Ultrasound energy rapidly labels stem/progenitor cells with nanoparticle beacons without disrupting membrane integrity

Kathryn C. Partlow, Jason A. Brant, Jon N. Marsh, Jan Nolta, Michael S. Hughes, Gregory M. Lanza, Samuel A. Wickline

Research output: Chapter in Book/Report/Conference proceedingConference contribution

1 Citation (Scopus)

Abstract

Stem/progenitor cells participate in many pathological and regenerative processes, which can be studied in vivo with molecular imaging approaches. Labeling cells with contrast agents for non-invasive imaging and tracking typically requires long exposure times or adjunctive methods, such as electroporation or transfection agents that can compromise cell viability. We have previously utilized perfluorocarbon (PFC) nanoparticles (∼200 nm) for cell tracking, but this process entailed 12 hours of incubation to achieve efficient cellular labeling. We sought to develop an approach that reduces the prolonged labeling time by enhancing PFC nanoparticle-to-cell interactions using clinical levels of ultrasound energy. Methods: Stem/progenitor (CD34 +CD133+CD31+) cells were derived from human umbilical cord mononuclear cells grown in fibronectincoated OptiCell™ cassettes. Ultrasound (US) was applied using a medical imaging system (Acuson Sequoia) and broadband (23MHz) phased array transducer, which was coupled to cells in a heated (37°C) waterbath. The transducer was advanced mechanically to expose the entire surface to calibrated levels of US energy (MI: 1.9, frequency: 2MHz). Estimated exposure time for individual cells was ∼5min. Results: Flow cytometry revealed US application greatly improved labeling when compared with cells not exposed to US (55±9% vs. 17±12% respectively, p<0.001). This approaches the labeling efficiency achieved in the 12-hr incubation method (71±4%). Under conditions of energy (ATP) depletion (20mM sodium azide, 50mM 2-deoxyglucose), augmentation of labeling with US application was prevented (3.6±0.8% vs. 4.0±1.6%, with and without US, respectively). US exposure did not compromise cell membrane integrity based on calcein dye exclusion. Cell viability was equivalent for the untreated and US-exposed cells (∼90% viable each). We conclude that ultrasound-enhanced cell labeling with PFC nanoparticles is safe and rapid, achieving sufficient labeling with only 5 minutes of exposure at clinical frequencies and power levels. The labeling process depends on active cellular transport mechanisms (i.e., ATP) and is quite distinct from typical acoustic delivery methods, which must alter or disrupt the cell membrane to achieve delivery (e.g., sonoporation, cavitation). This unique approach should facilitate investigation of regenerative therapeutics by providing a safe adjunctive method to label cells for real-time tracking.

Original languageEnglish (US)
Title of host publicationProceedings - IEEE Ultrasonics Symposium
Pages1768-1771
Number of pages4
DOIs
StatePublished - 2007
Externally publishedYes
Event2007 IEEE Ultrasonics Symposium, IUS - New York, NY, United States
Duration: Oct 28 2007Oct 31 2007

Other

Other2007 IEEE Ultrasonics Symposium, IUS
CountryUnited States
CityNew York, NY
Period10/28/0710/31/07

Fingerprint

Stem cells
Labels
Labeling
Ultrasonics
Nanoparticles
Membranes
Adenosinetriphosphate
Cells
Cell membranes
Transducers
Molecular imaging
Flow cytometry
Medical imaging
Cavitation
Imaging systems
Dyes
Acoustics
Sodium
Imaging techniques

Keywords

  • Cell tracking
  • Contrast agent
  • Endothelial progenitor cells
  • Nanoparticles

ASJC Scopus subject areas

  • Engineering(all)

Cite this

Partlow, K. C., Brant, J. A., Marsh, J. N., Nolta, J., Hughes, M. S., Lanza, G. M., & Wickline, S. A. (2007). Ultrasound energy rapidly labels stem/progenitor cells with nanoparticle beacons without disrupting membrane integrity. In Proceedings - IEEE Ultrasonics Symposium (pp. 1768-1771). [4410018] https://doi.org/10.1109/ULTSYM.2007.445

Ultrasound energy rapidly labels stem/progenitor cells with nanoparticle beacons without disrupting membrane integrity. / Partlow, Kathryn C.; Brant, Jason A.; Marsh, Jon N.; Nolta, Jan; Hughes, Michael S.; Lanza, Gregory M.; Wickline, Samuel A.

Proceedings - IEEE Ultrasonics Symposium. 2007. p. 1768-1771 4410018.

Research output: Chapter in Book/Report/Conference proceedingConference contribution

Partlow, KC, Brant, JA, Marsh, JN, Nolta, J, Hughes, MS, Lanza, GM & Wickline, SA 2007, Ultrasound energy rapidly labels stem/progenitor cells with nanoparticle beacons without disrupting membrane integrity. in Proceedings - IEEE Ultrasonics Symposium., 4410018, pp. 1768-1771, 2007 IEEE Ultrasonics Symposium, IUS, New York, NY, United States, 10/28/07. https://doi.org/10.1109/ULTSYM.2007.445
Partlow KC, Brant JA, Marsh JN, Nolta J, Hughes MS, Lanza GM et al. Ultrasound energy rapidly labels stem/progenitor cells with nanoparticle beacons without disrupting membrane integrity. In Proceedings - IEEE Ultrasonics Symposium. 2007. p. 1768-1771. 4410018 https://doi.org/10.1109/ULTSYM.2007.445
Partlow, Kathryn C. ; Brant, Jason A. ; Marsh, Jon N. ; Nolta, Jan ; Hughes, Michael S. ; Lanza, Gregory M. ; Wickline, Samuel A. / Ultrasound energy rapidly labels stem/progenitor cells with nanoparticle beacons without disrupting membrane integrity. Proceedings - IEEE Ultrasonics Symposium. 2007. pp. 1768-1771
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abstract = "Stem/progenitor cells participate in many pathological and regenerative processes, which can be studied in vivo with molecular imaging approaches. Labeling cells with contrast agents for non-invasive imaging and tracking typically requires long exposure times or adjunctive methods, such as electroporation or transfection agents that can compromise cell viability. We have previously utilized perfluorocarbon (PFC) nanoparticles (∼200 nm) for cell tracking, but this process entailed 12 hours of incubation to achieve efficient cellular labeling. We sought to develop an approach that reduces the prolonged labeling time by enhancing PFC nanoparticle-to-cell interactions using clinical levels of ultrasound energy. Methods: Stem/progenitor (CD34 +CD133+CD31+) cells were derived from human umbilical cord mononuclear cells grown in fibronectincoated OptiCell™ cassettes. Ultrasound (US) was applied using a medical imaging system (Acuson Sequoia) and broadband (23MHz) phased array transducer, which was coupled to cells in a heated (37°C) waterbath. The transducer was advanced mechanically to expose the entire surface to calibrated levels of US energy (MI: 1.9, frequency: 2MHz). Estimated exposure time for individual cells was ∼5min. Results: Flow cytometry revealed US application greatly improved labeling when compared with cells not exposed to US (55±9{\%} vs. 17±12{\%} respectively, p<0.001). This approaches the labeling efficiency achieved in the 12-hr incubation method (71±4{\%}). Under conditions of energy (ATP) depletion (20mM sodium azide, 50mM 2-deoxyglucose), augmentation of labeling with US application was prevented (3.6±0.8{\%} vs. 4.0±1.6{\%}, with and without US, respectively). US exposure did not compromise cell membrane integrity based on calcein dye exclusion. Cell viability was equivalent for the untreated and US-exposed cells (∼90{\%} viable each). We conclude that ultrasound-enhanced cell labeling with PFC nanoparticles is safe and rapid, achieving sufficient labeling with only 5 minutes of exposure at clinical frequencies and power levels. The labeling process depends on active cellular transport mechanisms (i.e., ATP) and is quite distinct from typical acoustic delivery methods, which must alter or disrupt the cell membrane to achieve delivery (e.g., sonoporation, cavitation). This unique approach should facilitate investigation of regenerative therapeutics by providing a safe adjunctive method to label cells for real-time tracking.",
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