SU-F-J-220: Micro-CT Based Quantification of Mouse Brain Vasculature: The Effects of Acquisition Technique and Contrast Material

2016 ◽  
Vol 43 (6Part12) ◽  
pp. 3459-3459
Author(s):  
C Tipton ◽  
M Lamba ◽  
Z Qi ◽  
K LaSance ◽  
C Tipton
2002 ◽  
Vol 282 (5) ◽  
pp. R1267-R1279 ◽  
Author(s):  
Michael D. Bentley ◽  
Maria C. Ortiz ◽  
Erik L. Ritman ◽  
J. Carlos Romero

Appropriate nephron function is dependent on the intrarenal arrangement of blood vessels. The preferred and primary means to study the architecture of intrarenal circulation has been by filling it with opaque substances such as india ink, radio-opaque contrast material, or various polymers for study by light or scanning electron microscopy. With such methodologies, superficial vessels may obscure deep vessels and little quantitative information may be obtained. Serial-section microtomy has not been practical because of problems relating to alignment and registration of adjacent sections, lost sections, and preparation time and effort. Microcomputed tomography (micro-CT) overcomes such limitations and provides a means to study the three-dimensional architecture of filled vessels within an intact rodent kidney and to obtain more quantitative information. As an example of micro-CT's capabilities, we review the use of micro-CT to study the alterations in renal microvasculature caused by the development of liver cirrhosis after chronic bile duct ligation. In this example, micro-CT evidence shows a selective decrease in cortical vascular filling in the kidney, with a maintenance of medullary vascular filling. These changes may contribute to the salt and water retention that accompanies cirrhosis. These results indicate that micro-CT is a promising method to evaluate renal vascular architecture in the intact rodent kidney relative to physiological and pathological function.


2021 ◽  
Vol 2021 ◽  
pp. 1-15
Author(s):  
Wei-Wei Lin ◽  
Lin-Tao Xu ◽  
Yi-Sheng Chen ◽  
Ken Go ◽  
Chenyu Sun ◽  
...  

Background. The critical role of vascular health on brain function has received much attention in recent years. At the single-cell level, studies on the developmental processes of cerebral vascular growth are still relatively few. Techniques for constructing gene regulatory networks (GRNs) based on single-cell transcriptome expression data have made significant progress in recent years. Herein, we constructed a single-cell transcriptional regulatory network of mouse cerebrovascular cells. Methods. The single-cell RNA-seq dataset of mouse brain vessels was downloaded from GEO (GSE98816). This cell clustering was annotated separately using singleR and CellMarker. We then used a modified version of the SCENIC method to construct GRNs. Next, we used a mouse version of SEEK to assess whether genes in the regulon were coexpressed. Finally, regulatory module analysis was performed to complete the cell type relationship quantification. Results. Single-cell RNA-seq data were used to analyze the heterogeneity of mouse cerebrovascular cells, whereby four cell types including endothelial cells, fibroblasts, microglia, and oligodendrocytes were defined. These subpopulations of cells and marker genes together characterize the molecular profile of mouse cerebrovascular cells. Through these signatures, key transcriptional regulators that maintain cell identity were identified. Our findings identified genes like Lmo2, which play an important role in endothelial cells. The same cell type, for instance, fibroblasts, was found to have different regulatory networks, which may influence the functional characteristics of local tissues. Conclusions. In this study, a transcriptional regulatory network based on single-cell analysis was constructed. Additionally, the study identified and profiled mouse cerebrovascular cells using single-cell transcriptome data as well as defined TFs that affect the regulatory network of the mouse brain vasculature.


2019 ◽  
Vol 2019 ◽  
pp. 1-7 ◽  
Author(s):  
Jana Mrzílková ◽  
Matěj Patzelt ◽  
Pasquale Gallina ◽  
Zdeněk Wurst ◽  
Martin Šeremeta ◽  
...  

Micro-CT imaging is a well-established morphological method for the visualization of animal models. We used ethanol fixation of the mouse brains to perform high-resolution micro-CT scans showing in great details brain grey and white matters. It was possible to identify more than 50 neuroanatomical structures on the 5 selected coronal sections. Among white matter structures, we identified fornix, medial lemniscus, crossed tectospinal pathway, mammillothalamic tract, and the sensory root of the trigeminal ganglion. Among grey matter structures, we identified basal nuclei, habenular complex, thalamic nuclei, amygdala, subparts of hippocampal formation, superior colliculi, Edinger–Westphal nucleus, and others. We suggest that micro-CT of the mouse brain could be used for neurohistological lesions evaluation as an alternative to classical neurohistology because it does not destroy brain tissue.


2008 ◽  
Vol 28 (8) ◽  
pp. 1449-1459 ◽  
Author(s):  
Julie Cattelotte ◽  
Pascal André ◽  
Mélissa Ouellet ◽  
Fanchon Bourasset ◽  
Jean-Michel Scherrmann ◽  
...  

The in situ mouse brain perfusion method for measuring blood—brain barrier permeability was adapted to assess transport of solutes at the blood—brain and blood—eye barriers. The procedure was checked with radiolabeled markers in oxygenated bicarbonate-buffered fluid infused for 30 to 120 secs via a carotid artery. Vascular flow estimated with diazepam was 2.2-fold lower in the eye than in the brain. The vascular volume and the integrity markers sucrose and inulin indicated that a perfusion flow rate of 2.5 mL/min preserved the physical integrity of these organs. However, the brain vasculature integrity was more sensitive to acute perfusion pressure than the eye vasculature. The functional capacities of blood barriers were assessed with d-glucose; its transport followed Michaelis—Menten kinetics with an apparent Km of 7.6 mmol/L and a Vmax of 23 μmol/sec per g in the brain, and a Km of 22.9 mmol/L and a Vmax of 40 μmol/sec per g in the eye. The transport of cholesterol to the brain and eye was significantly enhanced by adding the Abca1 inhibitor probucol, suggesting an Abca1-mediated efflux at the mouse brain and eye blood barriers. Thus in situ carotid perfusion is suitable for elucidating transport processes at the blood—brain and blood-eye barriers.


Biomaterials ◽  
2010 ◽  
Vol 31 (9) ◽  
pp. 2617-2626 ◽  
Author(s):  
Wei Lu ◽  
Qian Huang ◽  
Geng Ku ◽  
Xiaoxia Wen ◽  
Min Zhou ◽  
...  

Author(s):  
Scott Trinkle ◽  
Sean Foxley ◽  
Narayanan Kasthuri ◽  
Patrick La Rivière

2019 ◽  
Author(s):  
Mihail Ivilinov Todorov ◽  
Johannes C. Paetzold ◽  
Oliver Schoppe ◽  
Giles Tetteh ◽  
Velizar Efremov ◽  
...  

SUMMARYTissue clearing methods enable imaging of intact biological specimens without sectioning. However, reliable and scalable analysis of such large imaging data in 3D remains a challenge. Towards this goal, we developed a deep learning-based framework to quantify and analyze the brain vasculature, named Vessel Segmentation & Analysis Pipeline (VesSAP). Our pipeline uses a fully convolutional network with a transfer learning approach for segmentation. We systematically analyzed vascular features of the whole brains including their length, bifurcation points and radius at the micrometer scale by registering them to the Allen mouse brain atlas. We reported the first evidence of secondary intracranial collateral vascularization in CD1-Elite mice and found reduced vascularization in the brainstem as compared to the cerebrum. VesSAP thus enables unbiased and scalable quantifications for the angioarchitecture of the cleared intact mouse brain and yields new biological insights related to the vascular brain function.GRAPHICAL ABSTRACTSupporting material of VesSAP is available athttp://DISCOtechnologies.org/VesSAP


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