Methods for measuring the capacity of cortical Layer-4 representation

Author(s):  
M. Erdem Isenkul ◽  
Olcay Kursun ◽  
Oleg V. Favorov
Keyword(s):  
Development ◽  
2000 ◽  
Vol 127 (13) ◽  
pp. 2863-2872 ◽  
Author(s):  
A.R. Desai ◽  
S.K. McConnell

During early stages of cerebral cortical development, progenitor cells in the ventricular zone are multipotent, producing neurons of many layers over successive cell divisions. The laminar fate of their progeny depends on environmental cues to which the cells respond prior to mitosis. By the end of neurogenesis, however, progenitors are lineally committed to producing upper-layer neurons. Here we assess the laminar fate potential of progenitors at a middle stage of cortical development. The progenitors of layer 4 neurons were first transplanted into older brains in which layer 2/3 was being generated. The transplanted neurons adopted a laminar fate appropriate for the new environment (layer 2/3), revealing that layer 4 progenitors are multipotent. Mid-stage progenitors were then transplanted into a younger environment, in which layer 6 neurons were being generated. The transplanted neurons bypassed layer 6, revealing that layer 4 progenitors have a restricted fate potential and are incompetent to respond to environmental cues that trigger layer 6 production. Instead, the transplanted cells migrated to layer 4, the position typical of their origin, and also to layer 5, a position appropriate for neither the host nor the donor environment. Because layer 5 neurogenesis is complete by the stage that progenitors were removed for transplantation, restrictions in laminar fate potential must lag behind the final production of a cortical layer. These results suggest that a combination of intrinsic and environmental cues controls the competence of cortical progenitor cells to produce neurons of different layers.


2019 ◽  
Author(s):  
Hongyoon Choi ◽  
Yoori Choi ◽  
Do Won Hwang ◽  
Dong Soo Lee

ABSTRACTThere is a growing evidence that a subset of microglia, disease-associated microglia (DAM), is crucially involved in the onset and progression of Alzheimer Disease (AD). However, it has been challenging to comprehensively know how DAM affects neuronal loss and reconstitute the complicated cellular composition. Here, we describe the relationship between neuronal reconfiguration and microglia by digitally dissecting the human brain transcriptome. We observed DAM enrichment associated with neuronal loss and the degree of amyloid deposits, which was commonly found in different brain regions. The neuronal subtype analyses showed that DAM enrichment was correlated with the proportion of two excitatory neurons located in the cortical layer 4. The direction of these relations was opposite, which implied excitatory neuronal reconfiguration in the specific cortical layer. Our results suggested immune reaction represented by DAM might mediate the reconfiguration of cellular components in AD, which may eventually have implications for diagnostics and therapeutics.One sentence summaryThe enrichment of disease-associated microglia signature is associated with the reconfiguration of neuronal subtypes, particularly excitatory neurons in the cortical layer 4.


2021 ◽  
Author(s):  
Haruka Sato ◽  
Jun Hatakeyama ◽  
Takuji Iwasato ◽  
Kimi Araki ◽  
Nobuhiko Yamamoto ◽  
...  

AbstractNeuronal abundance and thickness of each cortical layer is specific to each area, but how this fundamental feature arises during development remains poorly understood. While some of area-specific features are controlled by intrinsic cues such as morphogens and transcription factors, the exact influence and mechanisms of action by extrinsic cues, in particular the thalamic axons, have not been fully established. Here we identify a thalamus-derived factor, VGF, which is indispensable for thalamocortical axons to maintain the proper amount of layer 4 neurons in the mouse sensory cortices. This process is prerequisite for further maturation of the primary somatosensory area, such as barrel field formation instructed by a neuronal activity-dependent mechanism. Our results also provide an insight into regionalization of brain in that highly site-specific axon projection anterogradely confers further regional complexity upon the target field through locally secreting signaling molecules from axon terminals.


2018 ◽  
Author(s):  
Philip O’Herron ◽  
John Woodward ◽  
Prakash Kara

AbstractWith the advent of two-photon imaging as a tool for systems neuroscience, the mouse has become a preeminent model system for studying sensory processing. One notable difference that has been found however, between mice and traditional model species like cats and primates is the responsiveness of the cortex. In the primary visual cortex of cats and primates, nearly all neurons respond to simple visual stimuli like drifting gratings. In contrast, imaging studies in mice consistently find that only around half of the neurons respond to such stimuli. Here we show that visual responsiveness is strongly dependent on the cortical depth of neurons. Moving from superficial layer 2 down to layer 4, the percentage of responsive neurons increases dramatically, ultimately reaching levels similar to what is seen in other species. Over this span of cortical depth, neuronal response amplitude also increases and orientation selectivity moderately decreases. These depth dependent response properties may be explained by the distribution of thalamic inputs in mouse V1. Unlike in cats and primates where thalamic projections to the granular layer are constrained to layer 4, in mice they spread up into layer 2/3, qualitatively matching the distribution of response properties we see. These results show that the analysis of neural response properties must take into consideration not only the overall cortical lamina boundaries but also the depth of recorded neurons within each cortical layer. Furthermore, the inability to drive the majority of neurons in superficial layer 2/3 of mouse V1 with grating stimuli indicates that there may be fundamental differences in the role of V1 between rodents and other mammals.


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