3D Ultrastructural segmentation of human microvasculature reveals new insights in pericyte-endothelial cell interactions.
The 1 match
- [1] § Methods › Using the 3D-Unet for semantic segmentation ↔ DeepLearningTrainingMatlab/main_train3dUnet_7class.m, lines 58–69 · score 0.81 · max epochs, mini batch, validation frequency, trained, Unet
Paper
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The authors' code
MATLAB · 74 lines · 2.7 KB · no license · 1 match
- % get directory name where the training data is found
- imageDir = fullfile('C:\Users\TEV4\DLtraining\','VesTS_3Dmulticlass');
- %% Create data stores for Training data
- % create an image datastore
- volReader = @(x) matRead(x);
- volLoc = fullfile(imageDir,'imagesTr');
- volds = imageDatastore(volLoc, ...
- 'FileExtensions','.mat','ReadFcn',volReader);
- % create a pixelLabel datastore for Training data
- lblLoc = fullfile(imageDir,'labelsTr');
- classNames = ["background","BM","Lumen","Nuclei","Mito","ER","Unknown"];
- pixelLabelID = [0 1 2 3 4 5 6];
- pxds = pixelLabelDatastore(lblLoc,classNames,pixelLabelID, ...
- 'FileExtensions','.mat','ReadFcn',volReader);
- % create random patch datastore for Training data
- patchSize = [164 164 100];
- patchPerImage = 60;
- miniBatchSize = 12;
- patchds = randomPatchExtractionDatastore(volds,pxds,patchSize, ...
- 'PatchesPerImage',patchPerImage);
- patchds.MiniBatchSize = miniBatchSize;
- %% Create datastores for Validation data
- % repeat creating datastores for the validation data
- volLocVal = fullfile(imageDir,'imagesVal');
- voldsVal = imageDatastore(volLocVal, ...
- 'FileExtensions','.mat','ReadFcn',volReader);
- lblLocVal = fullfile(imageDir,'labelsVal');
- pxdsVal = pixelLabelDatastore(lblLocVal,classNames,pixelLabelID, ...
- 'FileExtensions','.mat','ReadFcn',volReader);
- dsVal = randomPatchExtractionDatastore(voldsVal,pxdsVal,patchSize, ...
- 'PatchesPerImage',patchPerImage);
- dsVal.MiniBatchSize = miniBatchSize;
- %% Create Unet Layers
- numChannels = 1;
- inputPatchSize = [patchSize numChannels];
- numClasses = 7;
- [lgraph,outPatchSize] = unet3dLayers(inputPatchSize,numClasses,'ConvolutionPadding','valid');
- %% data augmentation
- dataSource = 'Training';
- dsTrain = transform(patchds,@(patchIn)augmentAndCrop3dPatch(patchIn,outPatchSize,dataSource));
- dataSource = 'Validation';
- dsVal = transform(dsVal,@(patchIn)augmentAndCrop3dPatch(patchIn,outPatchSize,dataSource));
- inputLayer = image3dInputLayer(inputPatchSize,'Normalization','none','Name','ImageInputLayer');
- lgraph = replaceLayer(lgraph,'ImageInputLayer',inputLayer);
- %% training options
- options = trainingOptions('adam', ...
- 'MaxEpochs',200, ...
- 'InitialLearnRate',5e-4, ...
- 'LearnRateSchedule','piecewise', ...
- 'LearnRateDropPeriod',5, ...
- 'LearnRateDropFactor',0.95, ...
- 'ValidationData',dsVal, ...
- 'ValidationFrequency',400, ...
- 'Plots','training-progress', ...
- 'Verbose',false, ...
- 'MiniBatchSize',miniBatchSize);
- %% train network
- modelDateTime = string(datetime('now','Format',"yyyy-MM-dd-HH-mm-ss"));
- [net,info] = trainNetwork(dsTrain,lgraph,options);
- save(strcat("trained3DUNet-",modelDateTime,"-Epoch-",num2str(options.MaxEpochs),".mat"),'net');
main_train3dUnet_7class.m at commit f873001, no license · at the source
Overview
Abstract
Introduction: Capillary structure remains incompletely characterized at the nanoscale level. Advances in 3D electron microscopy datasets provide new opportunities to systematically examine microvascular architecture and cellular interactions.
Methods: We performed 3D image segmentation of human cerebral cortex microvasculature using the publicly available H01 Release dataset. This initial analysis focused on descriptive and quantitative characterization of the basement membrane, peg-and-socket cell interactions, and other subcellular features.
Results: We identified several novel structural features. In addition to known bidirectional peg-and-socket connections between pericytes (PCs) and endothelial cells (ECs), we observed similar structures between neighboring ECs and at interfaces where ECs form junctions with themselves. PC pegs showed an unexpected preference for proximity to EC nuclei and were enriched at PC edges. The PC endoplasmic reticulum (ER) frequently contacted the plasma membrane on the lumen-facing surface, particularly at sites corresponding to sockets of EC pegs. We also identified electron-lucent pockets (ELPs) at interfaces between ECs and PCs, as well as within the basement membrane.
Discussion: These findings expand current understanding of capillary ultrastructure by revealing previously unrecognized interactions between vascular cells and novel subcellular features. The observed structural features may have functional implications for signaling, stability, and vascular mechanics, warranting further investigation.
Reproduced under the paper's license (CC BY), from the paper cited above.
Repository
Its files are read in the Code ↔ Paper reader above, with 1 match between paragraphs and lines of code.
timvanderleest/Vessel-Ultrastructure-Analysis
f873001e5e1f87622b7f0996a7c58ba0eda556c4, 5 April 2026Availability: 1 check, the latest on 28 September 2026: the link answers
- 28 September 2026: the link answers
5 files
- DeepLearningTrainingMatl
ab/ , MATLAB, 36 linesaugmentAndCrop3dPatch.m - DeepLearningTrainingMatl
ab/ , MATLAB, 74 lines, 1 matchmain_train3dUnet_7class. m - DeepLearningTrainingMatl
ab/ , MATLAB, 5 linesmatRead.m - DownloadH01VesselRawImag
es/ , Python, 49 linesmain.py - README.md, Text, 2 lines
The paper's code and data availability statement is in the Data section.
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Data
No dataset and no data link were found in the paper.
Data availability statement
Matlab codes developed for our analysis pipeline are available through Github (https://
Reproduced under the paper's license (CC BY), from the paper cited above.
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Version 2, 28 September 2026
- Funding: added Good Ventures Foundation
Version 1, 28 September 2026: the first record
Recorded: type, language, journal, volume, pages, dates, 2 authors, 5 keywords, 25 references.
Cite
This paper
Vanderleest, T. E., & Arboleda-Velasquez, J. F. (2026). 3D Ultrastructural segmentation of human microvasculature reveals new insights in pericyte-endothelial cell interactions. Frontiers in cell and developmental biology, 14, 1788958. https://
BibTeX
@article{vanderleest2026
author = {Vanderleest, Timothy E. and Arboleda-Velasquez, Joseph F.},
title = {{3D Ultrastructural segmentation of human microvasculature reveals new insights in pericyte-endothelial cell interactions}},
journal = {Frontiers in cell and developmental biology},
year = {2026},
month = may,
volume = {14},
pages = {1788958},
publisher = {Frontiers Media SA},
issn = {2296-634X},
doi = {10.3389/
url = {https://
pmid = {42205677},
pmcid = {PMC13201225}
}
RIS
TY - JOUR
AU - Vanderleest, Timothy E.
AU - Arboleda-Velasquez, Joseph F.
TI - 3D Ultrastructural segmentation of human microvasculature reveals new insights in pericyte-endothelial cell interactions
T2 - Frontiers in cell and developmental biology
J2 - Front Cell Dev Biol
PY - 2026
DA - 2026/
VL - 14
SP - 1788958
SN - 2296-634X
PB - Frontiers Media SA
DO - 10.3389/
UR - https://
LA - en
ER -
CSL-JSON
{
"id": "10.3389/
"type": "article-journal",
"title": "3D Ultrastructural segmentation of human microvasculature reveals new insights in pericyte-endothelial cell interactions",
"container-title": "Frontiers in cell and developmental biology",
"author": [
{
"family": "Vanderleest",
"given": "Timothy E."
},
{
"family": "Arboleda-Velasquez",
"given": "Joseph F."
}
],
"container-title-short":
"volume": "14",
"page": "1788958",
"DOI": "10.3389/
"PMID": "42205677",
"PMCID": "PMC13201225",
"ISSN": "2296-634X",
"publisher": "Frontiers Media SA",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
[
2026,
5,
12
]
]
}
}
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