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MRI Contrast Agents Alter Proliferation of Stem Cells

By MedImaging International staff writers
Posted on 29 Nov 2010
When scientists tested three different labeling agents on three different stem cell populations to determine what effect the labeling agents had on stem cell phenotype, biologic behavior, and migration abilities, they discovered changes in stem cell proliferation depending on the type of contrast agent used.

The team of researchers from Belgium and Spain tested USPIO (ultra small superparamagnetic iron oxide) contrast agents Resovist, Endorem, and Sinerem on mouse embryonic stem cells (mESCs), rat multipotent adult progenitor cells (rMAPCs), and mouse mensenchymal stem cells (mMSCs).

Their study is available on-line in November 2010 in the journal Cell Transplantation (published issue 19:8). The researchers, from the Stem Cell Institute, K.U. Leuven (Leuven, Belgium) and the University of Valencia (Spain), discovered the labeling efficiency with each of the (U)SPIOs varied considerably when different stem cell populations were compared. "This means that labeling methods will likely need to be optimized for every cell type,” said Dr. Annelies Crabbe, from the Stem Cell Institute, K.U. Leuven (Katholieke Universiteit Leuven). "Over time we saw a dilution of (U)SPIOs and a decrease of iron in the cells.”

Noninvasive imaging plays a significant post-transplantation role in stem cell research, but questions regarding whether the contrast agents used to monitor transplanted stem cells in vivo via magnetic resonance imaging (MRI) have an impact on the cells had mostly gone unanswered until this study. On the issue of whether (U)SPIO labeling has a biologic affects on cells, the researchers discovered "no significant alterations” in cell phenotypes and that the label "does not significantly alter stem cell differentiation.”

"Sinerem decreased proliferation of mMSC while both Sinerem and Endorem affected the proliferation rate of rMAPC, although prolonged culture, until seven days, resulted in restoration of the proliferation rate,” noted Dr. Crabbe. "We also found that higher concentrations of Sinerem and Endorem were needed for cell labeling to achieve similar MRI detectability.”

The researchers concluded that it would be necessary to evaluate the efficiency of cell labeling for every new contrast agent combination aimed at being followed in vivo by MRI. Moreover, the effect on biologic behavior of cells should be examined. They noted that their results were limited to examining the effects of labeling on proliferation, not differentiation.

"Although labeling of stem cells with MRI is promising, there are some limitations,” concluded Dr. Crabbe. "More optimal particles are needed that can be taken up without the need of potentially toxic agents. Also, there is the problem of particle dilution over time as cells divide. When grafted cells continue to proliferate, loss of signal occurs.”

According to Dr. Julio Voltarelli, professor of clinical medicine and clinical immunology at the University of Sao Pãul (Brazil) and section editor for Cell Transplantation there has been a knowledge gap regarding the survival and distribution of stem cell populations used for in vivo therapy. "Many studies have tried to close this gap by using radioactive or nonradioactive labeling of the cells in order to follow their fate in the organism,” said Dr. Voltarelli. "However, this paper demonstrates that such labeling may alter stem cell behavior, such as proliferative potential, and give biased information when compared to nonlabeled cells.”

Resovist was developed by the diagnostic imaging business of Bayer Schering Pharma, AG (Berlin, Germany); Endorem by Guerbet (Sulzbach, Germany); and Sinerem was manufactured by Amag Pharmaceuticals, Inc.(Cambridge, MA, USA).

Related Links:

Stem Cell Institute, K.U. Leuven
University of Valencia



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