Biochemical Pharmacology, Journal Year: 2025, Volume and Issue: unknown, P. 116964 - 116964
Published: May 1, 2025
Language: Английский
Biochemical Pharmacology, Journal Year: 2025, Volume and Issue: unknown, P. 116964 - 116964
Published: May 1, 2025
Language: Английский
Cell, Journal Year: 2023, Volume and Issue: 186(24), P. 5411 - 5427.e23
Published: Nov. 1, 2023
Neurons build synaptic contacts using different protein combinations that define the specificity, function, and plasticity potential of synapses; however, diversity proteomes remains largely unexplored. We prepared synaptosomes from 7 transgenic mouse lines with fluorescently labeled presynaptic terminals. Combining microdissection 5 brain regions fluorescent-activated synaptosome sorting (FASS), we isolated analyzed 18 synapse types. discovered ∼1,800 unique synapse-type-enriched proteins allocated thousands to types synapses (https://syndive.org/). identify shared modules highlight proteomic hotspots for specialization. reveal common features striatal dopaminergic proteome discover signatures relate functional properties interneuron classes. This study provides a molecular systems-biology analysis framework integrate information subtypes interest cellular or circuit-level experiments.
Language: Английский
Citations
58Neuron, Journal Year: 2024, Volume and Issue: 112(12), P. 2015 - 2030.e5
Published: April 9, 2024
Synchronous neuronal activity is a hallmark of the developing brain. In mouse cerebral cortex, decorrelates during second week postnatal development, progressively acquiring characteristic sparse pattern underlying integration sensory information. The maturation inhibition seems critical for this process, but interneurons involved in crucial transition network cortex remain unknown. Using vivo longitudinal two-photon calcium imaging period that precedes change from highly synchronous to decorrelated activity, we identify somatostatin-expressing (SST+) as modulators switch mice. Modulation SST+ cells accelerates or delays decorrelation cortical process involves regulating parvalbumin-expressing (PV+) interneurons. critically link inputs with local circuits, controlling neural dynamics while modulating other into nascent circuits.
Language: Английский
Citations
20Nature, Journal Year: 2024, Volume and Issue: 629(8011), P. 402 - 409
Published: April 17, 2024
Abstract Throughout life, neuronal networks in the mammalian neocortex maintain a balance of excitation and inhibition, which is essential for computation 1,2 . Deviations from balanced state have been linked to neurodevelopmental disorders, severe disruptions result epilepsy 3–5 To balance, microcircuits composed excitatory inhibitory neurons sense alterations neural activity adjust connectivity function. Here we identify signalling pathway adult mouse that activated response increased network activity. Overactivation signalled through an increase levels BMP2, growth factor well known its role as morphogen embryonic development. BMP2 acts on parvalbumin-expressing (PV) interneurons transcription SMAD1, controls array glutamatergic synapse proteins components perineuronal nets. PV-interneuron-specific disruption BMP2–SMAD1 accompanied by loss innervation PV cells, underdeveloped nets decreased excitability. Ultimately, this impairment functional recruitment disrupts cortical excitation–inhibition with mice exhibiting spontaneous epileptic seizures. Our findings suggest developmental repurposed stabilize brain.
Language: Английский
Citations
19Proceedings of the National Academy of Sciences, Journal Year: 2024, Volume and Issue: 121(17)
Published: April 16, 2024
A key feature of excitatory synapses is the existence subsynaptic protein nanoclusters (NCs) whose precise alignment across cleft in a transsynaptic nanocolumn influences strength synaptic transmission. However, whether properties vary between functioning different cellular contexts unknown. We used combination confocal and DNA-PAINT super-resolution microscopy to directly compare organization shared scaffold proteins at two important synapses—those forming onto principal neurons (Ex→Ex synapses) those parvalbumin-expressing interneurons (Ex→PV synapses). As Ex→Ex synapses, we find that Ex→PV presynaptic Munc13-1 postsynaptic PSD-95 both form NCs demonstrate alignment, underscoring nanostructure as conserved organizational principles synapses. Despite general conservation these features, observed specific differences characteristics pre- nanostructure. contained larger PSDs with fewer when accounting for size than Furthermore, were denser. The identity cell was also represented organization, hosted puncta less dense but more numerous NCs. Moreover, measured spatial variability synapse types, revealing over distinct range distances compared conclude while are shared, cell-specific elements nanodomain likely contribute functional diversity
Language: Английский
Citations
13European Neuropsychopharmacology, Journal Year: 2024, Volume and Issue: 82, P. 44 - 52
Published: March 14, 2024
Parvalbumin-expressing (PV+) interneurons represent one of the most abundant subclasses cortical interneurons. Owing to their specific electrophysiological and synaptic properties, PV+ are essential for gating pacing activity excitatory neurons. In particular, critically involved in generating maintaining rhythms gamma frequency, which complex cognitive functions. Deficits have been frequently reported postmortem studies schizophrenia patients, alterations oscillations a prominent feature disease. Here, I summarise main features review clinical preclinical linking developmental dysfunction with pathophysiology schizophrenia.
Language: Английский
Citations
12Proceedings of the National Academy of Sciences, Journal Year: 2024, Volume and Issue: 121(25)
Published: June 13, 2024
Cortical networks exhibit complex stimulus–response patterns that are based on specific recurrent interactions between neurons. For example, the balance excitatory and inhibitory currents has been identified as a central component of cortical computations. However, it remains unclear how required synaptic connectivity can emerge in developing circuits where synapses neurons simultaneously plastic. Using theory modeling, we propose wide range response properties arise from single plasticity paradigm acts at all connections—Hebbian learning is stabilized by synapse-type-specific competition for limited supply resources. In plastic circuits, this enables formation decorrelation inhibition-balanced receptive fields. Networks develop an assembly structure with stronger connections similarly tuned normalization orientation-specific center-surround suppression, reflecting stimulus statistics during training. These results demonstrate self-organize into functional suggest essential role competitive development circuits.
Language: Английский
Citations
9Cell Reports, Journal Year: 2025, Volume and Issue: 44(5), P. 115628 - 115628
Published: April 30, 2025
Language: Английский
Citations
1Frontiers in Neurology, Journal Year: 2023, Volume and Issue: 14
Published: Sept. 7, 2023
Individuals with autism spectrum disorder (ASD) exhibit a diverse range of behavioral features and genetic backgrounds, but whether different forms involve convergent pathophysiology brain function is unknown. Here, we analyze evidence for deficits in neural circuit across multiple transgenic mouse models ASD. We focus on sensory areas neocortex, where differences may underlie atypical processing, central feature autism. Many distinct circuit-level theories ASD have been proposed, including increased excitation–inhibition (E–I) ratio hyperexcitability, hypofunction parvalbumin (PV) interneuron circuits, impaired homeostatic plasticity, degraded coding, others. review these assess the degree convergence each. Behaviorally, our analysis reveals that innate detection behavior heightened discrimination many models. Neurophysiologically, PV E–I are prevalent only rarely generate hyperexcitability excess spiking. Instead, tuning other aspects coding commonly explain behavior. Two phenotypic clusters opposing signatures evident Such clustering could suggest physiological subtypes autism, which facilitate development tailored therapeutic approaches.
Language: Английский
Citations
14Current Opinion in Neurobiology, Journal Year: 2024, Volume and Issue: 84, P. 102840 - 102840
Published: Jan. 29, 2024
Astrocytes interact with various cell types, including neurons, vascular cells, microglia, and peripheral immune cells. These interactions are crucial for regulating normal brain functions as well modulating neuroinflammation in pathological conditions. Recent transcriptomic proteomic studies have identified critical molecules involved astrocytic crosstalk other shedding light on their roles maintaining homeostasis both healthy diseased perform these through either direct or indirect physical associations neuronal synapses vasculature. Furthermore, astrocytes can communicate such T natural killer secreted during neuroinflammation. In this review, we discuss the molecular basis of underlying mechanisms astrocyte communication We propose that function a central hub inter-connecting vasculatures, cells brains.
Language: Английский
Citations
5Cold Spring Harbor Perspectives in Biology, Journal Year: 2024, Volume and Issue: 16(5), P. a041501 - a041501
Published: Feb. 5, 2024
Ben Verpoort1,2 and Joris de Wit1,2 1VIB-KU Leuven Center for Brain Disease Research, 3000 Leuven, Belgium 2KU Department of Neurosciences, Institute, Correspondence: joris.dewit{at}kuleuven.be
Language: Английский
Citations
4