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Kurosawa, M.

Publications and source records attributed to Kurosawa, M..

3 recordsLinked to original sources

Structure-Function Coupling Aligns with a Unimodal-to-Transmodal Gradient in the Mouse Cortex

Understanding how anatomical connectivity shapes brain activity is essential for clarifying brain function and disorders. In the human brain, the regional heterogeneity in structure-function (S-F) coupling is well characterized by measuring correlations between structural and functional connectivity. However, it remains unclear whether the same principles apply to the mouse cortex, where biological mechanisms can be studied directly. Here, we mapped S-F coupling across the mouse cortex by combining high-resolution structural connectivity derived from axonal tracing with resting-state functional connectivity measured by wide-field calcium imaging. Our findings revealed that structural connectivity imposes a robust yet regionally variable constraint on functional connectivity. As in humans, the S-F coupling was strong in primary sensorimotor areas and weaker in association areas, demonstrating a gradient from unimodal-to-transmodal cortical organization. This spatial variation covaried with intrinsic cellular properties, including myelination, excitation-inhibition balance, synaptic density, and gene expression profiles, but did not align with the anatomically defined cortical hierarchy. Our findings highlight graded S-F coupling as a common organizational principle in both the mouse and human cortex, providing a framework for future mechanistic studies using mouse models.

neuroscience↗

OVGP1 is an oviductal fluid factor essential particularly for early embryonic development in golden hamsters

The mammalian oviductal lumen is a specialized chamber that provides an environment that strictly regulates fertilization an early embryogenesis, the regulatory mechanisms to gametes/zygote are still largely unknown. In this report, we studied the oviductal regulation of early embryonic development using Ovgp1 (a gene encoding an oviductal humoral factor, OVGP1)-knockout (KO) hamsters. The experimental results revealed the following: 1) Female Ovgp1-KO hamsters fail to produce any litters at all; 2) In the oviducts from KO animal, fertilized eggs are sometimes identified, but their morphology shows abnormal features; 3) The number of implantations in the KO females is evidently low; 4) Even if implantations occur, the embryos develop abnormally and eventually become embryonic lethal; and 5) Ovgp1-KO females transferred to wild-type females produce KO egg-derived litters, but the reverse experiment does not. These results suggest that OVGP1-mediated physiological events are crucial for early embryonic development in vivo. This animal model shows that the fate of the fertilized egg is not only genetically determined, but that the surrounding oviductal microenvironment plays a pivotal role in normal embryonic development. Summary statementDeficiency an oviductal humoral factor (OVGP1) caused female infertility in the golden hamsters. The presence or absence of OVGP1 has significant physiological effects on early embryonic development in vivo.

developmental biology↗

Astrocyte GluN2C NMDA receptors control basal synaptic strengths of hippocampal CA1 pyramidal neurons in the stratum radiatum

Experience-dependent plasticity is a key feature of brain synapses for which neuronal N-Methyl-D-Aspartate receptors (NMDARs) play a major role, from developmental circuit refinement to learning and memory. Astrocytes also express NMDARs although their exact function has remained controversial. Here we identify a circuit function for GluN2C NMDAR, a subtype highly expressed in astrocytes, in layer-specific tuning of synaptic strengths in mouse hippocampal CA1 pyramidal neurons. Interfering with astrocyte NMDAR or GluN2C NMDAR activity reduces the range of presynaptic strength distribution specifically in the stratum radiatum inputs without an appreciable change in the mean presynaptic strength. Mathematical modeling shows that narrowing of the width of presynaptic release probability distribution compromises the expression of long-term synaptic plasticity. Our findings suggest a novel feedback signaling system that uses astrocyte GluN2C NMDARs to adjust basal synaptic weight distribution of Schaffer collateral inputs, which in turn impacts computations performed by the CA1 pyramidal neuron.

neuroscience↗