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Related Concept Videos

Vision01:24

Vision

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Vision is the result of light being detected and transduced into neural signals by the retina of the eye. This information is then further analyzed and interpreted by the brain. First, light enters the front of the eye and is focused by the cornea and lens onto the retina—a thin sheet of neural tissue lining the back of the eye. Because of refraction through the convex lens of the eye, images are projected onto the retina upside-down and reversed.
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The eye is a spherical, hollow structure composed of three tissue layers. The outer layer — the fibrous tunic, comprises the sclera — a white structure — and the cornea, which is transparent. The sclera encompasses some of the ocular surface, most of which is not visible. However, the 'white of the eye' is distinctively visible in humans compared to other species. The cornea, a clear covering at the front of the eye, enables light penetration. The eye's middle...
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Visual System01:26

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Light enters the eye through the cornea, a transparent, dome-shaped surface covering the surface of the eyeball that helps to direct and focus incoming light. This light is then channeled toward the pupil, an adjustable opening whose size is controlled by the iris. The iris, a pigmented muscle, regulates the amount of light entering the eye by contracting or dilating the pupil, thereby ensuring optimal light levels for clear vision.
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Spatial profiling of the interplay between cell type- and vision-dependent transcriptomic programs in the visual

Fangming Xie1, Saumya Jain1,2, Runzhe Xu1

  • 1Department of Biological Chemistry, David Geffen School of Medicine, University of California, Los Angeles, CA 90095.

Proceedings of the National Academy of Sciences of the United States of America
|February 13, 2025
PubMed
Summary
This summary is machine-generated.

Early visual experience shapes how neurons organize in the mammalian brain. Visual deprivation alters gene expression in layer 2/3 (L2/3) cells, impacting their identity and spatial distribution in the visual cortex.

Keywords:
cortexgradientsspatial transcriptomicstranscriptomicsvision

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Area of Science:

  • Neuroscience
  • Developmental Biology
  • Genomics

Background:

  • The impact of early sensory experience on neocortical organization at the cellular level remains unclear.
  • Previous work showed that functional and molecular profiles of layer 2/3 (L2/3) cells in the primary visual cortex (V1) depend on visual input.
  • Understanding critical period plasticity is crucial for comprehending brain development.

Purpose of the Study:

  • To investigate the spatial organization of L2/3 cell types in V1 in relation to visual experience.
  • To elucidate the molecular mechanisms by which visual deprivation affects L2/3 cell types.
  • To map the influence of vision on cortical cell-type distribution during development.

Main Methods:

  • Spatial transcriptomic profiling of V1 L2/3 cells using approximately 500 genes.
  • Comparison of gene expression and spatial organization between normally reared and dark-reared mice.
  • Integration of spatial transcriptomics with single-nucleus RNA sequencing data.

Main Results:

  • Spatial transcriptomics revealed the zonation of L2/3 cell types along the pial-ventricular axis in V1.
  • Visual deprivation induced two distinct transcriptomic changes: a cell state shift (orthogonal to cell identity) and a shift in cell-type identity within the L2/3 manifold.
  • The first gene program involved immediate-early genes and metabolic genes, while the second affected cell-type-specific genes.

Conclusions:

  • Visual experience is a key factor in patterning L2/3 cell types and their spatial organization in the V1 during critical developmental periods.
  • Multitasking theory provides a framework for understanding the continuous gene expression profiles and zonation of L2/3 cell types.
  • The study reveals distinct molecular mechanisms through which visual input shapes cortical circuitry at a cellular resolution.