AI Article Synopsis

  • - The study focuses on imaging the blood-brain barrier (BBB) using advanced techniques in order to better understand its 3D structure in both human and rat brain tissue.
  • - Researchers used the CUBIC clearing method along with confocal and two-photon microscopes to visualize and reconstruct the BBB, revealing uneven expression of certain proteins in human brain endothelial cells.
  • - Findings indicated that astrocytes only partially cover blood vessels, highlighting significant structural differences between the 3D BBB and previously understood 2D models, and suggesting that tissue clearing and 3D imaging could enhance our understanding of biological structures.

Article Abstract

The blood-brain barrier (BBB) is part of the neurovascular unit (NVU) which plays a key role in maintaining homeostasis. However, its 3D structure is hardly known. The present study is aimed at imaging the BBB using tissue clearing and 3D imaging techniques in both human brain tissue and rat brain tissue. Both human and rat brain tissue were cleared using the CUBIC technique and imaged with either a confocal or two-photon microscope. Image stacks were reconstructed using Imaris. Double staining with various antibodies targeting endothelial cells, basal membrane, pericytes of blood vessels, microglial cells, and the spatial relationship between astrocytes and blood vessels showed that endothelial cells do not evenly express CD31 and Glut1 transporter in the human brain. Astrocytes covered only a small portion of the vessels as shown by the overlap between GFAP-positive astrocytes and Collagen IV/CD31-positive endothelial cells as well as between GFAP-positive astrocytes and CD146-positive pericytes, leaving a big gap between their end feet. A similar structure was observed in the rat brain. The present study demonstrated the 3D structure of both the human and rat BBB, which is discrepant from the 2D one. Tissue clearing and 3D imaging are promising techniques to answer more questions about the real structure of biological specimens.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11368551PMC
http://dx.doi.org/10.1155/2024/4482931DOI Listing

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