Border Cell Arrangement

Border cell arrangement is the spatial organization of a specialized group of cells at a tissue boundary during development, where coordinated positioning supports tissue formation and remodeling. In developmental biology, arrangement depends on cell-cell adhesion, polarity, and signaling that regulate how cells maintain contact, orient relative to neighboring tissues, and, in some systems, move collectively toward a target. Studying these patterns helps researchers connect cellular organization with morphogenesis, including the formation of organs and epithelial structures. Border cell arrangement also provides a framework for investigating how disrupted adhesion or signaling can alter developmental outcomes.

Border Cell Arrangement - Related Videos

Education

JoVE Core - Anatomy and Physiology

Fascicle Arrangement in Skeletal Muscles

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2025

Fascicles are bundles of muscle fibers in a skeletal muscle. Muscle fascicle arrangement is directly associated with the power and range of motion of various muscles. The configuration of these fascicles can vary, leading to different functional outcomes. The four primary types of muscle based on fascicle arrangement are: Parallel Muscles: In this type, fascicles run parallel to the long axis of the muscle. Examples include the biceps brachii and the rectus abdominis. When parallel muscles...

Research

JoVE Journal - Developmental Biology

Spatially Compact Arrangement of Larval Zebrafish Sections for Spatial Transcriptomic Analysis

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2025

Here, we present a method for aligning and cryosectioning multiple Zebrafish (Danio rerio) larvae samples and collecting them on a single slide for spatial transcriptomic analysis.

Research

JoVE Journal - Neuroscience
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Combined Optogenetic and Freeze-fracture Replica Immunolabeling to Examine Input-specific Arrangement of Glutamate Receptors in the Mouse Amygdala

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Cited by 6 •

2016

This article illustrates how the expression of neurotransmitter receptors can be quantified and the pattern analyzed at synapses with identified pre and postsynaptic elements using a combination of viral transduction of optogenetic tools and the freeze-fracture replica immunolabeling technique.

Research

JoVE Journal - Biology
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In utero and ex vivo Electroporation for Gene Expression in Mouse Retinal Ganglion Cells

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Cited by 30 •

2009

Here we present two techniques for manipulating gene expression in murine retinal ganglion cells (RGCs) by in utero and ex vivo electroporation. These techniques enable one to examine how alterations in gene expression affect RGC development, axon guidance, and functional properties.

Analyzing Murine Schwann Cell Development Along Growing Axons

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Cited by 1 •

2012

Here we describe a Schwann cell (SC) migration assay in which SCs are able to develop along extending axons.

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