Lu Hui-Chen, She Wei-Chi, Plas Daniel T, Neumann Paul E, Janz Roger, Crair Michael C
Division of Neuroscience and Program in Developmental Biology, Baylor College of Medicine, One Baylor Plaza S-603, Houston, Texas 77030, USA.
Nat Neurosci. 2003 Sep;6(9):939-47. doi: 10.1038/nn1106.
Cortical map formation requires the accurate targeting, synaptogenesis, elaboration and refinement of thalamocortical afferents. Here we demonstrate the role of Ca2+/calmodulin-activated type-I adenylyl cyclase (AC1) in regulating the strength of thalamocortical synapses through modulation of AMPA receptor (AMPAR) trafficking using barrelless mice, a mutant without AC1 activity or cortical 'barrel' maps. Barrelless synapses are stuck in an immature state that contains few functional AMPARs that are rarely silent (NMDAR-only). Long-term potentiation (LTP) and long-term depression (LTD) at thalamocortical synapses require postsynaptic protein kinase A (PKA) activity and are difficult to induce in barrelless mice, probably due to an inability to properly regulate synaptic AMPAR trafficking. Consistent with this, both the extent of PKA phosphorylation on AMPAR subunit GluR1 and the expression of surface GluR1 are reduced in barrelless neurons. These results suggest that activity-dependent mechanisms operate through an AC1/PKA signaling pathway to target some synapses for consolidation and others for elimination during barrel map formation.
皮质图谱的形成需要丘脑皮质传入纤维的精确靶向、突触形成、细化和完善。在这里,我们使用无桶小鼠(一种没有AC1活性或皮质“桶状”图谱的突变体),证明了Ca2+/钙调蛋白激活的I型腺苷酸环化酶(AC1)在通过调节AMPA受体(AMPAR)转运来调节丘脑皮质突触强度中的作用。无桶小鼠的突触处于不成熟状态,含有很少的功能性AMPAR,很少处于沉默状态(仅NMDAR)。丘脑皮质突触的长时程增强(LTP)和长时程抑制(LTD)需要突触后蛋白激酶A(PKA)的活性,并且在无桶小鼠中很难诱导,这可能是由于无法正确调节突触AMPAR的转运。与此一致的是,在无桶神经元中,AMPAR亚基GluR1上的PKA磷酸化程度和表面GluR1的表达均降低。这些结果表明,在桶状图谱形成过程中,活性依赖机制通过AC1/PKA信号通路作用于某些突触以进行巩固,而作用于其他突触以进行消除。