Lalonde Jasmin, Lachance Pascal E D, Chaudhuri Avi
Department of Psychology, McGill University, Montréal, Québec, Canada H3A 1B1.
J Neurosci. 2004 Jan 14;24(2):554-64. doi: 10.1523/JNEUROSCI.1668-03.2004.
Elevation of intracellular Ca2+ levels activates calcium/calmodulin-dependent protein kinase (CaMK) IV, which in turn plays an important role in neuroprotection and neuroplasticity. The possibility that CaMKIV is similarly involved in neocortical tissue has not been examined previously, especially with regard to the plastic nature of ocular dominance features in the primary visual cortex (area V1). We addressed this question by way of monocular enucleation (ME) to disrupt sensory input and examine CaMKIV expression changes in monkey area V1. Immunohistochemical staining of area V1 in normal infants showed a nuclear presence of CaMKIV, which did not changed after ME. However, a striking set of layer- and time-dependent changes in nuclear CaMKIV expression was observed in adult area V1 after ME. A strong increase in nuclear CaMKIV levels was evident in cortical layers II/III and VI after 1 d of ME and in layer IVC after 5 d of ME. These specific laminar changes persisted after 30 d of ME and, most notably, showed a columnar profile in which CaMKIV expression was linked to open-eye columns. Real-time quantitative reverse transcription-PCR and Western blot analysis showed that total amounts of CaMKIV mRNA and protein remained unchanged after ME, suggesting that a nuclear translocation may occur from the cytoplasm. Finally, double-label immunohistochemical staining with a pyramidal cell marker (SMI-32) showed that CaMKIV was absent in this subtype, whereas coincidental expression with GABA, parvalbumin, and calretinin, but not calbindin, showed its clear presence in a subset of interneurons. We propose that CaMKIV activity within diverse groups of cortical interneurons may play an important role in adaptive plastic reorganization of adult neocortical tissue.
细胞内钙离子(Ca2+)水平升高会激活钙/钙调蛋白依赖性蛋白激酶(CaMK)IV,而CaMKIV反过来在神经保护和神经可塑性中发挥重要作用。此前尚未研究CaMKIV是否同样参与新皮质组织,特别是在初级视觉皮层(V1区)眼优势特征的可塑性方面。我们通过单眼摘除(ME)来中断感觉输入,并研究猴V1区CaMKIV表达的变化,从而解决了这个问题。正常婴儿V1区的免疫组织化学染色显示CaMKIV存在于细胞核中,ME后其并未改变。然而,在成年猴V1区ME后,观察到细胞核CaMKIV表达出现了一组显著的层和时间依赖性变化。ME后1天,皮质II/III层和VI层细胞核CaMKIV水平明显升高,ME后5天,IVC层细胞核CaMKIV水平明显升高。这些特定的层状变化在ME后30天仍然存在,最值得注意的是,呈现出柱状分布,其中CaMKIV表达与睁眼柱相关。实时定量逆转录聚合酶链反应和蛋白质免疫印迹分析表明,ME后CaMKIV mRNA和蛋白质的总量保持不变,这表明可能发生了从细胞质到细胞核的转运。最后,用锥体细胞标记物(SMI-32)进行的双重标记免疫组织化学染色显示,该亚型中不存在CaMKIV,而与γ-氨基丁酸、小白蛋白和钙视网膜蛋白同时表达,但不与钙结合蛋白同时表达,表明其在一部分中间神经元中明显存在。我们认为,不同组皮质中间神经元内的CaMKIV活性可能在成年新皮质组织的适应性可塑性重组中发挥重要作用。