长期抑郁
神经科学
受体
磷脂酶C
C级GPCR
代谢受体
长时程增强
生物
代谢型谷氨酸受体
化学
细胞生物学
NMDA受体
谷氨酸受体
生物化学
AMPA受体
作者
Se‐Young Choi,Jeff Chang,Bin Jiang,Geun Hee Seol,Sun-Seek Min,Jung‐Soo Han,Hee‐Sup Shin,Michela Gallagher,Alfredo Kirkwood
标识
DOI:10.1523/jneurosci.4084-05.2005
摘要
Long-term depression (LTD) in sensory cortices depends on the activation of NMDA receptors. Here, we report that in visual cortical slices, the induction of LTD (but not long-term potentiation) also requires the activation of receptors coupled to the phospholipase C (PLC) pathway. Using immunolesions in combination with agonists and antagonists, we selectively manipulated the activation of α1 adrenergic, M1 muscarinic, and mGluR5 glutamatergic receptors. Inactivation of these PLC-coupled receptors prevents the induction of LTD, but only when the three receptors were inactivated together. LTD is fully restored by activating any one of them or by supplying intracellular d -myo-inositol-1,4,5-triphosphate (IP 3 ). LTD was also impaired by intracellular application of PLC or IP 3 receptor blockers, and it was absent in mice lacking PLCβ1, the predominant PLC isoform in the forebrain. We propose that visual cortical LTD requires a minimum of PLC activity that can be supplied independently by at least three neurotransmitter systems. This essential requirement places PLC-linked receptors in a unique position to control the induction of LTD and provides a mechanism for gating visual cortical plasticity via extra-retinal inputs in the intact organism.
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