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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

The preliminary inquiry confirms that subarachnoid hemorrhage (SAH) causes brain pericyte demise. Evaluating pericyte contractility post-SAH requires differentiation between viable and non-viable brain pericytes. Hence, a procedure has been developed to label viable and non-viable brain pericytes concurrently in brain sections, facilitating observation using a high-resolution confocal microscope.

Abstract

Pericytes are crucial mural cells situated within cerebral microcirculation, pivotal in actively modulating cerebral blood flow via contractility adjustments. Conventionally, their contractility is gauged by observing morphological shifts and nearby capillary diameter changes under specific circumstances. Yet, post-tissue fixation, evaluating vitality and ensuing pericyte contractility of imaged brain pericytes becomes compromised. Similarly, genetically labeling brain pericytes falls short in distinguishing between viable and non-viable pericytes, particularly in neurologic conditions like subarachnoid hemorrhage (SAH), where our preliminary investigation validates brain pericyte demise. A reliable protocol has been devised to surmount these constraints, enabling simultaneous fluorescent tagging of both functional and non-functional brain pericytes in brain sections. This labeling method allows high-resolution confocal microscope visualization, concurrently marking the brain slice microvasculature. This innovative protocol offers a means to appraise brain pericyte contractility, its impact on capillary diameter, and pericyte structure. Investigating brain pericyte contractility within the SAH context yields insightful comprehension of its effects on cerebral microcirculation.

Introduction

Brain pericytes, distinguished by their slender protuberances and protruding cell bodies, encircle the microcirculation1,2. While cerebral blood flow augmentation is predominantly driven by capillary dilation, smaller arteries exhibit slower rates of dilation3. Pericyte contractility exerts influence over capillary diameter and pericyte morphology, impacting vascular dynamics4. Contraction of brain pericytes leads to capillary constriction, and in pathological scenarios, excessive contraction may impede erythrocyte flow5. Various factors, ....

Protocol

The experimental protocol was approved by the Animal Ethics and Use Committee of Kunming Medical University (kmmu20220945). Sprague-Dawley (SD) rats of both sexes, 300-350 g, were used for the present study.

1. Inducing the SAH model

  1. Anesthetize the rats using 2% isoflurane and 100% oxygen. Maintain anesthesia by supplying continuous inhalation anesthesia with isoflurane (1%-3%). Secure the rat's head using a stereotaxic apparatus (see Table of Material.......

Representative Results

Under normal physiological conditions, brain pericytes generally do not undergo cell death. Figure 6 illustrates this phenomenon, with yellow indicating the presence of vital brain pericytes; brain pericytes show no staining with PI, indicating their viability. To further investigate whether pericytes remain attached to the microvasculature following cell death, methods were employed in a SAH rat model, and subsequent imaging was conducted.

Methods for imaging bot.......

Discussion

Developed are high-resolution confocal imaging techniques for visualizing vital brain pericytes, non-vital brain pericytes, and the microvasculature in brain slices. In acute rat brain slices, the process entails initial labeling of pericytes with TO-PRO-311, followed by microvascular endothelial cells with IB412; subsequently, identification of deceased pericytes is conducted using PI. This protocol is straightforward, reproducible, and highly applicable for functional res.......

Acknowledgements

The study was supported by grants from the National Natural Science Foundation of China (81960226,81760223); the Natural Science Foundation of Yunnan Province (202001AS070045,202301AY070001-011)

....

Materials

NameCompanyCatalog NumberComments
6-well plateABC biochemistryABC703006RT
Adobe PhotoshopAdobeAdobe Illustrator CS6 16.0.0RT
Aluminium foilMIAOJIE225 mm x 273 mmRT
CaCl2·2H2OSigma-AldrichC3881RT
Confocal imaging softwareNikonNIS-Elements 4.10.00RT
Confocal Laser Scanning MicroscopeNikonN-SIM/C2siRT
Gas tank (5% CO2, 95% O2)PENGYIDA40LRT
Glass Bottom Confocal DishesBeyotimeFCFC020-10pcsRT
GlucoseSigma-AldrichG5767RT
GlueEVOBONDKH-502RT
Ice machineXUEKEIMS-20RT
Image analysis softwareNational Institutes of HealthImage JRT
Inhalation anesthesia systemSCIENCEQAF700RT
Isolectin B 4-FITCSIGMAL2895–2MGStore aliquots at –20 °C
KClSigma-Aldrich7447–40–7RT
KH2PO4Sigma-AldrichP0662RT
MgSO4Sigma-AldrichM7506RT
NaClSigma-Aldrich7647–14–5RT
NaH2PO4·H2OSigma-Aldrich10049–21–5RT
NaHCO3Sigma-AldrichS5761RT
Pasteur pipetteNEST Biotechnology318314RT
Peristaltic PumpScientific Industries IncModel 203RT
Propidium (Iodide)Med Chem ExpressHY-D0815/CS-7538Store aliquots at –20 °C
Stereotaxic apparatusSCIENCEQART
Syringe pumpHarvard PUMPPUMP 11 ELITE NanomiteRT
Thermostatic water bathOLABOHH-2RT
Vibrating microtomeLeicaVT1200RT

References

  1. Dalkara, T., Gursoy-Ozdemir, Y., Yemisci, M. Brain microvascular pericytes in health and disease. Acta Neuropathologica. 122 (1), 1-9 (2011).
  2. Dore-Duffy, P., Cleary, K. Morphology and properties of pericytes. Methods in Molecul....

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Brain PericytesSubarachnoid HemorrhageVital And Non vital PericytesFluorescent LabelingBrain MicrovasculaturePericyte ContractilityCerebral Blood Flow

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