The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
EndoCAM: a novel endothelial cell-cell adhesion molecule.
Open accessAbstract
Cell-cell adhesion is controlled by many molecules found on the cell surface. In addition to the constituents of well-defined junctional structures, there are the molecules that are thought to play a role in the initial interactions of cells and that appear at precise times during development. These include the cadherins and cell adhesion molecules (CAMs). Representatives of these families of adhesion molecules have been isolated from most of the major tissues. The notable exception is the vascular endothelium. Here we report the identification of a cell surface molecule designated "endoCAM" (endothelial Cell Adhesion Molecule), which may function as an endothelial cell-cell adhesion molecule. EndoCAM is a 130-kD glycoprotein expressed on the surface of endothelial cells both in culture and in situ. It is localized to the borders of contiguous endothelial cells. It is also present on platelets and white blood cells. Antibodies against endoCAM prevent the initial formation of endothelial cell-cell contacts. Despite similarities in size and intercellular location, endoCAM does not appear to be a member of the cadherin family of adhesion receptors. The serologic and protease susceptibility characteristics of endoCAM are different from those of the known cadherins, including an endogenous endothelial cadherin. Although the precise biologic function of endoCAM has not been determined, it appears to be one of the molecules responsible for regulating endothelial cell-cell adhesion processes and may be involved in platelet and white blood cell interactions with the endothelium.
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Gumbiner, B., Stevenson, B., & Grimaldi, A. (1988) · The Journal of cell biology · doi:10.1083/jcb.107.4.1575 · Cited by 799
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A novel endothelial-specific membrane protein is a marker of cell-cell contacts.
Lampugnani, M. G., Resnati, M., Raiteri, M., Pigott, R., Pisacane, A., Houen, G., Ruco, L. P., & Dejana, E. (1992) · The Journal of cell biology · doi:10.1083/jcb.118.6.1511 · Cited by 632
Neuropathologic correlates of white matter hyperintensities
Young, V. G., Halliday, G. M., & Kril, J. J. (2008) · Neurology · doi:10.1212/01.wnl.0000319691.50117.54 · Cited by 336
The role of integrins in the maintenance of endothelial monolayer integrity.
Lampugnani, M. G., Resnati, M., Dejana, E., & Marchisio, P. C. (1991) · The Journal of cell biology · doi:10.1083/jcb.112.3.479 · Cited by 292
“Immunocytochemical topography of the ~x5 integrin chain (b) and of the intercellular adhesion molecule CD31/PECAM-I (d) in par[i'ally confluent EC. a and c show F-PHD staining of the same fields for F-actin.”
InfluentialThe shear stress of it all: the cell membrane and mechanochemical transduction
White, C. R., & Frangos, J. A. (2007) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2007.2128 · Cited by 255
Metadata
- Authors
- Albelda, S. M., Oliver, P. D., Romer, L. H., & Buck, C. A.
- Venue
- The Journal of cell biology
- Publisher
- Rockefeller University Press
- Published
- 1990-04-01
- Volume
- 110
- Issue
- 4
- Pages
- 1227-1237
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- OpenAlex
- W2095828707
- Cited by
- 402
- References
- 1
- FWCI
- 6.35
- Type
- journal article
- Language
- en
- Open access
- green
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- CoChat. (2026). Citation check: EndoCAM: a novel endothelial cell-cell adhesion molecule. https://app.cochat.ai/papers/10.1083/jcb.110.4.1227
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- Albelda, S. M., Oliver, P. D., Romer, L. H., & Buck, C. A. (1990). EndoCAM: a novel endothelial cell-cell adhesion molecule. The Journal of cell biology. https://doi.org/10.1083/jcb.110.4.1227
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.