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Expression of transferrin receptor and ferritin following ferumoxides-protamine sulfate labeling of cells: Implications for cellular magnetic resonance imaging

  • Edyta Pawelczyk(corresponding author)
    ,
  • ,
  • Sunil Pandit
    ,
  • Elbert Hu
    ,
  • Joseph A. Frank
*Corresponding author for this work
  • National Institutes of Health, Bethesda
    ,
  • Henry Ford Health System
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Ferumoxides-protamine sulfate (FE-Pro) complexes are used for intracellular magnetic labeling of cells to non-invasively monitor cell trafficking by in vivo MRI. FE-Pro labeling is non-toxic to cells; however, the effects of FE-Pro labeling on cellular expression of transferrin receptor (TfR- 1) and ferritin, proteins involved in iron transport and storage, has not been reported. FE-Pro-labeled human mesenchymal stem cells (MSCs), HeLa cells and primary macrophages were cultured from 1 week to 2 months and evaluated for TfR- 1 and ferritin gene expression by RT-PCR and protein levels were determined using Western blots. MTT (proliferation assay) and reactive oxygen species (ROS) analysis were performed. FE-Pro labeling of HeLa and MSCs resulted in a transient decrease in TfR- 1 mRNA and protein levels. In contrast, Fe-Pro labeling of primary macrophages resulted in an increase in TfR-1 mRNA but not in TfR-1 protein levels. Ferritin mRNA and protein levels increased transiently in labeled HeLa and macrophages but were sustained in MSCs. No changes in MTT and ROS analysis were noted. In conclusion, FE-Pro labeling elicited physiological changes of iron metabolism or storage, validating the safety of this procedure for cellular tracking by MRI.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 581-592 (12 pages)

Journal (Volume, Issue Number)

NMR in Biomedicine (Volume 19, Issue 5)

Publication milestones

  • Published - 08/2006

Publication status

Published - 08/2006

ISSN

0952-3480

Publication IDs

  • Scopus: 33747359371
  • PubMed: 16673357

Publication metrics

Metrics

Scopus
citations
SciVal
citations
107
Fractional count
1
Fractional count
0.20
Fractional count
4
Fractional count
0.80
Fractional count
1
Fractional count
1
SciVal
FWCI
3.64
SciVal
Author count
5
SciVal
Paper percentile
95
SciVal
Top percentile
5

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Citation count
110
Captures
39