The hippocampus at 50 micrometres
A human hippocampus scanned at fifty micrometres, the finest diffusion MRI of a human brain reported so far. In September 2026 a team at Zhejiang University put a five millimetre coronal block from the middle of a right hippocampus, from a woman of fifty with no brain disease, into a 14.1 tesla magnet for 78 hours and imaged it at 50 by 50 by 100 micrometres, close enough to the size of cells that the scan started to agree with the stains a pathologist would use. Then they did the same for a man of 91 with Alzheimer's. Below: what that voxel is against the real structure, the layers it could tell apart, and the three pathways of the memory circuit it traced without cutting anything. Drag to turn the hippocampus, scroll to zoom out along the fornix.
The two hippocampi are the population shape from the Melbourne Subcortex Atlas, so the lengths and voxel counts are real. The cables are the two bundles of a whole-brain tract atlas that end in the hippocampus, drawn in the same millimetres. The block through the middle marks where the specimen came from only roughly: the paper says mid-hippocampal, and no more than that is drawn.
The circuit it traced
Water in tissue moves more easily along fibres than across them, and diffusion MRI measures that. At 50 µm the paper's tractography followed the three legs of the hippocampal trisynaptic circuit in three dimensions: the perforant path, the mossy fibres and the Schaffer collaterals. The drawing here is a textbook section, not their data; press a leg to run a signal along it.
Inside the tissue
The scan itself has not been released, but the paper is open, so the panels the authors made from it can be walked here. Pick a layer, a pathway, a resolution or a comparison and the viewer flies to the authors' own panel for it, with what they say it shows. Drag to pan, scroll or pinch to zoom, double tap for the whole figure. Everything in this box is specimen data: one control block, one Alzheimer's block.
What the scan saw
Six laminae. Alveus, pyramidal cell layer, stratum radiatum, stratum lacunosum-moleculare, molecular layer and granule cell layer, segmented by hand on the scan, with the hilus inside. The molecular layer split into inner and outer, a distinction made by which fibres arrive there rather than by any visible edge.
Fibres that match the stains. Diffusion maps and tractography lined up with immunohistology for axons and dendrites, at a scale the paper describes as approaching cellular dimensions.
What 100 µm loses. Downsampling the same scan to 100 µm blurred the boundary between stratum radiatum and lacunosum-moleculare, attenuated the granule cell layer, and preferentially lost streamlines shorter than 10 mm. At 400 µm only grey and white matter contrast was left.
Less contrast between layers. The laminar pattern that is crisp in the control block was reduced in the Alzheimer's block, and the CA1 pyramidal cell layer was thinner.
Local breaks. Discontinuities in stratum radiatum and lacunosum-moleculare, and granule cell dendrites in the molecular layer that had lost their regular radial order.
Matched by pathology. The same regions showed changes on pathological staining, which is what gives a nondestructive scan its claim to be virtual histology.
Not shown, and why. One control block and one Alzheimer's block is a feasibility study, not a cohort, so nothing here draws an Alzheimer's hippocampus against a healthy one. The paper carries no data availability statement and the scan has not been released, so the layers and fibres above are a hand drawn section, badged as such, and the voxel comparisons use the atlas shape and the paper's one layer thickness. When the data are public this page will draw them.
By the numbers
| Quantity | Value | Source |
|---|---|---|
| Voxel, this paper | 50 × 50 × 100 µm | Shen et al. 2026, abstract |
| Field strength | 14.1 T | Shen et al. 2026 |
| Scan time per block | 78 hours | Shen et al. 2026, methods: b = 3000 s/mm², 20 directions, 16 averages |
| Block | 16 × 19 × 5 mm field of view | Shen et al. 2026, methods: middle of the right hippocampus |
| Specimens | 2 | A woman of 50 without brain disease; a man of 91 with Alzheimer's |
| Downsampled comparisons | 100, 200, 400 µm | Shen et al. 2026, figure 2 |
| Granule cell layer thickness | about 0.2 mm | Shen et al. 2026, results; locally as thin as 60 µm (Amaral et al. 2007) |
| Hippocampus length, front to back | … | Melbourne Subcortex Atlas mesh, measured on this page |
| 50 µm voxels along that length | … | Computed from the row above |
| Clinical voxel, for comparison | 1 mm | A typical 3 T structural scan |
Read the paper
Shen Y, Yu Z, Zhu Q, Zhao Z, Wang P, Yin Y, Jiang P, Wang C, Kong X, Zhang J, Wu D. Diffusion MR Microscopy of the Human Hippocampus at 50 μm Resolution at 14.1 T for 3D Virtual Histology. bioRxiv, posted 9 September 2026, not yet peer reviewed, CC BY 4.0. doi:10.64898/2026.09.04.749425. Zhejiang University, the National Human Brain Bank for Health and Disease, and collaborators in Hangzhou, Shanghai and Ningbo.
Zhao Z, Zhang L, Luo W, et al. Layer-specific microstructural patterns of anterior hippocampus in Alzheimer's disease with ex vivo diffusion MRI at 14.1 T. Human Brain Mapping 2022. doi:10.1002/hbm.26062. The same group's earlier work at 100 µm, the baseline this paper improves on.
Yeh FC. Population-based tract-to-region connectome of the human brain. Nature Communications 2022. doi:10.1038/s41467-022-32595-4. The fornix and parahippocampal cingulum, from the HCP1065 tract atlas, CC BY-SA 4.0, the same data as the white matter page.
Tian Y, Margulies DS, Breakspear M, Zalesky A. Topographic organization of the human subcortex unveiled with functional connectivity gradients. Nature Neuroscience 2020. doi:10.1038/s41593-020-00711-6. The hippocampus meshes, from the Melbourne Subcortex Atlas.
The figures in the tissue viewer are reproduced from the preprint under its CC BY 4.0 licence, unaltered apart from encoding; the boxes and captions are this site's.
Diffusion MRI cannot tell which way a signal travels along a fibre. The direction of the animated signal above follows the textbook, not the scan.