TY - JOUR
T1 - Targeting of liposomes carrying recombinant fragments of platelet membrane glycoprotein Ibα to immobilized von Willebrand factor under flow conditions
AU - Nishiya, Takako
AU - Murata, Mitsuru
AU - Handa, Makoto
AU - Ikeda, Yasuo
N1 - Funding Information:
We thank the Yoshitomi Pharmaceutical Industry (Osaka, Japan) for preparation of rGPIbα and vWf. We also thank Norihiko Yamagata and George Shih for technical assistance. This work was supported by Health Science Research Grants, Research on Advanced Medical Technology, Ministry of Health and Welfare, Japan.
PY - 2000/4/21
Y1 - 2000/4/21
N2 - Liposomes with covalently bound recombinant fragments of platelet membrane glycoprotein Ibα that retain the von Willebrand factor (vWf)-binding function (rGPIbα-liposomes) were prepared. Their interactions with an immobilized vWf surface under flow conditions were evaluated with a recirculating flow chamber, mounted on an epifluorescence microscope, which allows real-time visualization of fluorescence-labeled liposomes interacting with the surface. The interaction of rGPIbα-liposomes with the vWf surface was directly related to shear rate. At high densities of rGPIbα and vWf, rGPIbα-liposomes establishing contact with the vWf surface exhibited continuous displacement with decreased velocity relative to the hydrodynamic flow, depending on receptor density and matrix concentration. At lower densities of rGPIbα and vWf, rGPIbα-liposomes stopped only transiently, in the millisecond range, on the surface. This is the first study to demonstrate that the targeting of rGPIbα-liposomes is specific to the vWf surface under flow conditions. (C) 2000 Academic Press.
AB - Liposomes with covalently bound recombinant fragments of platelet membrane glycoprotein Ibα that retain the von Willebrand factor (vWf)-binding function (rGPIbα-liposomes) were prepared. Their interactions with an immobilized vWf surface under flow conditions were evaluated with a recirculating flow chamber, mounted on an epifluorescence microscope, which allows real-time visualization of fluorescence-labeled liposomes interacting with the surface. The interaction of rGPIbα-liposomes with the vWf surface was directly related to shear rate. At high densities of rGPIbα and vWf, rGPIbα-liposomes establishing contact with the vWf surface exhibited continuous displacement with decreased velocity relative to the hydrodynamic flow, depending on receptor density and matrix concentration. At lower densities of rGPIbα and vWf, rGPIbα-liposomes stopped only transiently, in the millisecond range, on the surface. This is the first study to demonstrate that the targeting of rGPIbα-liposomes is specific to the vWf surface under flow conditions. (C) 2000 Academic Press.
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U2 - 10.1006/bbrc.2000.2516
DO - 10.1006/bbrc.2000.2516
M3 - Article
C2 - 10772897
AN - SCOPUS:0034696813
SN - 0006-291X
VL - 270
SP - 755
EP - 760
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -