Developmental Regulation of Homeostatic Plasticity in Mouse Primary Visual Cortex

• Published in: The Journal of neuroscience Vol. 41; no. 48; pp. 9891 - 9905
• Main Authors: Wen, Wei, Turrigiano, Gina G.
• Format: Journal Article
• Language: English
• Published: United States Society for Neuroscience 01.12.2021
• Subjects: Animals; Circuits; Critical period; Deprivation; Developmental plasticity; Developmental stages; Excitability; Female; Homeostasis - physiology; Homeostatic plasticity; Male; Mice; Mice, Inbred C57BL; Neurogenesis - physiology; Neuronal Plasticity - physiology; Neurons; Plastic properties; Plasticity; Primary Visual Cortex - physiology; Pyramidal cells; Synaptic plasticity; Visual cortex; Visual deprivation; Visual observation; Visual plasticity; Visual system; homeostatic plasticity; DREADDs; intrinsic homeostatic plasticity; visual cortex; critical periods; synaptic scaling
• ISSN: 0270-6474; 1529-2401; 1529-2401
• DOI: 10.1523/JNEUROSCI.1200-21.2021

Homeostatic plasticity maintains network stability by adjusting excitation, inhibition, or the intrinsic excitability of neurons, but the developmental regulation and coordination of these distinct forms of homeostatic plasticity remains poorly understood. A major contributor to this information gap is the lack of a uniform paradigm for chronically manipulating activity at different developmental stages. To overcome this limitation, we used designer receptors exclusively activated by designer drugs (DREADDs) to directly suppress neuronal activity in layer2/3 (L2/3) of mouse primary visual cortex of either sex at two important developmental timepoints: the classic visual system critical period [CP; postnatal day 24 (P24) to P29], and adulthood (P45 to P55). We show that 24 h of DREADD-mediated activity suppression simultaneously induces excitatory synaptic scaling up and intrinsic homeostatic plasticity in L2/3 pyramidal neurons during the CP, consistent with previous observations using prolonged visual deprivation. Importantly, manipulations known to block these forms of homeostatic plasticity when induced pharmacologically or via visual deprivation also prevented DREADD-induced homeostatic plasticity. We next used the same paradigm to suppress activity in adult animals. Surprisingly, while excitatory synaptic scaling persisted into adulthood, intrinsic homeostatic plasticity was completely absent. Finally, we found that homeostatic changes in quantal inhibitory input onto L2/3 pyramidal neurons were absent during the CP but were present in adults. Thus, the same population of neurons can express distinct sets of homeostatic plasticity mechanisms at different development stages. Our findings suggest that homeostatic forms of plasticity can be recruited in a modular manner according to the evolving needs of a developing neural circuit. SIGNIFICANCE STATEMENT Developing brain circuits are subject to dramatic changes in inputs that could destabilize activity if left uncompensated. This compensation is achieved through a set of homeostatic plasticity mechanisms that provide slow, negative feedback adjustments to excitability. Given that circuits are subject to very different destabilizing forces during distinct developmental stages, the forms of homeostatic plasticity present in the network must be tuned to these evolving needs. Here we developed a method to induce comparable homeostatic compensation during distinct developmental windows and found that neurons in the juvenile and mature brain engage strikingly different forms of homeostatic plasticity. Thus, homeostatic mechanisms can be recruited in a modular manner according to the developmental needs of the circuit.