果表明,RhoGTP酶调节蛋白的特定组合在突触后棘突发育过程中暂时平衡RhoGTP酶活性。