The behavior of lipid debris left on cell surfaces from microbubble based ultrasound molecular imaging

Stuart Ibsen, Guixin Shi, Carolyn Schutt, Linda Shi, Kyle David Suico, Michael Benchimol, Viviana Serra, Dmitri Simberg, Michael Berns, Sadik Esener

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Lipid monolayer coated microbubbles are currently being developed to identify vascular regions that express certain surface proteins as part of the new technique of ultrasound molecular imaging. The microbubbles are functionalized with targeting ligands which bind to the desired cells holding the microbubbles in place as the remaining unbound microbubbles are eliminated from circulation. Subsequent scanning with ultrasound can detect the highly reflectant microbubbles that are left behind. The ultrasound scanning and detection process results in the destruction of the microbubble, creating lipid fragments from the monolayer. Here we demonstrate that microbubbles targeted to 4T1 murine breast cancer cells and human umbilical cord endothelial cells leave behind adhered fragments of the lipid monolayer after exposure to ultrasound with peak negative pressures of 0.18 and 0.8 MPa. Most of the observed fragments were large enough to be resistant to receptor mediated endocytosis. The fragments were not observed to incorporate into the lipid membrane of the cell over a period of 96 min. They were not observed to break into smaller pieces or significantly change shape but they were observed to undergo translation and rotation across the cell surface as the cells migrated over the substrate. These large fragments will apparently remain on the surface of the targeted cells for significant periods of time and need to be considered for their potential effects on blood flow through the microcapillaries and potential for immune system recognition.

Original languageEnglish (US)
Pages (from-to)2090-2098
Number of pages9
JournalUltrasonics
Volume54
Issue number8
DOIs
StatePublished - 2014
Externally publishedYes

Fingerprint

debris
lipids
fragments
cells
immune systems
scanning
blood flow
breast
destruction
cancer
membranes
proteins
ligands

Keywords

  • Lipid debris
  • Microbubble
  • Microbubble targeting
  • Ultrasound molecular imaging

ASJC Scopus subject areas

  • Acoustics and Ultrasonics

Cite this

The behavior of lipid debris left on cell surfaces from microbubble based ultrasound molecular imaging. / Ibsen, Stuart; Shi, Guixin; Schutt, Carolyn; Shi, Linda; Suico, Kyle David; Benchimol, Michael; Serra, Viviana; Simberg, Dmitri; Berns, Michael; Esener, Sadik.

In: Ultrasonics, Vol. 54, No. 8, 2014, p. 2090-2098.

Research output: Contribution to journalArticle

Ibsen, S, Shi, G, Schutt, C, Shi, L, Suico, KD, Benchimol, M, Serra, V, Simberg, D, Berns, M & Esener, S 2014, 'The behavior of lipid debris left on cell surfaces from microbubble based ultrasound molecular imaging', Ultrasonics, vol. 54, no. 8, pp. 2090-2098. https://doi.org/10.1016/j.ultras.2014.06.020
Ibsen, Stuart ; Shi, Guixin ; Schutt, Carolyn ; Shi, Linda ; Suico, Kyle David ; Benchimol, Michael ; Serra, Viviana ; Simberg, Dmitri ; Berns, Michael ; Esener, Sadik. / The behavior of lipid debris left on cell surfaces from microbubble based ultrasound molecular imaging. In: Ultrasonics. 2014 ; Vol. 54, No. 8. pp. 2090-2098.
@article{466181ddb089403e9314ac5e07be8506,
title = "The behavior of lipid debris left on cell surfaces from microbubble based ultrasound molecular imaging",
abstract = "Lipid monolayer coated microbubbles are currently being developed to identify vascular regions that express certain surface proteins as part of the new technique of ultrasound molecular imaging. The microbubbles are functionalized with targeting ligands which bind to the desired cells holding the microbubbles in place as the remaining unbound microbubbles are eliminated from circulation. Subsequent scanning with ultrasound can detect the highly reflectant microbubbles that are left behind. The ultrasound scanning and detection process results in the destruction of the microbubble, creating lipid fragments from the monolayer. Here we demonstrate that microbubbles targeted to 4T1 murine breast cancer cells and human umbilical cord endothelial cells leave behind adhered fragments of the lipid monolayer after exposure to ultrasound with peak negative pressures of 0.18 and 0.8 MPa. Most of the observed fragments were large enough to be resistant to receptor mediated endocytosis. The fragments were not observed to incorporate into the lipid membrane of the cell over a period of 96 min. They were not observed to break into smaller pieces or significantly change shape but they were observed to undergo translation and rotation across the cell surface as the cells migrated over the substrate. These large fragments will apparently remain on the surface of the targeted cells for significant periods of time and need to be considered for their potential effects on blood flow through the microcapillaries and potential for immune system recognition.",
keywords = "Lipid debris, Microbubble, Microbubble targeting, Ultrasound molecular imaging",
author = "Stuart Ibsen and Guixin Shi and Carolyn Schutt and Linda Shi and Suico, {Kyle David} and Michael Benchimol and Viviana Serra and Dmitri Simberg and Michael Berns and Sadik Esener",
year = "2014",
doi = "10.1016/j.ultras.2014.06.020",
language = "English (US)",
volume = "54",
pages = "2090--2098",
journal = "Ultrasonics",
issn = "0041-624X",
publisher = "Elsevier",
number = "8",

}

TY - JOUR

T1 - The behavior of lipid debris left on cell surfaces from microbubble based ultrasound molecular imaging

AU - Ibsen, Stuart

AU - Shi, Guixin

AU - Schutt, Carolyn

AU - Shi, Linda

AU - Suico, Kyle David

AU - Benchimol, Michael

AU - Serra, Viviana

AU - Simberg, Dmitri

AU - Berns, Michael

AU - Esener, Sadik

PY - 2014

Y1 - 2014

N2 - Lipid monolayer coated microbubbles are currently being developed to identify vascular regions that express certain surface proteins as part of the new technique of ultrasound molecular imaging. The microbubbles are functionalized with targeting ligands which bind to the desired cells holding the microbubbles in place as the remaining unbound microbubbles are eliminated from circulation. Subsequent scanning with ultrasound can detect the highly reflectant microbubbles that are left behind. The ultrasound scanning and detection process results in the destruction of the microbubble, creating lipid fragments from the monolayer. Here we demonstrate that microbubbles targeted to 4T1 murine breast cancer cells and human umbilical cord endothelial cells leave behind adhered fragments of the lipid monolayer after exposure to ultrasound with peak negative pressures of 0.18 and 0.8 MPa. Most of the observed fragments were large enough to be resistant to receptor mediated endocytosis. The fragments were not observed to incorporate into the lipid membrane of the cell over a period of 96 min. They were not observed to break into smaller pieces or significantly change shape but they were observed to undergo translation and rotation across the cell surface as the cells migrated over the substrate. These large fragments will apparently remain on the surface of the targeted cells for significant periods of time and need to be considered for their potential effects on blood flow through the microcapillaries and potential for immune system recognition.

AB - Lipid monolayer coated microbubbles are currently being developed to identify vascular regions that express certain surface proteins as part of the new technique of ultrasound molecular imaging. The microbubbles are functionalized with targeting ligands which bind to the desired cells holding the microbubbles in place as the remaining unbound microbubbles are eliminated from circulation. Subsequent scanning with ultrasound can detect the highly reflectant microbubbles that are left behind. The ultrasound scanning and detection process results in the destruction of the microbubble, creating lipid fragments from the monolayer. Here we demonstrate that microbubbles targeted to 4T1 murine breast cancer cells and human umbilical cord endothelial cells leave behind adhered fragments of the lipid monolayer after exposure to ultrasound with peak negative pressures of 0.18 and 0.8 MPa. Most of the observed fragments were large enough to be resistant to receptor mediated endocytosis. The fragments were not observed to incorporate into the lipid membrane of the cell over a period of 96 min. They were not observed to break into smaller pieces or significantly change shape but they were observed to undergo translation and rotation across the cell surface as the cells migrated over the substrate. These large fragments will apparently remain on the surface of the targeted cells for significant periods of time and need to be considered for their potential effects on blood flow through the microcapillaries and potential for immune system recognition.

KW - Lipid debris

KW - Microbubble

KW - Microbubble targeting

KW - Ultrasound molecular imaging

UR - http://www.scopus.com/inward/record.url?scp=84906314505&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84906314505&partnerID=8YFLogxK

U2 - 10.1016/j.ultras.2014.06.020

DO - 10.1016/j.ultras.2014.06.020

M3 - Article

C2 - 25059435

AN - SCOPUS:84906314505

VL - 54

SP - 2090

EP - 2098

JO - Ultrasonics

JF - Ultrasonics

SN - 0041-624X

IS - 8

ER -