The most potent of these, known as effector memory T cells, are activated by a group of proteins known as human leukocyte antigens (HLAs) on
the surface of endothelial cells lining the donated organ's blood vessels.
The study, published in Proceedings of the National Academy of Sciences, found that rod - shaped nanoparticles — or nanorods — as opposed to spherical nanoparticles, appear to adhere more effectively to
the surface of endothelial cells that line the inside of blood vessels.
In contrast, the elongated nanorods have a larger surface area that is in contact with
the surface of the endothelial cells.
More of the antibodies that coat the nanorod can therefore bind receptors on
the surface of endothelial cells, and that leads to more effective cell adhesion and more effective drug delivery.
Not exact matches
Epithelial
cells form tissue layers that cover our skin and the inner
surfaces of most
of our internal organs, while
endothelial cells line the adjacent blood - transporting vessels and capillaries that support their functions.
Like a free pass, its presence on the
surface of lymphoma
cells facilitates their migration through the vessel walls between adjacent
endothelial cells.
To determine whether
endothelial cells — the
cells that line the interior
surface of blood vessels — directly influence breast cancer
cell growth, they then created unique organotypic models
of lung and bone marrow microvascular niches, in which
endothelial cells formed blood vessel - like structures in culture as they would in the original organ.
When zebrafish with the green fluorescing
endothelial gene matured, the researchers observed green FGPs on the
surface of the fish's brains — confirming that these
cells arose from
endothelial tissue.
In the current study, the researchers showed that FGPs are present on the
surface of the zebrafish brain and that these blood vessel - associated FGPs do not arise from the immune system, as had been previously thought, but from
endothelial cells themselves.
The team used light and electron microscopy to show that lymphatic
endothelial cells, which line the interior
surface of the lymph node capsule, contain a number
of channels that penetrate the whole thickness
of the
cells.
A specific lung - targeting molecule is attached to the carrier's
surface and the steriod, dexamethasone, an anti-inflammatory, is loaded into the nanogel, which then binds to lung
endothelial cells lining the inside wall
of the blood vessels where it rapidly delivers the drug.
That's because experiments conducted on the International Space Station involving
cells that line the inner
surfaces of blood vessels (
endothelial cells) show that microgravity accelerates cardiovascular disease and the biological aging
of these
cells.
He then injected human
endothelial cells into the collagen structures
of blood vessels to recolonise the
surfaces of blood vessels.
Phase - contrast images
of organ - derived
endothelial cells (37 °C) on Matrigel
surface (A) and after 4 h
of incubation with DiI - Ac - LDL (B).
As expected, all
of the
endothelial cell lines showed diminished constitutive expression
of E-selectin (data not shown) and VCAM - 1 (Fig. 4C) ⇓ in comparison with
surface levels
of ICAM - 1 (Fig. 4B) ⇓.
Established
cell lines exhibited several inherent
endothelial properties, including the expression
of constitutive and inducible levels
of endothelial cell adhesion molecules E-selectin, intercellular adhesion molecule - 1, and vascular
cell adhesion molecule - 1, internalization
of acetylated low - density lipoprotein, and formation
of loop structures on Matrigel
surfaces.
Each
of the
endothelial cell lines demonstrated an ability to orient into capillary - like structures when placed onto a Matrigel
surface (Fig. 5A) ⇓.
We also noted constitutive
surface expression
of the tyrosine kinase receptors Tie - 2, FGFR - 1, and Flk - 1 on proliferating and resting
endothelial cells (data not shown).
We also found that the EphB4 receptor expressed on the
surface of breast cancer
cells can promote tumor xenograft growth by enhancing blood vessel formation through interactions with its preferred ligand, ephrin - B2, present in tumor
endothelial cells.
Cytoadhesion
of P. falciparum in the brain leads to a large number
of deaths each year and is a consequence
of exported parasite proteins, some
of which modify the erythrocyte cytoskeleton while others such as PfEMP1 project onto the erythrocyte
surface where they bind to
endothelial cells.
Elevated plasma concentrations
of soluble forms
of endothelial adhesion molecules, released from shedding or proteolytic cleavage from the
endothelial cell surface, are considered useful indicators
of endothelial dysfunction and activation (20, 25).