Anatomical identification of a corticocortical top-down recipient inhibitory circuitry by enhancer-restricted transsynaptic tracing DOI Creative Commons

Yusuke Atsumi,

Yasuhiro Oisi, Maya Odagawa

et al.

Frontiers in Neural Circuits, Journal Year: 2023, Volume and Issue: 17

Published: Aug. 30, 2023

Despite the importance of postsynaptic inhibitory circuitry targeted by mid/long-range projections (e.g., top-down projections) in cognitive functions, its anatomical properties, such as laminar profile and neuron type, are poorly understood owing to lack efficient tracing methods. To this end, we developed a method that combines conventional adeno-associated virus (AAV)-mediated transsynaptic with distal-less homeobox (Dlx) enhancer-restricted expression system label neurons. We called "Dlx Interneuron-SpECific Tracing" (DISECT). applied DISECT corticocortical circuit from secondary motor cortex (M2) primary somatosensory (S1) wild-type mice. First, injected AAV1-Cre into M2, which enabled Cre recombinase M2-input recipient S1 Second, AAV1-hDlx-flex-green fluorescent protein (GFP) transduce GFP neurons Cre-dependent manner. succeeded exclusively labeling S1. Laminar analysis labeled via indicated were distributed superficial deep layers This distribution was aligned density axons projecting M2. further classified types using immunohistochemistry

Language: Английский

Bidirectional control of neurovascular coupling by cortical somatostatin interneurons DOI Creative Commons

B. Peer Mohamed,

Jill X. O’Reilly,

Sandrine Picaud

et al.

bioRxiv (Cold Spring Harbor Laboratory), Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 6, 2024

ABSTRACT Neurovascular coupling, linking neuronal activity to cerebral blood flow, is altered early in neurological disorders and underlies functional brain imaging. This process involves numerous cellular players. Among them inhibitory interneurons receive increasing attention, but how they control flow remains elusive. study elucidates the mechanisms by which somatostatin bidirectionally neurovascular coupling. Patch clamp recordings in, ex vivo, cortical slices from mice expressing channelrhodopsin-2 interneurons, revealed that these neurons are supralinearly activated at low-frequencies (< 5 Hz) efficiently photostimulated frequencies up 20 Hz. Ex vivo vascular imaging showed low-frequency (2 photostimulation triggered vasodilation whereas high-frequency (20 induced vasoconstriction. Histochemistry subpopulations of expressed nitric oxide synthase, and/or neuropeptide Y a greater extent. Consistently, pharmacological investigations release activation soluble guanylate cyclase. In contrast, vasoconstriction Y1 receptor. These findings provide valuable insights into coupling help understand mechanism underlying signals.

Language: Английский

Citations

0

Anatomical identification of a corticocortical top-down recipient inhibitory circuitry by enhancer-restricted transsynaptic tracing DOI Creative Commons

Yusuke Atsumi,

Yasuhiro Oisi, Maya Odagawa

et al.

Frontiers in Neural Circuits, Journal Year: 2023, Volume and Issue: 17

Published: Aug. 30, 2023

Despite the importance of postsynaptic inhibitory circuitry targeted by mid/long-range projections (e.g., top-down projections) in cognitive functions, its anatomical properties, such as laminar profile and neuron type, are poorly understood owing to lack efficient tracing methods. To this end, we developed a method that combines conventional adeno-associated virus (AAV)-mediated transsynaptic with distal-less homeobox (Dlx) enhancer-restricted expression system label neurons. We called "Dlx Interneuron-SpECific Tracing" (DISECT). applied DISECT corticocortical circuit from secondary motor cortex (M2) primary somatosensory (S1) wild-type mice. First, injected AAV1-Cre into M2, which enabled Cre recombinase M2-input recipient S1 Second, AAV1-hDlx-flex-green fluorescent protein (GFP) transduce GFP neurons Cre-dependent manner. succeeded exclusively labeling S1. Laminar analysis labeled via indicated were distributed superficial deep layers This distribution was aligned density axons projecting M2. further classified types using immunohistochemistry

Language: Английский

Citations

0