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NeuroscienceNature Methods
Peer-reviewed journal article

A versatile miniature two-photon microscope enabling multicolor deep-brain imaging

Runlong WuiD, Chunzhu ZhaoiD, Shan QiuiD, Yufei ZhuiD, Lifeng ZhangiD, Qiang FuiD, Yanhui HuiD, Dakun WuiD, Fei YuiD, Fangxu ZhouiD, Haipeng HuangiD, Yunfeng ZhangiD, Xianhua WangiD, Aimin WangiD, Heping ChengiD

Abstract

Here we present the FHIRM-TPM 3.0, a 2.6 g miniature two-photon microscope capable of multicolor deep-brain imaging in freely behaving mice. The system was integrated with a broadband anti-resonant hollow-core fiber featuring low transmission loss, minimal dispersion from 700-1060 nm, and high tolerance of laser power. By correcting chromatic and spherical aberrations and optimizing the fluorescence collection aperture, we achieved cortical neuronal imaging at depths exceeding 820 m and, using a GRIN lens, hippocampal Ca2+ imaging at single dendritic spine resolution. Moreover, we engineered three interchangeable parfocal objectives, allowing for a tenfold scalable field-of-view up to 1x0.8 mm{superscript 2}, with lateral resolutions ranging from 0.68 to 1.46 m. By multicolor imaging at excitation wavelengths of 780 nm, 920 nm and 1030 nm, we investigated mitochondrial and cytosolic Ca2+ activities relative to the deposition of amyloid plaques in the cortex of awake APP/PS1 transgenic mice. Thus, the FHIRM-TPM 3.0 provides a versatile imaging system suitable for diverse brain imaging scenarios.

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02 /Specification & Classification

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