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Updated: Jan 7, 2026

Optical Coherence Tomography: Imaging Mouse Retinal Ganglion Cells In Vivo
Published on: September 22, 2017
Precise biometric measurement of the mouse eye using optical coherence tomography based on optic-nerve-head imaging
Sisi Chen1, Peifeng Zhang1, Haiyao Wang1
1Eye Hospital and School of Ophthalmology and Optometry, Wenzhou Medical University, Oujiang Laboratory (Zhejiang Lab for Regenerative Medicine, Vision and Brain Health), Wenzhou, Zhejiang, 325000, China; National Engineering Research Center of Ophthalmology and Optometry, Eye Hospital, Wenzhou Medical University, Wenzhou, 325027, China.
None:
Due to the availability of various mouse strains with well-defined genomes, mice have become pivotal models for ocular developmental research. Accurate and highly repeatable biometric measurements are crucial for investigating myopia in experimental animals. This study aimed to develop a precise methodology for comprehensive assessment of ocular biometrics in mice. We developed the custom-built spectral domain optical coherence tomography (SD-OCT) system with an axial resolution of 4.3 μm, and an imaging depth of 4.1 mm in tissue. Three-dimensional biometric parameters exhibited superior precision (standard deviation = 5-6 μm, intraclass correlation coefficients (ICC) ≥ 0.78) compared to each two-dimensional parameter (standard deviation = 6-10 μm, ICC ≥0.62). Excellent repeatability was observed in the measurement of anterior chamber depth, vitreous chamber depth, retinal thickness, and axial thickness in mouse eyes, with ICC≥ 0.79 for optic nerve head (ONH) localization results, surpassing the classical non-ONH method (ICC ≥0.62, except for retinal thickness where ICC is 0.33). Notably, ICC and within-subject standard deviation of AL were 0.978 and 5.14 μm, respectively, in ONH localization results, while these values were 0.873 and 11.69 μm, respectively, in classical non-ONH results. Based on the custom-built SD-OCT, this study proposes a precise in vivo ocular biometric measurement method for mouse using the combination of a radial 3D scan mode and novel ONH localization imaging, which provides a useful method for the study of ocular physiology and pathological growth.

