Novel Peripherally Derived Neural-Like Stem Cells as Therapeutic Carriers for Treating Glioblastomas

Author:

Birbrair Alexander1234,Sattiraju Anirudh56,Zhu Dongqin57,Zulato Gilberto5,Batista Izadora5,Nguyen Van T.5,Messi Maria Laura3,Solingapuram Sai Kiran Kumar6,Marini Frank C.8,Delbono Osvaldo3,Mintz Akiva56

Affiliation:

1. a Ruth L. and David S. Gottesman Institute for Stem Cell and Regenerative Medicine, Albert Einstein College of Medicine, Bronx, New York, USA

2. b Department of Cell Biology, Albert Einstein College of Medicine, Bronx, New York, USA

3. c Department of Internal Medicine-Gerontology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA

4. d Department of Pathology, Federal University of Minas Gerais, Minas Gerais, Brazil

5. e Department of Radiology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA

6. f Brain Tumor Center of Excellence, Comprehensive Cancer Center of Wake Forest University, Winston-Salem, North Carolina, USA

7. g Department of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA

8. h Wake Forest Institute for Regenerative Medicine, Winston-Salem, North Carolina, USA

Abstract

Abstract Glioblastoma (GBM), an aggressive grade IV astrocytoma, is the most common primary malignant adult brain tumor characterized by extensive invasiveness, heterogeneity, and angiogenesis. Standard treatment options such as radiation and chemotherapy have proven to be only marginally effective in treating GBM because of its invasive nature. Therefore, extensive efforts have been put forth to develop tumor-tropic stem cells as viable therapeutic vehicles with potential to treat even the most invasive tumor cells that are harbored within areas of normal brain. To this end, we discovered a newly described NG2-expressing cell that we isolated from a distinct pericyte subtype found abundantly in cultures derived from peripheral muscle. In this work, we show the translational significance of these peripherally derived neural-like stem cells (NLSC) and their potential to migrate toward tumors and act as therapeutic carriers. We demonstrate that these NLSCs exhibit in vitro and in vivo GBM tropism. Furthermore, NLSCs did not promote angiogenesis or transform into tumor-associated stromal cells, which are concerns raised when using other common stem cells, such as mesenchymal stem cells and induced neural stem cells, as therapeutic carriers. We also demonstrate the potential of NLSCs to express a prototype therapeutic, tumor necrosis factor α-related apoptosis-inducing ligand and kill GBM cells in vitro. These data demonstrate the therapeutic potential of our newly characterized NLSC against GBM.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

Reference45 articles.

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