Grin Lens Imaging

GRIN lens imaging is an optical method that uses a gradient-index (GRIN) lens to capture images from regions that conventional microscopy cannot readily reach, making it valuable for investigating deep biological tissue. The lens contains a precisely varying refractive index that bends light through the rod and relays an image from its distal surface to an external camera or microscope, often through a compact endoscope. In neuroscience, implanted GRIN lenses enable fluorescence imaging of neuronal structure and activity in deep brain areas, including calcium signals, during behavior. This approach supports longitudinal studies of neural circuits while preserving access to freely moving animals.

Grin Lens Imaging - Related Videos

Research

JoVE EoE - Danio rerio (zebrafish)

Eye Lens Dissection: A Technique to Observe Zebrafish Lens Morphology

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2023

This video describes the protocol which is developed to dissect adult and larval zebrafish lenses to analyze cortical lens morphology and structural integrity of the lens sutures.

Real-Time Microendoscopic Calcium Imaging in a Freely Moving Mouse

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2025

Source: Lee, H. et. al., Successful In vivo Calcium Imaging with a Head-Mount Miniaturized Microscope in the Amygdala of Freely Behaving Mouse. J. Vis. Exp. (2020)This video demonstrates in vivo calcium imaging in a mouse using a gradient refractive index, or GRIN lens, and a miniaturized microscope. The setup combines head fixation within a frictionless mobile cage system, stimulating neurons and triggering calcium ion influx. The GRIN lens captures calcium signaling in the brain, enabling...

Simulating the Mechanics of Lens Accommodation via a Manual Lens Stretcher

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Cited by 9 •

2018

We present an efficient method of studying lens accommodation by using a manual lens stretcher. The protocol mimics physiological accommodation by pulling the zonules connected around the lens capsule, thereby, stretching the lens.

Field-Deployable Lens-Free Imaging Platform for Rapid Label-Free Analysis of Natural Killer Cell Activation

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Cited by 1 •

2025

This protocol describes a label-free method for the rapid single-cell analysis of natural killer (NK) cell count and activity using lens-free shadow imaging technology. This method quantifies morphological changes in individual NK cells by computerized analysis of their diffraction patterns.

Research

JoVE Journal - Bioengineering
Free Sample

High-resolution Fiber-optic Microendoscopy for in situ Cellular Imaging

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Cited by 84 •

2011

In many biological and clinical situations it is advantageous to study cellular processes as they evolve in their native microenvironment. Here we describe the assembly and use of a low-cost fiber-optic microscope which can provide real time imaging in cell culture, animal studies, and clinical patient studies.

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