Alan Gutman-Wei
@alangutmanwei.bsky.social
25 followers 61 following 7 posts
postdoc @ hobertlab.org studying synaptic remodeling in the C elegans nervous system | PhD neuroscience @jhu.edu
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alangutmanwei.bsky.social
Check out our preprint for details! We also look at the development of layer 6 corticothalamic neuron dendrites, which differ from axons in both time course and activity dependence, the maturation of PV interneuron physiology and connectivity, and more (end)
alangutmanwei.bsky.social
Synaptogenesis is selective for parvalbumin interneurons within layer 6, and in translaminar connections to layer 4. This is despite these interneurons being far less abundant than neighboring excitatory neurons in both layers (6/7)
alangutmanwei.bsky.social
Do excitatory neurons selectively innervate their targets from the beginning, or make synapses promiscuously and then eliminate the off-target ones? We find that layer 6 corticothalamic neurons selectively form functional synapses to parvalbumin interneurons (5/7)
Example traces of patch clamp recordings of layer 6 corticothalamic neurons with parvalbumin interneurons, or with other layer 6 corticothalamic neurons, at P7 and at P15.
alangutmanwei.bsky.social
How does developmental neuronal activity affect axon arbor growth? We found that hyperpolarizing layer 6 corticothalamic neurons increased axon arbor elaboration specifically in layer 6, but not in layers 4 or 5 (4/7)
Example reconstructions of a control and a Kir2.1-expressing layer 6 corticothalamic neuron, showing increased axonal arborization in the Kir2.1-expressing cell
alangutmanwei.bsky.social
When and how do layer 6 corticothalamic neurons elaborate their intracortical axon branches? Using sparse labeling and lightsheet imaging we found two stages of outgrowth separated by a period of stasis in the first two postnatal weeks (3/7)
alangutmanwei.bsky.social
We focused on layer 6 corticothalamic neurons, which have a striking preference for connections to inhibitory interneurons that express parvalbumin over other excitatory cell types. In mice, this synaptic preference for inhibitory neurons can regulate cortical responses to sensory input (2/7)