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Morphology Favors an Endothelial Cell Pathway for Longitudinal Conduction within Arterioles
Open accessAbstract
We examined the morphological parameters of arteriolar endothelial and smooth muscle cell dimensions and gap junctional surface areas to obtain an indication of the coupling capacity of each cell type. Silver nitrate staining was utilized to define cell borders of endothelial and smooth muscle cells in arterioles of several vascular beds from two species. From video images of silver-stained arterioles, the mean endothelial cell length of hamster cheek pouch arterioles (diameter 20 to 110 microns) was found to be 141 +/- 2 microns. Mean endothelial cell width was 7 +/- 0.2 microns in the same arterioles. Mean smooth muscle cell length in hamster cheek pouch arterioles of diameter 80 to 150 microns was 66 +/- 3 microns, with an average cell width of 8 +/- 0.2 microns. Dimensions of both endothelial and smooth muscle cells varied moderately with arteriole size and tissue type, but no general trends were seen. Based on the measured dimensions and the specific orientation of cell types within the arteriole, it was calculated that in hamster cheek pouch arterioles (60 microns diameter), 6 or 7 endothelial cell lengths would constitute a 1-mm segment of vessel, whereas approximately 140 smooth muscle cell widths would be required to span the same length. Estimates of connexin43 gap junctional plaque surface areas in each cell type suggest that endothelial cell junctional surface area is approximately eight times that of smooth muscle cells. Thus, combined measurement of cell dimensions and orientation with estimates of junctional plaque density leads to the conclusion that the endothelial cell layer forms a more permissive pathway for longitudinal conduction of signals through the blood vessel.
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Citations
Cited by
Signaling Mechanisms Underlying the Vascular Myogenic Response
Davis, M. J., & Hill, M. A. (1999) · Physiological Reviews · doi:10.1152/physrev.1999.79.2.387 · Cited by 992
Cell Densities in the Mouse Brain: A Systematic Review
Keller, D., Erö, C., & Markram, H. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00083 · Cited by 380
Dora, K. A., Doyle, M. P., & Duling, B. R. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.12.6529 · Cited by 332
Self-citationChen, K., Pittman, R. N., & Popel, A. S. (2008) · Antioxidants & Redox Signaling · doi:10.1089/ars.2007.1959 · Cited by 326
Emerson, G. G., & Segal, S. S. (2000) · Circulation Research · doi:10.1161/01.res.87.6.474 · Cited by 299
Metadata
- Authors
- Haas, T. L., & Duling, B. R.
- Venue
- Microvascular Research
- Publisher
- Elsevier BV
- Published
- 1997-03
- Volume
- 53
- Issue
- 2
- Pages
- 113-120
- ISSN
- 0026-2862 (ISSN-L)
- OpenAlex
- W2019485640
- Cited by
- 171
- References
- 0
- FWCI
- 2.36
- Type
- journal article
- Language
- en
- Open access
- hybrid
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- Haas, T. L., & Duling, B. R. (1997). Morphology Favors an Endothelial Cell Pathway for Longitudinal Conduction within Arterioles. Microvascular Research. https://doi.org/10.1006/mvre.1996.1999
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