Competition and Homeostasis of Excitatory and Inhibitory Connectivity in the Adult Mouse Visual Cortex

被引:5
作者
Saiepour, M. Hadi [1 ]
Chakravarthy, Sridhara [1 ]
Min, Rogier [1 ]
Levelt, Christiaan N. [1 ]
机构
[1] Royal Netherlands Acad Arts & Sci KNAW, Netherlands Inst Neurosci, Dept Mol Visual Plast, NL-1105 Amsterdam, Netherlands
关键词
BDNF; cell autonomous; inhibition; parvalbumin; TrkB; ACTIVITY-DEPENDENT REGULATION; OCULAR DOMINANCE PLASTICITY; NEUROTROPHIC FACTOR; SPONTANEOUS NEUROTRANSMISSION; MONOCULAR DEPRIVATION; SYNAPTIC-TRANSMISSION; NEURONS; SYNAPSES; RESPONSES; POOL;
D O I
10.1093/cercor/bhu245
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
During cortical development, synaptic competition regulates the formation and adjustment of neuronal connectivity. It is unknown whether synaptic competition remains active in the adult brain and how inhibitory neurons participate in this process. Using morphological and electrophysiological measurements, we show that expressing a dominant-negative form of the TrkB receptor (TrkB.T1) in the majority of pyramidal neurons in the adult visual cortex does not affect excitatory synapse densities. This is in stark contrast to the previously reported loss of excitatory input which occurs if the exact same transgene is expressed in sparse neurons at the same age. This indicates that synaptic competition remains active in adulthood. Additionally, we show that interneurons not expressing the TrkB.T1 transgene may have a competitive advantage and obtain more excitatory synapses when most neighboring pyramidal neurons do express the transgene. Finally, we demonstrate that inhibitory synapses onto pyramidal neurons are reduced when TrkB signaling is interfered with in most pyramidal neurons but not when few pyramidal neurons have this deficit. This adjustment of inhibitory innervation is therefore not a cell-autonomous consequence of decreased TrkB signaling but more likely a homeostatic mechanism compensating for activity changes at the population level.
引用
收藏
页码:3713 / 3722
页数:10
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