Over the past few years, issues related to the commitment and potential of reservoir precursor cells that reside in most tissues have been revisited. Many reports have documented either plasticity or de-differentiation of a number of precursor cells isolated from several tissues, including bone marr
Brain engraftment and therapeutic potential of stem/progenitor cells derived from mouse skin
β Scribed by Patrizia Tunici; Jeff W. M. Bulte; Maria Grazia Bruzzone; Pietro Luigi Poliani; Laura Cajola; Marina Grisoli; Trevor Douglas; Gaetano Finocchiaro
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 295 KB
- Volume
- 8
- Category
- Article
- ISSN
- 1099-498X
- DOI
- 10.1002/jgm.866
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Skin stem/progenitor cells (SKPs) derive from the dermis and in culture can generate mesodermal and neural progenies. To investigate their potential for the treatment of brain diseases, we first injected SKPs into the brain of syngeneic mice. Brain histology indicated that most SKPs remained undifferentiated and clustered at the injection site, while, in vitro, 17% of SKPs expressed neural markers, as assessed by flow cytometry. After labeling with magnetodendrimers, murine and human SKPs were detected by magnetic resonance imaging even 5 months after brain injection. To evaluate their therapeutic potential on malignant gliomas, ILβ4 SKPs (i.e. SKPs transduced by a lentiviral vector carrying the cDNA of the antiβglioma cytokine interleukinβ4) were injected into GL261 experimental gliomas. ILβ4βSKPs prolonged significantly the survival of tumorβbearing mice: furthermore, GL261 gliomas attracted SKPs originally injected into the contralateral hemisphere. Thus, prolonged survival, capacity for transgene expression, and lack of uncontrolled proliferation suggest that SKPs warrant further consideration as therapeutic tools for brain tumors and, possibly, other neurological disorders. Copyright Β© 2006 John Wiley & Sons, Ltd.
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