[HTML][HTML] The current status of somatostatin-interneurons in inhibitory control of brain function and plasticity

I Scheyltjens, L Arckens - Neural plasticity, 2016 - hindawi.com
I Scheyltjens, L Arckens
Neural plasticity, 2016hindawi.com
The mammalian neocortex contains many distinct inhibitory neuronal populations to balance
excitatory neurotransmission. A correct excitation/inhibition equilibrium is crucial for normal
brain development, functioning, and controlling lifelong cortical plasticity. Knowledge about
how the inhibitory network contributes to brain plasticity however remains incomplete.
Somatostatin-(SST-) interneurons constitute a large neocortical subpopulation of
interneurons, next to parvalbumin-(PV-) and vasoactive intestinal peptide-(VIP-) …
The mammalian neocortex contains many distinct inhibitory neuronal populations to balance excitatory neurotransmission. A correct excitation/inhibition equilibrium is crucial for normal brain development, functioning, and controlling lifelong cortical plasticity. Knowledge about how the inhibitory network contributes to brain plasticity however remains incomplete. Somatostatin- (SST-) interneurons constitute a large neocortical subpopulation of interneurons, next to parvalbumin- (PV-) and vasoactive intestinal peptide- (VIP-) interneurons. Unlike the extensively studied PV-interneurons, acknowledged as key components in guiding ocular dominance plasticity, the contribution of SST-interneurons is less understood. Nevertheless, SST-interneurons are ideally situated within cortical networks to integrate unimodal or cross-modal sensory information processing and therefore likely to be important mediators of experience-dependent plasticity. The lack of knowledge on SST-interneurons partially relates to the wide variety of distinct subpopulations present in the sensory neocortex. This review informs on those SST-subpopulations hitherto described based on anatomical, molecular, or electrophysiological characteristics and whose functional roles can be attributed based on specific cortical wiring patterns. A possible role for these subpopulations in experience-dependent plasticity will be discussed, emphasizing on learning-induced plasticity and on unimodal and cross-modal plasticity upon sensory loss. This knowledge will ultimately contribute to guide brain plasticity into well-defined directions to restore sensory function and promote lifelong learning.
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