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Near-isotropic, reconstructed volume electron microscopy (FIB-SEM) of mouse liver (jrc_mus-liver-2)

Version 2 2024-09-17, 20:32
Version 1 2023-07-28, 19:32
dataset
posted on 2024-09-17, 20:32 authored by CellMap Project TeamCellMap Project Team, Zhiyuan Lu, Stephan PreibischStephan Preibisch, Wei Qiu, Eric T. Trautman, Nirmala Iyer, Shu-Hsien Shu

Sample: Wild-type, 8 week old mouse, strain: C57BL/6 from Jackson Lab

Sample Description: This dataset features isotropic 3D electron microscopy data of the mouse liver (jrc_mus-liver-2). The sample was obtained from an 8-week-old wild-type C57BL/6 mouse strain, sourced from Jackson Laboratory. Euthanasia was performed in accordance with IACUC guidelines, with perfusion conducted by Shu-Hsien Shu.

The sample preparation involved cutting 1.5 mm punches from 100 µm-thick vibratome slices. High-pressure freezing (HPF) was performed using the Wohlwend HPF. Freeze substitution (FS) was carried out with 0.5% OsO₄, 0.1% uranyl acetate, and 20 mM 1,2,4 triazole in acetone, followed by acetone rinses. The sample was infiltrated with increasing concentrations of Durcupan in acetone, followed by three exchanges with 100% Durcupan. The embedding was completed in 100% Durcupan and cured at 60°C for 48 hours.

Shu-Hsien Shu was responsible for the perfusion, while Nirmala Iyer (HHMI/Janelia) handled HPF, freeze substitution, and resin embedding. Zhiyuan Lu (HHMI/Janelia) trimmed the sample for FIBSEM, and Wei Qiu (HHMI/Janelia) performed the imaging. Post-processing was completed by Eric Trautman and Stephan Preibisch (HHMI/Janelia).

This dataset provides a detailed view of the cellular architecture of a young mouse liver, contributing valuable data for research in hepatology and related areas.

Protocol: Mouse euthanasia was performed as IACUC guidelines. Perfusion by Shu-Hsien.1.5 mm punches were cut out of 100µm thick vibratome slices and HPF using the Wohlwend HPF. FS using 0.5% OsO4, 0.1% UA,20mM 1,2,4 triazole in acetone. Acetone rinses followed by infiltration with increasing concentrations of Durcupan in Acetone and 3 exchanges of 100% Durcupan. Embedding in 100% Durcupan and curing at 60 degrees for 48 hours.

Contributions: Sample preparation by Shu-Hsien Shu (perfusion) and Nirmala Iyer (HHMI/ Janelia) - HPF FS and resin embedding. Trimmed for FIBSEM by Zhiyuan Lu (HHMI/Janelia), and imaged by Wei Qiu (HHMI/Janelia) and post-processing by Eric Trautman and Stephan Preibisch (HHMI/Janelia).

Acquisition ID: jrc_mus-liver-2

Voxel size (nm): 8.0 x 8.0 x 8.0 (X, Y, Z)

Data dimensions (µm): 82.208, 92.088, 101.704 (X, Y, Z)

Imaging start date: 2022-10-20

Dataset URL (Redirect): https://data.janelia.org/zX4wO

Visualization Website: https://openorganelle.janelia.org/datasets/jrc_mus-liver-2

Imaging duration (days): 9

Scanning speed (MHz): 3.000

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